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去甲肾上腺素能和内源性阿片肽途径对雄性大鼠促黄体生成素分泌的调节

Noradrenergic and endogenous opioid pathways in the regulation of luteinizing hormone secretion in the male rat.

作者信息

Miller M A, Clifton D K, Steiner R A

出版信息

Endocrinology. 1985 Aug;117(2):544-8. doi: 10.1210/endo-117-2-544.

Abstract

Endogenous opioid pathways (EOPs) appear to play a role in the tonic regulation of pulsatile LH secretion. The mechanism by which EOPs influence LH release is not known. However, the observation that acute chemical disruption of the noradrenergic (NE) system by alpha-receptor-blocking agents or NE synthesis inhibitors blocks the LH increase occurring in response to naloxone (NAL) suggests that the ability of EOPs to influence LH secretion may depend upon a functional NE system. We hypothesized that if EOPs required an interacting NE system to influence LH secretion, then rats that have ascending NE tract lesions would not respond to NAL with an increase in LH. To test this hypothesis, we challenged NE-lesioned and sham-lesioned rats with NAL. Young adult male rats received either a NE lesion or a sham lesion and 6 weeks later were implanted with jugular catheters. On the following day, four baseline blood samples (400 microliters at 10-min intervals) were taken from NE-lesioned and sham-lesioned rats. All rats were then challenged with 2 mg/kg NAL, iv, and four subsequent blood samples were taken. NAL significantly increased LH levels (P less than 0.01) in both the NE-lesioned (n = 7) and sham-lesioned (n = 8) rats. Mean LH responses above baseline for these groups were 0.52 +/- 0.12 ng RP-2/ml and 0.38 +/- 0.07 ng/ml, respectively. Failure of the NE lesions to block the LH response to NAL was not due to the presence of active residual NE fibers, because pretreatment with the alpha-receptor blocker phenoxybenzamine (20 mg/kg, iv) failed to block the NAL response in the NE-lesioned animals (n = 8), whereas it did so in the sham-lesioned animals (n = 7). The mean LH response from baseline after phenoxybenzamine pretreatment was -0.01 +/- 0.01 ng/ml for the sham-lesioned group and 0.53 +/- 0.24 ng/ml for the NE-lesioned group. These results indicate that EOPs do not require noradrenergic mediation to influence LH secretion in the adult male rat.

摘要

内源性阿片肽通路(EOPs)似乎在促性腺激素释放激素(LH)脉冲式分泌的紧张性调节中发挥作用。EOPs影响LH释放的机制尚不清楚。然而,α受体阻滞剂或去甲肾上腺素(NE)合成抑制剂对去甲肾上腺素能(NE)系统的急性化学破坏会阻断因纳洛酮(NAL)而出现的LH升高,这一观察结果表明,EOPs影响LH分泌的能力可能取决于一个功能性的NE系统。我们假设,如果EOPs需要一个相互作用的NE系统来影响LH分泌,那么上行NE束受损的大鼠对NAL的反应就不会出现LH升高。为了验证这一假设,我们用NAL对NE损伤和假损伤的大鼠进行了挑战。年轻成年雄性大鼠接受了NE损伤或假损伤,6周后植入颈静脉导管。第二天,从NE损伤和假损伤的大鼠身上采集了四个基线血样(每隔10分钟采集400微升)。然后所有大鼠静脉注射2mg/kg NAL进行挑战,并采集随后的四个血样。NAL显著提高了NE损伤组(n = 7)和假损伤组(n = 8)大鼠的LH水平(P < 0.01)。这些组高于基线的平均LH反应分别为0.52±0.12 ng RP-2/ml和0.38±0.07 ng/ml。NE损伤未能阻断LH对NAL的反应并非由于存在活跃的残余NE纤维,因为用α受体阻滞剂苯氧苄胺(20mg/kg,静脉注射)预处理未能阻断NE损伤动物(n = 8)对NAL的反应,而在假损伤动物(n = 7)中则可以阻断。苯氧苄胺预处理后,假损伤组从基线开始的平均LH反应为-0.01±0.01 ng/ml,NE损伤组为0.53±0.24 ng/ml。这些结果表明,在成年雄性大鼠中,EOPs影响LH分泌不需要去甲肾上腺素能介导。

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