Metformin regulates TRPM6, a potential explanation for magnesium imbalance in type 2 diabetes patients

Can J Physiol Pharmacol. 2020 Jun;98(6):400-411. doi: 10.1139/cjpp-2019-0570. Epub 2020 Feb 4.

Abstract

Metformin therapy is associated with lower serum magnesium (Mg2+) levels in type 2 diabetes patients. The TRPM6 channel determines the fine-tuning of Mg2+ (re)absorption in intestine and kidney. Therefore, we aimed to investigate the short- and long-term effects of metformin on TRPM6. Patch clamp recordings and biotinylation assays were performed upon 1 h of incubation with metformin in TRPM6-transfected HEK293 cells. Additionally, 24 h of treatment of mDCT15 kidney and hCaco-2 colon cells with metformin was applied to measure the effects on endogenous TRPM6 expression by quantitative real-time PCR. To assess Mg2+ absorption, 25Mg2+ uptake measurements were performed using inductively coupled plasma mass spectrometry. Short-term effects of metformin significantly increased TRPM6 activity and its cell surface trafficking. In contrast, long-term effects significantly decreased TRPM6 mRNA expression and 25Mg2+ uptake. Metformin lowered TRPM6 mRNA levels independently of insulin- and AMPK-mediated pathways. Moreover, in type 2 diabetes patients, metformin therapy was associated with lower plasma Mg2+ concentrations and fractional excretion of Mg2+. Thereby, short-term metformin treatment increases TRPM6 activity explained by enhanced cell surface expression. Conversely, long-term metformin treatment results in downregulation of TRPM6 gene expression in intestine and kidney cells. This long-term effect translated in an inverse correlation between metformin and plasma Mg2+ concentration in type 2 diabetes patients.

Keywords: AMPK; TRPM6; diabetes; diabète; intestin; intestine; kidney; magnesium; magnésium; metformin; metformine; rein.

MeSH terms

  • Animals
  • Biological Transport / drug effects
  • Caco-2 Cells
  • Diabetes Mellitus, Type 2 / metabolism*
  • Down-Regulation / drug effects
  • HEK293 Cells
  • Humans
  • Magnesium / blood
  • Magnesium / metabolism*
  • Metformin / pharmacology*
  • Mice
  • RNA, Messenger / genetics
  • TRPM Cation Channels / genetics
  • TRPM Cation Channels / metabolism*
  • Time Factors

Substances

  • RNA, Messenger
  • TRPM Cation Channels
  • TRPM6 protein, human
  • Metformin
  • Magnesium