Ohashi S, Kaji H, Abe H, Chihara K
Department of Medicine, Kobe University School of Medicine, Japan.
Life Sci. 1995;57(18):1655-66. doi: 10.1016/0024-3205(95)02145-9.
To elucidate whether GHR and GHBP are coordinately regulated or not, we studied the effect of fasting with or without GH administration on the GHR and GHBP mRNAs in the liver as well as in extrahepatic tissues in rats. Tissues were collected from 7-week-old male rats by decapitation 1,3, and 7 days after the start of fasting. Liver GHR mRNA levels were not affected 1 day after the start of fasting but progressively decreased for the subsequent 3 and 7 days of fasting as compared with those in control rats fed ad libitum. In contrast, liver GHBP mRNA levels significantly rose after 1 day fasting, returned to the control level after 3 days and further reduced after 7 days of fasting. Changes in GHBP mRNA level after fasting were different among the tissues. A transient increase in GHBP mRNA levels was observed in muscle and heart as well as liver, while the GHBP mRNA levels in fat tissues did not change throughout 7 days of fasting. Next, bovine GH(bGH) was administered ip to the fasted rats and control fed rats for either 1 day(100 micrograms [corrected], tid) or 5 days(150 micrograms [corrected], daily). In fed rats, liver GHR mRNA level was significantly increased by 1 day bGH treatment, but after 5 days treatment with bGH it was not different from the level in saline-injected control. Accordingly, net increment of plasma IGF-I was 296.0 ng/ml with 1 day bGH treatment and 234.2 ng/ml with bGH administration for 5 days. In fasted rats, liver GHR mRNA level did not changed after 1 day treatment with bGH, but markedly decreased 5 days after bGH administration. Net increment of plasma IGF-I was slightly reduced to 284 ng/ml with 1 day treatment with bGH, and markedly decreased to 37.0 with bGH administration for 5 days. The effect of GH administration on liver GHBP mRNA level was virtually absent in either fasting or fed state. These findings suggest that GHR and GHBP mRNAs in the liver are expressed in different ways and that expression of GHBP mRNA is differently regulated among tissues.
为了阐明生长激素受体(GHR)和生长激素结合蛋白(GHBP)是否受到协同调节,我们研究了禁食以及禁食同时给予生长激素(GH)对大鼠肝脏和肝外组织中GHR和GHBP mRNA的影响。在禁食开始后的第1、3和7天,通过断头处死7周龄雄性大鼠并采集组织。禁食开始1天后,肝脏GHR mRNA水平未受影响,但在随后禁食的3天和7天中,与自由进食的对照大鼠相比逐渐下降。相反,禁食1天后肝脏GHBP mRNA水平显著升高,禁食3天后恢复到对照水平,禁食7天后进一步降低。禁食后GHBP mRNA水平的变化在不同组织中有所不同。在肌肉、心脏以及肝脏中观察到GHBP mRNA水平短暂升高,而脂肪组织中的GHBP mRNA水平在整个7天的禁食过程中没有变化。接下来,对禁食大鼠和对照进食大鼠腹腔注射牛生长激素(bGH),持续1天(100微克[校正后],每日3次)或5天(150微克[校正后],每日1次)。在进食大鼠中,bGH处理1天后肝脏GHR mRNA水平显著升高,但在bGH处理5天后与注射生理盐水的对照水平没有差异。因此,bGH处理1天血浆胰岛素样生长因子-I(IGF-I)的净增量为296.0纳克/毫升,bGH给药5天为234.2纳克/毫升。在禁食大鼠中,bGH处理1天后肝脏GHR mRNA水平没有变化,但在bGH给药5天后显著下降。bGH处理1天血浆IGF-I的净增量略有降低至284纳克/毫升,bGH给药5天则显著降至37.0纳克/毫升。无论在禁食还是进食状态下,给予GH对肝脏GHBP mRNA水平几乎没有影响。这些发现表明,肝脏中的GHR和GHBP mRNA以不同方式表达,并且GHBP mRNA的表达在不同组织中受到不同调节。