首页> 外文期刊>Brain research >The 5-HT(1A) receptor agonist, 8-OH-DPAT, attenuates stress-induced anorexia in conjunction with the suppression of hypothalamic serotonin release in rats.
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The 5-HT(1A) receptor agonist, 8-OH-DPAT, attenuates stress-induced anorexia in conjunction with the suppression of hypothalamic serotonin release in rats.

机译:5-HT(1A)受体激动剂8-OH-DPAT与大鼠下丘脑5-羟色胺释放的抑制作用相结合,可减轻压力引起的厌食症。

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The effect of the selective 5-HT(1A) receptor agonist 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT) on stress-induced anorexia and serotonin (5-HT) release in the rat hypothalamus was studied with brain microdialysis. Subcutaneous injection of 8-OH-DPAT (1 mg/kg) significantly attenuated the immobilization-induced anorexia for 3 h, but had no effect during the following 9 h. Injection of 8-OH-DPAT itself had no effect on basal release of 5-HT, while it significantly blocked the immobilization-induced 5-HT release in the lateral hypothalamus. The results suggest that 8-OH-DPAT attenuated the stress-induced anorexia through the activation of 5-HT(1A) autoreceptors in dorsal raphe nucleus.
机译:选择性5-HT(1A)受体激动剂8-羟基-2-(二-正丙基氨基)四氢萘(8-OH-DPAT)对应激诱导的厌食和5-羟色胺(5-HT)释放的影响下丘脑通过脑微透析进行了研究。皮下注射8-OH-DPAT(1 mg / kg)可以显着减弱固定化引起的厌食症3 h,但在随后的9 h中无效。注射8-OH-DPAT本身对5-HT的基础释放没有影响,但它显着阻断了固定诱导的下丘脑外侧的5-HT释放。结果表明8-OH-DPAT通过活化背缝核中的5-HT(1A)自体受体减弱了应激诱导的厌食症。

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