Kanchana Kengkoom MS*, Aunchalee Sirimontaporn MS*, Uthai Sotanaphun PhD**, Orapin Gerdprasert DVM, PhD***, Punnee Nusuetrong PhD****
Affiliation : * National Laboratory Animal Center, Mahidol University, Nakhon Pathom, Thailand ** Department of Pharmacognosy, Faculty of Pharmacy, Silpakorn University, Nakhon Pathom, Thailand *** Department of Anatomy, Faculty of Medicine, Srinakharinwirot University, Bangkok, Thailand **** Department of Physiology, Faculty of Medicine, Srinakharinwirot University, Bangkok, Thailand
Background : Phikud Navakot (PN) is a set of nine medicinal plants and the main ingredient of “Yahom Navakot”, a
traditional Thai herbal formula for treatment of cardiovascular symptoms.
Objective : To investigate the cardioprotective effects of PN on myocardial ischemia/reperfusion (IR) in male Sprague Dawley
rats.
Material and Method: Rats were randomly divided into 7 groups: sham, IR, and IR orally pretreated with PN (10, 50, 100,
200, and 400 mg/kg BW) for 7 days. After treatment, IR induction was performed by left coronary artery (LCA) ligation for
30 min, followed by reperfusion for 24 h. At the end of the experiment, blood was collected for hematological and biochemical
parameters, and hearts were immediately removed for histopathological examination and Western blot analysis.
Results : IR induction caused ST elevation in the electrocardiogram and an increase in serum troponin I (TnI), confirming
myocardial damage. In addition, histopathological changes of ischemic myocardium showed inflammation, infiltration, and
edema. Oral administration of PN (10, 50, 100, 200, and 400 mg/kg BW) for 7 days prior to IR simulation showed no change
on serum TnI and histopathology of cardiac tissues, when compared to IR group. However, Western blot analysis showed that
IR rats pretreated with PN (10 mg/kg BW) significantly increased (p<0.05) pERK/ERK ratio, meanwhile pretreated with PN
(50-200 mg/kg BW) up-regulated (p<0.05) the protein expression of HO-1, when compared with IR group.
Conclusion : The present study implied that 7-day pretreatment of PN failed to protect cardiac tissues against IR injury
induced by LCA ligation. Investigation at molecular level found however that PN up-regulated the expression of protective
proteins pERK/ERK ratio and HO-1 in cardiac tissues, suggesting molecular mechanism of PN in cardioprotection against
IR injury.
Keywords : Phikud Navakot, Yahom, Left coronary artery ligation, Troponin, HO-1, ERK1/2
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