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大鼠盐食欲调控中的外侧臂旁核与血清素能机制

Lateral parabrachial nucleus and serotonergic mechanisms in the control of salt appetite in rats.

作者信息

Menani J V, Thunhorst R L, Johnson A K

机构信息

Department of Psychology, University of Iowa, Iowa City 52242-1407, USA.

出版信息

Am J Physiol. 1996 Jan;270(1 Pt 2):R162-8. doi: 10.1152/ajpregu.1996.270.1.R162.

Abstract

This study investigated the effects of bilateral injections of serotonergic receptor agonist and antagonist into the lateral parabrachial nucleus (LPBN) on the ingestion of water and 0.3 M NaCl induced by intracerebroventricular angiotensin II (ANG II) or by combined subcutaneous injections of the diuretic furosemide (Furo) and the angiotensin-converting enzyme inhibitor captopril (Cap). Rats had stainless steel cannulas implanted bilaterally into the LPBN and into the left lateral ventricle. Bilateral LPBN pretreatment with the serotonergic 5-HT1/5-HT2 receptor antagonist methysergide (4 micrograms/200 nl each site) increased 0.3 M NaCl and water intakes induced by intracerebroventricular ANG II (50 ng/microliter) and 0.3 M NaCl intake induced by subcutaneous Furo + Cap. Pretreatment with bilateral LPBN injections of a serotonergic 5-HT2A/2C receptor agonist DOI (5 micrograms/200 nl) significantly reduced 0.3 M NaCl intake induced by subcutaneous Furo + Cap. Pretreatment with methysergide or DOI into the LPBN produced no significant changes in the water intake induced by subcutaneous Furo + Cap. These results suggest that serotonergic mechanisms associated with the LPBN may have inhibitory roles in water and sodium ingestion in rats.

摘要

本研究调查了向外侧臂旁核(LPBN)双侧注射5-羟色胺能受体激动剂和拮抗剂,对由脑室内注射血管紧张素II(ANG II)或联合皮下注射利尿剂速尿(Furo)和血管紧张素转换酶抑制剂卡托普利(Cap)诱导的水和0.3M氯化钠摄取的影响。大鼠双侧植入不锈钢套管,分别通向LPBN和左侧脑室。用5-羟色胺能5-HT1/5-HT2受体拮抗剂美西麦角(每个位点4微克/200纳升)对LPBN进行双侧预处理,可增加由脑室内注射ANG II(50纳克/微升)诱导的0.3M氯化钠和水的摄取量,以及由皮下注射Furo + Cap诱导的0.3M氯化钠摄取量。用5-羟色胺能5-HT2A/2C受体激动剂DOI(5微克/200纳升)对LPBN进行双侧注射预处理,可显著降低由皮下注射Furo + Cap诱导的0.3M氯化钠摄取量。向LPBN注射美西麦角或DOI进行预处理,对由皮下注射Furo + Cap诱导的水摄取量没有显著影响。这些结果表明,与LPBN相关的5-羟色胺能机制可能在大鼠水和钠摄取中起抑制作用。

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