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. 2023 Feb 24;14:1098570. doi: 10.3389/fimmu.2023.1098570

Table 3.

Key findings of preclinical studies on the metabolism of Metrnl.

Year Ref. Animal/Cell models Key findings
Glucose
2014 (15) Normal Promote white fat browning, increase thermogenic in adipose tissue, improve glucose tolerance
2015 (59) HFD-induced obese Antagonize insulin sensitivity at least via PPARγ pathway
2018 (58) HFD-induced obese Improve impaired insulin functions, rescue glucose intolerance, reduce weight gains
2020 (62) Obese, diabetes Improve glucose metabolism via calcium-dependent AMPKα2/GLUT4/HDAC5
2021 (22) Non-obese diabetes Delay the onset of diabetes, improve islet function
2021 (78) Diabetes Ameliorate pancreas islet β-cell functions via WNT/β-catenin pathway.
Lipid
2017 (104) Human adipocytes Promote adipose tissue accumulation, inhibite adipocyte differentiation, decrease during adipogenesis
2018 (105) HFD-induced obese Decrease fat accumulation
2020 (20) H9C2 cells Decrease myocardial ischemia/reperfusion injury and endoplasmic stress via AMPK-PAK2
2020 (106) Knockout mice Adipose Metrnl regulate blood TG, liver Metrnl regulate HDL-C
2020 (107) Cardiac injury Attenuate oxidative damage, apoptosis, and cardiac dysfunction via cAMP/PKA/SIRT1 pathway
2021 (95) 3T3-L1 cells A transient reduce during adipocyte differentiation, decreased by omega-3 and omega-6 fatty acids
2021 (108) Cardiac hypertrophy Prevent cardiomyocyte hypertrophy and dysfunction, autocrine actions, a biomarker of heart failure
2022 (48) Cardial infarction Promote angiogenesis and infarct repair, a high-affinity ligand of KIT receptor
Bone and skeletal muscle
2020 (21) Muscle injury Promote muscle regeneration, regulate muscle satellite cells proliferation
2022 (109) Bone fracture Osteoinductive, promote bone fracture healing, strongest expression by osteoblasts