Study on vascular mechanisms underlying the hypotensive effect of Sorghum halepense (L.) Pers.


Journal

Pakistan journal of pharmaceutical sciences
ISSN: 1011-601X
Titre abrégé: Pak J Pharm Sci
Pays: Pakistan
ID NLM: 9426356

Informations de publication

Date de publication:
Sep 2020
Historique:
entrez: 9 4 2021
pubmed: 10 4 2021
medline: 19 11 2021
Statut: ppublish

Résumé

Sorghum halepense L (Poaceae), ordinarily it is known as Johnson grass and locally as baru. This study was designed to find the vascular mechanisms underlying the hypotensive activity of S. halepense. In this study, effect of S. halepense seed extract/fractions on various blood pressure parameters were evaluated in normal and fructose induced hypertensive rats by invasive technique. Possible underlying hypotensive mechanism of active fraction was determined by using various pharmacological inhibitors. S. halepense extract/fractions vasorelaxant effect were also evaluated on rat aorta rings in organ bath and various intracellular signaling pathway inhibitors were used for determination of underlying mechanisms. S. halepense extract/fractions produced blood pressure lowering effect with most significant effect by its aqueous soluble fraction at dose of 10mg/kg. This effect was attenuated by pretreatment of atropine. Aqueous soluble fraction produced endothelium dependent vasorelaxation in rat aortic rings that was inhibited by pretreatment of atropine after phenylephrine induced contraction. The vasorelaxant effect of aqueous soluble fraction was attenuated by potassium channel blockers and also produced inhibitory effect on calcium entry through calcium channels. It also suppressed phenylephrine induced contraction like verapamil. By HPLC analysis found vanillic acid and naringinin in it. In conclusion, aqueous soluble fraction of S.halepense possess phytoconstituents which may be responsible for hypotensive and vasorelaxant effect of Sorghum halepense.

Identifiants

pubmed: 33832894

Substances chimiques

Antihypertensive Agents 0
Flavanones 0
Plant Extracts 0
Vasodilator Agents 0
Fructose 30237-26-4
Vanillic Acid GM8Q3JM2Y8
naringenin HN5425SBF2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2219-2230

Auteurs

Amna Batool (A)

Department of Pharmacology Faculty of Pharmaceutical Sciences, Government College University Faisalabad, Pakistan.

Muhammad Saleem (M)

Department of Pharmacology Faculty of Pharmaceutical Sciences, Government College University Faisalabad, Pakistan/Punjab University college of Pharmacy, University of the Punjab, Lahore, Pakistan.

- Alamgeer (-)

Punjab University college of Pharmacy, University of the Punjab, Lahore, Pakistan.

Hafiz Muhammad Irfan (HM)

Laboratory of Cardiovascular Research and Integrative Pharmacology, College of Pharmacy, University of Sargodha, Pakistan.

Waqas Younis (W)

Department of Pharmacy The University of Lahore, Lahore.

Nasser Hadal Alotaibi (NH)

College of Pharmacy, Jouf University, Aljouf, Sakaka, Saudi Arabia.

Khalid Saad Alharbi (KS)

College of Pharmacy, Jouf University, Aljouf, Sakaka, Saudi Arabia.

Syed Nasir Abbas Bukhari (SNA)

College of Pharmacy, Jouf University, Aljouf, Sakaka, Saudi Arabia.

Marcello Locatelli (M)

Department of Pharmacy, University G. Annunzio of Chieti-Pescara, Chieti, Italy.

Hammad Saleem (H)

Institute of Pharmaceutical Sciences (IPS), University of Veterinary & Animal Sciences (UVAS), Lahore, Pakistan.

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Classifications MeSH