Hepatic Cannabinoid Receptor Type 1 Mediates Alcohol-Induced Regulation of Bile Acid Enzyme Genes Expression Via CREBH

Dipanjan Chanda, Yong Hoon Kim, Tiangang Li, Jagannath Misra, Don Kyu Kim, Jung Ran Kim, Joseph Kwon, Won Il Jeong, Sung Hoon Ahn, Tae Sik Park, Seung-Hoi Koo, John Y L Chiang, Chul Ho Lee, Hueng Sik Choi

Research output: Contribution to journalArticle

20 Citations (Scopus)

Abstract

Bile acids concentration in liver is tightly regulated to prevent cell damage. Previous studies have demonstrated that deregulation of bile acid homeostasis can lead to cholestatic liver disease. Recently, we have shown that ER-bound transcription factor Crebh is a downstream effector of hepatic Cb1r signaling pathway. In this study, we have investigated the effect of alcohol exposure on hepatic bile acid homeostasis and elucidated the mediatory roles of Cb1r and Crebh in this process. We found that alcohol exposure or Cb1r-agonist 2-AG treatment increases hepatic bile acid synthesis and serum ALT, AST levels in vivo alongwith significant increase in Crebh gene expression and activation. Alcohol exposure activated Cb1r, Crebh, and perturbed bile acid homeostasis. Overexpression of Crebh increased the expression of key bile acid synthesis enzyme genes via direct binding of Crebh to their promoters, whereas Cb1r knockout and Crebh-knockdown mice were protected against alcohol-induced perturbation of bile acid homeostasis. Interestingly, insulin treatment protected against Cb1r-mediated Crebh-induced disruption of bile acid homeostasis. Furthermore, Crebh expression and activation was found to be markedly increased in insulin resistance conditions and Crebh knockdown in diabetic mice model (db/db) significantly reversed alcohol-induced disruption of bile acid homeostasis. Overall, our study demonstrates a novel regulatory mechanism of hepatic bile acid metabolism by alcohol via Cb1r-mediated activation of Crebh, and suggests that targeting Crebh can be of therapeutic potential in ameliorating alcohol-induced perturbation of bile acid homeostasis.

Original languageEnglish
Article numbere68845
JournalPLoS One
Volume8
Issue number7
DOIs
Publication statusPublished - 2013 Jul 22

Fingerprint

Cannabinoid Receptors
bile acids
Bile Acids and Salts
Gene expression
alcohols
Alcohols
Gene Expression
gene expression
liver
Liver
homeostasis
Enzymes
enzymes
Homeostasis
Chemical activation
cannabinoid receptors
Insulin
synthesis
gene activation
Deregulation

ASJC Scopus subject areas

  • Agricultural and Biological Sciences(all)
  • Biochemistry, Genetics and Molecular Biology(all)
  • Medicine(all)

Cite this

Hepatic Cannabinoid Receptor Type 1 Mediates Alcohol-Induced Regulation of Bile Acid Enzyme Genes Expression Via CREBH. / Chanda, Dipanjan; Kim, Yong Hoon; Li, Tiangang; Misra, Jagannath; Kim, Don Kyu; Kim, Jung Ran; Kwon, Joseph; Jeong, Won Il; Ahn, Sung Hoon; Park, Tae Sik; Koo, Seung-Hoi; Chiang, John Y L; Lee, Chul Ho; Choi, Hueng Sik.

In: PLoS One, Vol. 8, No. 7, e68845, 22.07.2013.

Research output: Contribution to journalArticle

Chanda, D, Kim, YH, Li, T, Misra, J, Kim, DK, Kim, JR, Kwon, J, Jeong, WI, Ahn, SH, Park, TS, Koo, S-H, Chiang, JYL, Lee, CH & Choi, HS 2013, 'Hepatic Cannabinoid Receptor Type 1 Mediates Alcohol-Induced Regulation of Bile Acid Enzyme Genes Expression Via CREBH', PLoS One, vol. 8, no. 7, e68845. https://doi.org/10.1371/journal.pone.0068845
Chanda, Dipanjan ; Kim, Yong Hoon ; Li, Tiangang ; Misra, Jagannath ; Kim, Don Kyu ; Kim, Jung Ran ; Kwon, Joseph ; Jeong, Won Il ; Ahn, Sung Hoon ; Park, Tae Sik ; Koo, Seung-Hoi ; Chiang, John Y L ; Lee, Chul Ho ; Choi, Hueng Sik. / Hepatic Cannabinoid Receptor Type 1 Mediates Alcohol-Induced Regulation of Bile Acid Enzyme Genes Expression Via CREBH. In: PLoS One. 2013 ; Vol. 8, No. 7.
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AU - Kwon, Joseph

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AU - Koo, Seung-Hoi

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