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一氧化氮合酶抑制剂诱导大鼠胃排空延迟。

Delayed gastric emptying induced by inhibitors of nitric oxide synthase in rats.

作者信息

Plourde V, Quintero E, Suto G, Coimbra C, Taché Y

机构信息

CURE/UCLA Digestive Disease Center, VA Medical Center.

出版信息

Eur J Pharmacol. 1994 Apr 21;256(2):125-9. doi: 10.1016/0014-2999(94)90236-4.

Abstract

The effect of the nitric oxide (NO) synthase inhibitor, NG-nitro-L-arginine methyl ester, on gastric emptying of a non-nutrient solution was investigated in conscious rats. NG-Monomethyl-L-arginine (10 mg/kg i.v.) and NG-nitro-L-arginine methyl ester (3 or 10 mg/kg i.v.) inhibited the 20-min rate of gastric emptying of liquids by 34%, 69% and 84% respectively, whereas the 0.3 mg/kg of NG-nitro-L-arginine methyl ester or 3 mg/kg of NG-monomethyl-L-arginine had no effect. The inhibitory effect of NG-nitro-L-arginine methyl ester (3 mg/kg) was prevented by L-arginine (300 mg/kg i.v.), but not by D-arginine (300 mg/kg i.v.). NG-Nitro-L-arginine methyl ester (0.3-10 mg/kg) induced a dose-related increase in mean blood pressure up to 161 +/- 10 mm Hg. Spontaneous hypertensive rats with a mean blood pressure of 180 +/- 5 mm Hg had a gastric emptying rate of 51.9 +/- 6.1%. These data indicate that NO synthase inhibitors given i.v. at doses that inhibit NO synthase, delay gastric emptying through mechanisms which are unrelated to changes in arterial blood pressure.

摘要

在清醒大鼠中研究了一氧化氮(NO)合酶抑制剂NG-硝基-L-精氨酸甲酯对非营养溶液胃排空的影响。NG-单甲基-L-精氨酸(10毫克/千克静脉注射)和NG-硝基-L-精氨酸甲酯(3或10毫克/千克静脉注射)分别使液体的20分钟胃排空率降低34%、69%和84%,而0.3毫克/千克的NG-硝基-L-精氨酸甲酯或3毫克/千克的NG-单甲基-L-精氨酸则无作用。L-精氨酸(300毫克/千克静脉注射)可阻止NG-硝基-L-精氨酸甲酯(3毫克/千克)的抑制作用,但D-精氨酸(300毫克/千克静脉注射)则不能。NG-硝基-L-精氨酸甲酯(0.3 - 10毫克/千克)可使平均血压呈剂量相关升高,最高可达161±10毫米汞柱。平均血压为180±5毫米汞柱的自发性高血压大鼠的胃排空率为51.9±6.1%。这些数据表明,静脉注射抑制NO合酶的剂量的NO合酶抑制剂,通过与动脉血压变化无关的机制延迟胃排空。

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