作者
Tzu-Tang Wei,Mark Chandy,Masataka Nishiga,Angela Zhang,Kaavya Krishna Kumar,Dilip Thomas,Amit Manhas,Siyeon Rhee,Johanne Marie Justesen,Ian Y. Chen,Hung-Ta Wo,Saereh Khanamiri,Johnson Y. Yang,Frederick J. Seidl,Noah Z. Burns,Chun Liu,Nazish Sayed,Jiun‐Jie Shie,Chih-Fan Yeh,Kai‐Chien Yang,Edward Lau,Kara L. Lynch,Manuel A. Rivas,Brian K. Kobilka,Joseph C. Wu
摘要
Epidemiological studies reveal that marijuana increases the risk of cardiovascular disease (CVD); however, little is known about the mechanism. Δ9-tetrahydrocannabinol (Δ9-THC), the psychoactive component of marijuana, binds to cannabinoid receptor 1 (CB1/CNR1) in the vasculature and is implicated in CVD. A UK Biobank analysis found that cannabis was an risk factor for CVD. We found that marijuana smoking activated inflammatory cytokines implicated in CVD. In silico virtual screening identified genistein, a soybean isoflavone, as a putative CB1 antagonist. Human-induced pluripotent stem cell-derived endothelial cells were used to model Δ9-THC-induced inflammation and oxidative stress via NF-κB signaling. Knockdown of the CB1 receptor with siRNA, CRISPR interference, and genistein attenuated the effects of Δ9-THC. In mice, genistein blocked Δ9-THC-induced endothelial dysfunction in wire myograph, reduced atherosclerotic plaque, and had minimal penetration of the central nervous system. Genistein is a CB1 antagonist that attenuates Δ9-THC-induced atherosclerosis.