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链脲佐菌素诱导的糖尿病与大鼠心肌肌膜、主动脉和肝脏中腺苷酸环化酶的激素敏感性

Streptozotocin-induced diabetes and hormone sensitivity of adenylate cyclase in rat myocardial sarcolemma, aorta and liver.

作者信息

Srivastava A K, Anand-Srivastava M B

出版信息

Biochem Pharmacol. 1985 Jun 1;34(11):2013-7. doi: 10.1016/0006-2952(85)90324-7.

DOI:10.1016/0006-2952(85)90324-7
PMID:4039939
Abstract

Adenylate cyclase activity was investigated in myocardial sarcolemma, aorta particulate fractions, and liver plasma membranes from control and 5-day streptozotocin-induced diabetic rats. The basal adenylate cyclase activity was increased in heart sarcolemma from diabetic rats, whereas the extent of stimulation by glucagon, dopamine, isoproterenol, epinephrine, sodium fluoride and forskolin was decreased markedly. The decreased responsiveness was associated with a decrease in Vmax but not in the activation constant. In contrast, GTP stimulated adenylate cyclase in control and diabetic myocardial sarcolemma to the same extent. In addition, the basal adenylate cyclase activity was not altered significantly in aorta particulate fraction of liver plasma membranes from diabetic rats, but the stimulation of adenylate cyclase by catecholamines and forskolin (in the case of aorta) and by adenosine, glucagon, NaF and forskolin (in the case of liver) was diminished markedly. These data suggest that, in streptozotocin-induced diabetes, the responsiveness of adenylate cyclase to various hormones and agents (fluoride and forskolin) which act through receptor-independent mechanisms is decreased.

摘要

研究了对照大鼠和经链脲佐菌素诱导糖尿病5天的大鼠的心肌肌膜、主动脉微粒体部分及肝细胞膜中的腺苷酸环化酶活性。糖尿病大鼠心肌肌膜中的基础腺苷酸环化酶活性增加,而胰高血糖素、多巴胺、异丙肾上腺素、肾上腺素、氟化钠和福斯高林的刺激程度则显著降低。反应性降低与Vmax降低有关,但与活化常数无关。相比之下,GTP对对照大鼠和糖尿病大鼠心肌肌膜中腺苷酸环化酶的刺激程度相同。此外,糖尿病大鼠主动脉微粒体部分及肝细胞膜中的基础腺苷酸环化酶活性无显著改变,但儿茶酚胺和福斯高林(在主动脉的情况下)以及腺苷、胰高血糖素、氟化钠和福斯高林(在肝脏的情况下)对腺苷酸环化酶的刺激显著减弱。这些数据表明,在链脲佐菌素诱导的糖尿病中,腺苷酸环化酶对通过非受体依赖机制起作用的各种激素和试剂(氟化物和福斯高林)的反应性降低。

相似文献

1
Streptozotocin-induced diabetes and hormone sensitivity of adenylate cyclase in rat myocardial sarcolemma, aorta and liver.链脲佐菌素诱导的糖尿病与大鼠心肌肌膜、主动脉和肝脏中腺苷酸环化酶的激素敏感性
Biochem Pharmacol. 1985 Jun 1;34(11):2013-7. doi: 10.1016/0006-2952(85)90324-7.
2
Altered responsiveness of adenylate cyclase to adenosine and other agents in the myocardial sarcolemma and aorta of spontaneously-hypertensive rats.自发性高血压大鼠心肌肌膜和主动脉中腺苷酸环化酶对腺苷及其他试剂的反应性改变。
Biochem Pharmacol. 1988 Aug 1;37(15):3017-22. doi: 10.1016/0006-2952(88)90291-2.
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Altered hormone sensitivity of adenylate cyclase in myocardial sarcolemma of renal hypertensive rats.肾性高血压大鼠心肌肌膜中腺苷酸环化酶激素敏感性的改变
Biochem Pharmacol. 1983 Oct 1;32(19):2857-62. doi: 10.1016/0006-2952(83)90389-1.
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Alloxan-induced diabetes reduces beta-adrenergic receptor number without affecting adenylate cyclase in rat ventricular membranes.四氧嘧啶诱导的糖尿病会减少大鼠心室膜中β-肾上腺素能受体的数量,而不影响腺苷酸环化酶。
J Cardiovasc Pharmacol. 1983 May-Jun;5(3):454-61. doi: 10.1097/00005344-198305000-00018.
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Regulation of adenylate cyclase by adenosine and other agonists in rat myocardial sarcolemma.大鼠心肌肌膜中腺苷及其他激动剂对腺苷酸环化酶的调节作用
Arch Biochem Biophys. 1985 Dec;243(2):439-46. doi: 10.1016/0003-9861(85)90520-x.
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Selective alteration of secretin-stimulated cardiac adenylate cyclase activity in streptozotocin-diabetic rats.链脲佐菌素诱导的糖尿病大鼠中促胰液素刺激的心脏腺苷酸环化酶活性的选择性改变。
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Determination of G-protein levels, ADP-ribosylation by cholera and pertussis toxins and the regulation of adenylyl cyclase activity in liver plasma membranes from lean and genetically diabetic (db/db) mice.测定瘦型和遗传性糖尿病(db/db)小鼠肝细胞膜中G蛋白水平、霍乱毒素和百日咳毒素介导的ADP核糖基化作用以及腺苷酸环化酶活性的调节。
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Regulation of adenylate cyclase by hormones and guanine nucleotides in normal, desensitized, and resensitized rabbit heart.正常、脱敏和再敏化兔心脏中激素和鸟嘌呤核苷酸对腺苷酸环化酶的调节
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Guanine nucleotide binding regulatory proteins and adenylate cyclase in livers of streptozotocin- and BB/Wor-diabetic rats. Immunodetection of Gs and Gi with antisera prepared against synthetic peptides.
J Clin Invest. 1989 Jun;83(6):2050-62. doi: 10.1172/JCI114116.
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Forskolin regulation of liver membrane adenylyl cyclase.福斯高林对肝细胞膜腺苷酸环化酶的调节作用。
Eur J Biochem. 1983 Oct 17;136(1):107-12. doi: 10.1111/j.1432-1033.1983.tb07712.x.

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Cells. 2020 Nov 26;9(12):2548. doi: 10.3390/cells9122548.
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