Skip to main content
Top
Published in: Journal of Translational Medicine 1/2016

Open Access 01-12-2016 | Research

Mechanisms underlying the antihypertensive properties of Urtica dioica

Authors: Rahila Qayyum, Hafiz Misbah-ud-Din Qamar, Shamim Khan, Umme Salma, Taous Khan, Abdul Jabbar Shah

Published in: Journal of Translational Medicine | Issue 1/2016

Login to get access

Abstract

Background

Urtica dioica has traditionally been used in the management of cardiovascular disorders especially hypertension. The aim of this study was to explore pharmacological base of its use in hypertension.

Methods

Crude methanolic extract of U. dioica (Ud.Cr) and its fractions (Ud.EtAc, Ud.nHex, Ud.Chl and Ud.Aq) were tested in vivo on normotensive and hypertensive rats under anesthesia for blood pressure lowering effect. In-vitro experiments on rat and rabbit aortae were employed to probe the vasorelaxation mechanism(s). The responses were measured using pressure and force transducers connected to PowerLab Data Acquisition System.

Results

Ud.Cr and fractions were found more effective antihypertensive in hypertensive rats than normotensive with remarkable potency exhibited by the ethyl acetate fraction. The effect was same in the presence of atropine. In isolated rat aortic rings, Ud.Cr and all its fractions exhibited l-NAME sensitive endothelium-dependent vasodilator effect and also inhibit K+ (80 mM)-induced pre-contractions. In isolated rabbit thoracic aortic rings Ud.Cr and its fractions induced relaxation with more potency against K+ (80 mM) than phenylephrine (1 µM) like verapamil, showing Ud.EtAc fraction the most potent one. Pre-incubation of aortic rings with Ud.Cr and its fractions exhibited Ca2+ channel blocking activity comparable with verapamil by shifting Ca2+ concentration response curves to the right. Ud.Cr and its fractions also ablated the intracellular Ca2+ release by suppressing PE peak formation in Ca2+ free medium. When tested on basal tension, the crude extract and all fractions were devoid of any vasoconstrictor effect.

Conclusions

These data indicate that crude methanolic extract and its fractions possess antihypertensive effect. Identification of NO-mediated vasorelaxation and calcium channel blocking effects explain the antihypertensive potential of U. dioica and provide a potential pharmacological base to its medicinal use in the management of hypertension.
Literature
1.
go back to reference Caliskaner Z, Karaayvaz M, Ozturk S. Misuse of a herb: stinging nettle (Urtica urens) induced severe tongue oedema. Complement Ther Med. 2004;12:57–8.CrossRefPubMed Caliskaner Z, Karaayvaz M, Ozturk S. Misuse of a herb: stinging nettle (Urtica urens) induced severe tongue oedema. Complement Ther Med. 2004;12:57–8.CrossRefPubMed
2.
go back to reference Anon. Reintroduction of nettle cultivation as a sustainable raw material for fibres and cellulose production. Department of Plant Production Biotechnology [online]; 1998. Anon. Reintroduction of nettle cultivation as a sustainable raw material for fibres and cellulose production. Department of Plant Production Biotechnology [online]; 1998.
3.
go back to reference Dreyer J, Dreyling G, Feldmann F. Cultivation of stinging nettle Urtica diocia L. with high fibre content as a raw material for the production of fibre and cellulose: qualitative and quantitative differentiation of ancient clones. J Appl Bot. 1996;70(1–2):28–39. Dreyer J, Dreyling G, Feldmann F. Cultivation of stinging nettle Urtica diocia L. with high fibre content as a raw material for the production of fibre and cellulose: qualitative and quantitative differentiation of ancient clones. J Appl Bot. 1996;70(1–2):28–39.
4.
go back to reference Whitney PJ, Gibbs G. The common stinging nettle: resource or risk? Biologist. 2006;53:178–82. Whitney PJ, Gibbs G. The common stinging nettle: resource or risk? Biologist. 2006;53:178–82.
5.
go back to reference Bisht S, Bhandari S, Bisht SN. Urtica dioica L., an undervalued, economically important plant. Agric Sci Res J. 2012;2:250–2. Bisht S, Bhandari S, Bisht SN. Urtica dioica L., an undervalued, economically important plant. Agric Sci Res J. 2012;2:250–2.
6.
go back to reference Garnier G, Bezanger-Beauquesne L, Debraux G. Inresources medicinenelous delaflore francase. Vegots Freres Paris. 1961; 1:1-34. Garnier G, Bezanger-Beauquesne L, Debraux G. Inresources medicinenelous delaflore francase. Vegots Freres Paris. 1961; 1:1-34.
7.
go back to reference Newall CA, Anderson LA, Philipson JD. Herbal medicines: a guide for health care professionals. London: The Pharmaceutical Press; 1996. p. 201–2. Newall CA, Anderson LA, Philipson JD. Herbal medicines: a guide for health care professionals. London: The Pharmaceutical Press; 1996. p. 201–2.
8.
go back to reference Ziyyat A, Legssyer A, Mekhfi H, Dassoule A, Serharouchni M, Benjellon W. Phytotherapy of hypertension in oriental Morroco. J Ethnopharmacol. 1997;58:45–54.CrossRefPubMed Ziyyat A, Legssyer A, Mekhfi H, Dassoule A, Serharouchni M, Benjellon W. Phytotherapy of hypertension in oriental Morroco. J Ethnopharmacol. 1997;58:45–54.CrossRefPubMed
9.
go back to reference Lahighi SH, Amini K, Moradi P, Asaadi K. Investigating the chemical composition of different parts extracts of bipod nettle Urtica dioica L. in Tonekabon region. Physiology. 2011;2:339–42. Lahighi SH, Amini K, Moradi P, Asaadi K. Investigating the chemical composition of different parts extracts of bipod nettle Urtica dioica L. in Tonekabon region. Physiology. 2011;2:339–42.
10.
go back to reference Palic R, Stojanovic G, Alagic S, Nikolic M, Lepojevic Z. Chemical composition and antimicrobial activity of the essential oil and CO2 extracts of the oriental tobacco, Prilep. Flavour Fragr J. 2002;17:323–6.CrossRef Palic R, Stojanovic G, Alagic S, Nikolic M, Lepojevic Z. Chemical composition and antimicrobial activity of the essential oil and CO2 extracts of the oriental tobacco, Prilep. Flavour Fragr J. 2002;17:323–6.CrossRef
11.
go back to reference Lalitharani S, Mohan VR, Regini GS. GC-MS analysis of ethanolic extract of Zanthoxylum rhetsa (roxb.) dc spines. J Herbal Med Toxicol. 2010;4:191–2. Lalitharani S, Mohan VR, Regini GS. GC-MS analysis of ethanolic extract of Zanthoxylum rhetsa (roxb.) dc spines. J Herbal Med Toxicol. 2010;4:191–2.
12.
go back to reference Roy S, Rao K, Bhuvaneswari CH, Giri A, Mangamoori LN. Phytochemical analysis of Andrographis paniculata extract and its antimicrobial activity. World J Microbiol Biotechnol. 2010;26:85–91.CrossRef Roy S, Rao K, Bhuvaneswari CH, Giri A, Mangamoori LN. Phytochemical analysis of Andrographis paniculata extract and its antimicrobial activity. World J Microbiol Biotechnol. 2010;26:85–91.CrossRef
13.
go back to reference Li RW, Leach DN, Myers P, Leach GJ, Lin GD, Brushett DJ, Waterman PG. Anti-inflammatory activity, cytotoxicity and active compounds of Tinospora smilacina Benth. Phytother Res. 2004;18:78–83.CrossRefPubMed Li RW, Leach DN, Myers P, Leach GJ, Lin GD, Brushett DJ, Waterman PG. Anti-inflammatory activity, cytotoxicity and active compounds of Tinospora smilacina Benth. Phytother Res. 2004;18:78–83.CrossRefPubMed
14.
go back to reference Ogunlesi M, Okiei W, Ademoye M, Osibote EA. Analysis of essential oil from the stem of Chansmanthera dependens. J Nat Prod. 2010;3:47–53. Ogunlesi M, Okiei W, Ademoye M, Osibote EA. Analysis of essential oil from the stem of Chansmanthera dependens. J Nat Prod. 2010;3:47–53.
15.
go back to reference Wagner H, Willer F, Kreher B. Biologically active compounds from Urtica dioica. Planta Med. 1989;55:452–4.CrossRefPubMed Wagner H, Willer F, Kreher B. Biologically active compounds from Urtica dioica. Planta Med. 1989;55:452–4.CrossRefPubMed
16.
go back to reference Reihemman K, Behnke B, Schulze-Osthoffs K. Plant extract from stinging nettle (Urtica dioica), an anti-rheumatic remedy inhibits the pro-inflammatory transcription factor NF- KappaB. FEBS Lett. 1999;442:89–94.CrossRef Reihemman K, Behnke B, Schulze-Osthoffs K. Plant extract from stinging nettle (Urtica dioica), an anti-rheumatic remedy inhibits the pro-inflammatory transcription factor NF- KappaB. FEBS Lett. 1999;442:89–94.CrossRef
17.
go back to reference Lichius JJ, Muth C. The inhibiting effect of Urtica dioica root extract on experimentally induced prostatic hyperplasia in mouse. Planta Med. 1997;63:307–10.CrossRefPubMed Lichius JJ, Muth C. The inhibiting effect of Urtica dioica root extract on experimentally induced prostatic hyperplasia in mouse. Planta Med. 1997;63:307–10.CrossRefPubMed
18.
go back to reference Tahri A, Yamani S, Leggsyer A. Acute natriuretic and hypotensive effects of continuous perfusion of aqueous extract of Urtica dioica in the rat. J Ethnopharmacol. 2000;73:95–100.CrossRefPubMed Tahri A, Yamani S, Leggsyer A. Acute natriuretic and hypotensive effects of continuous perfusion of aqueous extract of Urtica dioica in the rat. J Ethnopharmacol. 2000;73:95–100.CrossRefPubMed
19.
go back to reference Williamson EM, Okpako DT, Evans FJ. Pharmacological methods in phytotherapy research. Chichester: Wiley; 1998. Williamson EM, Okpako DT, Evans FJ. Pharmacological methods in phytotherapy research. Chichester: Wiley; 1998.
20.
go back to reference National Research Council. Guide for the care and use of laboratory animals. Washington, DC: National Academy Press; 1996. National Research Council. Guide for the care and use of laboratory animals. Washington, DC: National Academy Press; 1996.
21.
go back to reference Shah AJ, Gilani AH. Blood pressure-lowering and vascular modulator effects of Acorus calamus extract are mediated through multiple pathways. Cardiovasc Pharmacol. 2009;54:38–46.CrossRef Shah AJ, Gilani AH. Blood pressure-lowering and vascular modulator effects of Acorus calamus extract are mediated through multiple pathways. Cardiovasc Pharmacol. 2009;54:38–46.CrossRef
22.
go back to reference Lawler JE. Hypertension produced by a high sodium diet in the borderline hypertensive rat (BHR). Clin Exp Hypertens A. 1987;9(11):1713–31.PubMed Lawler JE. Hypertension produced by a high sodium diet in the borderline hypertensive rat (BHR). Clin Exp Hypertens A. 1987;9(11):1713–31.PubMed
23.
go back to reference Vasdev S, Gill V, Longerich L. Salt-induced hypertension in WKY rats: prevention by α-lipoic acid supplementation. Mol Cell Biochem. 2003;254:319–26.CrossRefPubMed Vasdev S, Gill V, Longerich L. Salt-induced hypertension in WKY rats: prevention by α-lipoic acid supplementation. Mol Cell Biochem. 2003;254:319–26.CrossRefPubMed
24.
go back to reference Taqvi SI. Blood pressure lowering and vasomodulator effects of piperine. J Cardiovasc Pharmacol. 2008;52(5):452–8.CrossRefPubMed Taqvi SI. Blood pressure lowering and vasomodulator effects of piperine. J Cardiovasc Pharmacol. 2008;52(5):452–8.CrossRefPubMed
25.
go back to reference Ghayur MN, Gilani AH, Afridi MB. Cardiovascular effects of ginger aqueous extract and its phenolic constituents are mediated through multiple pathways. Vasc Pharmacol. 2005;43:234–41.CrossRef Ghayur MN, Gilani AH, Afridi MB. Cardiovascular effects of ginger aqueous extract and its phenolic constituents are mediated through multiple pathways. Vasc Pharmacol. 2005;43:234–41.CrossRef
26.
go back to reference Chan SS, Choi AO, Jones RL, Lin G. Mechanisms underlying the vasorelaxing effects of butylidenephthalide, an active constituent of Ligusticum chuanxiong, in rat isolated aorta. Eur J Pharmacol. 2006;537:111–7.CrossRefPubMed Chan SS, Choi AO, Jones RL, Lin G. Mechanisms underlying the vasorelaxing effects of butylidenephthalide, an active constituent of Ligusticum chuanxiong, in rat isolated aorta. Eur J Pharmacol. 2006;537:111–7.CrossRefPubMed
27.
go back to reference Arunlakhshana O, Schild HO. Some quantitative uses of drug antagonists. Br J Pharmacol. 1959;14:48–58. Arunlakhshana O, Schild HO. Some quantitative uses of drug antagonists. Br J Pharmacol. 1959;14:48–58.
28.
go back to reference Joen-Rong S. Pharmacological effects of rutaecarpine, an alkaloid isolated from Evodia rutaecarpa. Cardiovasc Drug Rev. 1999;17:237–45. Joen-Rong S. Pharmacological effects of rutaecarpine, an alkaloid isolated from Evodia rutaecarpa. Cardiovasc Drug Rev. 1999;17:237–45.
29.
go back to reference Martin E, Davis K, Bian K. Cellular signaling with nitric oxide and cyclic guanosine monophosphate. Semin Perinatol. 2000;24:2–6.CrossRefPubMed Martin E, Davis K, Bian K. Cellular signaling with nitric oxide and cyclic guanosine monophosphate. Semin Perinatol. 2000;24:2–6.CrossRefPubMed
30.
31.
go back to reference Bragulat E, de la Sierra A, Antonio MT. Effect of salt intake on endothelium derived factors in a group of patients with essential hypertension. Clin Sci. 2001;101:73–8.CrossRefPubMed Bragulat E, de la Sierra A, Antonio MT. Effect of salt intake on endothelium derived factors in a group of patients with essential hypertension. Clin Sci. 2001;101:73–8.CrossRefPubMed
32.
go back to reference Godfraind T, Miller R, Wibo M. Calcium antagonism and calcium entry blockade. Pharmacol Rev. 1986;3:321–416. Godfraind T, Miller R, Wibo M. Calcium antagonism and calcium entry blockade. Pharmacol Rev. 1986;3:321–416.
33.
go back to reference Koike K, Takayanagi I, Takiguchi S. Ca2+-blocking action of stereoisomers of CI-951, (+)-CI-951, (NC)-1500 and (−)-CI-951 in the isolated muscle preparations. Gen Pharmacol. 1992;23:207–10.CrossRefPubMed Koike K, Takayanagi I, Takiguchi S. Ca2+-blocking action of stereoisomers of CI-951, (+)-CI-951, (NC)-1500 and (−)-CI-951 in the isolated muscle preparations. Gen Pharmacol. 1992;23:207–10.CrossRefPubMed
34.
go back to reference Boyd RA, Giacomini JC, Giacomini KM. Species differences in the negative inotropic response of 1, 4-dihydropyridine calcium channel blockers in myocardium. J Cardiovasc Pharmacol. 1988;12:650–7.CrossRefPubMed Boyd RA, Giacomini JC, Giacomini KM. Species differences in the negative inotropic response of 1, 4-dihydropyridine calcium channel blockers in myocardium. J Cardiovasc Pharmacol. 1988;12:650–7.CrossRefPubMed
35.
go back to reference Suszkiw JB, Murawsky MM, Fortner RC. Heterogeneity of presynaptic calcium channels revealed by species differences in the sensitivity of synaptosomal 45Ca entry to ω-conotoxin. Biochem Biophys Res Commun. 1987;145:1283–6.CrossRefPubMed Suszkiw JB, Murawsky MM, Fortner RC. Heterogeneity of presynaptic calcium channels revealed by species differences in the sensitivity of synaptosomal 45Ca entry to ω-conotoxin. Biochem Biophys Res Commun. 1987;145:1283–6.CrossRefPubMed
36.
go back to reference Patil PN. The classical competitive antagonism of phentolamine on smooth muscle preparations, investigated by two procedures. Auton Autacoids Pharmacol. 2007;27:71–7.CrossRef Patil PN. The classical competitive antagonism of phentolamine on smooth muscle preparations, investigated by two procedures. Auton Autacoids Pharmacol. 2007;27:71–7.CrossRef
37.
go back to reference Tudzynski P, Correia T, Keller U. Biotechnology and genetics of ergot. Appl Microbiol Biotechnol. 2001;57:593–605.CrossRefPubMed Tudzynski P, Correia T, Keller U. Biotechnology and genetics of ergot. Appl Microbiol Biotechnol. 2001;57:593–605.CrossRefPubMed
38.
go back to reference Wang GJ, Liao JF, Kadonk H. Calcium-antagonizing activity of S-petasin, a hypotensive sesquiterpene from Petasites formosanus, on inotropic and chronotropic responses in isolated rat atria and cardiac myocytes. Naunyn Schmiedebergs Arch Pharmacol. 2004;369:322–9.CrossRefPubMed Wang GJ, Liao JF, Kadonk H. Calcium-antagonizing activity of S-petasin, a hypotensive sesquiterpene from Petasites formosanus, on inotropic and chronotropic responses in isolated rat atria and cardiac myocytes. Naunyn Schmiedebergs Arch Pharmacol. 2004;369:322–9.CrossRefPubMed
Metadata
Title
Mechanisms underlying the antihypertensive properties of Urtica dioica
Authors
Rahila Qayyum
Hafiz Misbah-ud-Din Qamar
Shamim Khan
Umme Salma
Taous Khan
Abdul Jabbar Shah
Publication date
01-12-2016
Publisher
BioMed Central
Published in
Journal of Translational Medicine / Issue 1/2016
Electronic ISSN: 1479-5876
DOI
https://doi.org/10.1186/s12967-016-1017-3

Other articles of this Issue 1/2016

Journal of Translational Medicine 1/2016 Go to the issue