Abstract |
To investigate the effort of mitochondrial calcium transport and calcium-induced membrane permeability transition in alleviating atherosclerosis. The experimental mice were divided into three groups: the control group (C57BL/6 mice with normal diet), the atherosclerosis group ( apolipoprotein E-deficient ( ApoE-/-) mice with high-fat diet) and the mitochondrial targeting agent group ( ApoE-/- mouse with high-fat diet). The mean fluorescence intensity of Ca2+ in the atherosclerosis group is significantly higher than control group and mitochondrial targeting agent group. But the mean fluorescence intensity of Ca2+- ATPase is lower than other groups. The macrophage recruitment (F4/80 positive area) and the expression of tumor necrosis factor alpha, interleukin-6, pyrin domain containing protein 3, intercellular cell adhesion molecule-1, p38 mitogen-activated protein kinase and Jun kinase 1/2 phosphorylation in the atherosclerosis group are higher that other groups. Treatment with mitochondrial targeting agents reduced the levels of elevated cyt C and cleaved caspase-3 in atherosclerotic mice (p<0.05). Mitochondrial targeting agents interfere with mitochondrial calcium transport and calcium-induced membrane permeability transition, inhibit MAPK/JNK pathway activation, inhibit foam cell formation and alleviate the process of atherosclerosis.
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Authors | Sisi Chen, Jianing Wang, Lei Zhang, Hao Xia |
Journal | Journal of investigative medicine : the official publication of the American Federation for Clinical Research
(J Investig Med)
Vol. 69
Issue 6
Pg. 1156-1160
(08 2021)
ISSN: 1708-8267 [Electronic] England |
PMID | 33906902
(Publication Type: Journal Article)
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Copyright | © American Federation for Medical Research 2021. No commercial re-use. See rights and permissions. Published by BMJ. |
Chemical References |
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Topics |
- Animals
- Atherosclerosis
(drug therapy)
- Calcium
(metabolism)
- Calcium Signaling
- Mice
- Mice, Inbred C57BL
- Mice, Knockout, ApoE
- Mitochondria
(drug effects, metabolism)
- Permeability
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