Anand-Srivastava M B, Johnson R A
J Neurochem. 1980 Oct;35(4):905-14. doi: 10.1111/j.1471-4159.1980.tb07089.x.
An adenosine-sensitive adenylate cyclase has been characterized from rat brain striatum. In whole homogenates as well as in particulate fractions, N6-phenylisopropyl adenosine (PIA), 2-chloroadenosine, and adenosine N'-oxide were equipotent in stimulating adenylate cyclase. Although GTP inhibited basal as well as PIA-stimulated activity of whole homogenates, the enzyme showed an absolute dependency on GTP for stimulation by PIA, dopamine, epinephrine, and norepinephrine in a particulate fraction derived from discontinuous sucrose gradient centrifugation. Adenosine exerts two effects on this adenylate cyclase, stimulation at low concentrations and inhibition at high concentrations, suggesting the presence of two adenosine binding sites. The stimulation of adenylate cyclase by PIA was dependent on the concentration of Mg2+. The degree of stimulation by PIA was greater at a low concentration of MG2+, which suggests that stimulation by PIA was accompanied by increasing the apparent affinity for Mg2+. Activation of adenylate cyclase by PIA was blocked by theophylline or 3-isobutyl-1-methylxanthine (IBMX). The pH optimum for basal or (PIA + GTP)-stimulated activities was broad, with a peak between 8.5 and 9.5. In the presence of GTP, stimulation by an optimal concentration of PIA was additive, with maximal stimulation by the catecholamines. Phospholipase A2 treatment at a concentration of 1 U/ml for 5 min completely abolished the stimulatory effect of dopamine, whereas PIA-stimulated activity remained unaltered. These data suggest that rat brain striatum either has a single adenylate cyclase, which is stimulted by catecholamines and adenosine by distinct mechanisms, or has different cyclase populations, stimulated by either adenosine or catecholamines.
已从大鼠脑纹状体中鉴定出一种对腺苷敏感的腺苷酸环化酶。在全匀浆以及颗粒组分中,N6-苯基异丙基腺苷(PIA)、2-氯腺苷和腺苷N'-氧化物在刺激腺苷酸环化酶方面具有同等效力。尽管GTP抑制全匀浆的基础活性以及PIA刺激的活性,但在通过不连续蔗糖梯度离心获得的颗粒组分中,该酶显示出对GTP的绝对依赖性,以实现PIA、多巴胺、肾上腺素和去甲肾上腺素的刺激作用。腺苷对这种腺苷酸环化酶有两种作用,低浓度时刺激,高浓度时抑制,这表明存在两个腺苷结合位点。PIA对腺苷酸环化酶的刺激作用取决于Mg2+的浓度。在低浓度Mg2+时,PIA的刺激程度更大,这表明PIA的刺激伴随着对Mg2+表观亲和力的增加。PIA对腺苷酸环化酶的激活作用被茶碱或3-异丁基-1-甲基黄嘌呤(IBMX)阻断。基础活性或(PIA + GTP)刺激活性的最适pH范围较宽,峰值在8.5至9.5之间。在存在GTP的情况下,最佳浓度的PIA的刺激作用是相加的,儿茶酚胺可产生最大刺激。以1 U/ml的浓度进行5分钟的磷脂酶A2处理完全消除了多巴胺的刺激作用,而PIA刺激的活性保持不变。这些数据表明,大鼠脑纹状体要么具有单一的腺苷酸环化酶,其通过不同机制被儿茶酚胺和腺苷刺激,要么具有不同的环化酶群体,分别被腺苷或儿茶酚胺刺激。