Haenen G R, Van Dansik P, Vermeulen N P, Timmerman H, Bast A
Department of Pharmacochemistry, Subfaculty of Chemistry, Vrije Universiteit, Amsterdam, The Netherlands.
Free Radic Res Commun. 1988;4(4):243-9. doi: 10.3109/10715768809055149.
A membrane preparation of calf heart left ventricle has been used to study the effect of radical stress on the beta-adrenoceptor complex. To this end the membranes were incubated for 30 minutes with several concentrations of hydrogen peroxide. This resulted in a dose dependent peroxidation of the membrane lipids. Preincubation with hydrogen peroxide in the concentration range 10(-7)-10(-3) M caused an increase in specific (-)-[125I]-Iodocyanopindolol binding, possibly due to a decrease in membrane fluidity as a result of lipid peroxidation, thus making the receptor protein more accessible. Higher concentrations H2O2 reduced the specific (-)-[125I]-Iodocyanopindolol binding, which is most likely the effect of deterioration of the receptor protein by the more pronounced radical stress induced by these higher concentrations. Also adenylate cyclase activity was affected by radical stress. Basal cyclic-AMP production and cyclic-AMP production induced by NaF (10(-2) M) or guanylylimidodiphosphate (10(-4) M), was suppressed after pretreatment with concentrations of H2O2 above 10(-4) M. This indicates a higher sensitivity of the adenylate cyclase toward radical stress when compared to the receptor protein. Our results show that radical stress can perturb beta-adrenoceptor function considerably in the heart.
利用小牛心脏左心室的膜制剂研究自由基应激对β - 肾上腺素能受体复合物的影响。为此,将膜与几种浓度的过氧化氢孵育30分钟。这导致膜脂质发生剂量依赖性过氧化。在10(-7)-10(-3)M浓度范围内用过氧化氢预孵育会导致特异性(-)-[125I]-碘氰吲哚洛尔结合增加,这可能是由于脂质过氧化导致膜流动性降低,从而使受体蛋白更容易接近。较高浓度的H2O2会降低特异性(-)-[125I]-碘氰吲哚洛尔结合,这很可能是由于这些较高浓度诱导的更明显的自由基应激使受体蛋白降解所致。腺苷酸环化酶活性也受到自由基应激的影响。在用高于10(-4)M浓度的H2O2预处理后,基础环磷酸腺苷(cAMP)产生以及由氟化钠(10(-2)M)或鸟苷酰亚胺二磷酸(10(-4)M)诱导的cAMP产生均受到抑制。这表明与受体蛋白相比,腺苷酸环化酶对自由基应激更敏感。我们的结果表明,自由基应激可显著扰乱心脏中的β - 肾上腺素能受体功能。