Vasorelaxant and blood pressure lowering effects of alchemilla vulgaris: A comparative study of methanol and aqueous extracts
S Takir1, IH Altun2, B Sezgi3, S Suzgec-Selcuk4, A Mat5, BS Uydes-Dogan1
1 Department of Pharmacology, Faculty of Pharmacy, Istanbul University, Istanbul, Turkey
2 Department of Pharmacology, Faculty of Pharmacy, Istanbul University, Istanbul, Netherlands
3 Department of Pharmaceutical Sciences, Medicinal Chemistry and Chemical Biology Section, ▀ Faculty, Utrecht University, Utrecht, Turkey
4 Department of Pharmacognosy, Faculty of Pharmacy, Marmara University, Turkey
5 Department of Pharmacognosy, Faculty of Pharmacy, Istanbul University, Istanbul, Turkey
|Date of Submission||18-Mar-2014|
|Date of Acceptance||14-May-2014|
|Date of Web Publication||21-Jan-2015|
Department of Pharmacology, Faculty of Pharmacy, Istanbul University, Beyaz?t, 34116, Istanbul
Source of Support: None, Conflict of Interest: None
| Abstract|| |
Background: In the last decade, a growing interest particularly in determining the cardiovascular effects of herbal extracts took place among researchers. Objective: Herein, we aimed to investigate the microvascular and blood pressure lowering effects of two differently processed extracts of the same herb, Alchemilla vulgaris (Rosaceaea), which was revealed to contain high levels of vasoactive compounds. Materials and Methods: For the purpose, endothelium intact rat mesenteric arteries were mounted in a myograph system and contracted with prostaglandin F 2α (PGF 2α: 3 × 10−5 M) or potassium chloride (K + : 40 mM). Then, aqueous and methanol extracts were added at 0.01-10 mg/ml concentrations in a cumulative manner. Results: Both extracts produced relaxations in PGF 2α (3 × 10−5 M) precontracted arteries which were insensitive to the inhibitors of endothelium derived vasoactive substances namely, L G -nitro-L-arginine (10−4 M), ODQ (10−5 M) and indomethacin (10−5 M) or removal of endothelium. Opposite vascular effects were observed when extracts were applied in K + precontracted arteries. In addition, oral administration of the methanol extract of Alchemilla vulgaris, but not the aqueous extract, reduced blood pressure significantly in L-NAME hypertensive rats. Conclusion: Our results demonstrated that the methanol extract of Alchemilla vulgaris has more prominent and favourable vascular effects in normal and experimental hypertensive conditions reinforcing its traditional use in cardiovascular disorders, in particular hypertension. These results most likely give rise to further studies to reveal its mechanism of action and clinical value of this herb.
Keywords: Alchemilla vulgaris, blood pressure, extract, mesenteric artery, vasodilatation
|How to cite this article:|
Takir S, Altun I H, Sezgi B, Suzgec-Selcuk S, Mat A, Uydes-Dogan B S. Vasorelaxant and blood pressure lowering effects of alchemilla vulgaris: A comparative study of methanol and aqueous extracts. Phcog Mag 2015;11:163-9
|How to cite this URL:|
Takir S, Altun I H, Sezgi B, Suzgec-Selcuk S, Mat A, Uydes-Dogan B S. Vasorelaxant and blood pressure lowering effects of alchemilla vulgaris: A comparative study of methanol and aqueous extracts. Phcog Mag [serial online] 2015 [cited 2021 Jun 13];11:163-9. Available from: http://www.phcog.com/text.asp?2015/11/41/163/149733
| Introduction|| |
Hypertension is the leading cause of mortality and morbidity, especially in developing countries. In the last decade, a growing interest particularly in determining the cardiovascular effects of herbal extracts took place among researchers. In several experimental studies, the plant extracts rich in polyphenolic compounds and flavonoids were shown to induce vasorelaxant, antioxidant and hypotensive effects. ,
Alchemilla vulgaris (A. vulgaris; lady's mantle), a member of the Rosaceaea family, has traditionally been used to treat bleeding, eczema, inflammation, diarrhoea, ulcers, skin rashes, menstruation disorders and oedema in Europe. , It is also used as herbal tea for hypertension , and as infusion for diabetes.  Liquid extracts of A. vulgaris were shown to contain flavonoid glycosides composed of quercetin derivatives  and gallic acid.  It is very well known that the amount of bioactive compounds in plant extracts is subject to change according to several factors such as growth stages, cultivation, insect invasion, season of collection and the method of extraction.  In order to obtain standardization in medicinal plant extracts, all these factors especially the method of extraction should be under rigorous control. Indeed, a comparative study evaluating the effects of two differently processed extracts of the same herb parallelly in in vitro and in vivo experimentation is scarcely documented so far.  Herein, we compared the effects of aqueous and methanol extracts of A. vulgaris on systolic blood pressure and isolated microvessels of rats. We recently determined that, the methanol and aqueous extracts of A. vulgaris display opposite vascular effects, i.e. relaxation versus contraction, respectively, on isolated rat thoracic aorta possibly due to their different phenolic contents. In relation, total flavonoid and quercetin amount was found much higher in the methanol extract while gallic acid in the aqueous extracts.  Quercetin, the most abundant flavonoid in medicinal plants, also in A. vulgaris, was demonstrated to improve endothelium-dependent relaxation and reduce the contractile responses in rat thoracic aortas. , It was suggested to be more potent in mesenteric vascular bed compared to aorta  and decrease the elevated blood pressure noticeably when given orally.  Hence, in this study, we first aimed to identify the effectiveness of two differently processed extracts of A. vulgaris in small resistance arterial tone, which contribute importantly to the modulation of blood pressure, by comparing the direct effects of methanol and aqueous extracts in isolated rat mesenteric arteries. Then, in order to clarify the possible preventive influence of A. vulgaris on the elevation of blood pressure, the effects of orally administered methanol and aqueous extracts were determined on systolic blood pressure in L-NAME induced hypertensive rats.
| Materials and methods|| |
Preparation of extracts
To obtain methanol extract, the dried aerial parts of A. vulgaris herb (product no: 22140), purchased from Jacob Hooy and Co. BV in the Netherlands, exhausted in Soxhlet apparatus for 18 h and lyophilized after condensation in rotavopor. For the aqueous extract, plant material let to maceration at room temperature for 24 h. Then, under reverse refrigerant water bath exhausted for 6 h and lyophilized after blowing of the water. The major vasoactive constituents in methanol and aqueous extracts of Alchemilla vulgaris were previously determined by HPLC-DAD analysis. 
Characteristics of the animals
Male Wistar albino rats with an average weight of 200-250 g (10-12 weeks) were used. The animals were obtained from Experimental Medicine and Research Institute (DETAE) of Istanbul University and all experimental procedures utilized were approved by Local Animal Experimentation Ethics Committee of Istanbul University (04/11/2010, decision no: 161). Rats were housed under standard temperature of 20°C ± 2°C and humidity of 60-70% on a 12:12 h light/dark cycle with free access to standard rat chow and tap water.
The rats were sacrificed by stunning followed by decapitation. The mesenteric arteries were carefully excised and placed in cold Krebs Ringer-bicarbonate solution of the following composition (mM): NaCl 118, KCl 4.7, KH 2 PO 4 1.2, NaHCO 3 25, MgSO 4 .7H 2 O 1.2, CaCl 2 2.5, glucose 10 and disodium EDTA 0.026. Mesenteric arteries were cleaned of fat and surrounding tissues under a stereomicroscope (Model 2000, Zeiss, Germany). Four mesenteric artery preparations were mounted in parallel in a multichamber wire Myograph System (Model 610M, DMT, Aarhus, Denmark). Two stainless steel wires 40μm in diameter were treaded into the lumen of mesenteric arteries and then fixed to the mounting devices of a force transducer and a micrometer. The mesenteric arteries were equilibrated for 1 h in Krebs-Ringer bicarbonate solution at 37°C and gassed with 5% CO 2 + 95% O 2 (pH = 7.4). Thereafter, mesenteric arteries were set to a normalized internal circumference L 1 ( 0.9L 100 ) in accordance to passive wall tension-internal circumference relationship under a passive transmural pressure of 100 mmHg.  Normalized mesenteric arteries were contracted twice with potassium chloride (K + ; 120 mM) plus noradrenaline (NA; 10−4 M) to check the viability and standardization of the preparations. Preparations which developed a tension less than 0.5 mN/mm were discarded. Following the standardization, concentration-response curves of prostaglandin F 2α (PGF 2α; 10−8 -10−4 M) and K + (10-120 mM) were obtained. The presence of functional endothelium and the vascular relaxation capacities of the vessels were checked by the cumulative administration of acetylcholine (Ach; 10−8 -10−4 M) and sodium nitroprusside (SNP; 10−8 -10−4 M) to induce relaxation on PGF 2α (3 × 10−5 M) contracted mesenteric arteries.
The direct vascular effects of A. vulgaris extracts were investigated in mesenteric arteries of rats precontracted with differently acting contractile agents namely; PGF 2α (3 × 10−5 M) or K + (40 mM). Increasing concentrations (0.01-10 mg/ml) of the extracts were administered cumulatively when the contractions to PGF 2α or K + reached a plateau. The role of endothelium in vascular relaxant effects of the extracts were investigated in mesenteric arteries removed of endothelium or pretreated with putative inhibitors of endothelial vasodilators such as, nitric oxide (NO) synthase inhibitor, L G -nitro-L-arginine (L-NOARG, 10−4 M), guanylate cyclase inhibitor, ODQ (10−5 M) or cyclooxygenase inhibitor, indomethacin (10−5 M) for 20 min. 
In separate sets of experiments, the effects of both extracts on the contractile reactivity of mesenteric arteries were examined. In these experiments, concentration-response curves of PGF 2α (10−8 -10−4 M) and K + (10-120 mM) were obtained both in the presence and absence of the extracts and compared each other. For the purpose, mesenteric arteries were pretreated either with extracts (10 mg/ml) or vehicle (Krebs) for 20 min.
In vivo experiments
Rats were randomly divided into four groups. Group 1 served as control and received tap water for 5 weeks. Group 2, 3 and 4 received nonselective NO synthase inhibitor, L-NAME (60 mg/kg/day) for 5 weeks. Group 3 received methanol extract (300 mg/kg/day) and group 4 received aqueous extract (300 mg/kg/day)  for 2 weeks, starting at the 3 rd week of L-NAME (60 mg/kg/day) administrations. L-NAME was freshly prepared on each day and administrated in 35-40 ml of tap water which was determined as the daily water consumed per rat in our preliminary experiments. Each extract was given orally by intragastric gavage under light ether anaesthesia. Systolic blood pressure was measured by tail-cuff (PowerLab, ADInstruments, United Kingdom) and averages of four consecutive pressure measurements were calculated.
All drugs used in the experiments were purchased from Sigma-Aldrich (Taufkirchen, Germany) except for ODQ (Tocris, Germany). The stock solutions of ODQ were prepared in dimethylsulfoxide whereas indomethacin was prepared in 5% (w/v) sodium bicarbonate solution. Acetylcholine and noradrenaline were dissolved in 0.001 N HCl and ascorbic acid (1 mg/ml) was added to noradrenaline solution to prevent oxidation. All other drugs as well as methanol and aqueous extracts of A. vulgaris were dissolved in distilled water.
Data were presented as "mean ± standard error of the mean" while "n" is the number of rats or mesenteric artery rings used in the experiments. The contractile responses to spasmogens were expressed as "mN/mm". The relaxant responses were indicated as "%" decreases while the contractile responses were expressed as "%" increases of the precontractile tone. Sensitivities of the arteries to spasmogens and dilators were calculated as the effective concentration that elicit 50% of the maximal response (pD 2 ) by using nonlinear regression curve fit and expressed as "-Log EC 50". Statistical analyses were determined by Student's paired and unpaired t-tests as well as by one-way analysis of variance (ANOVA) followed by Tukey Kramer post-hoc test where appropriate. A "P < 0.05" was considered statistically significant.
| Results|| |
Characteristics of mesenteric arteries
The length (1.73 ± 0.02 mm) and internal diameter (280.60 ± 7.83 μm) of rat mesenteric arteries used in the experiments were all comparable within the preparations (n = 36). The maximal relaxant responses to Ach and SNP were determined as 93.08 ± 1.73% and 90.20 ± 1.49% (n = 36), respectively. In endothelium denuded rings, the maximal relaxation to Ach was abolished (8.54 ± 2.5%, n = 12, P < 0.05) whereas no change was observed in the response to SNP (90.21 ± 2.02%, n = 12, P > 0.05).
Effects of methanol and aqueous extracts
Cumulative addition of methanol and aqueous extracts (0.01-10 mg/ml) to the myograph system, produced concentration-dependent relaxations in mesenteric arteries precontracted submaximally with PGF 2α (3 × 10 −5 M: 1.07 ± 0.17 mN/mm and 1.04 ± 0.15 mN/mm, n = 8, respectively, P > 0.05). The maximal relaxation responses to the methanol (E max : 80.86 ±3.01%, n = 8) and aqueous extracts (E max : 79.68 ± 4.26%, n = 8) of A. vulgaris were comparable [Figure 1]a. On the other hand, cumulative addition of the methanol extract (0.01-10mg/ml) produced concentration-dependent relaxations (E max : 62.68 ± 9.29%, n = 7) whereas the aqueous extract induced contractions (E max : 37.29 ± 6.27%, n = 10) in mesenteric arteries precontracted with K + (40 mM) [Figure 1]b. In these experiments, the precontraction level obtained with K + (40 mM: 1.00 ± 0.10 mN/mm, n = 7 and 0.79 ± 0.10 mN/mm, n = 10, respectively, P > 0.05) were comparable in mesenteric arteries.
|Figure 1: The effects of methanol (▀) and aqueous extracts (▴) of Alchemilla vulgaris (0.01-10 mg/ml) on (a) PGF2α (3 × 10-5 M) or (b) K+ (40 mM) precontracted rat mesenteric arteries. n = 7-10. *P < 0.05, **P < 0.01 and ***P < 0.001 versus aqueous extract analysis of variance|
Click here to view
The role of endothelium and endothelium-derived vasodilator factors
Incubation of mesenteric arteries with L-NOARG (10 −4 M), ODQ (10 −5 M) and indomethacin (10 −5 M) for 20 min or removal of the endothelium, did not significantly modify the relaxation responses obtained with the methanol extract of A. vulgaris [Figure 2]. Similar results were obtained on the relaxation responses of the aqueous extract either in the presence of these inhibitors or after the removal of endothelium [Figure 3].
|Figure 2: The effects of nitric oxide synthase inhibitor, LG-nitro- L-arginine (10-4 M), guanylate cyclase inhibitor, ODQ (10-5 M), cyclooxygenase inhibitor, indomethacin (10-5 M) or removal of endothelium on the responses induced by methanol extract of Alchemilla vulgaris (0.01-10 mg/ml) in rat mesenteric arteries precontracted with PGF2α (3 × 10−5 M). n = 6-8. P > 0.05 versus corresponding control, paired Student's t-test|
Click here to view
|Figure 3 : The effects of nitric oxide synthase inhibitor, LG-nitro- L-arginine (10-4 M), guanylate cyclase inhibitor, ODQ (10-5 M), cyclooxygenase inhibitor, indomethacin (10-5 M) or removal of endothelium on the responses induced by aqueous extract of Alchemilla vulgaris (0.01-10 mg/ml) in rat mesenteric arteries precontracted with PGF2α (3 × 10-5 M). n = 6-8. P > 0.05 versus corresponding control, paired Student's t-test|
Click here to view
Effects of the methanol and aqueous extracts on vascular reactivity
In mesenteric arteries pretreated with methanol extract (10 mg/ml, 20 min) the maximum contractile responses of PGF 2α and K + were significantly reduced. There was also a significant reduction in pD 2 value of PGF 2α but not that of K + . On the other hand, pretreatment of the mesenteric arteries with the aqueous extract (10 mg/ml, 20 min) of A. vulgaris significantly decreased the maximum contractile response of PGF 2α although an increase was observed in the maximum contraction level of K + . While, the pD 2 values of PGF 2α and K + were comparable [Table 1].
|Table 1: The maximum contractile response (Emax: mN/mm) and pD2 values of PGF2α and K+ in the presence or absence of methanol (+M.E.) and aqueous (+A.E.) extracts of A. vulgaris |
Click here to view
Effects on blood pressure levels in L-NAME-induced hypertensive rats
Daily administration of L-NAME to the rats significantly increased systolic blood pressure levels compared to the age-matched controls. Chronic treatment of rats with methanol extract (300 mg/kg/day) for 2 weeks with the continued administration of L-NAME, statistically significant decreased the blood pressure level compared to untreated L-NAME induced hypertensive rats. However, treatment with the aqueous extract (300 mg/kg/day) for 2 weeks was ineffective to decrease significantly the elevated blood pressure in L-NAME induced hypertensive rats although; a partial prevention was notable in the gradual increase of systolic blood pressure [Table 2].
|Table 2: Blood pressure (mm/Hg) levels of control, L-NAME induced hypertensive and methanol (+M.E.) and aqueous (A.E.) extracts of A. vulgaris treated rats |
Click here to view
| Discussion|| |
In recent years a growing interest took place in the alternative therapies due to the increased evidence of drug related problems including ineffectiveness, low efficacy, developing resistance or serious adverse effects. In relation, many researchers paid more attention to investigate the effectiveness of medicinal plants especially rich in polyphenolic compounds and vasoactive flavonoids in disease conditions. Supportively, it was revealed that consumption of polyphenolic compounds and flavonoids in the diet decrease the risk of cardiovascular diseases.  Besides, in several experimental studies favourable effects of polyphenolic compounds and flavonoids in terms of antioxidant, antiinflammatory, vasorelaxant and blood pressure lowering effects were demonstrated. ,, In studies investigating the pharmacological effects of medicinal plants generally liquid extracts that prepared by different extraction methods are used. As the vasoactive compound ingredient and their amounts determined in the plant extracts could vary in accordance to the extraction methods, evaluating the pharmacological effects of two differently processed extracts of the same herb is important for an accurate assessment. In this study, we investigated the effects of methanol and aqueous extracts of A. vulgaris paralelly in an in vitro and in vivo experimentation performed in rats, i.e. influences on isolated microvessels and systolic blood pressure. Herein, we originally found that (1) the methanol extract of A. vulgaris, induced a pronounced vasorelaxation response either in PGF 2α or K + precontracted rat mesenteric arteries whereas, the aqueous extract induced contrasting effects depending on the contractile agent used to increase vascular tone (2) in PGF 2α precontracted mesenteric arteries the relaxation responses obtained with methanol and aqueous extracts of A. vulgaris were independent from the endothelium and endothelial vasodilators (3) in vitro pretreatment effects of methanol and aqueous extracts on the contractile reactivity to spasmogens were reinforcing their direct influences on rat mesenteric arteries (4) oral administration of the methanol extract (10 mg/ml) for 2 weeks reduced the elevated blood pressure in L-NAME hypertensive rats whereas the aqueous extract (10 mg/ml) did not have a prominent effect.
PGF 2α and K + are spasmogens acting via different cellular mechanisms. PGF 2α constricts arteries mainly through the activation of receptor-operated calcium channels whereas K + induces contraction by depolarization of vascular smooth muscle cell membrane to provide Ca +2 influxes.  Our findings revealed that the methanol and aqueous extracts of A. vulgaris display similar relaxation responses against the receptor-operated spasmogen mediated contraction. Interestingly, contrasting effect, in terms of relaxation versus contraction, were obtained with these extracts when a receptor-independent spasmogen was used to induce contraction in isolated mesenteric arteries. Indeed, this diverse direct effectiveness of the extracts was supported with the findings obtained in pretreatment experiments. Thus, in parallel to acute vascular effects, pretreatment of rat mesenteric arteries with either methanol or aqueous extract (10 mg/ml, 20 min.) reduced significantly the maximal contractile response to PGF 2α whereas, opposite effects were observed against the vasoreactivity to K + . Hence, our results demonstrated that methanol and aqueous extracts of A. vulgaris is effective in decreasing the vascular contractile tone induced by PGF 2α while, the aqueous extract evoked an increase in the contractility in particular, to a receptor independent spasmogen in rat mesenteric arteries.
Different responses obtained with the methanol and aqueous extracts of A. vulgaris in rat mesenteric arteries might be related with the differences in the phenolic composition of the extracts. The liquid extracts of A. vulgaris were previously shown to contain flavonoid glycosides composed of quercetin derivatives  and gallic acid.  Supportively, in our recent study, we also determined that the flavonoid amount of A. vulgaris is much higher in the methanol than the aqueous extract and as analysed by HPLC-DAD both extracts contained quercetin and gallic acid as the major vasoactive constituents.  Of these constituents, quercetin was demonstrated to induce relaxations  whereas; gallic acid was reported to produce contractions in isolated rat aorta.  Indeed, all these previous data are supporting our current findings in rat mesenteric arteries. Thus, much higher gallic acid content of the aqueous extract compared to the methanol extract might be one of the mechanisms that mediate its contractile responses in mesenteric arteries. Interestingly, opposite vascular effects of the extracts were apparent especially in K + precontracted arteries. Thus, it is possible that the vascular activity of flavonoids in the aqueous extract is diminished or abolished in the presence of high K + . Besides, we also noticed that the maximal relaxation response to methanol extract was significantly diminished in K + precontracted mesenteric arteries compared to PGF 2α contracted arteries. Previously, weak or negligible vasorelaxant effects of several flavonoids, including quercetin, has been reported in K + contracted rat aortic rings in contrary to the pronounced relaxations against phenylephrine induced contractions.  Then, in concern with quercetin, it was suggested that the presence of -OH substitution at C-5 atom increases its selectivity towards a receptor operated spasmogen compared to a nonreceptor operated spasmogen, i.e. K + .  This interpretation likely to support the differences in the relaxant responses of methanol extract, which contain quercetin as the major flavonoid, between PGF 2α and K + precontracted mesenteric arteries. Concerning the aqueous extract, high amount of gallic acid content in addition to the aforementioned low effectiveness of quercetin in the presence of high K + possibly explains its contractile influence in K + precontracted mesenteric arteries. Moreover, it is also known that relaxant properties of vasoactive substances acting via opening K + channels are remarkably diminished at high K + contractions.  Comparatively, the diminished or abolished relaxant influences of the methanol and aqueous extracts, respectively, in K + contracted arteries may also suggest the involvement of K + channel activation in their mechanism of action which requires further investigation.
The vascular endothelium controls vascular tone via release of relaxant and contractile factors.  In the present study, we tested the probable role of endothelium in the vascular effects of the extracts. The relaxation responses to methanol and aqueous extracts were not changed in the presence of putative inhibitors of endothelium namely, L-NOARG, ODQ and indomethacin, in rat mesenteric arteries. The results obtained in endothelium denuded mesenteric arteries were also in parallel. These findings suggested that the endothelial vasodilators, namely, NO and prostacyclin probably do not mediate the acute relaxant effects of the methanol and aqueous extracts of A. vulgaris in mesenteric arteries. In literature, the relaxant effects of various flavonoids have been reported to be mediated either endothelium dependent  or independent  mechanisms. Quercetin, which is found in both extracts, was shown to induce endothelium-independent relaxations in isolated resistance mesenteric vascular bed.  In addition, vasorelaxing effects of several flavonoids including quercetin, were reported to be inhibited in the presence of K + channel blockers.  Hence, it is reasonable to suggest that K + channel activation may contribute to the endothelium-independent relaxant effects of A. vulgaris extracts in mesenteric arteries which is one of the goal of our further investigation.
The preventive role of long term A. vulgaris treatment on increased blood pressure was evaluated in L-NAME induced hypertensive rats. Oral administration of the methanol extracts but not the aqueous extract for 2 weeks significantly diminished the elevated blood pressure in accordance to its vasorelaxant effects in mesenteric arteries. We suggested that the prominent vascular relaxant and blood pressure lowering effects of the methanol extract of A. vulgaris is possibly due to its high flavonoid content, in particular quercetin. While, ineffectiveness in lowering blood pressure in L-NAME induced hypertensive rats as well as the augmentation of the contractile tone in the K + contracted arteries with the aqueous extract of A. vulgaris could be related to its low flavonoid content and high amount of gallic acid. Thus, the varying vascular effects of the aqueous and methanol extracts of A. vulgaris in rat mesenteric arteries either in vitro or in vivo experimentation is most likely to be related to distinct flavonoid composition resulted from different extraction process.
In conclusion, our results demonstrated that the methanol extract of A. vulgaris has more prominent and favourable vascular effects in normal and experimentally hypertensive conditions. The methanol extract instead of aqueous extract might have usage in cardiovascular disorders, especially in hypertension. These results most likely give rise to further studies to reveal its mechanism of action and clinical value of this herb.
| Acknowledgments|| |
Part of this work was presented at the 10 th International Symposium on Resistance Arteries (ISRA) 8-12 May 2011.
| References|| |
Ghosh D, Scheepens A. Vascular action of polyphenols. Mol Nutr Food Res 2009;53:322-31.
Grassi D, Desideri G, Ferri C. Flavonoids: Antioxidants against atherosclerosis. Nutrients 2010;2:889-902.
D'Agostino M, Dini I, Ramondo E, Senatore F. Flavonoid glycosides of Alchemilla vulgaris
L. Phytother Res 1998;12:S162-3.
Condrat D, Mosoarca C, Zamfir AD, Criºan F, Szabo MR, Lupea AX. Qualitative and quantitative analysis of gallic acid in Alchemilla vulgaris
, Allium ursinum
, Acorus calamus
and Solidago virga-aurea
by chip-electrospray ionization mass spectrometry and high performance liquid chromatography. Cent Eur J Chem 2010;8:530-5.
Nihoul-Ghenne L. Presence of Alchemilla alpina
L. Together with Alchemilla vulgaris
L. In a tea for high blood pressure. J Pharm Belg 1950;5:335-8.
Pieroni A, Giusti ME, Quave CL. Cross-cultural ethnobiology in the Western Balkans: Medical ethnobotany and ethnozoology among Albanians and Serbs in the Pešter Plateau, Sand×ak, South-Western Serbia. Hum Ecol 2011;39:333-49.
Swanston-Flatt SK, Day C, Bailey CJ, Flatt PR. Traditional plant treatments for diabetes. Studies in normal and streptozotocin diabetic mice. Diabetologia 1990;33:462-4.
Ding W, Yang T, Liu F, Tian S. Effect of different growth stages of Ziziphora clinopodioides
Lam. on its chemical composition. Pharmacogn Mag 2014;10:S1-5.
Phillips OA, Mathew KT, Oriowo MA. Antihypertensive and vasodilator effects of methanolic and aqueous extracts of Tribulus terrestris
in rats. J Ethnopharmacol 2006;104:351-5.
Takir S, Sezgi B, Süzgeç-Selçuk S, Eroglu-Özkan E, Beukelman KJ, Mat A, et al.
Endothelium-dependent vasorelaxant effect of Alchemilla vulgaris
methanol extract: A comparison with the aqueous extract in rat aorta. Nat Prod Res 2014; 28:1-4.
Roghani M, Baluchnejadmojarad T, Vaez-Mahdavi MR, Roghani-Dehkordi F. Mechanisms underlying quercetin-induced vasorelaxation in aorta of subchronic diabetic rats: An in vitro
study. Vascul Pharmacol 2004;42:31-5.
Ajay M, Achike FI, Mustafa AM, Mustafa MR. Direct effects of quercetin on impaired reactivity of spontaneously hypertensive rat aortae: Comparative study with ascorbic acid. Clin Exp Pharmacol Physiol 2006;33:345-50.
Pérez-Vizcaíno F, Ibarra M, Cogolludo AL, Duarte J, Zaragozá-Arnáez F, Moreno L, et al.
Endothelium-independent vasodilator effects of the flavonoid quercetin and its methylated metabolites in rat conductance and resistance arteries. J Pharmacol Exp Ther 2002;302:66-72.
Duarte J, Pérez-Palencia R, Vargas F, Ocete MA, Pérez-Vizcaino F, Zarzuelo A, et al.
Antihypertensive effects of the flavonoid quercetin in spontaneously hypertensive rats. Br J Pharmacol 2001;133:117-24.
Mulvany MJ, Halpern W. Contractile properties of small arterial resistance vessels in spontaneously hypertensive and normotensive rats. Circ Res 1977;41:19-26.
Uydes-Dogan BS, Takir S, Ozdemir O, Kolak U, Topçu G, Ulubelen A. The comparison of the relaxant effects of two methoxylated flavones in rat aortic rings. Vascul Pharmacol 2005;43:220-6.
Plotnikov MB, Aliev OI, Andreeva VY, Vasil'ev AS, Kalinkina GI. Effect of Alchemilla vulgaris
extract on the structure and function of erythrocyte membranes during experimental arterial hypertension. Bull Exp Biol Med 2006;141:708-11.
Jia H, Liu JW, Ufur H, He GS, Liqian H, Chen P. The antihypertensive effect of ethyl acetate extract from red raspberry fruit in hypertensive rats. Pharmacogn Mag 2011;7:19-24.
Godfraind T, Miller RC. Actions of prostaglandin F2 alpha and noradrenaline on calcium exchange and contraction in rat mesenteric arteries and their sensitivity to calcium entry blockers. Br J Pharmacol 1982;75:229-36.
Sanae F, Miyaichi Y, Hayashi H. Potentiation of vasoconstrictor response and inhibition of endothelium-dependent vasorelaxation by gallic acid in rat aorta. Planta Med 2002;68:690-3.
Ajay M, Gilani AU, Mustafa MR. Effects of flavonoids on vascular smooth muscle of the isolated rat thoracic aorta. Life Sci 2003;74:603-12.
Nelson MT, Quayle JM. Physiological roles and properties of potassium channels in arterial smooth muscle. Am J Physiol 1995;268:C799-822.
Vanhoutte PM, Rubanyi GM, Miller VM, Houston DS. Modulation of vascular smooth muscle contraction by the endothelium. Annu Rev Physiol 1986;48:307-20.
Duarte J, Pérez Vizcaíno F, Utrilla P, Jiménez J, Tamargo J, Zarzuelo A. Vasodilatory effects of flavonoids in rat aortic smooth muscle. Structure-activity relationships. Gen Pharmacol 1993;24:857-62.
Calderone V, Chericoni S, Martinelli C, Testai L, Nardi A, Morelli I, et al.
Vasorelaxing effects of flavonoids: Investigation on the possible involvement of potassium channels. Naunyn Schmiedebergs Arch Pharmacol 2004;370:290-8.
[Figure 1], [Figure 2], [Figure 3]
[Table 1], [Table 2]