Curcuma oil reduces endothelial cell-mediated inflammation in postmyocardial ischemia/reperfusion in rats

• Published in: Journal of cardiovascular pharmacology Vol. 64; no. 3; p. 228
• Main Authors: Manhas, Amit, Khanna, Vivek, Prakash, Prem, Goyal, Dipika, Malasoni, Richa, Naqvi, Arshi, Dwivedi, Anil K, Dikshit, Madhu, Jagavelu, Kumaravelu
• Format: Journal Article
• Language: English
• Published: United States 01.09.2014
• Subjects: Animals; Cell Line; Curcuma - chemistry; Disease Models, Animal; E-Selectin - metabolism; Endothelial Cells - drug effects; Endothelial Cells - metabolism; Enzyme-Linked Immunosorbent Assay; Humans; Inflammation - drug therapy; Inflammation - pathology; Male; Monocytes - drug effects; Monocytes - metabolism; Myocardial Reperfusion Injury - drug therapy; Myocardial Reperfusion Injury - physiopathology; Oils, Volatile - pharmacology; Rats; Rats, Wistar; Real-Time Polymerase Chain Reaction
• ISSN: 1533-4023
• DOI: 10.1097/FJC.0000000000000110

Endothelial cells initiated inflammation persisting in postmyocardial infarction needs to be controlled and moderated for avoiding fatal complications. Curcuma oil (C.oil, Herbal Medicament), a standardized hexane soluble fraction of Curcuma longa has possessed neuroprotective effect. However, its effect on myocardial ischemia/reperfusion (MI/RP) and endothelial cells remains incompletely defined. Here, using in vivo rat MI/RP injury model and in vitro cellular approaches using EA.hy926 endothelial cells, enzyme-linked immunosorbent assay, real-time polymerase chain reaction, and myograph, we provide evidence that with effective regimen and preconditioning of rats with C.oil (250 mg/kg, PO), before and after MI/RP surgery protects rats from MI/RP-induced injury. C.oil treatment reduces left ventricular ischemic area and endothelial cell-induced inflammation, specifically in the ischemic region (*P < 0.0001) and improved endothelial function by reducing the expression of proinflammatory genes and adhesion factors on endothelial cells both in vitro and in vivo. Furthermore, mechanistic studies have revealed that C.oil reduced the expression of adhesion factors like E-selectin (#P = 0.0016) and ICAM-1 ($P = 0.0069) in initiating endothelial cells-induced inflammation. In line to the real-time polymerase chain reaction expression data, C.oil reduced the adhesion of inflammatory cells to endothelial cells as assessed by the interaction of THP-1 monocytes with the endothelial cells using flow-based adhesion and under inflammatory conditions. These studies provide evidence that salutary effect of C.oil on MI/RP could be achieved with pretreatment and posttreatment of rats, C.oil reduced MI/RP-induced injury by reducing the endothelial cell-mediated inflammation, specifically in the ischemic zone of MI/RP rat heart.