Clin Hypertens.  2014 ;20(3):6. 10.1186/s40885-014-0006-1.

Depressor action and vasorelaxation of methylene chloride fraction extracted from Rubus coreanum

Affiliations
  • 1Department of Anesthesiology and Pain Medicine, School of Medicine, Chosun University, Gwangju, Korea.
  • 2Department of Leisure and Sport, College of Public Health and Welfare, Dongshin University, Naju, Korea.
  • 3Department of Pharmacology, School of Medicine, Chosun University, 309 Pilmun-daero, Dong-gu, Gwangju 501-759, Korea. dylim@chosun.ac.kr

Abstract

INTRODUCTION
The present study was designed to examine whether methylene chloride (CH2Cl2) fraction extracted from Rubus coreanum affects the contractility of the isolated thoracic aortic strips and blood pressure of normotensive rats.
METHODS
One of the common carotid arteries or of the femoral arteries was catheterized with a polyethylene tubing. The tubing was connected to a pressure transducer, and pulse of the mean arterial blood pressure was recorded on a biological polygraph continuously.
RESULTS
The CH2Cl2 fraction (range, 200 to 800 microg/mL) significantly depressed both phenylephrine (PE, 10 microM)- and high K+ (56 mM)-induced contractile responses of the isolated thoracic aortic strips in a concentration-dependent fashion. In the simultaneous presence of N(omega)-nitro-L-arginine methyl ester hydrochloride (L-NAME) (an inhibitor of nitric oxide [NO] synthase, 300 microM) and the CH2Cl2 fraction (400 microg/mL), both PE- and high K+-induced contractile responses were recovered to the significant level of the corresponding control response in comparison with inhibition of CH2Cl2 fraction treatment alone. Moreover, in the simultaneous presence of the CH2Cl2 fraction after pretreatment with 0.4% CHAPS (3-[(3-cholamidopropyl) dimethylammonio]-1-propane sulfonate), both PE- and high K+-induced contractile responses were recovered to the significant level of the corresponding control response compared to the inhibitory response of CH2Cl2 fraction treatment alone. Also, in anesthetized rats, the CH2Cl2 fraction (range, 0.3 to 3.0 mg/kg) injected into a femoral vein dose-dependently produced depressor responses. This hypotensive action of the CH2Cl2 fraction was greatly inhibited after treatment with phentolamine (1 mg/kg), chlorisondamine (1 mg/kg), L-NAME (3 mg/kg/30 min), or sodium nitroprusside (30 microg/kg/30 min). Intravenous infusion of the CH2Cl2 fraction (range, 1.0 to 10.0 mg/kg/30 min) markedly inhibited norepinephrine-induced pressor responses. DISCUSSION: Taken together, these results demonstrate that the CH2Cl2 fraction causes vascular relaxation in the isolated rat thoracic aortic strips as well as hypotensive action in anesthetized rats. These vasorelaxation and hypotension of the CH2Cl2 fraction seem to be mediated at least by the increased NO production through the activation of NO synthase of the vascular endothelium and the inhibitory adrenergic modulation.

Keyword

Rubus coreanum (Bokboonja); Methylene chloride (CH2Cl2) fraction; Vasorelaxation; Depressor action; Adrenergic alpha1-receptor blockade; Activation of NO synthase

MeSH Terms

Animals
Arterial Pressure
Blood Pressure
Carotid Artery, Common
Catheters
Chlorisondamine
Endothelium, Vascular
Femoral Artery
Femoral Vein
Hypotension
Infusions, Intravenous
Methylene Chloride*
NG-Nitroarginine Methyl Ester
Nitric Oxide
Nitric Oxide Synthase
Nitroprusside
Phentolamine
Phenylephrine
Polyethylene
Rats
Relaxation
Transducers, Pressure
Vasodilation*
Chlorisondamine
Methylene Chloride
NG-Nitroarginine Methyl Ester
Nitric Oxide
Nitric Oxide Synthase
Nitroprusside
Phentolamine
Phenylephrine
Polyethylene
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