Key result
Pretreatment with kaempferol improved myocardial function, reduced infarct size and apoptosis, and modulated biochemical markers in isolated rat hearts with ischemia/reperfusion injury.
Why the study?
Does pretreatment with kaempferol improve myocardial function and reduce injury in isolated rat hearts subjected to ischemia/reperfusion?
Does pretreatment with kaempferol improve myocardial function and reduce injury in isolated rat hearts subjected to ischemia/reperfusion?
Kaempferol provides cardioprotection against ischemia/reperfusion injury in rat hearts via antioxidant activity and inhibition of GSK-3β.
Hypothesis-generating in isolated rat hearts; leaves open translation to human ischemia/reperfusion injury.
OBJECTIVE: This study aimed to evaluate the protective effect of kaempferol against myocardial ischemia/reperfusion (I/R) injury in rats. METHOD: Left ventricular developed pressure (LVDP) and its maximum up/down rate (±dp/dt max) were recorded as myocardial function. Infarct size was detected with 2,3,5-triphenyltetrazolium chloride staining. Cardiomyocyte apoptosis was determined using terminal deoxynucleotidyl nick-end labeling (TUNEL). The levels of creatine kinase (CK), lactate dehydrogenase (LDH), malondialdehyde (MDA), superoxide dismutase (SOD), glutathione/glutathione disulfide (GSH/GSSG) ratio, and tumor necrosis factor-alpha (TNF-α) were determined using enzyme linked immunosorbent assay (ELISA). Moreover, total glycogen synthase kinase-3β (GSK-3β), phospho-GSK-3β (P-GSK-3β), precaspase-3, cleaved caspase-3, and cytoplasm cytochrome C were assayed using Western blot analysis. RESULTS: Pretreatment with kaempferol significantly improved the recovery of LVDP and ±dp/dt max, as well as increased the levels of SOD and P-GSK-3β and GSH/GSSG ratio. However, the pretreatment reduced myocardial infarct size and TUNEL-positive cell rate, as well as decreased the levels of cleaved caspase-3, cytoplasm cytochrome C, CK, LDH, MDA, and TNF-α. CONCLUSION: These results suggested that kaempferol provides cardioprotection via antioxidant activity and inhibition of GSK-3β activity in rats with I/R.
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Zhou et al. (2015) studied Myocardial ischemia/reperfusion injury. Kaempferol was evaluated on Myocardial function (LVDP, ±dp/dt max), infarct size, apoptosis, and biochemical markers. Pretreatment with kaempferol improved myocardial function, reduced infarct size and apoptosis, and modulated biochemical markers in isolated rat hearts with ischemia/reperfusion injury.
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