Ex-vivo antihypertensive and calcium channel blocking activity of Androsace foliosa n-hexane leaves fraction on isolated rabbit aorta.

Journal: Pakistan journal of pharmaceutical sciences
PMID:

Abstract

Hypertension is persistent elevation in blood pressure for 3-4 weeks. Estimated global prevalence of hypertension suggested that by the Year 2025 (29%) of adult worldwide are suffering from hypertension (1.56 billion). Hypertension complications are hemorrhage, atherosclerosis, renal artery stenosis, angina pectoris end organ damage, cardiomyopathy, myocardial infarction and retinopathy. Along with other drug class Calcium channel blocker are also used for the treatment of hypertension. In this study the possible action of the n-hexane leaves fraction of the Androsace foliosa on isolated rabbit aorta was examined. Antihypertensive activity was examined in the existence of standard agonist like phenylephrine and antagonist like Verapamil. Phenylephrine (PE 1μM) high K was used to steady the tissue materials. Additionally to observe the calcium channel blocking effect the tissues were treated with n-hexane segment of A. foliosa leaves. Aortic tissues were treated 4-5intervals with Ca free preparation earlier to control calcium reaction curve (CRCs). Verapamil is utilized as standard calcium channel inhibitory mediator and is used as an antagonist. The Af. n-hexane leaves fraction completely inhibited the precontractions induced by Phenylephrine (1μM) and K (80 mM) precontractions, with EC standards of 1.0mM (0.3-1.0mg/mL) and 4.90mM (1-3mg/mL), respectively. Androsace foliosa n-hexane leaves fraction was tested for calcium channel inhibitory effect on isolated rabbit aorta. A. foliosa n- hexane leaves segment at the dosage of 1mg/mL block the calcium channel approximately (35±5%). Consequence indicates that A. foliosa n-hexane leaves segment block calcium channel in the similar manner as compared to the standard calcium channel blocker drug (verapamil).

Authors

  • Jawad Zaheer
    Department of Pharmacy, University of Poonch, Rawalakot, Azad Kashmir, Pakistan.
  • Abida Kausar
    Department of Botany, Government College Women University, Faisalabad, Pakistan.
  • Hina Kanwal
    Department of Botany, Government College Women University, Faisalabad, Pakistan.
  • Noreen Akhtar
    Department of Botany, Government College Women University, Faisalabad, Pakistan.
  • Aisha Ilyas
    Department of Botany, Government College Women University, Faisalabad, Pakistan.
  • Zil-I-Huma Nazlli
    Department of Chemistry, Government College Women University, Faisalabad.
  • Ayesha Riaz
    Department of Zoology, Government College Women University, Faisalabad, Pakistan.
  • Syed Muhammad Ali Shah
    Department of Eastern Medicine, Government College University, Faisalabad, Pakistan.
  • Muhammad Akram
    Department of Eastern Medicine, Government College University, Faisalabad, Pakistan.
  • Muhammad Usman Sarwar
    Department of Eastern Medicine, Government College University, Faisalabad, Pakistan.
  • Abdul Hamid Khan
    Department of Eastern Medicine, University of Poonch, Rawalakot Azad Kashmir, Pakistan.
  • Fahad Said Khan
    Department of Eastern Medicine, Government College University, Faisalabad, Pakistan.
  • Farhan Asad
    Department of Eastern Medicine, Government College University, Faisalabad, Pakistan.
  • Hina Anwar
    Department of Eastern Medicine, Government College University, Faisalabad, Pakistan.
  • Madeeha Anwar
    Department of Microbiology, Government College University, Faisalabad, Pakistan.