Mice lacking the M3 muscarinic acetylcholine receptor are hypophagic and lean

Masahisa Yamada, Tsuyoshi Miyakawa, Alokesh Duttaroy, Akihiro Yamanaka, Toru Moriguchi, Ryosuke Makita, Masaharu Ogawa, Chieh J. Chou, Bing Xia, Jacqueline N. Crawley, Christian C. Felder, Chu Xia Deng, Jürgen Wess

Research output: Contribution to journalArticlepeer-review

331 Citations (Scopus)


Members of the muscarinic acetylcholine receptor family (M1-M5) have central roles in the regulation of many fundamental physiological functions. Identifying the specific receptor subtype(s) that mediate the diverse muscarinic actions of acetylcholine is of considerable therapeutic interest, but has proved difficult primarily because of a lack of subtype-selective ligands. Here we show that mice deficient in the M3 muscarinic receptor (M3R -/- mice) display a significant decrease in food intake, reduced body weight and peripheral fat deposits, and very low levels of serum leptin and insulin. Paradoxically, hypothalamic messenger RNA levels of melanin-concentrating hormone (MCH), which are normally upregulated in fasted animals leading to an increase in food intake, are significantly reduced in M3R -/- mice. Intra-cerebroventricular injection studies show that an agouti-related peptide analogue lacked orexigenic (appetite-stimulating) activity in M3R -/- mice. However, M3R -/- mice remained responsive to the orexigenic effects of MCH. Our data indicate that there may be a cholinergic pathway that involves M3-receptor-mediated facilitation of food intake at a site downstream of the hypothalamic leptin/melanocortin system and upstream of the MCH system.

Original languageEnglish
Pages (from-to)207-212
Number of pages6
Issue number6825
Publication statusPublished - 08-03-2001
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • General


Dive into the research topics of 'Mice lacking the M3 muscarinic acetylcholine receptor are hypophagic and lean'. Together they form a unique fingerprint.

Cite this