Adenosine stimulates hepatic glycogenolysis via adrenal glands-liver crosstalk in mice

PLoS One. 2018 Dec 21;13(12):e0209647. doi: 10.1371/journal.pone.0209647. eCollection 2018.

Abstract

Adenosine signaling is involved in glucose metabolism in hepatocytes and myocytes in vitro. However, no information is available regarding the effect of adenosine on glucose metabolism in vivo. Thus, we examined how extracellular adenosine acts on glucose metabolism using mice. Subcutaneous injections of adenosine (10, 25, and 50 mg/kg bodyweight) dose-dependently increased blood glucose levels, with the peak occurring at 30 min post injection. At 30 min after adenosine injection (25 mg/kg bodyweight), glycogen content in the liver, but not the skeletal muscle, was significantly decreased. Hepatic glycogen depletion by fasting for 12 h suppressed the increase of blood glucose levels at 30 min after adenosine injection. These results suggest that adenosine increases blood glucose levels by stimulating hepatic glycogenolysis. To investigate the effect of adenosine on the adrenal gland, we studied the glycogenolysis signal in adrenalectomized (ADX) mice. Adenosine significantly increased the blood glucose levels in sham mice but not in the ADX mice. The decrease in hepatic glycogen content induced by adenosine in the sham mice was partially suppressed in the ADX mice. The level of plasma corticosterone, the main glucocorticoid in mice, was significantly increased in the sham mice by adenosine but its levels were low in ADX mice injected with either PBS or adenosine. These results suggest that adenosine promotes secretion of corticosterone from the adrenal glands, which causes hepatic glycogenolysis and subsequently the elevation of blood glucose levels. Our findings are useful for clarifying the physiological functions of adenosine in glucose metabolism in vivo.

MeSH terms

  • Adenosine / metabolism*
  • Adrenal Glands / metabolism*
  • Adrenal Glands / pathology
  • Adrenal Glands / surgery
  • Adrenalectomy
  • Animals
  • Corticosterone / blood*
  • Fasting
  • Glucose / metabolism
  • Glycogenolysis / genetics
  • Hepatocytes / metabolism
  • Hepatocytes / pathology
  • Insulin / metabolism
  • Liver / metabolism*
  • Liver / pathology
  • Liver Glycogen / metabolism
  • Mice

Substances

  • Insulin
  • Liver Glycogen
  • Glucose
  • Adenosine
  • Corticosterone

Grants and funding

The authors received no specific funding for this work.