Effect of thyroid status on phosphatidylinositols in rat heart.

Cardioscience Pub Date : 1993-12-01
G Jakab, E Kiss, E G Kranias, I Edes
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Abstract

The incorporation of 32Pi into phosphatidylinositols and inositol trisphosphates was studied in Langendorff-perfused hearts from hypothyroid, euthyroid and hyperthyroid rats. The hearts were perfused with modified Krebs buffer containing [32P]orthophosphate and the degree of 32P-labeling of phosphatidylinositol, phosphatidylinositol 4-monophosphate, phosphatidylinositol 4,5-bisphosphate, inositol trisphosphates and phosphatidic acid was measured. Hyperthyroidism was associated with increases in rates of rise and fall of left ventricular systolic pressure, sarcoplasmic reticular Ca(2+)-ATPase activity and 32P-labeling of phosphatidylinositols, inositol trisphosphates and phosphatidic acid. These measurements were significantly decreased in hypothyroid hearts. The tissue levels of inositol 1,4,5-trisphosphate isoform were found to be significantly higher in hyperthyroid hearts and lower in hypothyroid hearts than in euthyroid ones. Examination of phosphoinositide-specific phospholipase C activity in the perfused hearts revealed that hyperthyroidism was associated with an increase in the membrane-associated enzymatic activity, assayed at physiological calcium concentrations, while hypothyroidism was associated with a decrease in this activity as compared with control hearts. These findings indicate that alterations in the thyroid state of the myocardium may be associated with changes in basal phosphoinositide turnover which may contribute to alterations in myocardial contraction.

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甲状腺状态对大鼠心脏磷脂酰肌醇的影响。
在langendorff灌注的甲状腺功能减退、甲状腺功能正常和甲状腺功能亢进大鼠心脏中,研究了32Pi在磷脂酰肌醇和肌醇三磷酸中的掺入情况。用含[32P]正磷酸盐的改良Krebs缓冲液灌注心脏,测定磷脂酰肌醇、4-单磷酸磷脂酰肌醇、4,5-二磷酸磷脂酰肌醇、三磷酸肌醇和磷脂酸的32P标记度。甲状腺机能亢进与左室收缩压升高和下降的速率、肌浆网状Ca(2+)- atp酶活性以及磷脂酰肌醇、三磷酸肌醇和磷脂酸的32p标记增加有关。这些指标在甲状腺功能减退的心脏中显著降低。肌醇1,4,5-三磷酸异构体的组织水平在甲状腺功能亢进的心脏中明显高于正常甲状腺功能的心脏,而在甲状腺功能低下的心脏中明显低于正常甲状腺功能的心脏。对灌注心脏中磷酸肌醇特异性磷脂酶C活性的检查显示,在生理钙浓度下,甲状腺机能亢进与膜相关酶活性的增加有关,而与对照心脏相比,甲状腺功能减退与膜相关酶活性的降低有关。这些发现表明,心肌甲状腺状态的改变可能与基础磷酸肌肽转换的变化有关,这可能导致心肌收缩的改变。
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