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摘除大鼠颌下-舌下腺后,异丙肾上腺素诱导的大鼠腮腺和胰腺DNA及RNA合成受到抑制。

Inhibition of isoproterenol-induced DNA and RNA synthesis in rat parotid and pancreas following removal of submandibular-sublingual glands.

作者信息

Schneyer C A, Humphreys-Beher M

机构信息

Department of Physiology and Biophysics, University of Alabama, Birmingham 35294.

出版信息

Cell Tissue Res. 1989;256(2):361-3. doi: 10.1007/BF00218893.

Abstract

[3H] thymidine incorporation into DNA of the parotid (PA) gland of adult and 20-day-old rats and into DNA of the pancreas (PANC) of 20-day-old rats was increased markedly following a 2-day regimen of isoproterenol (ISO) administration. However, when the submandibular-sublingual (SM-SL) glands had been removed just prior to initiation of the ISO injections, the [3H] thymidine incorporation into PA and PANC was inhibited, and cpm/mg protein of these organs was even lower than that of organs of untreated rats with SM-SL glands present. Removal of the PA glands just prior to initiation of the ISO regimen had no effect on the ISO-induced [3H] thymidine incorporation into DNA of PANC but partially inhibited that of the submandibular (SM) gland. It is suggested that the inhibitory effects on DNA and RNA synthesis that follow removal of SM-SL glands are attributable to the growth factors (epidermal growth factor and nerve growth factor) found in the rat SM gland. These factors appear to regulate normal DNA synthetic activity of exocrine glands as well as beta 1-adrenoceptor mediated DNA synthesis. Cellular hypertrophy induced by the ISO was less markedly affected by absence of the SM glands, but a partial inhibition of [3H] uridine incorporation into RNA of PA of adult rats also occurred when SM-SL glands were removed prior to initiation of the ISO-regimen.

摘要

在成年大鼠和20日龄大鼠腮腺(PA)以及20日龄大鼠胰腺(PANC)中,给予异丙肾上腺素(ISO)2天方案后,[3H]胸苷掺入DNA的量显著增加。然而,在开始注射ISO之前刚刚切除下颌下腺-舌下腺(SM-SL),则PA和PANC中[3H]胸苷的掺入受到抑制,并且这些器官的每毫克蛋白质的计数每分钟(cpm/mg蛋白)甚至低于存在SM-SL腺的未处理大鼠器官。在开始ISO方案之前刚刚切除PA腺,对ISO诱导的[3H]胸苷掺入PANC的DNA没有影响,但部分抑制了下颌下腺(SM)的掺入。提示切除SM-SL腺后对DNA和RNA合成的抑制作用归因于大鼠SM腺中发现的生长因子(表皮生长因子和神经生长因子)。这些因子似乎调节外分泌腺的正常DNA合成活性以及β1-肾上腺素能受体介导的DNA合成。ISO诱导的细胞肥大受SM腺缺失的影响较小,但在开始ISO方案之前切除SM-SL腺时,成年大鼠PA中[3H]尿苷掺入RNA也会出现部分抑制。

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