Yamaguchi M, Koike K, Yoshimoto Y, Ikegami H, Miyake A, Tanizawa O
Department of Obstetrics and Gynecology, Osaka University Medical School, Japan.
Endocrinol Jpn. 1991 Aug;38(4):357-61. doi: 10.1507/endocrj1954.38.357.
The effects of human recombinant interleukin-1 beta and -6 and tumor necrosis factor-alpha (TNF-alpha) on the releases of PRL and dopamine were examined using monolayer cultures of rat pituitary cells and hypothalamic cells. The release of PRL from rat pituitary cells in 30 min was increased about 2-fold (p less than 0.05) by 10(5) U/l interleukin-1 beta, 10(5) U/l interleukin-6 or 100 micrograms/l TNF-alpha. TNF-alpha at 100 micrograms/l significantly increased PRL release within 5 min incubation and this effect continued throughout the next 30 min of incubation. Incubation for 5 min with TNF-alpha caused dose-dependent stimulation of PRL release. These cytokines did not modulate [3H]-dopamine release from primary cultures of hypothalamic cells. These results suggest that these cytokines stimulate PRL release directly at the pituitary gland, without modifying the release of dopamine from the hypothalamus.
利用大鼠垂体细胞和下丘脑细胞的单层培养物,研究了人重组白细胞介素-1β、白细胞介素-6和肿瘤坏死因子-α(TNF-α)对催乳素(PRL)和多巴胺释放的影响。10⁵ U/l白细胞介素-1β、10⁵ U/l白细胞介素-6或100 μg/l TNF-α可使大鼠垂体细胞在30分钟内PRL的释放增加约2倍(p<0.05)。100 μg/l的TNF-α在孵育5分钟内可显著增加PRL释放,且在接下来的30分钟孵育过程中这种作用持续存在。用TNF-α孵育5分钟可引起PRL释放的剂量依赖性刺激。这些细胞因子并未调节下丘脑细胞原代培养物中[³H] -多巴胺的释放。这些结果表明,这些细胞因子直接在垂体水平刺激PRL释放,而不改变下丘脑多巴胺的释放。