Burger A, Bellersheim M
Naunyn Schmiedebergs Arch Pharmacol. 1976 Dec;296(1):47-57. doi: 10.1007/BF00498839.
Noradrenaline-storing granules, a mitochondrial fraction and a microsomal fraction of bovine splenic nerve trunks were prepared by differential centrifugation. These particulate fractions were characterized by their noradrenaline content, succinate dehydrogenase and glucose-6-phosphatase activity. In the presence of ATP-Mg2+ all three fractions accumulated 45Ca2+ during incubation with 0.1 mM 45 CaCl2, buffered with potassium phosphate or glycylglycine (pH 7.5; 28 degrees C). The accumulated 45 Ca2+ was not removable by EGTA, and the uptake was absent at 0 degrees C or after destruction of the particles by sonication. The behaviour of the 45 Ca2+ -uptake into all three fractions against varying ATP-concentrations, metabolic inhibitors (pentachlorophenol, desaspidine, 2,4-dinitrophenol, N-ethylmaleimide, p-chloromercuribenzoate, sodium azide, amobarbital) and drugs (phenoxybenzamine, verapamil, prenylamine, reserpine, bretylium, phentolamine) was studied. Under nearly all conditions there were differences between the 45 Ca2+ -uptake into mitochondria and that into microsomes, which suggests two distinct uptake processes. The 45 Ca2+ -uptake into the granule fraction behaved intermediate between the two other fractions under many conditions, but not under all. Therefore, it is not possible to explain the 45 Ca2+ -uptake into the granule fraction as being due to contamination with mitochondria and microsomes; an inherent ATP-Mg2+ -dependent 45Ca2+ -uptake into the nerve granules must be postulated, which is not directly coupled with the noradrenaline transport into these particles. A particulate fraction (14000-100000 g), containing noradrenaline granules, was prepared from the vas deferens of the rat. Incubation with 5 X 10(-6) M (-)-noradrenaline and 0.1 mM 45Ca2+ showed that the particles of this fraction take up noradrenaline and 45Ca2+. The uptake of both was dependent on ATP-Mg2+. The ATP-Mg2+ -dependent uptake of both noradrenaline and 45Ca2+ was substantially reduced in the corresponding tissue fraction prepared from denervated vasa deferentia.
通过差速离心法制备了牛脾神经干的去甲肾上腺素储存颗粒、线粒体组分和微粒体组分。这些颗粒组分通过其去甲肾上腺素含量、琥珀酸脱氢酶和葡萄糖-6-磷酸酶活性来表征。在ATP-Mg2+存在的情况下,在与0.1 mM 45CaCl2一起孵育期间,所有三个组分都积累了45Ca2+,孵育用磷酸钾或甘氨酰甘氨酸缓冲(pH 7.5;28℃)。积累的45Ca2+不能被EGTA去除,并且在0℃或通过超声处理破坏颗粒后摄取不存在。研究了所有三个组分对45Ca2+的摄取行为,针对不同的ATP浓度、代谢抑制剂(五氯苯酚、地杀平、2,4-二硝基苯酚、N-乙基马来酰亚胺、对氯汞苯甲酸、叠氮化钠、异戊巴比妥)和药物(酚苄明、维拉帕米、普尼拉明、利血平、溴苄铵、酚妥拉明)。在几乎所有条件下,线粒体和微粒体对45Ca2+的摄取之间存在差异,这表明存在两种不同的摄取过程。在许多条件下,但并非所有条件下,颗粒组分对45Ca2+的摄取表现介于其他两个组分之间。因此,不可能将颗粒组分对45Ca2+的摄取解释为由于线粒体和微粒体的污染;必须假定神经颗粒中存在一种固有的ATP-Mg2+依赖性45Ca2+摄取,它与去甲肾上腺素向这些颗粒中的转运没有直接偶联。从大鼠输精管制备了一个含有去甲肾上腺素颗粒的颗粒组分(14000-100000 g)。与5×10(-6) M (-)-去甲肾上腺素和0.1 mM 45Ca2+一起孵育表明,该组分的颗粒摄取去甲肾上腺素和45Ca2+。两者的摄取都依赖于ATP-Mg2+。在去神经输精管制备的相应组织组分中,去甲肾上腺素和45Ca2+的ATP-Mg2+依赖性摄取显著降低。