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神经垂体中的钙与刺激分泌偶联。V. Ca2+离子载体A23187和X537 A对血管加压素释放和45Ca2+外流的影响;与钠及维拉帕米类似物(D600)的相互作用

Calcium and stimulus secretion coupling in the neurohypophysis. V. The effects of the Ca2+ ionophores A23187 and X537 A on vasopressin release and 45Ca2+ efflux; interactions with sodium and a verapamil analogue (D600).

作者信息

Robinson I C, Russell J T, Thorn N A

出版信息

Acta Endocrinol (Copenh). 1976 Sep;83(1):36-49.

PMID:60866
Abstract

Slices from ox neurohypophyses were incubated in a calcium-free medium with the ionophores A23187 or X537A. X537A (5 X 10(-5) mol/l) caused a marked release of vasopressin, neurophysin and protein to the medium. A23187 (2 X 10(-5) mol/l) did not cause any release by itself, but when Ca2+ was added to the medium in the presence of the ionophore, an increase in the release of vasopressin, neuorphysin and protein occurred. Release of lactate dehydrogenase and peptidase were not affected by the ionophores. The secretion caused by A23187 was abolished by D600 (a verapamil analogue) (2 X 10(-5) mol/l) whereas the effect of X537A was unchanged. The effects of X537A were strongly inhibited by removal of sodium from the medium. Re-addition of sodium to the medium caused a marked release. Gramicidin (10(-6) or 5 X 10(-5) mol/l) had no effect on secretion. Efflux of 45Ca2+ from pre-loaded slices was drastically reduced in a sodium-free medium. X537A caused an increase in the efflux rate of 45Ca2+ both in medium with a normal concentration of sodium and when slices had been incubated in a sodium-free medium. A23187 and X537A both released 45Ca2+ from a neurohypophyseal mitochondrial fraction. When sodium in a concentration of 20 mmol/l was added to this fraction, the Ca2+ accumulation was inhibited. This effect was reduced by inorganic phosphate up to a concentration of 2 mmol/l.

摘要

将牛神经垂体切片置于含有离子载体A23187或X537A的无钙培养基中进行孵育。X537A(5×10⁻⁵mol/L)可使血管加压素、神经垂体素和蛋白质显著释放到培养基中。A23187(2×10⁻⁵mol/L)本身不会引起任何释放,但当在离子载体存在的情况下向培养基中添加Ca²⁺时,血管加压素、神经垂体素和蛋白质的释放会增加。乳酸脱氢酶和肽酶的释放不受离子载体影响。D600(维拉帕米类似物)(2×10⁻⁵mol/L)可消除A23187引起的分泌,而X537A的作用不受影响。从培养基中去除钠可强烈抑制X537A的作用。向培养基中重新添加钠会导致显著释放。短杆菌肽(10⁻⁶或5×10⁻⁵mol/L)对分泌无影响。在无钠培养基中,预加载切片中⁴⁵Ca²⁺的流出量大幅减少。X537A在正常钠浓度的培养基中以及切片在无钠培养基中孵育后,均可使⁴⁵Ca²⁺的流出率增加。A23187和X537A均可从神经垂体线粒体组分中释放⁴⁵Ca²⁺。当向该组分中添加浓度为20mmol/L的钠时,Ca²⁺积累受到抑制。这种作用在无机磷酸盐浓度高达2mmol/L时会减弱。

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