Attenuation of methylation of catecholamines and treatment with a coenzyme of catechol-O-methyltransferase in spontaneously hypertensive rats (SHR)

被引:17
作者
Imai, K
Tsunoda, M
Takezawa, K
Mitsuhashi, K
Santa, T
Nagashima, K
Katayama, K
Ohmori, K
机构
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Bunkyo Ku, Tokyo 1130033, Japan
[2] Kyowa Hakko Kogyo Co Ltd, Drug Dev Res Labs, Pharmaceut Res Inst, Nagaizumi, Shizuoka 4118731, Japan
来源
PROCEEDINGS OF THE JAPAN ACADEMY SERIES B-PHYSICAL AND BIOLOGICAL SCIENCES | 1999年 / 75卷 / 07期
关键词
norepinephrine; catechol-O-methyltransferase; blood pressure; S-adenosyl-L-methionine; hypertension;
D O I
10.2183/pjab.75.224
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We have previously demonstrated that the release of plasma norepinephrine (NE) in response to blood pressure reduction induced by calcium antagonist was substantially decreased in spontaneously hypertensive rats (SHR), as compared to the age-matched normotensive Wistar Kyoto (WKY) rats. Here we examined extraneuronal methylation of NE: to normetanephrine (NLN) by catechol-O-methyl-transferase (COMT). In the face of an acute hypotension by benidipine, the ratio of the increase of NMN to the increase of NE in plasma was lower in SHR than in WKY rat. The finding suggests that the extraneuronal inactivation of the released NE is blunted in SHR, namely, COMT is deactivated in this hypertensive rats. To define the role of NE methylation in hypertension, S-adenosyl-L-methionine (SAMe; 1.0 mg/kg, i.v.), a coenzyme of COMT, was administered to SHR. The treatment induced a greater antihypertensive effect, along with a greater decrease of NE and a larger increase of NMN in SHR. The data suggest that SAMe may be used as a possible remedy for hypertension.
引用
收藏
页码:224 / 227
页数:4
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