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人生长激素对猪脂肪组织基质血管细胞血清补充培养和无血清培养中前脂肪细胞发育的影响。

The influence of human growth hormone on preadipocyte development in serum-supplemented and serum-free cultures of stromal-vascular cells from pig adipose tissue.

作者信息

Hausman G J, Martin R J

机构信息

USDA-ARS, Richard B. Russell Agricultural Research Center, Athens, GA 30613.

出版信息

Domest Anim Endocrinol. 1989 Oct;6(4):331-7. doi: 10.1016/0739-7240(89)90027-1.

Abstract

The influence of human growth hormone (hGH) on the differentiation of preadipocytes was examined in primary cultures of stromal-vascular (s-v) cells from porcine adipose tissue. In these experiments, cells were exposed to test media for 7-8 days after seeding and plating for two days in fetal bovine serum. In serum-free (insulin, transferrin and selenium) cultures hGH (1 and 10 nM) reduced the number and size of fat cell clusters (P less than .05) by 50% relative to controls (no hGH). Differentiation of preadipocytes was assayed by labelling dividing cells with tritiated thymidine under identical conditions and then exposing cultures to test media for seven days. Fat cells were then separated from the other cells and radioactivity was determined in each fraction. In serum containing (2% pig serum) cultures hGH (10 nM) inhibited (P less than .05) the differentiation of labelled preadipocytes. In cultures with serum and with 1 microM insulin and in serum-free cultures, 1 and 10 nM hGH reduced (P less than .05) the levels of glycerol phosphate dehydrogenase (GPDH) specific activity by approximately 50%. However, hGH (1 and 10 nM) had no affect on GPDH activity in cultures with serum but without insulin. These studies indicate that hGH significantly impedes porcine preadipocyte development in vitro. Therefore, the decreased rate of adipose tissue growth observed in pigs chronically treated with GH could be due in part to impaired preadipocyte growth.

摘要

在猪脂肪组织基质血管(s-v)细胞的原代培养中,研究了人生长激素(hGH)对前脂肪细胞分化的影响。在这些实验中,细胞接种并在胎牛血清中培养两天后,暴露于测试培养基中7 - 8天。在无血清(胰岛素、转铁蛋白和硒)培养中,hGH(1和10 nM)使脂肪细胞簇的数量和大小相对于对照组(无hGH)减少了50%(P < 0.05)。在前脂肪细胞分化实验中,在相同条件下用氚标记胸腺嘧啶核苷标记正在分裂的细胞,然后将培养物暴露于测试培养基中7天。然后将脂肪细胞与其他细胞分离,并测定每个部分的放射性。在含血清(2%猪血清)培养中,hGH(10 nM)抑制(P < 0.05)标记的前脂肪细胞的分化。在含血清且添加1 microM胰岛素的培养以及无血清培养中,1和10 nM hGH使甘油磷酸脱氢酶(GPDH)比活性水平降低了约50%(P < 0.05)。然而,hGH(1和10 nM)对含血清但无胰岛素培养中的GPDH活性没有影响。这些研究表明,hGH在体外显著阻碍猪前脂肪细胞的发育。因此,长期用生长激素治疗的猪脂肪组织生长速率降低可能部分归因于前脂肪细胞生长受损。

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