Caughey B, Kirshner N
J Neurochem. 1987 Aug;49(2):563-73. doi: 10.1111/j.1471-4159.1987.tb02901.x.
The in vivo storage relationship between catecholamines and ATP in chromaffin vesicles of cultured bovine adrenal medulla cells was investigated using drugs that block vesicular catecholamine uptake. Three-day treatments with reserpine and tetrabenazine causing 85-90% depletion of catecholamines resulted in 41-46% reductions in cellular ATP content. Subcellular fractionation of reserpine-treated cells indicated that the ATP is lost from the chromaffin vesicle pool. This was confirmed in experiments using metabolic inhibitors to differentiate the vesicular and extravesicular ATP pools. The vesicular ATP loss was not proportional to that of catecholamines, resulting in a reduction by 50% in the chromaffin vesicle mole ratio of catecholamines to ATP after 48 h of treatment. In metabolic labeling studies, it was found that reserpine treatment reduced the incorporation of [3H]adenosine into vesicular ATP selectively, but it reduced the incorporation of 32Pi into both the vesicular and extravesicular pools. The reduction of the [3H]adenosine incorporation was not due to diminished vesicular nucleotide uptake resulting from low catecholamine levels, because when the catecholamines were depleted by tetrabenazine pretreatment followed by removal of the drug before labeling, no reduction in [3H]adenosine incorporation was observed. When present during the labeling, tetrabenazine was found to be a reversible inhibitor of plasma membrane adenosine uptake. The observed loss of adenine nucleotides from catecholamine-depleted chromaffin vesicles in vivo provides evidence that interactions between ATP and catecholamines are important in the vesicular storage of high concentration of these compounds.
利用阻断囊泡儿茶酚胺摄取的药物,研究了培养的牛肾上腺髓质细胞嗜铬囊泡中儿茶酚胺与ATP的体内储存关系。用利血平和丁苯那嗪进行三天治疗,导致儿茶酚胺耗竭85 - 90%,细胞ATP含量降低41 - 46%。对利血平处理的细胞进行亚细胞分级分离表明,ATP从嗜铬囊泡池中丢失。在使用代谢抑制剂区分囊泡和囊泡外ATP池的实验中得到了证实。囊泡ATP的损失与儿茶酚胺的损失不成比例,导致处理48小时后嗜铬囊泡中儿茶酚胺与ATP的摩尔比降低了50%。在代谢标记研究中发现,利血平处理选择性地降低了[3H]腺苷掺入囊泡ATP,但它降低了32Pi掺入囊泡和囊泡外池。[3H]腺苷掺入的减少不是由于儿茶酚胺水平低导致囊泡核苷酸摄取减少,因为当儿茶酚胺通过丁苯那嗪预处理耗尽,然后在标记前去除药物时,未观察到[3H]腺苷掺入减少。当在标记过程中存在时,发现丁苯那嗪是质膜腺苷摄取的可逆抑制剂。体内观察到儿茶酚胺耗尽的嗜铬囊泡中腺嘌呤核苷酸的丢失提供了证据,表明ATP与儿茶酚胺之间的相互作用在这些化合物的高浓度囊泡储存中很重要。