Abstract Title:

Betulinic Acid Induces eNOS Expression via the AMPK-Dependent KLF2 Signaling Pathway.

Abstract Source:

J Agric Food Chem. 2020 Dec 9 ;68(49):14523-14530. Epub 2020 Nov 24. PMID: 33232606

Abstract Author(s):

Gi Ho Lee, Jin Song Park, Sun Woo Jin, Thi Hoa Pham, Tuyet Ngan Thai, Ji Yeon Kim, Chae Yeon Kim, Jae Ho Choi, Eun Hee Han, Hye Gwang Jeong

Article Affiliation:

Gi Ho Lee


Betulinic acid (BA) is a natural pentacyclic triterpenoid with protective effects against inflammation, metabolic diseases, and cardiovascular diseases. We have previously shown that BA prevents endothelial dysfunction by increasing nitric oxide (NO) synthesis through activating endothelial nitric oxide synthase (eNOS) in human endothelial cells. However, the effect of BA on eNOS expression remains unclear. Thus, the aim of our study was to investigate the intracellular pathways associated with the effect of BA to regulate eNOS expression in human endothelial cells. BA significantly increased eNOS expression in a time- and concentration-dependent manner. Additionally, BA upregulated the expression of the transcription factor KLF2, which is known to regulate eNOS expression. KLF2 silencing in human endothelial cells attenuated the ability of BA to upregulate eNOS. BA also increased levels of intracellular Ca, activating CaMKKβ, CaMKIIα, and AMPK. Inhibition of the TRPC calcium channel abolished BA-mediated effects on intracellular Calevels. Moreover, BA increased the phosphorylation levels of ERK5, HDAC5, and MEF2C. Pretreatment of cells with compound C (AMPK inhibitor), LMK235 (HDAC5 inhibitor), and XMD8-92 (ERK5 inhibitor) attenuated the BA-induced eNOS expression. Collectively, these findings suggest that BA induces eNOS expression by activating the HDAC5/ERK5/KLF2 pathway in endothelial cells. The data presented here provide strong evidence supporting the use of BA to prevent endothelial dysfunction and treat vascular diseases, such as atherosclerosis.

Study Type : Human In Vitro

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