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[24R,25-二羟基维生素D3对垂体切除大鼠肾脏碱性磷酸酶和γ-谷氨酰转移酶的体外作用]

[In vitro effects of 24R,25-dihydroxyvitamin D3 on alkaline phosphatase and gamma-glutamyltransferase in the kidney of hypophysectomized rats].

作者信息

Prelot M, Do T X, Giraul A, Thuillier A

机构信息

Laboratoires de Physiologie, de Biochimie appliquée (CHU), de Pharmacie clinique, UFR des Sciences Médicales et de Pharmaceutiques, Angers, France.

出版信息

Arch Int Physiol Biochim Biophys. 1991 Jun;99(3):269-73. doi: 10.3109/13813459109146934.

Abstract

The effects of 24R,25-dihydroxyvitamin D3 (24,25-(OH)2D3 on alkaline phosphatase (PAL), gamma-glutamyltransferase (GGT) and acid phosphatase (PAC) activities were investigated on renal cortex slices of hypophysectomized rats. Indeed after hypophysectomy renal 24,25-(OH)2D3 production was increased and renal PAL and GGT activities were decreased. After 5h incubation with physiological concentrations (0.1-10 nM) of 24,25-(OH)2D3 significant increases of PAL and GGT activities were produced. The maximum stimulation obtained with 1 nM was +23% for PAL and +26% for GGT as compared to controls. PAC was not modified. The time course of these effects was studied from 45 min to 8 h. In the presence of 24,25-(OH)2D3 (1 nM), delayed (3h) stimulation of PAL and GGT appeared. It reached the maximal value after 6h, +37% for PAL and +30% for GGT and persisted again at 8h. Cycloheximide added to incubation medium with steroid inhibited the stimulating effect on PAL only. Actinomycin D suppressed the induction of both enzymes, indicating that the observed actions of 24,25-(OH)2D3 depend on protein synthesis whose responsible mechanisms were different. These protein synthesis inhibitors did not modified enzymatic activities. Physiological significance of these renal effects is to be clarified.

摘要

研究了24R,25-二羟基维生素D3(24,25-(OH)2D3)对垂体切除大鼠肾皮质切片中碱性磷酸酶(PAL)、γ-谷氨酰转移酶(GGT)和酸性磷酸酶(PAC)活性的影响。事实上,垂体切除后,肾脏24,25-(OH)2D3的生成增加,而肾脏PAL和GGT活性降低。用生理浓度(0.1 - 10 nM)的24,25-(OH)2D3孵育5小时后,PAL和GGT活性显著增加。与对照组相比,1 nM的24,25-(OH)2D3产生的最大刺激作用为PAL增加23%,GGT增加26%。PAC活性未改变。从45分钟到8小时研究了这些作用的时间进程。在存在24,25-(OH)2D3(1 nM)的情况下,PAL和GGT出现延迟(3小时)刺激。6小时后达到最大值,PAL为37%,GGT为30%,并在8小时时再次持续。添加到含类固醇孵育培养基中的放线菌酮仅抑制对PAL的刺激作用。放线菌素D抑制这两种酶的诱导,表明观察到的24,25-(OH)2D3的作用依赖于蛋白质合成,但其负责机制不同。这些蛋白质合成抑制剂未改变酶活性。这些肾脏作用的生理意义有待阐明。

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