{"title":"氟刺激的纹状体和大脑皮层中腺苷酸环化酶活性的胞浆调节剂的差异效应。","authors":"R A Rabin, D C Bode, P B Molinoff","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The effects of sodium fluoride (NaF) and ethanol on adenylate cyclase activity were investigated in mouse and rat striatum and cerebral cortex. In a crude homogenate of striatum, NaF (10 mM) had no effect on adenylate cyclase activity even though guanyl-5'-yl-imidodiphosphate (GppNHp) increased enzyme activity by two-fold. Addition of 300 mM ethanol increased basal and GppNHp-stimulated activity and allowed expression of an effect of NaF. Stimulation of adenylate cyclase activity by NaF was also observed after sedimentation and resuspension of membranes. Readdition of the supernatant to washed membranes caused a decrease in maximal NaF-stimulated activity without any change in the concentration of NaF required for half-maximal stimulation. The inhibitory effect of the supernatant was resistant to heat but was eliminated by the addition of ethanol or perchloric acid. Inhibition of NaF-stimulated adenylate cyclase activity in striatal tissue was also observed when assays were carried out in the presence of a 20,000 X g supernatant prepared from cerebral cortex. NaF-stimulated activity in cortical tissue was, on the other hand, enhanced in the presence of a 20,000 X g supernatant prepared from either cortex or striatum. This suggests that there is a basic difference between the adenylate cyclase systems of these tissues.</p>","PeriodicalId":7671,"journal":{"name":"Alcohol and drug research","volume":"6 6","pages":"379-86"},"PeriodicalIF":0.0000,"publicationDate":"1985-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Differential effects of cytosolic modulators of fluoride-stimulated adenylate cyclase activity in striatum and cerebral cortex.\",\"authors\":\"R A Rabin, D C Bode, P B Molinoff\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The effects of sodium fluoride (NaF) and ethanol on adenylate cyclase activity were investigated in mouse and rat striatum and cerebral cortex. In a crude homogenate of striatum, NaF (10 mM) had no effect on adenylate cyclase activity even though guanyl-5'-yl-imidodiphosphate (GppNHp) increased enzyme activity by two-fold. Addition of 300 mM ethanol increased basal and GppNHp-stimulated activity and allowed expression of an effect of NaF. Stimulation of adenylate cyclase activity by NaF was also observed after sedimentation and resuspension of membranes. Readdition of the supernatant to washed membranes caused a decrease in maximal NaF-stimulated activity without any change in the concentration of NaF required for half-maximal stimulation. The inhibitory effect of the supernatant was resistant to heat but was eliminated by the addition of ethanol or perchloric acid. Inhibition of NaF-stimulated adenylate cyclase activity in striatal tissue was also observed when assays were carried out in the presence of a 20,000 X g supernatant prepared from cerebral cortex. NaF-stimulated activity in cortical tissue was, on the other hand, enhanced in the presence of a 20,000 X g supernatant prepared from either cortex or striatum. This suggests that there is a basic difference between the adenylate cyclase systems of these tissues.</p>\",\"PeriodicalId\":7671,\"journal\":{\"name\":\"Alcohol and drug research\",\"volume\":\"6 6\",\"pages\":\"379-86\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1985-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Alcohol and drug research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Alcohol and drug research","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
研究了氟化钠(NaF)和乙醇对小鼠和大鼠纹状体和大脑皮层腺苷酸环化酶活性的影响。在纹状体粗匀浆中,NaF (10 mM)对腺苷酸环化酶活性没有影响,而鸟酰-5′-酰基-咪胺二磷酸(GppNHp)使酶活性提高了两倍。添加300 mM乙醇增加了基础和gppnhp刺激的活性,并允许NaF的表达。在沉淀和重悬膜后,也观察到NaF对腺苷酸环化酶活性的刺激。将上清液注入洗过的膜后,最大NaF刺激活性降低,但半最大刺激所需的NaF浓度没有变化。上清的抑制作用耐热,但通过添加乙醇或高氯酸消除。当从大脑皮层制备的20,000 X g上清液存在时,也观察到纹状体组织中naf刺激的腺苷酸环化酶活性的抑制。另一方面,在皮层或纹状体制备的20,000 X g上清液存在时,皮质组织中naf刺激的活性增强。这表明这些组织的腺苷酸环化酶系统之间存在基本差异。
Differential effects of cytosolic modulators of fluoride-stimulated adenylate cyclase activity in striatum and cerebral cortex.
The effects of sodium fluoride (NaF) and ethanol on adenylate cyclase activity were investigated in mouse and rat striatum and cerebral cortex. In a crude homogenate of striatum, NaF (10 mM) had no effect on adenylate cyclase activity even though guanyl-5'-yl-imidodiphosphate (GppNHp) increased enzyme activity by two-fold. Addition of 300 mM ethanol increased basal and GppNHp-stimulated activity and allowed expression of an effect of NaF. Stimulation of adenylate cyclase activity by NaF was also observed after sedimentation and resuspension of membranes. Readdition of the supernatant to washed membranes caused a decrease in maximal NaF-stimulated activity without any change in the concentration of NaF required for half-maximal stimulation. The inhibitory effect of the supernatant was resistant to heat but was eliminated by the addition of ethanol or perchloric acid. Inhibition of NaF-stimulated adenylate cyclase activity in striatal tissue was also observed when assays were carried out in the presence of a 20,000 X g supernatant prepared from cerebral cortex. NaF-stimulated activity in cortical tissue was, on the other hand, enhanced in the presence of a 20,000 X g supernatant prepared from either cortex or striatum. This suggests that there is a basic difference between the adenylate cyclase systems of these tissues.