Table 1.
Hepatokines | Subjects | Places | Main Effects | Refs |
---|---|---|---|---|
Tsukushi | Mice | NAFLD | Reduce circulating high-density lipoprotein cholesterol. Lower cholesterol efflux capacity. Decrease cholesterol-to–bile acid conversion in the liver. |
Mouchiroud et al. [16] |
ANGPTL8 | Mice | Liver | Treat metabolic disorders. | Chen et al. [17] |
Selenoprotein P | Mice | Skeletal muscle | Inhibit the development of hyperglycemia in type 2 diabetes. Improve insulin resistance. |
Misu [18] |
LECT2 | Mice | Adipocytes | Stimulates inflammation and insulin resistance. | Jung et al. [19] |
FGF21 | Human | Plasma | Biomarkers of metabolic disease in human. | Keuper et al. [20] |
Fetuin-A | Human | Plasma | Positive association between plasma fetuin-A levels and risk of developing type 2 diabetes. | Wang et al. [21] |
ANGPTL4 | Human | Plasma | Significantly predict cardiovascular events independent of conventional cardiovascular risk factors. | Muendlein et al. [22] |
FST | Rat | Skeletal muscle | Increase anabolic, neurotrophic, and the progression of satellite cells. | Isaacs et al. [23] |
Asprosin | Rat | Adipose tissue | Protect against hyperinsulinism associated with metabolic syndrome. | Romere et al. [24,25] |
Heat shock protein 72 | Human | Skeletal muscle | Increase maximal voluntary eccentric contractions of biceps. | Yamada et al. [26] |
Abbreviations: ANGPTL8, angiopoietin-like protein 8; LECT2, Leukocyte cell-derived chemotaxin-2; ANGPTL4, angiopoietin-like protein 4; FST, follistatin; NAFLD, non-alcoholic fatty liver disease.