Effects of ketamine on contractile responses in vascular smooth muscle.
10.3349/ymj.1990.31.4.325
- Author:
Bok Soon KANG
1
;
Young Ho LEE
;
Taick Sang NAM
;
Dong Soo YEON
;
Soo Kwan HWNG
;
Kye Sook PARK
Author Information
1. Department of Physiology, Younsei University College of Medicine, Seoul, Korea.
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
Ketamine;
vascular smooth muscle contractility;
Ca++ mobilization;
rabbit thoracic aorta
- MeSH:
Animal;
Aorta, Thoracic;
Calcium/pharmacology;
Dose-Response Relationship, Drug;
Female;
Histamine/pharmacology;
Isometric Contraction/drug effects;
Ketamine/*pharmacology;
Male;
Muscle Contraction/*drug effects;
Muscle, Smooth, Vascular/*drug effects;
Norepinephrine/pharmacology;
Rabbits;
Support, Non-U.S. Gov't
- From:Yonsei Medical Journal
1990;31(4):325-332
- CountryRepublic of Korea
- Language:English
-
Abstract:
This study was designed to determine the effects of ketamine on contractions induced by norepinephrine (NE), K+ or histamine (Hist) and on agonist-induced calcium mobilization, in rabbit thoracic aorta with or without endothelium. Contractile responses to NE, K+ or Hist were markedly attenuated by prior exposure to ketamine. Subsequent addition of ketamine to the rabbit aorta undergoing an isometric contraction induced by NE, K+ or Hist also decreased the contractile responses in a calcium ion concentration-dependent manner. Preincubation with ketamine produced a concentration-dependent inhibition of contractile responses elicited by the addition of calcium ion (1.6 mM) to a Ca(++)-free depolarizing solution. However, the phasic contraction produced by NE with 2mM lanthanum pretreatment, which is release of intracellular calcium, was also inhibited by ketamine. Moreover, the tonic contraction produced by NE after depletion of the agonist-releasable pool of intracellular calcium, which is thought to be due to calcium influx, was depressed by ketamine. These data suggest that ketamine relaxes NE-contracted rings of rabbit thoracic aorta by decreasing calcium entry and by producing an extracellular calcium-independent relaxant effect.
