Yu DING, Hou-yong ZHU, Li-zong ZHANG, et al. Shexiang Tongxin Dropping Pill (麝香通心滴丸) Reduces Coronary Microembolization in Rats via Regulation of Mitochondrial Permeability Transition Pore Opening and AKT-GSK3β Phosphorylation. [J]. Chinese Journal of Integrative Medicine 27(7):527-533(2021)
DOI:
Yu DING, Hou-yong ZHU, Li-zong ZHANG, et al. Shexiang Tongxin Dropping Pill (麝香通心滴丸) Reduces Coronary Microembolization in Rats via Regulation of Mitochondrial Permeability Transition Pore Opening and AKT-GSK3β Phosphorylation. [J]. Chinese Journal of Integrative Medicine 27(7):527-533(2021) DOI: 10.1007/s11655-019-3176-6.
Shexiang Tongxin Dropping Pill (麝香通心滴丸) Reduces Coronary Microembolization in Rats via Regulation of Mitochondrial Permeability Transition Pore Opening and AKT-GSK3β Phosphorylation
摘要
Abstract
Objective:
2
To investigate the protective effects of Shexiang Tongxin Dropping Pill (麝香通心滴丸
STDP) following sodium laurate-induced coronary microembolization (CME) in rats.
Methods:
2
Forty rats were divided into 4 groups: the control (sham) group
CME group
low-dose STDP pretreatment group (20 mg•kg
-1
•d
-1
)
and high-dose STDP pretreatment group (40 mg•kg
-1
•d
-1
). The rats were intragastric administrated with STDP 2 weeks before operation. Moreover
the histopathological alterations were observed using optical microscopy and transmission electron microscopy. Antioxidant biomarkers were analyzed by enzyme-linked immunosorbent assay. Mitochondrial functions including the mitochondrial permeability transition pore (mPTP) mtDNA copy number were determined and proteins of AKT/GSK3β were analyzed by Western blot.
Results:
2
The rats in the CME group showed a significant increase in the fibrinogen-like protein 2 expression level and mitochondrial dysfunction and a decrease in the expression level of antioxidant biomarkers (superoxide dismutase and catalase
P
<
0.01 for all). In contrast
the rats in the low- and high-dose STDP pretreatment groups showed a significant decrease in coronary microthrombi (
P
<
0.05); moreover
STDP restored the antioxidant-related protein activities and mitochondrial function
inhibited mPTP opening
decreased AKT-Ser473 phosphorylation
and increased GSK3β-Ser9 phosphorylation (
P
<
0.05 or
P
<
0.01).
Conclusion:
2
STDP may be useful for treatment of CME
possibly via regulation of mPTP opening and AKT/GSK3β phosphorylation.
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