DHCR24 inhibitor SH42 increases desmosterol without preventing atherosclerosis development in mice

The liver X receptor (LXR) is considered a therapeutic target for atherosclerosis treatment, but synthetic LXR agonists generally also cause hepatic steatosis and hypertriglyceridemia. Desmosterol, a final intermediate in cholesterol biosynthesis, has been identified as a selective LXR ligand that suppresses inflammation without inducing lipogenesis. Δ24-Dehydrocholesterol reductase (DHCR24) converts desmosterol into cholesterol, and we previously showed that the DHCR24 inhibitor SH42 increases desmosterol to activate LXR and attenuate experimental peritonitis and metabolic dysfunction-associated steatotic liver disease. Here, we aimed to evaluate the effect of SH42 on atherosclerosis development in APOE∗3-Leiden.CETP mice and low-density lipoproteins (LDL) receptor knockout mice, models for lipid- and inflammation-driven atherosclerosis, respectively. In both models, SH42 increased desmosterol without affecting plasma lipids. While reducing liver lipids in APOE∗3-Leiden.CETP mice, and regulating populations of circulating monocytes in LDL receptor knockout mice, SH42 did not attenuate atherosclerosis in either model. [Display omitted] •DHCR24 inhibitor SH42 increases desmosterol in mice without causing hyperlipidemia•SH42 treatment decreases hepatic lipids in hyperlipidemic APOE∗3-Leiden.CETP mice•SH42 treatment lowers the abundance of blood monocytes in LDLr-KO mice•SH42 treatment does not affect atherosclerosis development in mice Cardiovascular medicine; Cellular physiology; Molecular genetics