Kappeler L, Gautron L, Layé S, Dantzer R, Zizzari P, Epelbaum J, Bluet-Pajot M T
UMR 549 Inserm, Université-Paris-René-Descartes, Faculté de Médecine, Paris, France.
J Neuroendocrinol. 2006 Jun;18(6):426-33. doi: 10.1111/j.1365-2826.2006.01435.x.
Cocaine- and amphetamine-regulated transcript (CART) mRNA and peptides are abundant in the adenohypophysis, but their role in pituitary function has not yet been elucidated. CART peptides were recently shown to colocalise with luteinising hormone (LH) or prolactin in rat anterior pituitary, and contradictory results concerning the peptide effects on pituitary hormonal secretions were obtained in vitro from pituitary cell cultures. Thus, we reinvestigated the expression of CART mRNA within the pituitary. Immunohistochemistry for pituitary hormones was performed on sections from adult male Wistar rats followed by in situ hybridisation using CART mRNA antisense 35S-labelled probes. The most represented CART-expressing cells were lactotrophs (42 +/- 1% of CART cells) and gonadotrophs (32 +/- 3%), followed by thyrotrophs (10 +/- 2%), corticotrophs (7 +/- 2%) and somatotrophs (6 +/- 1%). In the pars tuberalis, CART mRNA was easily detectable in gonadotrophs and lactotrophs and, to a lesser extent, in corticotrophs and thyrotrophs. CART peptide was quickly and potently released from perifused pituitary by depolarisation (K+ 30 mM for 15 min; 465 +/- 37% over basal release, n = 5). Gonadotrophin-releasing hormone and thyrotrophin-releasing hormone (0.1 microM) were also active to a lesser extent (138 +/- 11% and 71 +/- 17, n = 7, respectively). CART (0.1 microM) did not modify basal LH or prolactin release but selectively inhibited K+-induced LH release without affecting K+-induced prolactin secretion. Pituitary CART mRNA and content were sex dependent and varied during the oestrous cycle, being lower in dioestrous 2. Pituitary CART content also varied widely amongst rat strains being five to six-fold higher in Wistar and Fischer rats compared to Brown Norway and Lou C rats. Ageing differentially affected pituitary CART mRNA and content, resulting in a marked decrease in Lou C and an increase in Wistar and Sprague-Dawley rats. Taken together, these results suggest that pituitary CART expression is dependent of the sex steroid environment and may be physiologically involved in LH secretion.
可卡因和苯丙胺调节转录物(CART)mRNA及肽类在前叶垂体中含量丰富,但其在垂体功能中的作用尚未阐明。最近研究表明,CART肽在大鼠垂体前叶中与促黄体生成素(LH)或催乳素共定位,并且从垂体细胞培养物中体外实验获得了关于该肽对垂体激素分泌影响的相互矛盾的结果。因此,我们重新研究了垂体中CART mRNA的表达情况。对成年雄性Wistar大鼠的切片进行垂体激素免疫组织化学检测,随后使用CART mRNA反义35S标记探针进行原位杂交。表达CART的细胞中占比最多的是催乳素细胞(占CART细胞的42±1%)和促性腺激素细胞(32±3%),其次是促甲状腺激素细胞(10±2%)、促肾上腺皮质激素细胞(7±2%)和生长激素细胞(6±1%)。在结节部,促性腺激素细胞和催乳素细胞中很容易检测到CART mRNA,在促肾上腺皮质激素细胞和促甲状腺激素细胞中检测到的程度较低。通过去极化(30 mM K+处理15分钟)可快速且有效地从灌流垂体中释放CART肽(比基础释放量增加465±37%,n = 5)。促性腺激素释放激素和促甲状腺激素释放激素(0.1 μM)也有一定活性(分别为138±11%和71±17,n = 7)。CART(0.1 μM)不改变基础LH或催乳素的释放,但选择性抑制K+诱导的LH释放,而不影响K+诱导的催乳素分泌。垂体CART mRNA和含量存在性别差异,并且在发情周期中有所变化,在动情后期2含量较低。垂体CART含量在不同大鼠品系中也有很大差异,与棕色挪威大鼠和Lou C大鼠相比,Wistar大鼠和Fischer大鼠中的含量高五到六倍。衰老对垂体CART mRNA和含量的影响不同,导致Lou C大鼠中显著降低,而Wistar大鼠和Sprague-Dawley大鼠中升高。综上所述,这些结果表明垂体CART表达依赖于性类固醇环境,并且可能在LH分泌中发挥生理作用。