Anderson L L, Ford J J, Klindt J, Molina J R, Vale W W, Rivier J
Department of Animal Science, Iowa State University, Ames 50011.
Proc Soc Exp Biol Med. 1991 Feb;196(2):194-202. doi: 10.3181/00379727-196-43179.
Control of growth hormone (GH) and prolactin (PRL) release was investigated in hypophysial stalk-transected (HST) and stalk-intact pigs by determining the effects of analogs of GH-releasing factors (GHRF), somatostatin (SRIF), arginine, thyrotropin-releasing hormone, alpha-methyl-rho-tyrosine, and haloperidol. HST and control gilts were challenged with intravenous injections of human pancreatic GHRF(1-40)OH, thyrotropin-releasing hormone, and analogs of rat hypothalamic GHRF. HST animals remained acutely responsive to GHRF by releasing 2-fold greater quantities of GH than seen in controls. This occurred in spite of a 38% reduction in pituitary gland weight and a 32 and 55% decrease in GH concentration and total content. During SRIF infusion, GH remained at similar basal concentrations in HST and control gilts, but increased immediately after stopping SRIF infusion only in the controls. Releasable pituitary GH appears to accumulate during SRIF infusion. GHRF given during SRIF infusion caused a 2-fold greater release of GH than seen in animals receiving only GHRF. Arginine increased (P less than 0.05) GH release in controls, but not in HST gilts, which suggests that it acts through the central nervous system. Basal PRL concentrations were greater (P less than 0.05) in HST gilts than in control gilts. TRH acutely elevated circulating PRL (P less than 0.001) in HST gilts, suggesting that it acts directly on the pituitary gland. Haloperidol, a dopamine receptor antagonist, increased circulating PRL in controls but not in HST animals. alpha-Methyl-rho-tyrosine did not consistently increase circulating PRL, however, suggesting that it did not sufficiently alter turnover rate of the tyrosine hydroxylase pool. The results indicate that the isolated pituitary after HST remains acutely responsive to hypothalamic releasing and inhibiting factors for both GH and PRL release in the pig.
通过测定生长激素释放因子(GHRF)、生长抑素(SRIF)、精氨酸、促甲状腺激素释放激素、α-甲基-对酪氨酸和氟哌啶醇类似物的作用,研究了垂体柄横断(HST)和垂体柄完整的猪中生长激素(GH)和催乳素(PRL)释放的控制情况。对HST和对照后备母猪静脉注射人胰腺GHRF(1-40)OH、促甲状腺激素释放激素和大鼠下丘脑GHRF类似物进行刺激。HST动物对GHRF仍有急性反应,释放的GH量比对照组多两倍。尽管垂体重量减少了38%,GH浓度和总量分别降低了32%和55%,但仍出现这种情况。在SRIF输注期间,HST和对照后备母猪的GH保持在相似的基础浓度,但仅在对照组中,停止SRIF输注后GH立即增加。在SRIF输注期间,可释放的垂体GH似乎会积累。在SRIF输注期间给予GHRF导致GH释放量比仅接受GHRF的动物多两倍。精氨酸增加了(P<0.05)对照组的GH释放,但对HST后备母猪没有作用,这表明它是通过中枢神经系统起作用的。HST后备母猪的基础PRL浓度高于(P<0.05)对照后备母猪。TRH使HST后备母猪的循环PRL急性升高(P<0.001),表明它直接作用于垂体。多巴胺受体拮抗剂氟哌啶醇增加了对照组的循环PRL,但对HST动物没有作用。然而,α-甲基-对酪氨酸并没有持续增加循环PRL,这表明它没有充分改变酪氨酸羟化酶池的周转率。结果表明,HST后分离出的垂体对猪中GH和PRL释放的下丘脑释放和抑制因子仍有急性反应。