Soliman E B, Hashizume T, Ohashi S, Kanematsu S
Laboratory of Animal Breeding and Reproduction, Faculty of Agriculture, Iwate University, Morioka, Japan.
Domest Anim Endocrinol. 1997 Jan;14(1):39-46. doi: 10.1016/s0739-7240(96)00096-3.
The effects of the human growth hormone (GH)-releasing hormone (hGRF(1-44)-NH2: hGRF-44), bovine GRF (bGRF(1-44)-NH2: bGRF-44), and their analogs (hGRF(1-29)-NH2, [D-Ala2]- hGRF(1-29)-NH2, bGRF(1-29)-NH2,[D-Ala2,Ala15]-bGRF(1-29)-NH2) as well as rat GRF(rGRF) on bovine GH release from anterior pituitary (AP) cells were studied in vitro in steers. The AP cells were incubated for 2 hr with the GRFs after preincubation for 3.5 d. Both of the hGRF-44 and hGRF(1-29)-NH2 (hGRF-29) significantly stimulated GH release from cultured cells at doses from 10(-14) to 10(-8)M (P < 0.01). The analog [D-Ala2]-hGRF-29 significantly induced GH release in media at doses from 10(-18) to 10(-8) M (P < 0.01). The bGRF-44, bGRF(1-29)-NH2 (bGRF-29), and [D-Ala2, Ala15]-bGRF-29 significantly induced GH release in media at doses as low as 10(-18), 10(-17), and 10(-16)M, respectively (P < 0.01). At doses from 10(-11) to 10(-8)M, there were no significant differences in GH-releasing potency between the hGRFs and bGRFs. The rGRF significantly stimulated GH release at doses ranging from 10(-14) to 10(-8) M (P < 0.01). The linear regression tests showed that the hGRFs, bGRFs, and rGRF, at doses from 10(-14) to 10(-8)M, induced GH release in a dose-related manner (P < 0.01). These results suggest that the hGRF, bGRF, and their analogs, as well as rGRF, are potent secretagogues of GH release from adenohypophysial cells in vitro in cattle.
在体外对阉牛进行研究,观察了人类生长激素(GH)释放激素(hGRF(1 - 44)-NH2: hGRF - 44)、牛生长激素释放因子(bGRF(1 - 44)-NH2: bGRF - 44)及其类似物(hGRF(1 - 29)-NH2、[D - Ala2]-hGRF(1 - 29)-NH2、bGRF(1 - 29)-NH2、[D - Ala2,Ala15]-bGRF(1 - 29)-NH2)以及大鼠生长激素释放因子(rGRF)对牛垂体前叶(AP)细胞释放牛生长激素的影响。将AP细胞预孵育3.5天后,再与生长激素释放因子一起孵育2小时。hGRF - 44和hGRF(1 - 29)-NH2(hGRF - 29)在10(-14)至10(-8)M的剂量下均能显著刺激培养细胞释放生长激素(P < 0.01)。类似物[D - Ala2]-hGRF - 29在10(-18)至10(-8)M的剂量下能显著诱导培养基中生长激素的释放(P < 0.01)。bGRF - 44、bGRF(1 - 29)-NH2(bGRF - 29)和[D - Ala2, Ala15]-bGRF - 29分别在低至10(-18)、10(-17)和10(-16)M的剂量下能显著诱导培养基中生长激素的释放(P < 0.01)。在10(-11)至10(-8)M的剂量下,hGRF和bGRF之间的生长激素释放效力无显著差异。rGRF在10(-14)至10(-8)M的剂量范围内能显著刺激生长激素的释放(P < 0.01)。线性回归测试表明,hGRF、bGRF和rGRF在10(-14)至10(-8)M的剂量下,以剂量相关的方式诱导生长激素的释放(P < 0.01)。这些结果表明,hGRF、bGRF及其类似物以及rGRF在体外是牛腺垂体细胞释放生长激素的有效促分泌剂。