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缺氧新生大鼠心室肌细胞中的β受体-腺苷酸环化酶偶联

Beta-receptor-adenylate cyclase coupling in hypoxic neonatal rat ventricular myocytes.

作者信息

Thandroyen F T, Muntz K, Rosenbaum T, Ziman B, Willerson J T, Buja L M

机构信息

Department of Internal Medicine (Cardiology), University of Texas, Southwestern Medical Center, Dallas 75235.

出版信息

Am J Physiol. 1989 Apr;256(4 Pt 2):H1209-17. doi: 10.1152/ajpheart.1989.256.4.H1209.

Abstract

This study investigated the influence of hypoxia on alterations in the beta-adrenergic receptor-adenylate cyclase system. Cultured neonatal rat ventricular myocytes were subjected to normoxia (incubator PO2 135-145 mmHg) or hypoxia (incubator PO2 0-14 mmHg) and, in crude membrane preparations, beta-receptor binding properties were measured with [125I]iodocyanopindolol and adenylate cyclase activity by radioimmunoassay. Hypoxia of 30 min in duration caused no alteration in beta-receptor density (Bmax 75 +/- 11 vs. 71 +/- 12 fmol/mg protein) but increased adenylate cyclase activity under basal conditions and during stimulation with l-isoproterenol, 5'-guanylimidotriphosphate [Gpp(NH)p] 5 X 10(-5) M, NaF 10(-4) M, and forskolin 10(-4) M. For example, isoproterenol 10(-5) M + guanosine 5'-triphosphate (GTP) 5 X 10(-5) M gave 221 +/- 34 vs. 143 +/- 11 pmol.min-1.mg protein-1, P less than 0.05 hypoxia vs. normoxia. After 60 min of hypoxia, adenylate cyclase activity was no longer increased. Hypoxia of 120-150 min duration increased Bmax by 64% (73 +/- 8 to 120 +/- 11 fmol/mg protein, P less than 0.05 vs. normoxia) but decreased adenylate cyclase activity during stimulation with isoproterenol, NaF 10(-4) M, and forskolin 10(-4) M. For example, isoproterenol 10(-5) M + GTP 5 X 10(-5) M gave 107 +/- 12 vs. 148 +/- 11 pmol.min-1.mg protein-1, P less than 0.05 hypoxia vs. normoxia. Reoxygenation for 15 min following 120-150 min of hypoxia reversed the increased beta-receptor numbers and decreased adenylate cyclase activity.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究调查了缺氧对β-肾上腺素能受体-腺苷酸环化酶系统变化的影响。将培养的新生大鼠心室肌细胞置于常氧(培养箱PO₂ 135 - 145 mmHg)或缺氧(培养箱PO₂ 0 - 14 mmHg)环境中,在粗制膜制剂中,用[¹²⁵I]碘氰吲哚洛尔测定β受体结合特性,并用放射免疫分析法测定腺苷酸环化酶活性。持续30分钟的缺氧未导致β受体密度改变(Bmax 75 ± 11对71 ± 12 fmol/mg蛋白质),但在基础条件下以及用l-异丙肾上腺素、5'-鸟苷酰亚胺三磷酸[Gpp(NH)p] 5×10⁻⁵ M、NaF 10⁻⁴ M和福斯可林10⁻⁴ M刺激时,增加了腺苷酸环化酶活性。例如,10⁻⁵ M异丙肾上腺素 + 5×10⁻⁵ M鸟苷-5'-三磷酸(GTP)时,缺氧组为221 ± 34,常氧组为143 ± 11 pmol·min⁻¹·mg蛋白质⁻¹,缺氧组与常氧组相比P < 0.05。缺氧60分钟后,腺苷酸环化酶活性不再增加。持续120 - 150分钟的缺氧使Bmax增加64%(73 ± 8至120 ± 11 fmol/mg蛋白质,与常氧组相比P < 0.05),但在用异丙肾上腺素、10⁻⁴ M NaF和10⁻⁴ M福斯可林刺激时降低了腺苷酸环化酶活性。例如,10⁻⁵ M异丙肾上腺素 + 5×10⁻⁵ M GTP时,缺氧组为107 ± 12,常氧组为148 ± 11 pmol·min⁻¹·mg蛋白质⁻¹,缺氧组与常氧组相比P < 0.05。在120 - 150分钟缺氧后再给氧15分钟,可逆转增加的β受体数量和降低的腺苷酸环化酶活性。(摘要截断于250字)

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