Torsello A, Grilli R, Luoni M, Guidi M, Ghigo M C, Wehrenberg W B, Deghenghi R, Müller E E, Locatelli V
Department of Pharmacology, School of Medicine, University of Milan, Italy.
Eur J Endocrinol. 1996 Oct;135(4):481-8. doi: 10.1530/eje.0.1350481.
We have reported Hexarelin (HEXA), an analog of growth hormone-releasing peptide 6 (GHRP-6), potently stimulates growth hormone (GH) secretion in infant and adult rats. This study was undertaken to further investigate Hexarelin's mechanisms of action. In 10-day-old pups, treatments with HEXA (80 micrograms/kg, b.i.d.) for 3-10 days significantly enhanced, in a time-related fashion, the GH response to an acute HEXA challenge. Qualitatively similar effects were elicited in pups passively immunized against growth hormone-releasing hormone (GHRH) from birth. In adult male rats, a 5-day pretreatment with HEXA (150 micrograms/kg, b.i.d.) did not enhance the effect of the acute challenge, and the same pattern was present after a 5-day pretreatment in male rats with surgical ablation of the mediobasal hypothalamus (MBH-ablated rats). In addition, in adult sham-operated rats, Hexarelin (300 micrograms/kg, i.v.) induced a GH response greater (p < 0.05) than that induced by GHRH (2 micrograms/kg, i.v.). However, in MBH-ablated rats 7 days after surgery, GHRH was significantly (p < 0.05) more effective than HEXA, and 30 days after surgery HEXA and GHRH evoked similar rises of plasma GH. Finally, the in vitro Hexarelin (10(-6) mol/l) effect was transient while GHRH (10(-8) mol/l) induced a longer lasting and greater GH release. Three different mechanisms, not mutually exclusive, are postulated for Hexarelin stimulation of GH secretion in vivo: a direct action on the pituitary, though of minor relevance; an indirect action that involves release of GHRH, of relevance only in adult rats; and an action through the release of a still unknown hypothalamic "factor", which in infant and adult rats elicits GH release acting sinergistically with GHRH.
我们已报道生长激素释放肽6(GHRP - 6)的类似物Hexarelin(HEXA)能有效刺激幼龄和成年大鼠的生长激素(GH)分泌。本研究旨在进一步探究Hexarelin的作用机制。在10日龄幼鼠中,用HEXA(80微克/千克,每日两次)处理3至10天,以时间相关的方式显著增强了对急性HEXA刺激的GH反应。从出生就被动免疫生长激素释放激素(GHRH)的幼鼠也引发了定性相似的效应。在成年雄性大鼠中,用HEXA(150微克/千克,每日两次)进行5天预处理并未增强急性刺激的效果,并且在对中基底下丘脑进行手术切除的雄性大鼠(MBH切除大鼠)中进行5天预处理后也呈现相同模式。此外,在成年假手术大鼠中,Hexarelin(300微克/千克,静脉注射)诱导的GH反应比GHRH(2微克/千克,静脉注射)诱导的反应更大(p < 0.05)。然而,在手术后7天的MBH切除大鼠中,GHRH比HEXA显著更有效(p < 0.05),并且在手术后30天,HEXA和GHRH引起相似的血浆GH升高。最后,体外Hexarelin(10^(-6)摩尔/升)的作用是短暂的,而GHRH(10^(-8)摩尔/升)诱导了更持久且更大的GH释放。体内Hexarelin刺激GH分泌推测有三种不同机制,并非相互排斥:对垂体的直接作用,尽管相关性较小;涉及GHRH释放的间接作用,仅在成年大鼠中有相关性;以及通过释放一种仍未知的下丘脑“因子”的作用,该因子在幼龄和成年大鼠中与GHRH协同作用引发GH释放。