Effects of inhibitors of nitric oxide synthase on isolated uteri of fasting rats

被引:4
作者
Campos, ML [1 ]
Casalino-Matsuda, SM [1 ]
Linares, JA [1 ]
Goldraij, A [1 ]
机构
[1] Univ Nacl Cordoba, Fac Odontol, Catedra Fisiol, RA-5000 Cordoba, Argentina
来源
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS | 1998年 / 59卷 / 01期
关键词
D O I
10.1016/S0952-3278(98)90048-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The effects of inhibitors of nitric oxide synthase on the glucose metabolism of uteri isolated from 4-day underfed rats were studied. In control rats receiving normal feeding, the addition of indomethacin (5 x 10(-6) M); acetyl salicylic acid (10(-4)M); 400 mu M of N(G-)methyl-L-arginine, (L-NMMA) or 400 mu M of sodium nitroprusside (SNP), does not modify the production of (CO2)-C-14 from (UC)-C-14-glucose. On the contrary, in fasted rat uteri, indomethacin increases glucose oxidation significantly, while acetyl salicylic acid does not alter it. Also, the addition of L-NMMA has no effect. In another group of experiments, in the preparations containing indomethacin of uteri isolated from underfed rats, the addition of L-NMMA significantly changes the effect of indomethacin. Another inhibitor of nitric oxide synthase, N omega nitro-L-arginine methyl ester (L-NAME), or hemoglobin (2 mu g ml(-1)) a nitric oxide scavenger have the same effects while N omega nitro arginine-D-methyl ester (D-NAME) does not. However (SNP), a nitric oxide donor, does not alter the production of (CO2)-C-14 in uteri isolated from fasted rats. These results show that in underfed rats, indomethacin increases glucose oxidation independently from its inhibiting effect on cyclooxygenase. Specific inhibitors of nitric oxide synthase can reverse this effect.
引用
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页码:23 / 26
页数:4
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