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对因8-OH-DPAT敏感性不同而培育的大鼠进行脑5-HT1A受体放射自显影及低温反应研究。

Brain 5-HT1A receptor autoradiography and hypothermic responses in rats bred for differences in 8-OH-DPAT sensitivity.

作者信息

Knapp D J, Overstreet D H, Crews F T

机构信息

Skipper Bowles Center for Alcohol Studies, University of North Carolina School of Medicine, Chapel Hill, NC 27599-7178, USA.

出版信息

Brain Res. 1998 Jan 26;782(1-2):1-10. doi: 10.1016/s0006-8993(97)01127-x.

Abstract

Three rat lines were selectively bred for high (HDS), random (RDS), or low (LDS) hypothermic responses to the specific 5-HT1A receptor agonist 8-OH-DPAT. Forty-five minutes after 8-OH-DPAT administration (0.5 mg/kg), body temperatures dropped 3-5 degrees C in HDS rats, yet this dose produced only about 1.2 degrees C and 0.7 degree C drops in RDS and LDS rats, respectively. To investigate the relationship of body temperature of 5-HT1A receptor binding sites, autoradiographic analyses of [3H]8-OH-DPAT binding to 5-HT1A receptors in brains of these rats were conducted. Significant differences in binding were found in specific limbic cortical projection sites, with the HDS line having the greatest density of sites. Body temperature responses correlated significantly with [3H]8-OH-DPAT receptor binding in only a few areas of frontal cortex. Binding in many other brain regions, including the anterior and posterior hypothalami (regions long associated with body temperature regulation) and the raphe showed no significant differences among the lines. [3H]Ketanserin binding to cortical 5-HT2 receptors did not differ among the lines, except in the cingulate and superficial frontal cortices where HDS exhibited higher binding. These data suggest that differences in 5-HT1A receptor number may contribute to the exaggerated hypothermic response to 8-OH-DPAT in HDS rats. These studies also suggest that genetic regulation of receptor density may be brain region specific which should encourage future studies of the mechanisms of 5-HT1A receptor activity in brain and the action of drugs affecting this receptor.

摘要

三种大鼠品系被选择性培育,分别对特定的5-羟色胺1A受体激动剂8-羟基二苯丙胺(8-OH-DPAT)产生高体温降低反应(HDS)、随机体温降低反应(RDS)或低体温降低反应(LDS)。给予8-OH-DPAT(0.5毫克/千克)45分钟后,HDS大鼠的体温下降了3 - 5摄氏度,而该剂量在RDS和LDS大鼠中分别仅导致约1.2摄氏度和0.7摄氏度的体温下降。为了研究5-羟色胺1A受体结合位点的体温关系,对这些大鼠大脑中[3H]8-OH-DPAT与5-羟色胺1A受体的结合进行了放射自显影分析。在特定的边缘皮质投射位点发现结合存在显著差异,HDS品系的位点密度最大。体温反应仅在额叶皮质的少数区域与[3H]8-OH-DPAT受体结合显著相关。在许多其他脑区,包括与体温调节长期相关的下丘脑前部和后部以及中缝核,品系间的结合没有显著差异。[3H]酮色林与皮质5-羟色胺2受体的结合在品系间没有差异,除了在扣带回和额叶浅皮质,HDS表现出更高的结合。这些数据表明,5-羟色胺1A受体数量的差异可能导致HDS大鼠对8-OH-DPAT的过度体温降低反应。这些研究还表明,受体密度的基因调控可能具有脑区特异性,这应该会促进未来对脑内5-羟色胺1A受体活性机制以及影响该受体的药物作用的研究。

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