Skip to main content
Download PDF

Ophiocordyceps formosana improves hyperglycemia and depression-like behavior in an STZ-induced diabetic mouse model

BMC Complementary and Alternative Medicine volume 16, Article number: 310 (2016) Cite this article

Abstract

Background

A newly defined Cordyceps species, Ophiocordyceps formosana (O. formosana) has been implicated in multitudinous bioactivities, including lowering glucose and cholesterol levels and modulating the immune system. However, few literatures demonstrate sufficient evidence to support these proposed functions. Although the use of Cordyceps spp. has been previously addressed to improve insulin insensitivity and improve the detrimental symptoms of depression; its mechanistic nature remains unsettled. Herein, we reveal the effects of O. formosana in ameliorating hyperglycemia accompanied with depression.

Methods

Diabetes was induced in mice by employing streptozotocin(STZ), a chemical that is toxic to insulin-producing β cells of the pancreas. These streptozotocin (STZ)-induced diabetic mice showed combined symptoms of hyperglycemia and depressive behaviors. Twenty-four STZ-induced mice were randomly divided into 3 groups subjected to oral gavage with 100 μL solution of either PBS or 25 mg/mL Ophiocordyceps formosana extract (OFE) or 2 mg/mL rosiglitazone (Rosi, positive control group). Treatments were administered once per day for 28 days. An additional 6 mice without STZ induction were treated with PBS to serve as the control group. Insulin sensitivity was measured by a glucose tolerance test and levels of adiponectin in plasma and adipose tissue were also quantified. Behavioral tests were conducted and levels of monoamines in various brain regions relating to depression were evaluated.

Results

HPLC analysis uncovered three major constituents, adenosine, D-mannitol and cordycepin, within O. formosana similar to other prestigious medicinal Cordyceps spp.. STZ-induced diabetic mice demonstrated decreased body weight and subcutaneous adipose tissue, while these symptoms were recovered in mice receiving OFE treatment. Moreover, the OFE group displayed improved insulin sensitivity and elevated adiponectin within the plasma and adipose tissue. The anti-depressive effect of OFE was observed in various depression-related behavior tests. Concurrently, neurotransmitters, like 5-HT and dopamine in the frontal cortex, striatum and hippocampus were found to be up-regulated in OFE-treated mice.

Conclusions

Our findings illustrated, for the first time, the medicinal merits of O. formosana on Type I diabetes and hyperglycemia-induced depression. OFE were found to promote the expression of adiponectin, which is an adipokine involved in insulin sensitivity and hold anti-depressive effects. In addition, OFE administration also displayed altered levels of neurotransmitters in certain brain regions that may have contributed to its anti-depressive effect. Collectively, this current study provided insights to the potential therapeutic effects of O. formosana extracts in regards to hyperglycemia and its depressive complications.

Peer Review reports

Background

Type I diabetes (T1D) is an autoimmune disease caused by an immune response against the β cell antigens in the pancreas, which results in a lack of insulin, but an increase in blood and urine glucose levels [1]. In 2014, an estimate of 3 million people was reported to have T1D in the USA [2]. Current therapies for T1D place strong emphasis on insulin replacement or transplantation of insulin secreting tissues; however, numerous limitations and complications still remain. However, Gunawardana et al. [3] argued that adipose tissues are able to maintain glucose homeostasis in the absence of insulin; while adipokines have been shown to ameliorate both type 1 and 2 diabetic phenotypes in the absence of exogenous insulin by potentiating insulin receptor sensitivity [3–5]. Past literatures have shown a positive correlation between adiponectin levels and insulin sensitivity in T1D patients [6]; moreover, higher levels of adiponectin is found to be associated with lower prevalence of metabolic syndrome in T1DM [7]. In addition, STZ-induced type 1 diabetic mice displayed ameliorated hyperglycemic symptoms following adiponectin gene delivery into mice [3]. Consequently, an increase in the level of plasma adiponectin was found to improve insulin resistance [4].

Depression is commonly linked with hyperglycemia in T1D and T2D patients [8, 9] and is found to be more prevalent in T1D patients according to the Beck Depression Inventory Score [10]. Previous studies suggest that approximately 15 % of diabetic patients risk complications of clinical depression [8]. Thus, patients with type I diabetes also require the increased use of antidepressants [11]. Selective serotonin re-uptake inhibitors (SSRIs) are widely used as the first-line treatment for depression; however, several side effects, including nausea, anorexia and sexual dysfunction, are commonly observed [12, 13]. Unfortunately, SSRIs can lead to failure of glycemic control in diabetic patients. On the other hand, tricyclic antidepressants (TCAs) can also contribute to hyperglycemia in humans and mice [14]. Interestingly, a study showed that diabetic patients treated with Rosi for 12 weeks exhibited a significant decline in depressive severity as evaluated by the Hamilton Depression Rating Scale and the Clinical Global Impression Scale [15]. However, the side effects of Rosi include increase risk of myocardial infarction [16]. Thus, an effective alternative treatment with little or no side effects for T1D and depression-related complications is still in demand.

Many psychiatric disorders, such as anxiety and depression, can be ascribed to deficits in monoamine neurotransmitters [17, 18]. Thus, many antidepressants are aimed toward modulating the neurotransmission system by increasing the content and amount of monoamines (e.g., dopamine, 5-hydroxytryptamine, and norepinephrine) in the limbic regions of the brain. The hypothalamic serotonin is increased during insulin-induced hypoglycemia[19], indicating that glycemic homeostasis may be beneficial for ameliorating depression. As a result, adipokines (e.g., leptin and adiponectin) can promote insulin sensitivity as well as alleviate depressive behaviors [20, 21].

Some Cordyceps spp. have been used in traditional Chinese medicine (TCM) to lower blood pressure, glucose and cholesterol, as well as to modulate immune function [22]. Aside from ameliorating metabolic dysfunctions, Cordyceps spp. also improve psychological disorder like insomnia, dysphoria and sleep [23]. Even though the scientific reports to address Cordyceps spp. effectiveness as an antidepressant regimen [24] and an improvement of both hyperglycemia and depression in rodents treated with Ophiocordyceps sinensis [25], there is still inadequate number of scientific evidence in support of clinical use.

Our present study reported a close relationship in phylogenetic and secondary metabolism profiles between O. sinensis and O. formosana prompting the evaluation of the effects of O. formosana on hyperglycermia and depression. Herein, we addressed potential medicinal effects of O. formosana on hyperglycemia depression. By employing an STZ-induced diabetes mouse model, we identify the effects of OFE in comparison to Rosi via measuring glucose tolerance, and assessing the anxiety-like and depression-like behaviors of mice. The expressions of adiponectin in plasma and adipose tissue in situ were examined. In addition, the levels of several neurotransmitters were measured to correlate with the changes in psychological behaviors in response to Ophiocordyceps formosana treatments in STZ-induced diabetic mice.

Methods

Cultivation and extraction of Ophiocordyceps formosana

An epitypified Ophiocordyceps formosana (OF) was collected, identified, cultivated and maintained by Wang et al., as described in our previous study [26]. The voucher specimen of Ophiocordyceps formosana has been deposited in Leibniz-Institut DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH designated as Ophiocordyceps formosana MUCHO 815-DSM 32000. Ophiocordyceps formosana (OF) was maintained and cultivated according to our previous report [26]. OF was grown on potato dextrose agar (PDA) containing 0.4 % potato starch, 2 % dextrose, and 1.5 % agar (Difco Becton Dickinson, Sparks, MD, USA) at 25 °C for 28 days. The colonies were then collected, lyophilized, and pulverized by a homogenizer (SH100, KURABO International Co., Tokyo, Japan) at 1300 rpm. The preparation of Ophiocordyceps formosana extracts (OFE) was proceeded by the standard operating procedure as previously described [26, 27]. In brief, 1 gram of OF powder was mixed with deionized water at a ratio of 1:40 (w/v). Thereafter, the extractions were carried out in a hot water bath at 50 °C for 2 h along with sonication during the first 30 min. The samples were then centrifuged at 3000 g for 20 min. The supernatant fractions were sterilized through 0.22 μm filters (Millipore, USA), and stored at −80 °C. Each batch of OFE was subjected to content analyses by high-performance liquid chromatography (D2000 system, Hitachi Co., Tokyo, Japan).

HPLC analyses of Ophiocordyceps formosana extract (OFE)

The quality control of OFE was conducted by HPLC (D2000 system, Hitachi Co., Tokyo, Japan) utilizing a photodiarray detector (Primaide 1430, Hitachi Co., Tokyo, Japan). The analyses were performed using a RP-18 column (150252 Purospher®STAR RP-18 endcapped (5 μm) LiChroCART®250-4, Merck Co., New Jersey, USA.) at a flow rate of 1 mL/min. The mobile phase was 20 % methanol in H2O and the absorbance was detected at 260 nm. Two components in Cordecyps spp, adenosine (A9252, Sigma-Aldrich Co., St. Louis, Missouri, USA) and cordycepin (C3394, Sigma-Aldrich Co., St. Louis, Missouri, USA), were used as standards for quality controls.

STZ-induced diabetic mouse model

Thirty 8-week old male C57BL/6 mice (average weight = 20 ± 3 g) were purchased from the National Laboratory Animal Center (Taipei, Taiwan). The environment was maintained at 21 ± 3 °C, 50 ± 10 % relative humidity, and under a 12 h:12 h light/dark cycle with free access to food and water. All animal handling in this study are in accordance with a protocol approved by the Institutional Animal Care and Use Committee of National Taiwan University (IACUC approval NO. NTU-102-EL-37). All efforts were made to minimize animal suffering and to reduce the number of animals used, including that the animal sample size used for this current study was analyzed by G-power test with G*Power version 3.0.10.

The mice were first acclimatized for 7 days in the standard housing condition. After acclimatization, diabetes was induced by administrating streptozotocin (STZ) as previously described by Islam et al. [28, 29]. The STZ-induction mice were fasted for 6 h and before administered with 40 mg/kg STZ (S0130, Sigma-Aldrich Co., St. Louis, Missouri, USA) solution via intraperitoneal (IP). STZ was given once a day for 5 days with 2 subsequent days for recovery. A total of 30 mice were used in the present study with 24 mice as the STZ-induction group, while the remainder 6 served as the control group. A glucose tolerance test (GTT) was performed to confirm diabetes pathophysiology after STZ induction. STZ-induced mice were randomly divided into 3 groups (n = 8 mice/group) subjected to oral gavage with 100 μL solution of 25 mg/mL OFE, 2 mg/mL Rosi dissolved in PBS (R2408, Sigma-Aldrich Co., St. Louis, Missouri, USA) or PBS alone once per day for 28 days. An additional 6 mice without STZ induction were treated with PBS as the control group. Body weight and food intake were recorded daily during the experimental period. Mice are then sacrificed and islet cells were isolated and quantified as previously reported [30]. The subcutaneous white adipose tissue (SAT) was weighed and relative ratio of tissue-to-body weight was calculated. Moreover, blood samples were collected prior to sacrifice and stored at −80 °C for serological analyses, including mouse insulin ELISA kit (EMINS, Thermo Fisher Scientific, Waltham, Massachusetts, USA) and adiponectin ELISA kit (DY1119, R&D systems Ind., Minneapolis, Missouri, USA).

Intraperitoneal glucose tolerance test (IPGTT)

Glucose intolerance was measured by IPGTT as modified from Andrikopoulos et al. [31]. In brief, mice were fasted for 6 h prior to the 2 g/kg glucose administration by IP injection. IPGTT was performed before and after the above treatments (Fig. 1d, Day 17 and Day 54, respectively). Blood samples were collected from the tail at 0, 30, 60, and 120 min after glucose infusion to determine plasma glucose concentration utilizing a glucometer (Accu-Chek® active, Roche Diagnostics Ltd., Mannheim, Germany).

Fig. 1
figure 1

Experimental timeline and procedure. a Ophiocordyceps formosana (OF) was collected from fields in Taiwan. b Cultivation of OF mycelia on PDA plates with yellowish colonies. c Extracts of OF (OFE) were analyzed by a DAD-HPLC system. A representative HPLC profile of OFE allows quantitative analyses of the indicated components, including adenosine and cordycepin. d Scheme for experimental timeline and procedures. Eight week-old mice were first acclimated for 7 days prior to intraperitoneal (IP) injection with 40 mg/kg STZ solution for each mouse once a day for constitutive 5 days and recovery for 2 days. Six mice were injected with PBS as a sham-control group. To monitor anxiety and insulin resistance status for the STZ-treated and control group mice, at day 15, mice were conducted an anxiety behavior test by the open field test (OFT), and intraperitoneal glucose tolerance test (IPGTT) was performed before and after the above treatments (Day 17 and Day 54, respectively). The STZ-treated mice were then randomly divided into 3 different groups for oral gavage daily by 100 μL solution given of PBS, the 25 mg/mL OFE and 2 mg/mL Rosi, respectively. At day 48, several behavior tests, including OFT, EPM and TST, were used. All mice were then fasting for 6 h before evaluating insulin sensitivity by GTT. The mice were sacrifice after 1-day recovery from GTT

Full size image

Animal behavioral tests

A series of anxiety-like and depression-related behavior tests including open field test (OFT), elevated plus maze (EPM), and tail suspension tests (TST) are conducted to further characterize the depressive behavior associated with hyperglycemia as reported by previous literature [32–35].

An activity monitor enclosed in a sound-attenuated chamber equipped with ventilation was used to videotape all test sessions. Each mouse was individually placed in the center of an open-field apparatus (43.3 × 21.7 × 20.8 cm3, made of clear plexiglass) and allowed to explore freely for 60 min. Total travelled distance, duration, and velocity in the central and peripheral areas were analyzed by TopScan v2.0 software (Clever Sys Inc., Reston, VA, USA). The elevated plus maze is consisted of 2 open arms (30-L × 5-W cm2 in size) and 2 close arms enclosed by 50 cm high white acrylic walls. Open arms and close arms cross each other at right angle and is located 50 cm above the floor. All arms were made of white acrylic plates radiating from a central platform (5 × 5 cm2) to form a “+” sign. Each mouse was placed in the central platform area facing one of the closed arms. The motion trail and time spent in the apparatus were recorded for 5 min, and analyzed by TopScan v2.0 (Clever Sys Inc., Reston, VA, USA). Tail suspension test is used to assess the depressive behavior in animals. In brief, each mouse was taped by the tail (2–3 cm from the tip of the tail) and suspended for 6 min at 35 cm above the floor [36, 37]. The mouse was acoustically and visually isolated. The recorded data of all test sessions were used to calculate the immobility time, and subsequently the behavioral performance of each mouse was scored by three investigators. Immobility was defined as when all paws and the head of the mouse completely stop moving.

Immunohistolochemical analyses

Subcutaneous white adipose tissues (SAT) were isolated and immediately fixed with 4 % paraformaldehyde, then embedded into paraffin. Immunohistochemical analyses were performed for examining adiponectin expressions as described by Schindler et al. [38]. Tissue sections were first deparaffinized, and subjected to antigen retrieval at 95 °C for 15 min in antigen retrieval buffer (ab93680; Abcam, Cambridge, Massachusetts). Endogenous peroxidase activity was blocked with 0.3 % H2O2 in 80 % methanol for 30 min. The sections were then blocked with 1 % BSA and incubated with an anti-mouse adiponectin antibody (ab22554; Abcam, Cambridge, Massachusetts) for 18 h at 4 °C. Subsequently, the sections were incubated with a goat anti-mouse secondary antibody (K500711, DakoCytomation Ltd., CA, USA) for 30 min and visualized using a DakoCytomation EnVision® + Duallink system HRP (DAB+) kit (K4065, DakoCytomation Ltd., CA, USA). Slides were counterstained with hematoxylin, rinsed in ddH2O for 10 min, and mounted with glycerin gelatin (GG1, Sigma-Aldrich Co., St. Louis, Missouri, USA). Representative 40X images were photographed and presented. Five areas of a section were used for the signal intensity quantification. The signal intensity of adiponectin expression in SAT was calculated using Image J, an image-analysis program (NIH, Bethesda, MD, USA) [39].

Measurement of monoamine levels in mouse brains

The monoamine levels in various limbic regions were analyzed as described previously [40]. Briefly, brain was extracted and prefrontal cortex, striatum and hippocampus were isolated on an ice-chilled plate and weighed. The brain tissues were homogenized in 1 mL of extract solution consisting of 0.1 M HCl, 10−7 M ascorbic acid and 50 pg/μL isoproterenol. Homogenates were then centrifuged three times at 13200 rpm for 20 min at 4 °C and filtered through a 0.22 μm filter (Millipore, Bedford, USA). Supernatent was injected into a reverse C18 column (Hypersil GOLD aQ, 5 μm, 150 mm x 4.60 mm, Thermo Fisher Scientific, Inc., Massachusetts, USA). The concentrations of norepinephrine (NE, A7257, Sigma), dopamine (DA, H60255, Sigma), 3,4-dihydroxyphenylacetic acid (DOPAC, 850217, Sigma), 5-hydroxytryptamine (5-HT, H9523, Sigma), and 5-hydroxyindoleacetic acid (5-HIAA, H8876, Sigma) were measured by HPLC coupled with an electrochemical detector (P/N 70–9143 10 nA range, 1 Hz filter, and 0.7 V AppE cell ECD, Shiseido Co., Tokyo, Japan) equipped with an auto-sampler (WPS-3000, Shiseido Co., Tokyo, Japan). The mobile phase was 0.17 M NaH2PO4, 0.63 mM ethylenediaminetetraacetic acid (EDTA), 0.60 mM octane-1-sulfonic acid sodium salt, and 2 mM KCl in 20 % methanol, and adjusted to pH 3.30 with 85 % H3PO4. The flow rate was maintained in 0.6 mL/min. All the standards were purchased from Sigma (St. Louis, MO, USA) and dissolved in the extraction solution for HPLC. The standard curves ranged from 0.01 to 5.0 ppm, and the detection limit of this system was 0.1 pg for all samples.

Statistical analyses

Statistical significance was tested by one-way ANOVA and Tukey’s multiple comparison test (SAS institute, Cary, NC, USA). Data were expressed as mean ± S.E.M. p values ≤ 0.05 were considered statistically significant. The body weights were compared by the Student’s t test. Data were expressed as mean ± S.E.M. # represents p ≤ 0.05, and *** represents p ≤ 0.001.

Results

Extraction and chemical analyses of Ophiocordyceps formosana

Ophiocordyceps formosana (Cordyceps s.l.) was established, cultivated (Fig. 1a and b) then water extracted for bioactive compound analyses by HPLC (Fig. 1a-c). Like other known medicinal Cordyceps spp., the extract of O. formosana contained adenosine and cordycepin (Fig. 1c), potent bioactive components for medicinal use. Hence, we sought for its potential benefit on diabetic complications.

OFE ameliorates the characteristics of STZ-induced diabetic mice

To examine the medicinal benefit of the water extract of O. formosana on diabetes, an STZ-induced diabetic animal model was employed. Consistent with features of type I diabetes, STZ-induced diabetic mice displayed body weight loss (Fig. 2a) and a fasting plasma glucose value over 200 mg/dL (control = 119.5 ± 24.2 mg/dl and STZ-PBS = 392.2 ± 38.7 mg/dl, p ≤ 0.001) (Fig. 2d). In addition, the pancreatic β cell number was diminished in STZ-induced diabetic mice, but neither Rosi nor OFE treatment could rescue the number of β cells (data not shown). However, the body weight was regained and the subcutaneous adipose tissues (SAT) accumulated in the OFE-treated group compared to the PBS treated group. The OFE treated mice exhibited a better outcome than the Rosi-treated mice (Fig. 2b and c). Furthermore, the plasma glucose and area under curve (AUC) of the plasma glucose tolerance test (GTT) in the OFE treated STZ-induced diabetic mice was reduced, indicating that OFE could partially alleviate hyperglycemia induced by STZ (Fig. 2d). However, the concentration of plasma insulin did not show signs of recovery in OFE groups (Fig. 2e). These results suggest that OFE is potentially capable of ameliorating pathophysiological complications of STZ-induced diabetic mice, but not mediate insulin recovery.

Fig. 2
figure 2

Ophiocordyceps formosana ameliorated the hyperglycermic characteristic of STZ-induced diabetic mice. a Changes in body weight of mice. b Morphological appearance of visceral adiposity in mice. The arrows show the visualized adipose tissues. c The subcutaneous fat (SAT) to body weight ratio. d The glucose concentration in plasmas at the end of the experiment. e The insulin concentration in plasma at the end of the experiment. f The area under curve (AUC) of glucose tolerance test (GTT) after treatments. Data were expressed as mean ± S.E.M. # represents p ≤ 0.05, STZ-PBS vs. STZ-OFE and *** represents p ≤ 0.001, control vs. STZ-PBS, STZ-Rosi and STZ- OFE. Results of two groups were compared by the Student’s t test. One way ANOVA followed by Tukey’s post hoc test was performed for multiple comparisons. Mean in a row with different superscripts is significantly different (p ≤ 0.05). Values are mean ± SEM, n = 6 in control group and n = 8 in the all STZ-induced groups

Full size image

OFE increased adiponectin expression in plasma and adipose tissue

Adiponectin is an adipokine highly correlated with fat biogenesis and insulin sensitivity [4]. The level of adiponectin in plasma was decreased by STZ compared with the normal control group (Fig. 3a). As expected, the level of plasma adiponectin was significantly elevated by OFE treatment compared to PBS treatment. However, OFE or Rosi treatment failed to rescue plasma adiponectin level in comparison to the non-diabetic control group (Fig. 3A). The enlarged adipocyte size in STZ-diabetic mice was reduced in Rosi-treated mice and to a greater extent in OFE-treated mice (Fig. 3b). Moreover, STZ treatment lowered adiponectin level in subcutaneous adipose tissue, while Rosi treatment elevated adiponectin level and OFE treatment showed a greater increase compared to the non-diabetic controls (Fig. 3c). Taken together, our data imply that OFE may up-regulate the expression of adiponectin in SAT and plasma leading to the promotion of biogenesis of SAT in the diabetic mice.

Fig. 3
figure 3

Ophiocordyceps formosana upregulated adiponectin expressions in plasma and adipose tissues. a The levels of plasma adiponectin in different STZ-induced treated groups. b Immunohistochemical staining for adiponectin in adipose tissues. c The adiponectin-positive area of each treated group was quantified by Image J. Scale bar = 50 mm, under a 400x microscope. One-way ANOVA followed by Tukey’s post hoc test was performed for multiple comparisons. Mean in a row with different superscripts is significantly different (p ≤ 0.05). Values are mean ± SEM, n = 6 in control group and n = 8 in all STZ-treated groups

Full size image

OFE reduces the anxiety and depression-like behaviors in STZ-induced diabetic mice

To evaluate whether OFE confers benefits to the aforementioned psychological complications, we conducted animal behavioral tests, including open filed test (OFT), elevated plus maze (EPM) and tail suspension test (TST) [35]. The STZ-induced diabetic mice displayed anxiety- and depression-related behaviors compared to control group (Fig. 4), and the total travel distance decreased by STZ induction (Fig. 4a). Conversely, the STZ-induced diabetic mice treated with either Rosi or OFE showed an increased duration time spent in the central zone of the OFT (Fig. 4b). Moreover, the retention time spent in the open arms of the EPM was extended in the STZ-OFE group, indicating that OFE promoted exploratory behaviors (Fig. 4b and c). Similarly, results from the tail suspension test showed an extended motionless duration time in the STZ-PBS group (Fig. 4d), suggesting that the STZ-induced diabetic mice expressed depression-like behaviors. In contrast, the immobility time of the OFE group was similar to that of the non-diabetic mice (Fig. 4d). Collectively, our data demonstrated that OFE is potent to ameliorate anxiety and depression-related psychological complications associated with type I diabetes.

Fig. 4
figure 4

Ophiocordyceps formosana improved depressive-like behaviors in STZ-induced diabetic mice. a Locomotor activity in the open filed test (OFT) (b) The ratio of retention time in the central zone to total duration time in the OFT. c The ratio of the retention time in the open arm to total duration of the equipment (%) in the elevated plus maze (EPM). d The immobility time in the tail suspension test (TST). * represent p ≤ 0.05, Control-PBS vs. STZ-PBS. One way ANOVA followed by Tukey’s post hoc test was performed for multiple comparisons. Mean in a row with different superscripts is significantly different (p ≤ 0.05). Values are mean ± SEM, n = 6 in control group and n = 8 in all STZ-treated groups

Full size image

Evaluation of various neurotransmitters levels in different brain regions of STZ-induced diabetic mice treated by OFE

To elucidate the underlying mechanisms of OFE on alleviating the aforementioned psychological complications, levels of neurotransmitters (i.e., DA and 5HT) and their metabolites (i.e., DOPAC and 5HIAA) in the brain, including the hippocampus, the striatum and the prefrontal cortex, were measured by ECD-HPLC (Table 1). STZ-induced diabetic mice demonstrated reduced levels of DA, DOPAC, 5HT and 5HIAA in the three brain regions compared to control mice (Table 1). Intriguingly, neurotransmitter levels were recovered by either Rosi or OFE treatment, especially in the frontal cortex and striatum (Table 1), which may contribute to the changes in behaviors observed after Rosi and OFE treatment (Fig. 4). Noticeably, the amount of norepinephrine (NE) in the frontal cortex and hippocampus were increased by STZ-treatment, but not in the striatum. Our data suggest that OFE can alter the expression levels of neurotransmitters in dopaminergic and serotonergic pathways.

Table 1 Expressions of various neurotransmitters, including the frontal cortex, striatum and hippocampus of brain, in mice
Full size table

Discussion

Type 1 diabetic (T1D) patients suffer weight loss, increase fluid consumption and urination, as well as several mental complications, such as irritability, anxiety, and depression [41]. Unfortunately, current therapeutics like, β-cell transplantation, immunosuppressive regimens for pancreas transplantation or daily insulin injection [1], are served to alleviate most of the complications induced by T1D, but such treatments are limited and inefficient,. Hence, our current study employed a diabetic animal model induced by STZ to mimic the symptoms of hyperglycemia and depression as observed in T1D patients [42]. We found that the OFE treatment elevated adiponectin levels, various brain neurotransmitter expressions, and ameliorated various diabetes-related complications, including hyperglycermia and anxiety/depression (Fig. 5). Our results indicate the pharmacological potential for a newly established medicinal fungus, Ophiocordyceps formosana, as an alternative and complementary medicine.

Fig. 5
figure 5

Putative mechanisms for OFE in improving insulin resistance and depression. OFE promotes the expression of adiponectin, which is an adipokine involved in insulin sensitivity and anti-depression. In addition, the neurotransmitters (5-HT and dopamine) in brain regions were also elevated by OFE, which also leads to anti-depression

Full size image

Presently, several oral therapeutic regimens for treating diabetes-related hyperglycemia and depression have been widely developed and used. For instance, thiazolidinedione (TZDs) drugs, such as rosiglitazone (Rosi), have been reported to effectively control hyperglycemia in T2D [43]. In addition, Rosi has been shown to ameliorate depressive behaviors by reduction of plasma corticosterone levels [44]. However, several undesirable side effects, such as stomach pain, diarrhea, heart failure and edema, are often observed [45, 46]. Likewise, T1D patients show symptoms of depression can be treated with oral antidepressants [47, 48]. For instance, selective serotonin reuptake inhibitors (SSRIs) are the most widely prescribed antidepressants in spite of numerous adverse side effects [12]. Thus, there remains a need for regimens that can ameliorate the symptoms of T1D with fewer side effects. A natural product derived from an Ophiocordyceps sinensis relative, O. formosana has relatively lower toxicity in vitro [26] and as shown in this current study seems to be effective in the STZ mouse model for T1D. However, more studies remain needed to evaluate its safety and indications.

Like Ophiocordyceps sinensis [49], O. formosana exhibited a beneficial improvement in body weight of STZ-induced mice and an increase in SAT (Fig. 2). The extended plasma GTT in STZ-induced diabetic mice was partially corrected by either Rosi or O. formosana treatment (Fig. 2d). These results suggest that O. formosana not only promotes glucose metabolism, but also increases energy utilization in mice. Rosi is a PPAR-γ agonist capable of increasing adiponectin expression, synthesis and release [50]. Although adiponectin is exclusively secreted from adipocytes, it is a circulating hormone whose level in plasma is positively correlated with insulin sensitivity and inversely associated with obesity and T2D [21, 51]. Despite being highly expressed in most fat tissues, the level of adiponectin is lower in visceral adipose tissues than in subcutaneous abdominal adipose tissues (SAT), suggesting that SAT may be the major contributor to circulating adiponectins [52]. Consistently, our results showed that mice treated with 25 g/ml/day of OFE for 28 days had increased SAT as well as adiponectin in plasma and SAT (Fig. 3). We hypothesized that O. formosana ameliorates insulin resistance via up-regulation of adiponectin.

In addition to improvements in glucose sensitivity and adipogenesis, an increase in plasma adiponectins is reportedly associated with reduced depressive disorders in patients with diabetes [53, 54]. The intracerebroventricular infusion of recombinant globular adiponectin or recombinant full-length adiponectin reduced depressive-like behavioral effects in normal weighted mice [21]. Furthermore, adiponectins alleviate depression-like behaviors attributed to their neuroprotective activity and hippocampal neurogenesis modulation in mice [55]. Our observations demonstrated that the increase in adiponectin in plasma and adipose tissues by O.formosana may have attributed to the improvement in behavioral patterns in our mice treated with OFE.

O. formosana modulated monoamine neurotransmitters, including dopamine, 5-HT and norepinephrine (NE) in various brain regions, including the hippocampus, amygdala and striatum. These brain regions take part in regulating motion and rewarding as well as executive functions; therefore, their dysfunction has been implicated in depression [56, 57]. Depressive illness is linked with an insufficiency of brain monoamine neurotransmitters including dopamine, 5-HT and norepinephrine (NE) in these brain regions [12, 58]. Tail suspension test utilized to assess antidepressant-like activity in mice by observing their behavior under the inescapable stress of being suspended above ground [59]. Administration of OFE decreased immobility time and was accompanied by increased amounts of DA and 5-HT in the hippocampus and frontal cortex (Fig. 4d and Table 1). The striatum is essential in mediating anxiety and reducing motivation in patients with depression [60]. Two anxiety-related tests, EPM and OFT, displayed increases in retention time in the open arms and the central zone, respectively, in OFE-treated STZ-induced mice along with increased DA and 5-HT in the striatum (Table 1). Although there are conflicting reports, we found that the level of NE was increased in STZ-induced diabetic mice and is consistent with previous reports [61, 62]. The locomotor activity showed no significance between groups (data now shown), suggesting that the improvement of anti-depressive-like behaviors by OFE was not caused by hyperactivity. Taken together, O. formosana ameliorates both anxiety-like and depressive-like behaviors in STZ-induced diabetic mice. The increased levels of various neurotransmitters in some brain regions in these mice suggest that the changes in behaviors may result from modulation of neurotransmitters.

Rosiglitazone (Rosi) has been applied for the clinical treatment of T1D patients with depression [63]. After 12 weeks of treatment with Rosi, severity of depression based upon the Hamilton Depression Rating Scale and the Clinical Global Impression Scale was improved [15]. The results indicated that improvement of insulin resistance is a prospective treatment for alleviation of depression. Recently, an emerging relationship between inflammation and depression has led to the use of anti-inflammatory drugs to ameliorate the symptoms of depression [64, 65]. Here, we provide a new approach to ameliorate insulin insufficiency and depression mediated by Ophiocordyceps formosana; the mechanism was suggested to be via the upregulation of adiponectins. Although some minor components of Cordyceps spp., such as cordycepin, polysaccharides and trace elements like vanadium, are reported to be responsible for the antidepressant-like activities [25], further investigation is necessary to identify the constituents of Ophiocordyceps formosana rendering the anti-hyperglycemic and anti-depression activities.

Conclusion

To our knowledge, our current study demonstrated, for the first time, the medicinal merit of Ophiocordyceps formosana on T1D and hyperglycemia-induced depression. Our results revealed OFE improved glucose utilization by promoting adiponectin expression in STZ-induced diabetic mice. The administration of OFE also modulated the expression of monoamine neurotransmitters and their metabolites (i.e., 5-HT and DOPA). Collectively, this study provided a potential usage of O. formosana extracts to counteract hyperglycemia and depression complications.

Abbreviations

5-HT:

5-hydroxytrptamine

DOPA:

Dopamine

EPM:

Elevated plus maze

IPGTT:

Intraperitoneal glucose tolerance test

NE:

Norepinephrine

OFE:

Ophiocordyceps Formosana extract

OFT:

Open filed test

Rosi:

Rosiglitazone

SAT:

Subcutaneous white adipose tissue

SSRI:

Serotonin re-uptake inhibitor

STZ:

Streptozoticin

T1D:

Type 1 diabetes

T2D:

Type 2 diabetes

TCA:

Tricyclic antidepressants

TCM:

Traditional Chinese medicine

TST:

Tail suspension test

TZD:

Thiazolidinedione

References

  1. Atkinson MA, Eisenbarth GS. Type 1 diabetes: new perspectives on disease pathogenesis and treatment. Lancet. 2001;358(9277):221–9.

    Article  CAS  PubMed  Google Scholar 

  2. Chiang JL, Kirkman MS, Laffel LM, Peters AL. Type 1 diabetes through the life span: A position statement of the American Diabetes Association. Diabetes Care. 2014;37(7):2034–54.

    Article  PubMed  Google Scholar 

  3. Gunawardana SC, Piston DW. Reversal of type 1 diabetes in mice by brown adipose tissue transplant. Diabetes. 2012;61(3):674–82.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Fukushima M, Hattori Y, Tsukada H, Koga K, Kajiwara E, Kawano K, Kobayashi T, Kamata K, Maitani Y. Adiponectin gene therapy of streptozotocin‐induced diabetic mice using hydrodynamic injection. J Gene Med. 2007;9(11):976–85.

    Article  CAS  PubMed  Google Scholar 

  5. Fu Y, Luo N, Klein RL, Garvey WT. Adiponectin promotes adipocyte differentiation, insulin sensitivity, and lipid accumulation. J Lipid Res. 2005;46(7):1369–79.

    Article  CAS  PubMed  Google Scholar 

  6. Pereira RI, Snell-Bergeon JK, Erickson C, Schauer IE, Bergman BC, Rewers M, Maahs DM. Adiponectin dysregulation and insulin resistance in type 1 diabetes. J Clinical Endocrinol Metab. 2012;97(4):E642–7.

    Article  CAS  Google Scholar 

  7. Blaslov K, Bulum T, Zibar K, Duvnjak L. Relationship between Adiponectin Level, Insulin Sensitivity, and Metabolic Syndrome in Type 1 Diabetic Patients, Int. J Endocrinol. 2013;535906. 6 pages.

  8. Anderson RJ, Freedland KE, Clouse RE, Lustman PJ. The prevalence of comorbid depression in adults with diabetes a meta-analysis. Diabetes Care. 2001;24(6):1069–78.

    Article  CAS  PubMed  Google Scholar 

  9. Goldney RD, Phillips PJ, Fisher LJ, Wilson DH. Diabetes, depression, and quality of life a population study. Diabetes Care. 2004;27(5):1066–70.

    Article  PubMed  Google Scholar 

  10. Van Tilburg MA, McCaskill CC, Lane JD, Edwards CL, Bethel A, Feinglos MN, Surwit RS. Depressed mood is a factor in glycemic control in type 1 diabetes. Psychosom Med. 2001;63(4):551–5.

    Article  PubMed  Google Scholar 

  11. Gendelman N, Snell-Bergeon JK, McFann K, Kinney G, Wadwa RP, Bishop F, Rewers M, Maahs DM. Prevalence and correlates of depression in individuals with and without type 1 diabetes. Diabetes Care. 2009;32(4):575–9.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Bijlsma EY, Chan JS, Olivier B, Veening JG, Millan MJ, Waldinger MD, Oosting RS. Sexual side effects of serotonergic antidepressants: Mediated by inhibition of serotonin on central dopamine release? Pharmacol Biochem Behav. 2014;121:88–101.

    Article  CAS  PubMed  Google Scholar 

  13. Hu XH, Bull SA, Hunkeler EM, Ming E, Lee JY, Fireman B, Markson LE. Incidence and duration of side effects and those rated as bothersome with selective serotonin reuptake inhibitor treatment for depression: patient report versus physician estimate. J Clin Psychiatry. 2004;65(7):959–65.

    Article  CAS  PubMed  Google Scholar 

  14. Barnard K, Peveler RC, Holt RI. Antidepressant Medication as a Risk Factor for Type 2 Diabetes and Impaired Glucose Regulation Systematic review. Diabetes Care. 2013;36(10):3337–45.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Rasgon NL, Kenna HA, Williams KE, Powers B, Wroolie T, Schatzberg AF. Rosiglitazone add-on in treatment of depressed patients with insulin resistance: a pilot study. Sci World J. 2010;10:321–8.

    Article  CAS  Google Scholar 

  16. Nissen SE, Wolski K. Effect of rosiglitazone on the risk of myocardial infarction and death from cardiovascular causes. N Engl J Med. 2007;356(24):2457–71.

    Article  CAS  PubMed  Google Scholar 

  17. Schechter LE, Ring RH, Beyer CE, Hughes ZA, Khawaja X, Malberg JE, Rosenzweig-Lipson S. Innovative approaches for the development of antidepressant drugs: current and future strategies. NeuroRx. 2005;2(4):590–611.

    Article  PubMed  PubMed Central  Google Scholar 

  18. Richelson E. The clinical relevance of antidepressant interaction with neurotransmitter transporters and receptors. Psychopharmacology Bull. 2011;36(4):133–50.

    Google Scholar 

  19. Bivens CH, Lebovitz HE, Feldman JM. Inhibition of hypoglycemia-induced growth hormone secretion by the serotonin antagonists cyproheptadine and methysergide. N Engl J Med. 1973;289:236–9.

    Article  CAS  PubMed  Google Scholar 

  20. Trujillo M, Scherer P. Adiponectin–journey from an adipocyte secretory protein to biomarker of the metabolic syndrome. J Intern Med. 2005;257(2):167–75.

    Article  CAS  PubMed  Google Scholar 

  21. Liu J, Guo M, Zhang D, Cheng S-Y, Liu M, Ding J, Scherer PE, Liu F. Lu XY Adiponectin is critical in determining susceptibility to depressive behaviors and has antidepressant-like activity. Proc Natl Acad Sci U S A. 2012;109(30):12248–53.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Li CR, Fan MZ, Huang B, Wang SB, Li ZZ. The genus Cordyceps and its allies from Anhui I. Mycosystema. 2001;21(2):167–71.

    Google Scholar 

  23. Zhou X, Gong Z, Su Y, Lin J, Tang K. Cordyceps fungi: natural products, pharmacological functions and developmental products. J Pharm Pharmacol. 2009;61(3):279–91.

    Article  CAS  PubMed  Google Scholar 

  24. Nishizawa K, Torii K, Kawasaki A, Katada M, Ito M, Terashita K, Aiso S, Matsuoka M. Antidepressant-like effect of Cordyceps sinensis in the mouse tail suspension test. Biol Pharm Bull. 2007;30(9):1758–62.

    Article  CAS  PubMed  Google Scholar 

  25. Guo J, Li C, Wang J, Liu Y, Zhang J. Vanadium-enriched Cordyceps sinensis, a contemporary treatment approach to both diabetes and depression in rats. Evid Based Complement Alternat Med. 2011;2011:450316.

  26. Wang YW, Hong TW, Tai YL, Wang YJ, Tsai SH, Thi P: Evaluation of an epitypified Ophiocordyceps formosana (Cordyceps sl) for its pharmacological potential. Evid Based Complement Alternat Med. 2015. (In press).

  27. Chou SM, Lai WJ, Hong TW, Lai JY, Tsai SH, Chen YH, Yu SH, Kao CH, Chu R, Ding ST. Synergistic property of cordycepin in cultivated Cordyceps militaris-mediated apoptosis in human leukemia cells. Phytomedicine. 2014;21(12):1516–24.

    Article  CAS  PubMed  Google Scholar 

  28. Islam MS. Animal models of diabetic neuropathy: progress since 1960s. J Diabetes Res. 2013;149452:9.

    Google Scholar 

  29. Soria B, Roche E, Berná G, León-Quinto T, Reig JA, Martín F. Insulin-secreting cells derived from embryonic stem cells normalize glycemia in streptozotocin-induced diabetic mice. Diabetes. 2000;49(2):157–62.

    Article  CAS  PubMed  Google Scholar 

  30. Dorrell C, Grompe MT, Pan FC, Zhong Y, Canaday PS, Shultz LD, Greiner DL, Wright CV, Streeter PR, Grompe M. Isolation of mouse pancreatic alpha, beta, duct and acinar populations with cell surface markers. Mol Cell Endocrinol. 2011;339(1–2):144–50.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Andrikopoulos S, Blair AR, Deluca N, Fam BC, Proietto J. Evaluating the glucose tolerance test in mice. Am J Physiol Endocrinol Metab. 2008;295(6):1323–32.

    Article  Google Scholar 

  32. Lai W-S, Xu B, Westphal KG, Paterlini M, Olivier B, Pavlidis P, Karayiorgou M, Gogos JA. Akt1 deficiency affects neuronal morphology and predisposes to abnormalities in prefrontal cortex functioning. Proc Natl Acad Sci U S A. 2006;103(45):16906–11.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  33. Huang CH, Kuo MT, Lai WS. Characterization of behavioural responses in different test contexts after a single social defeat in male golden hamsters (Mesocricetus auratus). Behav Process. 2011;86(1):94–101.

    Article  Google Scholar 

  34. Cryan JF, Holmes A. The ascent of mouse: advances in modelling human depression and anxiety. Nat Rev Drug Discov. 2005;4(9):775–90.

    Article  CAS  PubMed  Google Scholar 

  35. O’Leary OF. Cryan JF The tail-suspension test: a model for characterizing antidepressant activity in mice. Mood and Anxiety Related Phenotypes in Mice. 2009;42:119–37.

    Article  Google Scholar 

  36. Steru L, Chermat R, Thierry B, Simon P. The tail suspension test: a new method for screening antidepressants in mice. Psychopharmacology (Berl). 1985;85(3):367–70.

    Article  CAS  Google Scholar 

  37. Can A, Dao DT, Terrillion CE, Piantadosi SC, Bhat S, Gould TD. The tail suspension test. J Vis Exp. 2012;59:3769.

    PubMed  Google Scholar 

  38. Schindler M, Fischer S, Thieme R, Fischer B, Santos AN. cAMP-responsive element binding protein: a vital link in embryonic hormonal adaptation. Endocrinology. 2013;154(6):2208–21.

    Article  CAS  PubMed  Google Scholar 

  39. Abràmoff MD, Magalhães PJ, Ram SJ. Image processing with Image J. Biophoton Int. 2004;11:36–42.

    Google Scholar 

  40. Hao CW, Lai WS, Ho CT, Sheen LY. Antidepressant-like effect of lemon essential oil is through a modulation in the levels of norepinephrine, dopamine, and serotonin in mice: Use of the tail suspension test. J Funct Foods. 2013;5(1):370–9.

    Article  CAS  Google Scholar 

  41. Hilakivi-Clarke L, Wozniak K, Durcan MJ, Linnoila M. Behavior of streptozotocin-diabetic mice in tests of exploration, locomotion, anxiety, depression and aggression. Physiol Behavior. 1990;48(3):429–33.

    Article  CAS  Google Scholar 

  42. Ohtani N, Ohta M, Sugano T. Microdialysis Study of Modification of Hypothalamic Neurotransmitters in Streptozotocin-Diabetic Rats. J Neurochem. 1997;69(4):1622–8.

    Article  CAS  PubMed  Google Scholar 

  43. Kintscher U. Law RE PPARγ-mediated insulin sensitization: the importance of fat versus muscle. Am J Physiol Endocrinol Metab. 2005;288(2):E287–91.

    Article  CAS  PubMed  Google Scholar 

  44. Ahmed AAE, Al-Rasheed NM, Al-Rasheed NM. Antidepressant-like effects of rosiglitazone, a PPARγ agonist, in the rat forced swim and mouse tail suspension tests. Behav Pharmacol. 2009;20(7):635–42.

    Article  CAS  Google Scholar 

  45. Home PD, Pocock SJ, Beck-Nielsen H, Gomis R, Hanefeld M, Jones NP, Komajda M, McMurray JJ. Rosiglitazone evaluated for cardiovascular outcomes—an interim analysis. N Engl J Med. 2007;357(1):28–38.

    Article  CAS  PubMed  Google Scholar 

  46. Nesto RW, Bell D, Bonow RO, Fonseca V, Grundy SM, Horton ES, Le Winter M, Porte D, Semenkovich CF, Smith S. Thiazolidinedione use, fluid retention, and congestive heart failure a consensus statement from the American Heart Association and American Diabetes Association. Circulation. 2003;108(23):2941–8.

    Article  PubMed  Google Scholar 

  47. Plener PL, Molz E, Berger G, Schober E, Mönkemöller K, Denzer C, Goldbeck L, Holl RW. Depression, metabolic contorl, and antidepressant medication in young patients with type 1 diabetes. 2015;16(1):58-66.

  48. Sawka AM, Burgart V, Zimmerman D. Loss of awareness of hypoglycemia temporally associated with selective serotonin reuptake inhibitors. Diabetes Care. 2001;24(10):1845–6.

    Article  CAS  PubMed  Google Scholar 

  49. Balon TW, Jasman AP, Zhu J-S. A fermentation product of Cordyceps sinensis increases whole-body insulin sensitivity in rats. J Altern Complement Med. 2002;8(3):315–23.

    Article  PubMed  Google Scholar 

  50. Boden G, Zhang M. Recent findings concerning thiazolidinediones in the treatment of diabetes. Expert Opin Investing Drugs. 2006;15(3):243–50.

    Article  CAS  Google Scholar 

  51. Whitehead J, Richards A, Hickman I, Macdonald G, Prins J. Adiponectin–a key adipokine in the metabolic syndrome. Diabetes Obes Metab. 2006;8(3):264–80.

    Article  CAS  PubMed  Google Scholar 

  52. Lihn AS, Bruun JM, He G, Pedersen SB, Jensen PF, Richelsen B. Lower expression of adiponectin mRNA in visceral adipose tissue in lean and obese subjects. Mol Cell Endocrinol. 2004;219(1–2):9–15.

    Article  CAS  PubMed  Google Scholar 

  53. Narita K, Murata T, Takahashi T, Kosaka H, Omata N, Wada Y. Plasma levels of adiponectin and tumor necrosis factor-alpha in patients with remitted major depression receiving long-term maintenance antidepressant therapy. Prog Neuropsychopharmacol Biol Psychiatry. 2006;30(6):1159–62.

    Article  CAS  PubMed  Google Scholar 

  54. Leo R, Di Lorenzo G, Tesauro M, Cola C, Fortuna E, Zanasi M, Troisi A, Siracusano A, Lauro R, Romeo F. Decreased plasma adiponectin concentration in major depression. Neurosci Lett. 2006;407(3):211–3.

    Article  CAS  PubMed  Google Scholar 

  55. Yau SY, Li A, Hoo RL, Ching YP, Christie BR, Lee TM, Xu A, So KF. Physical exercise-induced hippocampal neurogenesis and antidepressant effects are mediated by the adipocyte hormone adiponectin. Proc Natl Acad Sci U S A. 2014;111(44):15810–5.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  56. Krishnan V, Nestler EJ. The molecular neurobiology of depression. Nature. 2008;455(7215):894–902.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  57. Valente KD, Busatto FG. Depression and temporal lobe epilepsy represent an epiphenomenon sharing similar neural networks: clinical and brain structural evidences. Arq Neuropsiquiatr. 2013;71(3):183–90.

    Article  PubMed  Google Scholar 

  58. Lambert G, Johansson M, Ågren H, Friberg P. Reduced brain norepinephrine and dopamine release in treatment-refractory depressive illness: evidence in support of the catecholamine hypothesis of mood disorders. Arch Gen Psychiatry. 2000;57(8):787–93.

    Article  CAS  PubMed  Google Scholar 

  59. Dalvi A, Lucki I. Murine models of depression. Psychopharmacology (Berl). 1999;147(1):14–6.

    Article  CAS  Google Scholar 

  60. Berton O, Nestler EJ. New approaches to antidepressant drug discovery: beyond monoamines. Nat Reviews Neurosci. 2006;7:137–51.

    Article  CAS  Google Scholar 

  61. Liu I, Niu C, Chi T, Kuo D, Cheng J. Investigations of the mechanism of the reduction of plasma glucose by cold-stress in streptozotocin-induced diabetic rats. Neuroscience. 1999;92(3):1137–42.

    Article  CAS  PubMed  Google Scholar 

  62. Trulson M, Himmel C. Effects of insulin and streptozotocin-induced diabetes on brain norepinephrine metabolism in Rats. J Neurochem. 1985;44(6):1873–6.

    Article  CAS  PubMed  Google Scholar 

  63. Stone ML, Walker JL, Chisholm D, Craig ME, Donaghue KC, Crock P, Anderson D, Verge CF. The addition of rosiglitazone to insulin in adolescents with type 1 diabetes and poor glycaemic control: a randomized-controlled trial. Pediatr Diabetes. 2008;9(4 Pt 1):326–34.

    Article  CAS  PubMed  Google Scholar 

  64. Dantzer R, O’Connor JC, Freund GG, Johnson RW, Kelley KW. From inflammation to sickness and depression: when the immune system subjugates the brain. Nat Rev Neurosci. 2008;9(1):46–56.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  65. Miller AH, Maletic V, Raison CL. Inflammation and its discontents: the role of cytokines in the pathophysiology of major depression. Biol Psychiatry. 2009;65(9):732–41.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

We thank Dr. Tsai-Kun Li for giving excellent comments on this manuscript. It is grateful for the technique support from Ms. Yu-Ju Peng, Mr. Yu-Jen Chen, and Mr. Yen-Wen Wang.

Funding

This work was supported by Mucho Biotech. Inc.

Availability of data and materials

The datasets supporting the conclusions of this article are included within the article.

Authors’ contributions

TLS and STD contributed the concept and design of the study. CWH, TWH and YJW performed the experiments. TLS, CWH and KCC performed the statistical analysis and wrote the manuscript. RC and SHT provided the materials for the experiment. JCP, TYC, WSL, WCC, LYS and ST provided the techniques supported in the study. All authors read and approved the final manuscript.

Authors’ information

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Consent for publication

Not applicable in this session.

Ethics approval and consent to participate

All animal handling in this study are in accordance with a protocol approved by the Institutional Animal Care and Use Committee of National Taiwan University (IACUC approval NO. NTU-102-EL-37).

Author information

Author notes

    Authors and Affiliations

    1. Department of Animal Science and Technology, National Taiwan University, Taipei, 10617, Taiwan

      Chao-Wei Huang & Shih-Torng Ding

    2. Mucho Biotechnology Inc., Taipei, 10684, Taiwan

      Tzu-Wen Hong, Sheng-Hong Tsai & Richard Chu

    3. Department of Plant Pathology and Microbiology, National Taiwan University, Taipei, 10617, Taiwan

      Ying-Jing Wang, Ko-Chien Chen & Tang-Long Shen

    4. Department of Psychology, National Taiwan University, Taipei, 10617, Taiwan

      Ju-Chun Pei & Wen-Sung Lai

    5. Department of Athletics, National Taiwan University, Taipei, 10617, Taiwan

      Tai-Yuan Chuang

    6. Institute of Biotechnology, National Taiwan University, Taipei, 10617, Taiwan

      Shih-Torng Ding & Tang-Long Shen

    7. Institute of Food Science and Technology, National Taiwan University, Taipei, 10617, Taiwan

      Wei-Cheng Chen & Lee-Yan Sheen

    8. Graduate School of Comprehensive Human Sciences, University of Tsukuba 1-1-1, Tennodai, Tsukuba, 305-8575, Japan

      Satoru Takahashi

    Authors
    1. Chao-Wei Huang
      View author publications

      You can also search for this author in PubMed Google Scholar

    2. Tzu-Wen Hong
      View author publications

      You can also search for this author in PubMed Google Scholar

    3. Ying-Jing Wang
      View author publications

      You can also search for this author in PubMed Google Scholar

    4. Ko-Chien Chen
      View author publications

      You can also search for this author in PubMed Google Scholar

    5. Ju-Chun Pei
      View author publications

      You can also search for this author in PubMed Google Scholar

    6. Tai-Yuan Chuang
      View author publications

      You can also search for this author in PubMed Google Scholar

    7. Wen-Sung Lai
      View author publications

      You can also search for this author in PubMed Google Scholar

    8. Sheng-Hong Tsai
      View author publications

      You can also search for this author in PubMed Google Scholar

    9. Richard Chu
      View author publications

      You can also search for this author in PubMed Google Scholar

    10. Wei-Cheng Chen
      View author publications

      You can also search for this author in PubMed Google Scholar

    11. Lee-Yan Sheen
      View author publications

      You can also search for this author in PubMed Google Scholar

    12. Satoru Takahashi
      View author publications

      You can also search for this author in PubMed Google Scholar

    13. Shih-Torng Ding
      View author publications

      You can also search for this author in PubMed Google Scholar

    14. Tang-Long Shen
      View author publications

      You can also search for this author in PubMed Google Scholar

    Corresponding authors

    Correspondence to Shih-Torng Ding or Tang-Long Shen.

    Rights and permissions

    Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

    Reprints and Permissions

    About this article

    Verify currency and authenticity via CrossMark

    Cite this article

    Huang, CW., Hong, TW., Wang, YJ. et al. Ophiocordyceps formosana improves hyperglycemia and depression-like behavior in an STZ-induced diabetic mouse model. BMC Complement Altern Med 16, 310 (2016). https://doi.org/10.1186/s12906-016-1278-7

    Download citation

    • Received:

    • Accepted:

    • Published:

    • DOI: https://doi.org/10.1186/s12906-016-1278-7

    Keywords

    • Ophiocordyceps formosana
    • Insulin insensitivity
    • Depression

    BMC Complementary Medicine and Therapies

    ISSN: 2662-7671

    Contact us