Rivas R J, Nishioka R S, Bern H A
Gen Comp Endocrinol. 1986 Aug;63(2):245-51. doi: 10.1016/0016-6480(86)90162-0.
The control of release of two recently characterized forms of prolactin (PRL) of molecular mass 24 and 20 kDa was investigated. The rostral pars distalis of male tilapia was incubated singly in a hypotonic modified Krebs-Ringer bicarbonate medium in order to stimulate PRL release; for comparison, the proximal pars distalis containing growth hormone (GH) cells was incubated in isotonic medium with or without 1 microgram/ml cortisol to stimulate GH release. The release of both PRLs and GH into the medium was measured by sodium dodecyl sulfate (SDS)--polyacrylamide gel electrophoresis followed by densitometry. Both somatostatin and synthetic (Gillichthys) urotensin II, a partial somatostatin homolog and analog from the teleost caudal neurosecretory system, significantly inhibited the release of both PRLs. Somatostatin significantly inhibited GH release, but urotensin II had no significant effect.
对最近鉴定出的两种分子量分别为24 kDa和20 kDa的催乳素(PRL)释放的控制进行了研究。将雄性罗非鱼的吻端远侧部单独培养在低渗改良的克雷布斯-林格碳酸氢盐培养基中,以刺激PRL释放;作为比较,将含有生长激素(GH)细胞的近侧部在等渗培养基中培养,添加或不添加1微克/毫升皮质醇以刺激GH释放。通过十二烷基硫酸钠(SDS)-聚丙烯酰胺凝胶电泳,然后进行光密度测定,来测量PRL和GH释放到培养基中的量。生长抑素和合成的(吉利氏)尾加压素II(一种来自硬骨鱼尾神经分泌系统的部分生长抑素同系物和类似物)均显著抑制两种PRL的释放。生长抑素显著抑制GH释放,但尾加压素II没有显著影响。