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雄性大鼠对周期性给予胰岛素样生长因子-I(IGF-I)的生长激素细胞反应。

Somatotroph response to periodical IGF-I administration to male rats.

作者信息

Pellizas C G, Bonaterra M, De Paul A L, Aoki A, Coleoni A H, Torres A I

机构信息

Centro de Microscopía Electrónica, Facultad de Ciencias Médicas, Universidad Nacional de Córdoba, Argentina.

出版信息

Acta Histochem. 2000 Nov;102(4):439-51. doi: 10.1078/0065-1281-00570.

Abstract

Insulin-like growth factor I (IGF-I) downregulates growth hormone (GH) expression in pituitary cell cultures. However, in vivo different results were found depending on the experimental protocol used. We determined the kinetics of changes of pituitary and serum GH concentrations after subcutaneous IGF-I administration (240 microg/100 g body weight) to rats every 12 h for various periods. These parameters were correlated with changes in the somatotroph cell population. A significant increase in serum GH was registered at 6 h after IGF-I injection. At this time, some somatotroph cells exhibited ultrastructurally signs of high secretory activity, whereas adjacent somatotroph cells showed a quiescent appearance with sizeable stores of secretory granules. In contrast, serum GH levels remained unchanged at 1, 2 and 12 h after each IGF-I injection. Pituitary GH concentrations were comparable to control levels during the first 48 h and declined significantly at 72 h and 96 h of IGF-I treatment. After these prolonged periods of time of treatment, the size and extension of organelles involved in protein synthesis decreased and mature secretory granules in the cytoplasm increased significantly in GH-secreting cells. The somatotroph cell density remained unchanged even at 96 h of treatment. In conclusion, our results suggest that periodical IGF-I administration to rats does not inhibit GH secretion. Interestingly, IGF-I injections induced early and significant increases in serum GH levels. This result may be a consequence of a temporary stimulatory action on somatotroph cells concurrent with increased secretory activity.

摘要

胰岛素样生长因子I(IGF-I)可下调垂体细胞培养物中生长激素(GH)的表达。然而,在体内,根据所采用的实验方案会发现不同的结果。我们测定了每隔12小时给大鼠皮下注射IGF-I(240微克/100克体重)不同时间段后垂体和血清GH浓度的变化动力学。这些参数与生长激素细胞群体的变化相关。IGF-I注射后6小时血清GH显著升高。此时,一些生长激素细胞在超微结构上表现出高分泌活性的迹象,而相邻的生长激素细胞则呈现静止外观,有大量分泌颗粒储存。相反,每次IGF-I注射后1、2和12小时血清GH水平保持不变。在IGF-I治疗的前48小时垂体GH浓度与对照水平相当,在治疗72小时和96小时时显著下降。经过这些长时间的治疗后,参与蛋白质合成的细胞器的大小和范围减小,而分泌生长激素的细胞胞质中的成熟分泌颗粒显著增加。即使在治疗96小时时生长激素细胞密度仍保持不变。总之,我们的结果表明,对大鼠定期给予IGF-I不会抑制GH分泌。有趣的是,IGF-I注射导致血清GH水平早期显著升高。这一结果可能是对生长激素细胞的暂时刺激作用与分泌活性增加同时出现的结果。

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