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Effect of Dopamine Receptor 1 on Apoptosis of Cultured Neonatal Rat Cardiomyocytes in Simulated Ischaemia/Reperfusion
Author(s) -
Li Hongzhu,
Han Liping,
Jiang Chunming,
Li Hong,
Zhao Yajun,
Gao Jun,
Lin Yan,
Ma Shuxia,
Tian Ye,
Yang Baofeng,
Xu Changqing
Publication year - 2008
Publication title -
basic and clinical pharmacology and toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.805
H-Index - 90
eISSN - 1742-7843
pISSN - 1742-7835
DOI - 10.1111/j.1742-7843.2007.00177.x
Subject(s) - terminal deoxynucleotidyl transferase , lactate dehydrogenase , superoxide dismutase , apoptosis , agonist , malondialdehyde , fas ligand , receptor , medicine , endocrinology , biology , microbiology and biotechnology , chemistry , pharmacology , tunel assay , biochemistry , programmed cell death , oxidative stress , enzyme
Dopamine receptors exist in many tissues, including rat cardiac tissue. However, the physiological importance of dopamine receptors in the homeostatic regulation of cardiac function is unclear. In this study, a model of ischaemia/reperfusion was established by culturing primary neonatal rat cardiomyocytes in ischaemia‐mimetic solution for 2 hr, followed by incubation in normal culture medium for 24 hr. Lactate dehydrogenase activity, superoxide dismutase activity and malondialdehyde content were determined colorimetrically with a spectrophotometer. Apoptotic cell death was assayed by 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide assay, terminal deoxynucleotidyl transferase‐mediated dUTP‐biotin nick end labelling staining and flow cytometry, and morphological alterations were observed with transmission electron microscopy. The intracellular free calcium concentration ([Ca 2+ ] i ) was measured by confocal laser scanning microscopy. Finally, the expression of dopamine receptor 1 (DR1), caspase‐3, ‐8 and ‐9, Fas, Fas ligand and Bcl‐2 and the release of cytochrome c were analysed by Western blot. The results showed that DR1 expression was increased markedly during ischaemia/reperfusion. Treatment with 10 µM SKF‐38393 (DR1 agonist) significantly increased lactate dehydrogenase activity, decreased superoxide dismutase activity and increased malondialdehyde content in the culture medium. The DR1 agonist promoted the release of cytochrome c , accumulation of [Ca 2+ ] i , and apoptosis induced by ischaemia/reperfusion. Furthermore, SKF‐38393 up‐regulated the expression of caspase‐3, ‐8 and ‐9, Fas and Fas ligand, and down‐regulated Bcl‐2 expression. In contrast, 10 µM SCH‐23390 (DR1 antagonist) had no significant effects on the above indicators. In conclusion, DR1 activation is involved in the apoptosis of cultured neonatal rat cardiomyocytes in simulated ischaemia/reperfusion through the mitochondrial and death receptor pathways.