Skip to main content
. Author manuscript; available in PMC: 2019 May 1.
Published in final edited form as: Free Radic Biol Med. 2018 Feb 16;119:69–74. doi: 10.1016/j.freeradbiomed.2018.02.022

Table 1.

Genetic models of core clock gene disruption affecting β-cell function and glucose metabolism.

Gene disrupted Metabolic phenotype Refs.
Bmal1 (Global) Impaired gluconeogenesis, adipocyte differentiation, hyperlipidemia, glucose intolerance [34,50]
Bmal1 – since birth (Pancreas using Pdx-1 Cre) Hyperglycemia, hypoinsulinemia, glucose intolerance, β-cell dysfunction [34,35]
Bmal1 – since birth (β-cell specific using Rip-Cre) Hyperglycemia, hypoinsulinemia, glucose intolerance, β-cell dysfunction [36]
Bmal1 – only in adult (β-cell specific using Mip-Cre/ERT) Impaired compensatory hyperplasia in response to diet-induced obesity [75]
Bmal1 – only in adult (β-cell specific using Pdx1-CreER) Hyperglycemia, hypoinsulinemia, glucose intolerance, β-cell dysfunction [69]
Clock (Global) Hypertriglyceridemia, hypercholesterolemia, hyperglycemia, hyperleptinemia [52]
Cry1&2 (Global) Glucose intolerance [55]