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大鼠脑片背侧中缝核和下丘脑前部神经元上不同类型的蛙皮素受体(体外实验)

Different types of bombesin receptors on neurons in the dorsal raphe nucleus and the rostral hypothalamus in rat brain slices in vitro.

作者信息

Pinnock R D, Reynolds T, Woodruff G N

机构信息

Parke Davis Neuroscience Research Unit, Addenbrookes Hospital Site, Cambridge, UK.

出版信息

Brain Res. 1994 Aug 8;653(1-2):119-24. doi: 10.1016/0006-8993(94)90379-4.

DOI:10.1016/0006-8993(94)90379-4
PMID:7982044
Abstract

The actions of the peptides bombesin (BN), gastrin releasing peptide (GRP), neuromedin C (NMC), litorin and neuromedin B (NMB) were studied on neurons in slices of rat brain maintained in vitro to determine the BN receptor type present in different brain areas. Intracellular and extracellular recordings were made from hypothalamic neurons on the border of the periventricular nucleus (PVN) and suprachiasmatic nucleus (SCN) and from mesencephalic 5-HT sensitive neurons in the dorsal raphe nucleus. In the region of the brain containing the SCN and PVN, BN and the BN-related peptides excited 31 out of 77 neurons on which they were tested. There was little difference in the potency of the BN-related peptides as excitants of neurons, the EC50 being about 10 nM. The response to the peptides usually lasted between 5 and 15 min with little sign of desensitization. Using NMC, GRP and NMB as agonists, the equilibrium constant for the GRP receptor antagonist [D-Phe6]-BN-(6-13)-ethylamide was approximately 10 nM. The response to the peptides fully recovered on washout of the antagonist. The CCKB/gastrin receptor antagonist CI-988 (1 microM) had no effect on either GRP- or NMC-mediated excitation. In the dorsal nucleus 40 of 75 neurons were sensitive to the BN-related peptides. BN, [Tyr4]-BN, NMB and litorin, were 10-20 times more potent than GRP and NMC. The responses to the BN-related peptides were not blocked by the selective GRP receptor antagonists [D-Phe6]-BN-(6-13)-methylester, [DF5Phe6][D-Ala11]-BN-(6-13)-methylester and [D-Phe6]-BN-(6-13)- ethylamide.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

研究了蛙皮素(BN)、胃泌素释放肽(GRP)、神经介素C(NMC)、雨蛙肽和神经介素B(NMB)对体外培养的大鼠脑片神经元的作用,以确定不同脑区存在的BN受体类型。对位于室旁核(PVN)和视交叉上核(SCN)边界的下丘脑神经元以及中脑背缝核中5-羟色胺敏感神经元进行了细胞内和细胞外记录。在含有SCN和PVN的脑区,BN及与BN相关的肽在77个被检测的神经元中兴奋了31个。作为神经元兴奋剂,与BN相关的肽的效力差异不大,半数有效浓度(EC50)约为10 nM。对这些肽的反应通常持续5至15分钟,几乎没有脱敏迹象。使用NMC、GRP和NMB作为激动剂,GRP受体拮抗剂[D-苯丙氨酸6]-BN-(6-13)-乙酰胺的平衡常数约为10 nM。拮抗剂洗脱后,对肽的反应完全恢复。胆囊收缩素B/胃泌素受体拮抗剂CI-988(1 microM)对GRP或NMC介导的兴奋均无影响。在背核中,75个神经元中有40个对与BN相关的肽敏感。BN、[酪氨酸4]-BN、NMB和雨蛙肽的效力比GRP和NMC强10至20倍。对与BN相关的肽的反应未被选择性GRP受体拮抗剂[D-苯丙氨酸6]-BN-(6-13)-甲酯、[DF5苯丙氨酸6][D-丙氨酸11]-BN-(6-13)-甲酯和[D-苯丙氨酸6]-BN-(6-13)-乙酰胺阻断。(摘要截断于250字)

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