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禁食大鼠肝细胞中的细胞肿胀与糖原代谢

Cell swelling and glycogen metabolism in hepatocytes from fasted rats.

作者信息

Gustafson L A, Jumelle-Laclau M N, van Woerkom G M, van Kuilenburg A B, Meijer A J

机构信息

Department of Biochemistry, University of Amsterdam, The Netherlands.

出版信息

Biochim Biophys Acta. 1997 Jan 16;1318(1-2):184-90. doi: 10.1016/s0005-2728(96)00128-4.

Abstract

Cell swelling is known to increase net glycogen production from glucose in hepatocytes from fasted rats by activating glycogen synthase. Since both active glycogen synthase and phosphorylase are present in hepatocytes, suppression of flux through phosphorylase may also contribute to the net increase in glycogen synthesis by cell swelling. We have developed an isotopic procedure to estimate the fluxes through glycogen synthase and phosphorylase in intact hepatocytes and we have examined the effect of cell swelling on both enzyme fluxes. The following observations were made. (1) Hypotonic or glutamine-induced cell swelling increased net glycogen production by activating flux through glycogen synthase with little effect on phosphorylase flux. Proline, previously shown to increase glycogen synthesis more than could be accounted for by its ability to cause cell swelling, increased flux through glycogen synthase and inhibited phosphorylase flux. (2) Incorporation of [14C]glucose into glycogen preceded complete mixing of [14C]glucose with the intracellular pool of UDPglucose. It is concluded that cell swelling affects glycogen synthase only and that UDPglucose is compartmentalized.

摘要

已知细胞肿胀可通过激活糖原合酶增加禁食大鼠肝细胞中由葡萄糖产生的糖原净产量。由于活性糖原合酶和磷酸化酶都存在于肝细胞中,抑制磷酸化酶的通量也可能有助于细胞肿胀导致的糖原合成净增加。我们开发了一种同位素方法来估计完整肝细胞中糖原合酶和磷酸化酶的通量,并研究了细胞肿胀对这两种酶通量的影响。得到了以下观察结果。(1)低渗或谷氨酰胺诱导的细胞肿胀通过激活糖原合酶通量增加了糖原净产量,而对磷酸化酶通量影响很小。脯氨酸先前显示其增加糖原合成的程度超过了其引起细胞肿胀的能力所能解释的范围,它增加了糖原合酶通量并抑制了磷酸化酶通量。(2)[14C]葡萄糖掺入糖原之前,[14C]葡萄糖与细胞内UDP葡萄糖池并未完全混合。得出的结论是,细胞肿胀仅影响糖原合酶,并且UDP葡萄糖是分隔存在的。

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