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Protective effects of hydroalcoholic extract from rhizomes of Cynodon dactylon (L.) Pers. on compensated right heart failure in rats

BMC Complementary and Alternative Medicine volume 9, Article number: 28 (2009) Cite this article

Abstract

Background

The rhizomes of Cynodon dactylon are used for the treatment of heart failure in folk medicine. In the present study, we investigated the effects of hydroalcoholic extract of C. dactylon rhizomes on cardiac contractility in normal hearts and on cardiac functions in right-heart failure in rats.

Methods

Right-heart failure was induced by intraperitoneal injection of monocrotaline (50 mg/kg). Two weeks later, the animals were treated orally with different doses of the extract for fifteen days. At the end of the experiments cardiac functions and markers of myocardial hypertrophy were measured.

Results

The treated rats showed very less signs of fatigue, peripheral cyanosis and dyspnea. The survival rate was high in the extract treated groups (90%). Administration of C. dactylon in monocrotaline-injected rats led to profound improvement in cardiac functions as demonstrated by decreased right ventricular end diastolic pressure (RVEDP) and elevated mean arterial pressure. RVd P/d tmax, and RVd P/d t/P as indices of myocardial contractility were also markedly (p < 0.001; using one way ANOVA) increased by the extract. The extract reduced heart and lung congestion by decreasing tissue wet/dry and wet/body weight ratios (p < 0.01). In the isolated rat hearts, the extract produced a remarkable (P < 0.001) positive inotropic effect concomitant with a parallel decrease in LVEDP.

Conclusion

The results of this study indicated that C. dactylon exerted a strong protective effect on right heart failure, in part by positive inotropic action and improving cardiac functions.

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Background

Heart failure is a condition that impairs the ability of the heart to pump a sufficient amount of blood through the body. Treatment strategies have been focused mainly on the use of diuretics and cardiac glycosides. Although, such therapies relieve symptoms of the disease and stabilize patients but rarely improve survival [1]. In addition, pulmonary hypertension represents an important clinical problem that can results in development of right ventricular heart failure [2] and which is associated with a high rate of mortality [3]. It is now believed that medicinal plants can be a valuable source of assistance for prescription medicines and can be taken to aid recovery from serious disease such as heart failure. Digitalis purpurea is an excellent example of herbal use in conventional medicine. Digitalis purpurea contains cardioactive glycosides that effectively treat congestive heart failure [4]. Cynodon species are members of Cynodonteae tribe and Chloridoideae sub-family [5]. Cynodon dactylon (L.) pers. (C. dactylon; family poaceae), also known as Bermuda grass, Devil's Grass, Couch Grass, Triticum repens, and Indian Doab, is a resilient and perennial grass native to the warm temperate and tropical regions [5, 6]. It is populary named "Margh" in Iran. C. dactylon is claimed to have antidiabetic, antimicrobial [7], hypolipidemic [8], anti-inflammatory, and anti-emetic [9] properties. The plant is diuretic and traditionally known as a remedy for urinary infections, kidney stones, and congestion. The diuretic effect can be due to the presence of large amount of mannitol in this herb [10]. The root and rhizomes are also used in the treatment of depression, vomiting, cough, epilepsy, and hemorrhage [11]. It has been reported recently that the plant possesses protective effect against stroptozotocin induced hepatic injury in rats [12]. In North West of Iran, C. dactylon is named "chayer" and the aqueous extract obtained from its rhizomes is used as a cardiac tonic in heart failure and mostly believed that the extract has very curative effect on heart congestion diseases. The presence of glycosides and flavonoids has been shown in the alcoholic extract of the plant [13] and its curative effect may be attributed to the presence of these phytoconstituents. Recently, we have reported that the total extract of C. dactylon rhizomes has a potential protective effect against ischemic/reperfusion injury and improves recovery from the reperfusion insult in isolated rat heart [14]. To our knowledge, the effect of C. dactylon on heart failure has not been elucidated to date. Among the most widely studied animal models of right ventricular hypertrophy and failure is the administration of monocrotaline (MCT), which produces a relatively rapid (within a few weeks) pulmonary hypertension resulting in compensatory right ventricular hypertrophy and failure [15, 16]. The present study was carried out to investigate the effects of hydroalcoholic extract of C. dactylon rhizomes on myocardial responses in right ventricular heart failure as well as on cardiac contractility in isolated normal rat hearts.

Methods

Extract preparation

Rhizomes of C. dactylon were collected from the fields of Maragheh (Iran) in November and voucher samples were preserved for reference in the Herbarium of Department of Pharmacognosy, School of Pharmacy, Tabriz University of Medical Sciences. Powdered rhizomes (400 g) were extracted by maceration in MeOH/H2O (70:30, 3×1 liter) at room temperature for 3 days. The hydroalcoholic extracts were combined and concentrated in vacuo to yield 27 g dried extract. This hydroalcoholic extract was kept in refrigerator for all experiments.

Phytochemical screening

The crude extract of C. dactylon rhizomes was screened for the presence of different classes of compounds using the standard methods by some modifications [17, 18]. Thin Layer Chromatography procedures were performed using precoated silicagel plates (Merck; GF254, 0.25 mm) to confirm the results of screenings [19]. The following spray reagents were used for detection of respective classes of compounds: Neu's reagent for polyphenoles and flavonoids, Antimony trichloride in chloroform for steroidal saponins and sterols, Kedd reagent for cardiac glycosides, Dragendorrf's reagent for alkaloids, and 5% Ethanolic sodium hydroxide for anthraquinones [19, 20]. Since the dried extract contained mainly flavonoid glycosides, it was standardized in its flavonoid glycosides content (4.6%) by the reported method [21].

Characterization of fractions obtained from the total extract by HPLC

The dried total extract of C. dactylon rhizomes was fractionated by solid-phase extraction (SPE) method. The total extract (2 g) was dissolved in minimum possible volume of 20% of MeOH/H2O mixture and adsorbed on Sep-Pak (mega tube 10 g; Waters) cartridge and eluted by step gradient of MeOH/H2O mixtures (20%; 40%; 60%, 80; and 100%). The high content fractions (20% and 40%), based on weight, were characterized by HPLC finger print. The fractions dissolved in mobile phase and 20 μl of the samples were injected into the reverse phase column (C18). The mobile phase consisted of a gradient of 0–35% (over 35 min), 35–55% (over 15 mhn), and 55-0% (over 10 min) methanol in water (V/V) and was delivered at a flow rate of 1 ml/minute. The detection was performed at three wavelengths of 220, 280, and 350 nm.

Experimental animals

Male Wistar rats (110–120 g; 4 weeks old) were used in this study. The animals were given food and water ad libitum. They were housed in the Animal House of Tabriz University of Medical Sciences at a controlled ambient temperature of 25 ± 2°C with 50 ± 10% relative humidity and with a 12-h light/12-h dark cycle. This study was performed in accordance with the Guide for the Care and Use of Laboratory Animals of Tabriz University of Medical Sciences, Tabriz-Iran (National Institutes of Health Publication No 85-23, revised 1985).

Experimental protocol

Animals were randomized into six groups of 10 rats in each. Group 1 (normal control) received an intraperitoneal (i.p) injection of physiological saline (0.5 ml) and untreated for the whole period of the experiment (4 weeks). Group 2 was injected (i.p) a single dose of monocrotaline (50 mg/kg; MCT group) [22] and two weeks later they were given 1 ml vehicle [0.5% carboxy methyl cellulose (CMC)] orally, twice daily. Groups 3 to 6 were injected the same dose of MCT and two weeks later they received digoxin (0.01 mg/kg) or 50, 100, and 200 mg/kg (in 1 ml) of hydroalcoholic extract of C. dactylon rhizomes orally, twice daily continued for fifteen days. The extracts were suspended in CMC (0.5%). At the end of the experiments (4 weeks), hemodynamic measurements were taken and then the animals were sacrificed under deep anesthesia, and their hearts and lungs were removed. To assess the direct cardiac effects of the extract, in the other sets of experiments, wistar rat hearts (n = 6) were removed and mounted on a Langendorf apparatus and were exposed to different concentrations of the extract. Left ventricular developed pressure (LVDP), Left ventricular end diastolic pressure (LVEDP), and heart rate (HR) were recorded continuously during the experiment.

Hemodynamic measurements

Four weeks after MCT injection, the animals were anaesthetized with sodium pentobarbital (60 mg/kg; i.p). When the rats no longer responded to external stimuli, the trachea was cannulated for artificial respiration and systemic arterial blood pressure was recorded from a catheter inserted into the left carotid artery. A standard limb lead I ECG was monitored continuously throughout the experimental period. Mean Arterial Pressure (MAP) was calculated from the systolic and diastolic blood pressures trace. Heart rate (HR) was calculated from the ECG [23]. After recording the above mentioned parameters, the thorax was opened and the right ventricle was punctured with a 23-gauge needle attached to a pressure transducer. After stabilization, right ventricular systolic (RVSP) and end diastolic (RVEDP) pressures were recorded over 5 to 10 min. RV d P/d tmax and RV d P/d t/P as two indices of myocardial contractility were also calculated from RVSP. All parameters were continuously recorded using Powerlab system (AD Instruments, Australia).

Tissue weights

Following the hemodynamic measurements, animals were sacrificed by an overdose of pentobarbital. The hearts, lungs, livers, and kidneys were removed and weighed. Then, the tissues were cut into small pieces for drying at 55°C until a constant weight was reached. Wet to body weight ratios and wet to dry weight ratios of the tissues were calculated to assess the degree of the congestion.

Isolated heart perfusion

Rats were anaesthetized with sodium pentobarbital (60 mg/kg intraperitoneally) and given heparin sodium (300 IU). Hearts were rapidly excised and placed in ice-cold buffer and mounted on a constant pressure (100 mmHg) Langendorff-perfusion apparatus. They were perfused with modified Krebs-Henseleit bicarbonate buffer containing (in mM): NaCl 118.5, NaHCO3 25.0, KCl 4.8, MgSO4 1.2, KH2PO4 1.2, CaCl2 1.7 and D-glucose 12.0. All solutions were gassed with 95% O2/5% CO2 with pH maintained between 7.35 and 7.45 at 37°C. Temperature was continuously monitored by a thermo-probe inserted into the pulmonary artery and maintained between 36.5 and 37.5°C. A latex, fluidfilled, isovolumic balloon was introduced into the left ventricle through the left atrial appendage and connected to a pressure transducer (P-1000B; Narco Bio Instruments) and HR, LVDP, and LVEDP were recorded with a Narco Bio physiograph (MK-III-S, Narco Bio Systems, USA) [24]. The hearts were allowed to stabilize for 30 minutes before any interventions. Krebs containing different concentrations of the extract was perfused for 1 min at 30 min intervals and maximum responses were recorded. The effects of the extract were expressed as percentage change from pre-perfusion control values.

Statistics

Data were presented as mean ± SD. Comparisons between groups were made with Student's paired t-test or one way ANOVA as appropriate. If ANOVA analysis indicated significant differences, a Student-Newman-Keuls post test was performed to compare mean values between treatment groups and control. Differences between groups were considered significant at p < 0.05.

Results

Phytochemical screening

The finding of preliminary phytochemical screenings showed that the rhizomes of C. dactylon contain significant amounts of sugars, flavonoids, sterols and steroidal saponins while, the trace amount of alkaloids were also detectable. The presences of all above mentioned phytoconstituents have been reported previously [13, 25, 26]. HPLC fingerprints of two fractions (fraction 20% and fraction 40%) obtained from the total extract of C. dactylon rhizomes demonstrated different pattern (Figure 1a and 1b).

Figure 1
figure 1

HPLC fingerprints of fraction 20% (a) and fraction 40% (b) obtained from the total extract of C. dactylon rhizomes. The detection was performed at three wavelengths of 220 nm (upper trace); 280 nm (middle trace) and 350 nm (lower trace).

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General effects of C. dactylon extract in rats with right heart failure

Weight gain, which was greatly reduced after MCT administration (Table 1), was significantly high (p < 0.05 and p < 0.01) in the extract treated groups. A week after the administration of MCT, the rats showed a general loss of appetite (food intake reduced from 18 ± 3.3 g per rat to 7.5 ± 4 g per rat 14 days after MCT injection). Water consumption by these animals was also decreased (data not shown). Two weeks after the injection of MCT, the rats showed signs of fatigue and cyanosis of limbs and noses. Although, animals in MCT and MCT plus the extract treated groups showed fatigue and cyanosis, the extract treated rats exhibited an obvious improvement in their appearance and physical activity, even compared to digoxin treated rats. At the end of the experiments, MCT-injected rats (rats with heart failure) showed signs of tachypenea and dyspnea, while these signs were less apparent in the extract treated rats. So that, these symptoms were disappeared in the most of animals treated with 200 mg/kg of the extract. None of the control animals died during experiment period whereas, 2 of 10 rats (20%) from MCT group and groups treated with 50 and 100 mg/kg of the extract died during the experiment period. Mortality was as high as 40% in digoxin treated rats. The group treated with 200 mg/kg of the extract showed less mortality (10%).

Table 1 General animal characteristics parameters in the control group and in rats treated with MCT (i.p; Heart failure) or with MCT + C. Dactylon rhizomes hydroalcoholic extract (orally).
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Effecst of C. dactylon extract on tissue weights

In order to assess the extent of heart hypertrophy developed by the injection of MCT, ventricles wet to dry weight ratio as well as ventricles to body weight ratio were determined (Table 1). Both ratios were significantly higher (p < 0.01) in the rats four weeks after MCT treatment. Compared with MCT-treated rats, treatment with digoxin or the extract produced significant decline in the ventricles wet to dry weight ratio, where this reduction was very notable in groups treated with 100 and 200 mg/kg of C. dactylon extract (p < 0.01; Table 1). There was also a decrease in the ventricular to body weight ratio in the extract treated rats, but this reduction reached a significant (p < 0.01) level only by 200 mg/kg of the extract. In order to estimate the extent of proliferative pulmonary responses, wet to dry and wet to body weight ratios of lung was also determined. In comparison with control, wet to dry and wet to body weight ratios of lung were significantly (p < 0.01) high in MCT-injected rats. Compared with MCT group values, only treatment with 200 mg/kg of the extract reduced both ratios of the lungs significantly (P < 0.01; Table 1). There were no significant changes in either the liver or the kidneys wet to dry weight and to body weight ratios with any treatment (data not shown).

Effects of C. dactylon extract on hemodynamic responses

Mean arterial blood pressure (MAP) was significantly decreased from 63 ± 8 mmHg in control to 31 ± 3.5 mmHg in MCT group (p < 0.001; Figure 2a). Treatment with C. dactylon extract prevented the MCT induced reduction of MAP, as 200 mg/kg of the extract reversed the MAP from 31 ± 3.5 (mmHg) close to the control value of 60 ± 5.5 mmHg (p < 0.001; Figure 2a). Heart rate was also significantly (p < 0.001) reduced from 309 ± 25 (beats/min) in control to 250 ± 6 (beats/min) in MCT-injected rats. Treatment with 200 mg/kg of the extract increased the heart rate close to the control value of 290 ± 18 (beats/min; p < 0.01; Figure 2b). To further determine the degree of the right ventricular responses to MCT treatment, intraventricular pressures were measured. RVSP was significantly elevated by 61% (p < 0.001 vs. control) in MCT (heart failure) group. The degree of elevation was significantly attenuated by 50, 100, and 200 mg/kg of the extract to 35%, 21%, and 11%, respectively (p < 0.01 and p < 0.001; Figure 3a). In MCT group, RVEDP was markedly increased by 84% (p < 0.001 vs. control) while, it was lowered with concomitant administration of the extract. The extract with 100 mg/kg reduced this elevation from 9.4 ± 1.5 mmHg in MCT group to 7.3 ± 1.7 mmHg (p < 0.05; Figure 3b). Compared with the normal control, rats with right heart failure (MCT group) demonstrated a lower right ventricular maximal rate of pressure (RV d P/d tmax) and lower rate of pressure change at a fixed ventricular pressue (RV d P/d t/P) (p < 0.001; Figure 4). Similar to the digoxin treated rats, both of these indices of myocardial contractility, were markedly and dose dependently recovered by oral administration of the extract (P < 0.05 and p < 0.001; Figure 4).

Figure 2
figure 2

Mean arterial blood pressure (MAP; a) and heart rate (b) in the normal control group and in rats treated with MCT (heart failure) or with MCT + C. dactylon hydroalcoholic extract ( C. dac ). Values are mean ± S.D (n = 10). #p < 0.001 from respective control value; *p < 0.05, **p < 0.01, and ***p < 0.001 as compared with MCT treated group using one way ANOVA with Student-Newman-Keuls post hoc test.

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Figure 3
figure 3

Right ventricular systolic pressure (RVSP; a) and right ventricular end diastolic pressure (RVEDP; b) in the control group and in rats treated with MCT (heart failure) or with MCT + C. dactylon hydroalcoholic extract ( C. dac ). Values are mean ± S.D (n = 10). #p < 0.001 from respective control value; *p < 0.05, **p < 0.01, and ***p < 0.001 as compared with MCT treated group using one way ANOVA with Student-Newman-Keuls post hoc test.

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Figure 4
figure 4

Right ventricular maximal rate of pressure increase (RV d P/ d t max ; a) and the rate of pressure change at a fixed right ventricular pressure (RV d P/ d t/P; b) in the control group and in rats treated with MCT (rats with right heart failure) or with MCT + C. dactylon hydroalcoholic extract ( C. dac ). Values are mean ± S.D (n = 10). #p < 0.001 from respective control value; *p < 0.05, **p < 0.01, and ***p < 0.001 as compared with MCT treated group using one way ANOVA with Student-Newman-Keuls post hoc test.

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Direct effects of C. dactylon extract on isolated rat hearts

The extract produced a notable and concentration dependent increase in LVDP. A maximum increase of 51 ± 8% (p < 0.001) was obtained by 100 μg/ml of the extract (Figure 5a). The positive inotropic effect of the extract was concomitant with a parallel decrease in LVEDP (Figure 5a). Likewise, the extract produced a concentration dependent negative chronotropic effect on isolated rat hearts (Figure 5b).

Figure 5
figure 5

Direct Effect of the hydroalcoholic extract of C. dactylon on left ventricular developed pressure (LVDP; black square; a), left ventricular end diastolic pressure (LVEDP; open square; a), and heart rate (HR; black triangle; b) in isolated rat hearts. Symbols represent the mean ± SD values (n = 6) of maximum percentage changes in the parameters. *p < 0.05, **p < 0.01, and ***p < 0.001 significantly different from control values using Student's paired t-test.

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Discussion

Rhizomes of C. dactylon are being used traditionally for the treatment of congestive heart failures in some parts of Iran. However, little is known about its cardioprotective actions in cardiovascular diseases. In the present study, we investigated the therapeutic efficacy of the hydroalcoholic extract of rhizomes of the plant in rats with right heart failure induced by monocrotaline. Monocrotaline produces its effects primarily by injuring pulmonary vessels endothelium, resulting in pulmonary arterial pressure [27]. MCT-induced pulmonary hypertension is associated with development of compensated right ventricular hypertrophy, which progresses to failure within weeks [28]. In this study we started the treatment two weeks after MCT injection when, the heart failure was established. Thus, the results suggest that the favorable effect of C. dactylon is mainly due to the inhibition of the compensatory myocardial responses to MCT-induced pulmonary hypertension. The animals on C. dactylon treatment fared better than their untreated counterparts and exhibited an obvious improvement in their appearance and physical activity. Symptoms such as cyanosis, tachypenea, and dyspnea were almost disappeared in the most of the animals treated with the high dose of the extract. In addition, the beneficial effects were also clearly observed with respect to a variety of indices, including reduced myocardial hypertrophy, improved cardiac function, positive inotropic action, increase in myocardial contractility force, and parallel decrease in right ventricular end diastolic pressure. Furthermore, direct effect of hydroalcoholic extract of C. dactylon rhizomes on isolated rat hearts demonstrated that the extract produce a dose dependent and very significant increase of the contraction force by increasing the left ventricular developed pressure (LVDP) and parallel decrease of end diastolic pressure (LVEDP) and heart rate. In the treatment of heart failure it is very beneficial to improve the contractility of the heart and at the same time decrease the end diastolic pressure. Our preliminary phytochemical finding in this study revealed the presence of sugars, flavonoids, sterols and steroidal saponins in the hydroalcoholic extract obtained from C. dactylon rhizomes. Reactive oxygen species have been implicated in the progression of ventricular hypertrophy to congestive heart failure [29]. Plant flavonoids are antioxidant and scavenge oxygen free radicals, therefore suggesting their role in preventing of monocrotaline induced damages in this study. The other main components of the extract are steroidal saponins. Saponins are mainly plant-derived glycosides, occurring as triterpenoid or steroid saponins. Steroid saponins have been found to have some interesting biological and pharmacologic activities including cardiac tonic, diuretic, antibacterial, anti-inflammatory and hypocholesteremic influences [30, 31]. Furthermore, the sugar, probably mannitol, and saponins present in the extract have diuretic properties and can be useful in the treatment of congestion disorders such as heart failure.

Conclusion

The results of this study showed the beneficial effect of C. dactylon in rats with compensated right heart failure. We speculate that the extract produce its protective effects at least in part by direct improvement of cardiac performance. However, the precise mechanism for the salutary effect of C. dactylon on compensatory myocardial response needs to be determined especially in view of the right ventricular heart failure nature and finding the active ingredient(s).

References

  1. Rocco TP, Fang JC: Pharmacology of congestive heart failure. Goodman & Gilman's The Pharmacological Basis of Therapeutics. Edited by: Brunton LL, Lazo JS, Parker KL. 2006, New York: McGraw-Hill, 869-

    Google Scholar 

  2. Krowka MJ: Pulmonary hypertension: diagnostics and therapeutics. Mayo Clinic Proceedings. 2000, 75: 625-630. 10.4065/75.6.625.

    Article  CAS  PubMed  Google Scholar 

  3. Lilienfeld DE, Rubin LJ: Mortality from primary pulmonary hypertension in the United States, 1979–1996. Chest. 2000, 117: 796-800. 10.1378/chest.117.3.796.

    Article  CAS  PubMed  Google Scholar 

  4. Katzung BG, Parmley WW: Drug used in heart failure. Basic & Clinical Pharmacology. Edited by: Katzung BG. 2007, New York: McGraw-Hill, 201-202. 9

    Google Scholar 

  5. Bethel CM, Sciara EB, Estill JC, Bowers JE, Hanna W, Paterson AH: A framework linkage map of bermudagrass (Cynodon dactylon X transvaalensis) based on single-dose restriction fragments. Theor Appl genet. 2006, 112: 727-737. 10.1007/s00122-005-0177-y.

    Article  CAS  PubMed  Google Scholar 

  6. Auddy B, Ferreira M, Blasina F: Screening of antioxidant activity of three Indian medicinal plants, traditionally used for the management of neurodegenerative diseases. J Ethnopharmacol. 2003, 84: 131-138. 10.1016/S0378-8741(02)00322-7.

    Article  CAS  PubMed  Google Scholar 

  7. Singh SK, Kesari AN, Gupta RK, Jaiswal D, Watal G: Assessment of antidiabetic potential of C. dactylon extract in streptozotocin diabetic rats. J Ethnopharmacol. 2007, 114: 174-179. 10.1016/j.jep.2007.07.039.

    Article  PubMed  Google Scholar 

  8. Singh SK, Rai PK, Jaiswal D, Watal G: Evidence-based critical evaluation of glycemic potential of Cynodon dactylon. eCAM. 2008, 5 (4): 415-420.

    PubMed  Google Scholar 

  9. Ahmed S, Reza MS, Jabbar A: Antimicrobial activity of C. dactylon. Fitoterapia. 1994, 65: 463-464.

    Google Scholar 

  10. Bermuda grass is evil..... Bermuda grass is bug... [http://www.mdidea.com/products/proper/proper079paper.html]

  11. Miraldi E, Ferri S, Mostaghimi V: Botanical drugs and preparations in the traditional medicine of West Azerbaijan (Iran). J Ethnopharmacol. 2001, 75: 77-87. 10.1016/S0378-8741(00)00381-0.

    Article  CAS  PubMed  Google Scholar 

  12. Singh SK, Rai PK, Jaiswal D, Rai DK, Sharma B, Watal G: Protective effect of Cynodon dactylon against STZ induced hepatic injury in rats. J Ecophysiol Occup Hlth. 2008, 8: 195-199.

    CAS  Google Scholar 

  13. Garg VK, Khosa RL: Analgesic and anti-pyretic activity of aqueous extract of Cynodon dactylon. Pharmacologyonline. 2008, 3: 12-18.

    Google Scholar 

  14. Najafi M, Nazemiyeh H, Ghavimi H, Gharakhani A, Garjani A: Effects of hydroalcoholic extract of Cynodon dactylon (L.) pers. on ischemia/reperfusion-induced arrhythmias. Daru. 2008, 16 (4): 233-238.

    Google Scholar 

  15. Chen L, Gan XT, Haist JV, Feng Q, LU X, Chakrabarti S, Karmazyn M: Attenuation of compensatory right ventricular hypertrophyand heart failure following monocrotaline-induced pulmonary vascular injury by the Na+-H+ exchange inhibitor cariporide. J Pharmacol Exp Ther. 2001, 298: 469-476.

    CAS  PubMed  Google Scholar 

  16. Pichardo J, Palace V, Farahmand F, Pawan K: Myocardial oxidative stress changes during compensated right heart failure in rats. Mol Cell Biochem. 1999, 196: 51-57. 10.1023/A:1006914111957.

    Article  CAS  PubMed  Google Scholar 

  17. Mojab F, Kamalinejad M, Ghaderi N, Vahidipour HR: Phytochemical screening of some species of Iranian plants. Iranian J Pharmaceutic Res. 2003, 2: 77-82.

    CAS  Google Scholar 

  18. Harborne J: Phytochemical Methods: A Guide to Modern Techniques of Plant Analysis. 1998, London: Chapman & Hall;, 17-103.

    Google Scholar 

  19. Wagner H, Bladt S: Plant Drug Analysis: A Thin Layer Chromatography Atlas. 1996, Berlin Heidelberg: Springer-Verlag, 349-364. 2

    Chapter  Google Scholar 

  20. Stahl E: Thin Layer Chromatography: A laboratory handbook. 1969, Berlin Heidelberg: Springer-Verlag, 854-904.

    Chapter  Google Scholar 

  21. Lamaison JL, Carant A: The amount of main flavonoids in flowers and leaves of Crataegus monogyna Jacq. and Cratageus laevigata (Poiret) DC. (Rosacea). Pharma Acta Helv. 1996, 65: 315-320.

    Google Scholar 

  22. Pan LC, Wilson DW, Lame MW, Jones AD, Segall HJ: Corpulmonale is caused by monocrotaline and dehydromonocrotaline but not by glutathione or cysteine conjugates of dihydropyrrolizine. Toxicol Appl Pharmacol. 1993, 118: 87-97. 10.1006/taap.1993.1013.

    Article  CAS  PubMed  Google Scholar 

  23. Garjani A, nazemiyeh H, Maleki N, Valizadeh H: Effects of extracts from flowering tops of Crataegus meyeri A. Pojark. On ischaemic arrhythmias in anaesthetized rats. Phytother Res. 2000, 14: 428-431. 10.1002/1099-1573(200009)14:6<428::AID-PTR618>3.0.CO;2-L.

    Article  CAS  PubMed  Google Scholar 

  24. Najafi M, Garjani A: The effect of L-carnitine on arrhythmias in the ischemic rat heart. J Basic Med Sci. 2005, 8 (1): 38-44.

    CAS  Google Scholar 

  25. Patil MB, Jalalpure SS, Prakash NS, Kokate CK: Antiulcer properties of alcoholic extract of C. dactylon in rats. Acta Horticulturae. 2005, 680: 115-118.

    Article  Google Scholar 

  26. Aishah HS, Amri AMM, Ramlan MF, Mamat AS: Organic materials and nitrogen-potassium ratios for Bermuds tifdwarf (C. dactylon). Acta Horticulture. 1997, 450: 505-510.

    Article  Google Scholar 

  27. Schultze AE, Roth RA: Chronic pulmonary hypertension – the monocrotaline model and involvement of the hemostatic system. J Toxicol Environ Health B Crit Rev. 1998, 1: 271-346.

    Article  CAS  PubMed  Google Scholar 

  28. Hessel MHM, Steendijk P, Adel B, Schutte CI, Laarse AV: Characterization of right ventricular function after monocrotaline-induced pulmonary hypertension in the intact rat. Am J Physiol Heart Circ Physiol. 2006, 291: H2424-H2430. 10.1152/ajpheart.00369.2006.

    Article  CAS  PubMed  Google Scholar 

  29. Redout EM, Wagner MJ, Zuidwijk MJ, Boer C, Musters RJP, Hardeveld C, Paulus WJ, Simonides WS: Right-ventricular failure is associated with increased mitochondrial complex II activity and production of reactive oxygen species. Cardiovascular Research. 2007, 75: 770-781. 10.1016/j.cardiores.2007.05.012.

    Article  CAS  PubMed  Google Scholar 

  30. Francis G, Kerem Z, Makkar HPS, Becker K: The biological action of saponins in animal systems: a review. Br J Nutr. 2002, 88: 587-605. 10.1079/BJN2002725.

    Article  CAS  PubMed  Google Scholar 

  31. Lacaille-Dubois MA, Wagner H: A review of the biological and pharmacological activities of saponins. Phytomedicine. 1996, 2: 363-386.

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements

This study was supported by a grant from the Research Vice Chancellors of Tabriz University of Medical Sciences; Tabriz, Iran.

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Authors and Affiliations

  1. Department of pharmacology and Toxicology; School of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran

    Alireza Garjani, Arash Afrooziyan, Moslem Najafi, Ali Kharazmkia & Nasrin Maleki-Dizaji

  2. Department of Pharmacognosy, School of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran

    Hossein Nazemiyeh

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  1. Alireza Garjani
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Correspondence to Alireza Garjani.

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The authors declare that they have no competing interests.

Authors' contributions

AG designed and coordinated the study and also drafted the manuscript. AA carried out the hemodynamic measurements and the heart failure experiments. HN collaborated in the phytochemical procedures. MN helped in the animal experiments and acquisition of data. AK carried out the isolated heart perfusion experiments. NMD has been involved in revising the manuscript and performed the statistical analysis. All authors have read and approved the final manuscript.

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Garjani, A., Afrooziyan, A., Nazemiyeh, H. et al. Protective effects of hydroalcoholic extract from rhizomes of Cynodon dactylon (L.) Pers. on compensated right heart failure in rats. BMC Complement Altern Med 9, 28 (2009). https://doi.org/10.1186/1472-6882-9-28

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  • DOI: https://doi.org/10.1186/1472-6882-9-28

Keywords

  • Mean Arterial Blood Pressure
  • Body Weight Ratio
  • Left Ventricular Develop Pressure
  • Hydroalcoholic Extract
  • Carboxy Methyl Cellulose

BMC Complementary Medicine and Therapies

ISSN: 2662-7671

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