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一氧化氮参与急性给予锂盐对大鼠胃底非肾上腺素能非胆碱能介导舒张作用的影响。

Nitric oxide involvement in the effect of acute lithium administration on the nonadrenergic noncholinergic-mediated relaxation of rat gastric fundus.

作者信息

Ghasemi Mehdi, Karimollah Ali Reza, Dehpour Ahmad Reza

机构信息

Department of Pharmacology, School of Medicine, Medical Sciences/University of Tehran, Tehran 13145-784, Iran.

出版信息

Nitric Oxide. 2007 Nov-Dec;17(3-4):152-9. doi: 10.1016/j.niox.2007.08.002. Epub 2007 Aug 19.

Abstract

INTRODUCTION

Lithium has largely met its initial promise as the first drug to be discovered in the modern era of psychopharmacology. However, the mechanism for its action remains an enigma. The aim of the present study was to verify the effect of acute lithium administration on the nonadrenergic noncholinergic (NANC)-mediated relaxation of rat isolated gastric fundus and to evaluate the role of nitric oxide pathway in this manner.

MATERIALS AND METHODS

The isolated rat gastric fundus strips were precontracted with 0.5 microM serotonin and electrical field stimulation (EFS) was applied at 5 Hz frequency to obtain NANC-mediated relaxation in the presence or absence of lithium (0.1, 0.5, 1 and 5 mM). Also, effects of combining lithium (0.1 mM) with the NO synthase (NOS) inhibitor L-NAME (0.03 microM) or the guanylyl cyclase inhibitor ODQ (1 microM) on relaxant responses to EFS was investigated. Moreover, effects of combining lithium (1 mM) with 0.1 mM L-arginine (a precursor of NO) on neurogenic relaxation were assessed. Also, the effect of lithium (1 mM) on relaxation to sodium nitroprusside (SNP; 1 nM-0.1 mM) and glyceryltrinitrate (GTN; 0.1-10 microM) was investigated.

RESULTS

The NANC-mediated relaxation was significantly (P<0.001) reduced by lithium in a dose- and time-dependent manner. Combination of lithium (0.1 mM) with L-NAME (0.03 microM), which separately had partial inhibitory effect on relaxations, significantly (P<0.001) reduced the NANC-mediated relaxation of gastric fundus. ODQ (1 microM) significantly inhibited the neurogenic relaxations in the presence or absence of lithium (0.1 and 1 mM). Although L-arginine at 0.1 mM had no effect on relaxation to EFS, it prevented the inhibition by lithium (1 mM) of relaxant responses to EFS. Also, SNP and GTN produced concentration-dependent relaxation in precontracted rat gastric fundus which was not altered by lithium incubation (1 mM).

DISCUSSION

Our experiments indicated that lithium likely by interfering with L-arginine/NO pathway in nitrergic nerve can result in impairment of NANC-mediated relaxation of rat gastric fundus.

摘要

引言

锂作为现代精神药理学时代发现的第一种药物,在很大程度上实现了其最初的前景。然而,其作用机制仍然是个谜。本研究的目的是验证急性给予锂对大鼠离体胃底非肾上腺素能非胆碱能(NANC)介导的舒张作用,并评估一氧化氮途径在此过程中的作用。

材料与方法

将离体大鼠胃底条用0.5微摩尔血清素预收缩,以5赫兹频率施加电场刺激(EFS),在有或无锂(0.1、0.5、1和5毫摩尔)存在的情况下获得NANC介导的舒张。此外,研究了将锂(0.1毫摩尔)与一氧化氮合酶(NOS)抑制剂L-NAME(0.03微摩尔)或鸟苷酸环化酶抑制剂ODQ(1微摩尔)联合使用对EFS舒张反应的影响。此外,评估了将锂(1毫摩尔)与0.1毫摩尔L-精氨酸(一氧化氮的前体)联合使用对神经源性舒张的影响。同时,研究了锂(1毫摩尔)对硝普钠(SNP;1纳摩尔至0.1毫摩尔)和硝酸甘油(GTN;0.1至10微摩尔)舒张作用的影响。

结果

锂以剂量和时间依赖性方式显著(P<0.001)降低了NANC介导的舒张。锂(0.1毫摩尔)与L-NAME(0.03微摩尔)联合使用,它们单独对舒张有部分抑制作用,显著(P<0.001)降低了胃底的NANC介导的舒张。ODQ(1微摩尔)在有或无锂(0.1和1毫摩尔)存在的情况下均显著抑制神经源性舒张。尽管0.1毫摩尔的L-精氨酸对EFS的舒张无影响,但它可防止锂(1毫摩尔)对EFS舒张反应的抑制。此外,SNP和GTN在预收缩的大鼠胃底中产生浓度依赖性舒张,锂孵育(1毫摩尔)对此无改变。

讨论

我们的实验表明,锂可能通过干扰含氮神经中的L-精氨酸/一氧化氮途径,导致大鼠胃底NANC介导的舒张受损。

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