Department of Physiology, Mail Code 6523, School of Medicine, Southern Illinois University, Carbondale, IL 62901, USA.
Neuroscience. 2010 Mar 17;166(2):359-67. doi: 10.1016/j.neuroscience.2009.12.066. Epub 2010 Jan 4.
Endogenous opioid peptides are involved in prolactin release during lactation, in part by decreasing tuberoinfundibular dopaminergic (TIDA) neuronal activity. Both mu (mu) and kappa (kappa) opioid receptors have a role in the suckling-induced prolactin rise after 4-5 h up deprivation. The aim of this study was to investigate effects of mu opioid receptor antagonist, beta-funaltrexamine (beta-FNA), and kappa opioid receptor antagonist, nor-binaltorphimine (nor-BNI), on prolactin secretion and TIDA neuronal activity in lactating rats after 18 h pup deprivation. After 4 h separation from pups, the suckling-induced prolactin rise was abolished by 16 microg nor-BNI and 5 microg beta-FNA, coincident with increased dihydroxyphenylacetic acid (DOPAC):dopamine ratio in the stalk-median eminence (SME). However, after 18 h pups separation, these same doses of nor-BNI and beta-FNA did not alter the prolactin surge or DOPAC:dopamine ratios in the SME. Higher doses of nor-BNI (32 microg) and beta-FNA (10 microg) were required to inhibit suckling-induced prolactin secretion. beta-FNA (10 microg) increased the DOPAC:dopamine ratio in the SME, whereas nor-BNI (32 microg) treatment had no effect. The mu and kappa opioid receptor mRNA levels in the mediobasal hypothalamus were similar to suckled control rats after 4 h pup deprivation, but increased 1.4-fold after 18 h pup deprivation. These data support involvement of endogenous opioidergic systems in the suckling-induced prolactin rise after a prolonged (18 h) period of pup deprivation, as well as the shorter (4 h) pup deprivation period previously reported. Suppression of TIDA neuronal activity likely played a part in mu opioid receptor input to the suckling-induced prolactin rise after both 4 h and 18 h separation, whereas non-dopaminergic input was implicated with kappa opioid receptors after 18 h pup deprivation. Increased mu and kappa opioid receptors gene expression in the mediobasal hypothalamus may contribute to reduced effectiveness of opioid receptor antagonists to block suckling-induced prolactin release after 18 h pup deprivation.
内源性阿片肽参与哺乳期催乳素的释放,部分通过降低结节漏斗多巴胺能(TIDA)神经元的活性。μ(μ)和κ(κ)阿片受体在 4-5 小时吸吮诱导的催乳素升高中都有作用。本研究的目的是研究μ阿片受体拮抗剂β-氟纳曲胺(β-FNA)和κ阿片受体拮抗剂诺比那嗪(nor-BNI)对哺乳期大鼠在 18 小时幼仔剥夺后的催乳素分泌和 TIDA 神经元活性的影响。在与幼仔分离 4 小时后,16μg nor-BNI 和 5μg β-FNA 消除了吸吮诱导的催乳素升高,同时纹状体-中脑导水管周围灰质(SME)中二羟苯乙酸(DOPAC):多巴胺比值增加。然而,在 18 小时幼仔分离后,相同剂量的 nor-BNI 和β-FNA 并未改变 SME 中的催乳素激增或 DOPAC:多巴胺比值。更高剂量的 nor-BNI(32μg)和β-FNA(10μg)被需要抑制吸吮诱导的催乳素分泌。β-FNA(10μg)增加了 SME 中的 DOPAC:多巴胺比值,而 nor-BNI(32μg)处理则没有影响。中脑基底部的μ和κ阿片受体 mRNA 水平在与幼仔分离 4 小时后与哺乳对照组相似,但在与幼仔分离 18 小时后增加了 1.4 倍。这些数据支持内源性阿片肽系统参与了在长时间(18 小时)幼仔剥夺后吸吮诱导的催乳素升高,以及先前报道的较短(4 小时)幼仔剥夺期。TIDA 神经元活性的抑制可能在与幼仔分离 4 小时和 18 小时后对μ阿片受体输入到吸吮诱导的催乳素升高中起作用,而在 18 小时幼仔剥夺后则涉及非多巴胺能输入。中脑基底部 μ和κ阿片受体基因表达的增加可能导致在 18 小时幼仔剥夺后,阿片受体拮抗剂阻断吸吮诱导的催乳素释放的效果降低。