Effect of diazepam on the oxytocin induced contraction of the isolated rat uterus.
10.12701/yujm.1992.9.2.359
- Author:
Yoon Kee PARK
;
Sung Ho LEE
;
Oh Cheol KWON
;
Jeoung Hee HA
;
Kwang Youn LEE
;
Won Joon KIM
- Publication Type:Original Article
- Keywords:
Uterus;
GABA;
Contractility;
Diaszepam;
Calcium;
A23187
- MeSH:
Animals;
Baclofen;
Bicuculline;
Calcimycin;
Calcium;
Diazepam*;
Dislocations;
Estrogens;
Female;
GABA Agonists;
GABA-A Receptor Agonists;
GABA-A Receptor Antagonists;
GABA-B Receptor Agonists;
GABA-B Receptor Antagonists;
gamma-Aminobutyric Acid;
Humans;
Muscimol;
Ovariectomy;
Oxytocin*;
Picrotoxin;
Rats*;
Receptors, GABA;
Uterus*
- From:Yeungnam University Journal of Medicine
1992;9(2):359-381
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
This study was designed to investigate the effect of diazepam on the spontaneous contraction and oxytocin induced contraction of the isolated rat uterus. Female rat (Sprague-Dawley) pretreated with oophorectomy and 4 days administration of estrogen. Weighing about 200 g, was sacrificed by cervical dislocation, and the uteruses were isolated. A longitudinal muscle strip was placed in temperature controlled (37℃) muscle chamber containing Locke's solution and myographied isometrically. Diazepam inhibited the spontaneous contraction and oxytocin induced contraction of the isolated rat uterus in a concentration-dependent manner. GABA, muscimol, a GABA A receptor agonist, bicuculline, a competitive GABA A receptor antagonist, picrotoxin, a non competitive GABA A receptor antagonist, baclofen, a GABA B receptor agonist, and delta-aminovaleric acid, a GABA B receptor antagonist, did not affect on the spontaneous and oxytocin induced contraction of the isolated rat uterus. The inhibitory actions of diazepam on the spontaneous and oxytocin induced contraction were not affected by all the GABA receptor agonists and antagonists, but exceptionally potentiated by bicuculline. This potentiation-effect by bicuculline was not antagonized by muscumol. In normal calcium PSS, addition of calcium restored the spontaneous contraction preinhibited by diazepam and recovered the contractile of oxtrocin preinhibited by diazepam. A23187, a calcium inophore, enhanced the restoration of both the spontaneous and oxytocin induced contraction by addition of calcium. In calcium-free PSS, diazepam suppressed the restoration of spontaneous motility by addition of calcium but allowed the recovery of spontaneous motility to a considerable extent. Diazepam could not inhibit some development of contractility by oxytocin in calcium-free PSS, but inhibited the increase in contractility by subsequent addition of calcium. These results suggest that the inhibitory action of diazepam on the rat uterine motility does not depend on or related to GABA receptors and that diazepam inhibits the extracellular calcium influx to suppress the spontaneous and oxytocin induced contractilities.
