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内侧视前区6-羟基多巴胺损伤后的雄性大鼠交配行为:对重复给药的耐受性及行为的快速恢复

Male rat copulation following 6-OHDA lesions of the medial preoptic area: resistance to repeated administration and rapid behavioral recovery.

作者信息

Bazzett T, Lumley L, Bitran D, Markowski V, Warner R, Hull E

机构信息

Department of Psychology, SUNY, Buffalo 14260.

出版信息

Brain Res. 1992 May 15;580(1-2):164-70. doi: 10.1016/0006-8993(92)90940-b.

Abstract

Dopamine (DA) in the medial preoptic area (MPOA) has been shown to facilitate male rat sexual behavior. However, injections of the catecholamine (CA) neurotoxin 6-OHDA into the MPOA did not impair copulation in tests 3 days after injection. In the present study, three weekly (serial) injections produced no copulatory deficits compared to animals that received a single injection or to preinjection copulatory behavior scores. However, blocking CA synthesis, which did not impair control rats, produced deficits in both single and serial lesion animals, with significantly fewer serial than single lesion animals initiating copulation. Biochemical analysis of tissue punches showed no difference in MPOA concentrations of dopamine, norepinephrine, epinephrine, or the dopamine metabolite DOPAC between the two groups. Additional animals were tested at earlier intervals after 6-OHDA injections into the MPOA. Tests conducted 30 min after an MPOA injection of 6-OHDA revealed that all measures of copulation were impaired, relative to scores 24 h later. However, these scores were not significantly different from animals tested 30 min after a vehicle injection. A final group, tested 4 h after injection, showed impairment of all measures of copulation compared to vehicle injections and to tests 24 h later. Furthermore, in the tests 24 h later, 6-OHDA animals were not different from vehicle animals. Results from all experiments show that 6-OHDA injections into the MPOA impair copulation for at least 4 h, but that behavioral recovery is complete 24 h later. However, deficits can be reinstated by inhibiting DA synthesis, suggesting that increased synthesis in undamaged terminals contributed to behavioral recovery.

摘要

内侧视前区(MPOA)中的多巴胺(DA)已被证明可促进雄性大鼠的性行为。然而,向MPOA注射儿茶酚胺(CA)神经毒素6-羟基多巴胺(6-OHDA)后3天的测试中,并未损害交配行为。在本研究中,与接受单次注射的动物或注射前的交配行为评分相比,每周进行三次(连续)注射并未产生交配缺陷。然而,抑制CA合成(这对对照大鼠没有损害)在单次和连续损伤的动物中均产生了缺陷,开始交配的连续损伤动物明显少于单次损伤动物。组织打孔的生化分析显示,两组之间MPOA中的多巴胺、去甲肾上腺素、肾上腺素或多巴胺代谢物3,4-二羟基苯乙酸(DOPAC)的浓度没有差异。在向MPOA注射6-OHDA后,对其他动物在更早的时间间隔进行了测试。在MPOA注射6-OHDA后30分钟进行的测试显示,与24小时后的评分相比,所有交配指标均受到损害。然而,这些评分与注射溶媒后30分钟测试的动物没有显著差异。最后一组在注射后4小时进行测试,与注射溶媒以及24小时后测试相比,所有交配指标均受到损害。此外,在24小时后的测试中,6-OHDA处理的动物与溶媒处理的动物没有差异。所有实验结果表明,向MPOA注射6-OHDA至少在4小时内会损害交配行为,但24小时后行为恢复完全。然而,通过抑制DA合成可以恢复缺陷,这表明未受损终末中合成的增加有助于行为恢复。

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