Adiponectin

Adiponectin is a 244-amino-acid-long polypeptide (protein). It has four distinct regions: The first is a short signal sequence that targets the hormone for secretion outside the cell; next is a short region that varies between species; the third is a 65-amino acid region with similarity to collagenous proteins; the last is a globular domain. Overall, this protein shows similarity to the complement 1Q factors (C1Q), but when the three-dimensional structure of the globular region was determined, a striking similarity to TNFα was observed, despite unrelated protein sequences.[7]

Adiponectin is a protein hormone that modulates a number of metabolic processes, including glucose regulation and fatty acid oxidation.[8][9][10] Adiponectin is secreted from adipose tissue (and also from the placenta in pregnancy[11]) into the bloodstream and is very abundant in plasma relative to many hormones. High adiponectin levels correlate with a lower risk of diabetes mellitus type 2.[12] Plasma levels of adiponectin are lower in obese subjects than in lean subjects.[13] Many studies have found adiponectin to be inversely correlated with body mass index in patient populations.[14] However, a meta analysis was not able to confirm this association in healthy adults.[15] Circulating adiponectin concentrations increase during caloric restriction in animals and humans, such as in patients with anorexia nervosa. Furthermore, a recent study suggests that adipose tissue within bone marrow, which increases during caloric restriction, contributes to elevated circulating adiponectin in this context.[16]

Transgenic mice with increased adiponectin show reduced adipocyte differentiation and increased energy expenditure associated with mitochondrial uncoupling.[17] The hormone plays a role in the suppression of the metabolic derangements that may result in type 2 diabetes,[14] obesity, atherosclerosis,[10] non-alcoholic fatty liver disease (NAFLD) and an independent risk factor for metabolic syndrome.[18] Adiponectin in combination with leptin has been shown to completely reverse insulin resistance in mice.[19] Adiponectin enhances insulin sensitivity primarily though regulation of fatty acid oxidation and suppression of hepatic glucose production .[20]

Adiponectin is secreted into the bloodstream, where it accounts for about 0.01% of all plasma protein at around 5-10 μg/mL. In adults, plasma concentrations are higher in females than males, and are reduced in diabetics compared to nondiabetics. Weight reduction significantly increases circulating concentrations.[21]

Adiponectin automatically self-associates into larger structures. Initially, three adiponectin molecules bind together to form a homotrimer. The trimers continue to self-associate and form hexamers or dodecamers. Like the plasma concentration, the relative levels of the higher-order structures are sexually dimorphic, where females have increased proportions of the high-molecular-weight forms. Recent studies showed that the high-molecular-weight form may be the most biologically active form regarding glucose homeostasis.[13] High-molecular-weight adiponectin was further found to be associated with a lower risk of diabetes with similar magnitude of association as total adiponectin.[22] However, coronary artery disease has been found to be positively associated with high molecular weight adiponectin, but not with low molecular weight adiponectin.[23]

Adiponectin exerts some of its weight-reduction effects via the brain. This is similar to the action of leptin;[24] adiponectin and leptin can act synergistically.

Adiponectin promoted synaptic and memory function in the brain.[25] Humans with lower levels of adiponectin have reduced cognitive function.[25]

Adiponectin binds to a number of receptors. So far, two receptors have been identified with homology to G protein-coupled receptors, and one receptor similar to the cadherin family:[26][27]

• Adiponectin receptor 1 (AdipoR1)
• Adiponectin receptor 2 (AdipoR2)
• T-cadherin - CDH13

These have distinct tissue specificities within the body and have different affinities to the various forms of adiponectin. AdipoR1 is enriched in skeletal muscle, whereas AdipoR2 is enriched in liver.[6] Six months of exercise has been shown in rats to double muscle AdipoR1.[6]

The receptors affect the downstream target AMP kinase, an important cellular metabolic rate control point. Expression of the receptors is correlated with insulin levels, as well as reduced in mouse models of diabetes, particularly in skeletal muscle and adipose tissue.[28][29]

In 2016, the University of Tokyo announced that it would launch an investigation into claims of fabrication of AdipoR1 and AdipoR2 identification data, as accused by an anonymous person/group called Ordinary_researchers.[30]

Adiponectin was first characterised in 1995 in differentiating 3T3-L1 adipocytes (Scherer PE et al.).[31] In 1996 it was characterised in mice as the mRNA transcript most highly expressed in adipocytes.[5] In 2007, adiponectin was identified as a transcript highly expressed in preadipocytes[32] (precursors of fat cells) differentiating into adipocytes.[32][33]

The human homologue was identified as the most abundant transcript in adipose tissue. Contrary to expectations, despite being produced in adipose tissue, adiponectin was found to be decreased in obesity.[10][14][24][9] This downregulation has not been fully explained. The gene was localised to chromosome 3q27, a region highlighted as affecting genetic susceptibility to type 2 diabetes and obesity. Supplementation by differing forms of adiponectin was able to improve insulin control, blood glucose and triglyceride levels in mouse models.

The gene was investigated for variants that predispose to type 2 diabetes.[24][32][34][35][36][37] Several single nucleotide polymorphisms in the coding region and surrounding sequence were identified from several different populations, with varying prevalences, degrees of association and strength of effect on type 2 diabetes. Berberine, an isoquinoline alkaloid, has been shown to increase adiponectin expression,[38] which partly explains its beneficial effects on metabolic disturbances. Mice fed the omega-3 fatty acids eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) have shown increased plasma adiponectin.[39] Curcumin, capsaicin, gingerol, and catechins have also been found to increase adiponectin expression.[40]

Phylogenetic distribution includes expression in birds[41] and fish.[42]

Adiponectin effects:

• glucose flux
  • decreased gluconeogenesis
  • increased glucose uptake[10][24][35]
• lipid catabolism[35]
  • β-oxidation[24]
  • triglyceride clearance[24]
• protection from endothelial dysfunction (important facet of atherosclerotic formation)
• insulin sensitivity
• weight loss
• control of energy metabolism.[35]
• upregulation of uncoupling proteins[17]
• reduction of TNF-alpha
• promotion of reverse cholesterol transport[43]

Regulation of adiponectin

• Obesity is associated with decreased adiponectin.[9]
  • The exact mechanism of regulation is unknown, but adiponectin could be regulated by post-translational mechanisms in cells.[44]

A low level of adiponectin is an independent risk factor for developing:

• Metabolic syndrome[18]
• Diabetes mellitus[8][24][32][34][36][37]
• Dyslipidemia[8]
• Obesity[9]
• Hypertension[45]

Lower levels of adiponectin are associated with ADHD in adults.[46]

Adiponectin levels were found to be increased in rheumatoid arthritis patients responding to DMARDs or TNF inhibitor therapy.[47]

A low adiponectin to leptin ratio has been found in patients with COVID-19 pneumonia compared to healthy controls.[48]

Exercise induced release of adiponectin increased hippocampal growth and led to antidepressive symptoms in mice.[49]

Several studies have found a positive correlation in caffeine consumption and increased adiponectin levels, although the mechanism for this is unknown and requires more research.[50]

• Human ADIPOQ genome location and ADIPOQ gene details page in the UCSC Genome Browser.
• Overview of all the structural information available in the PDB for UniProt: Q15848 (Human Adiponectin) at the PDBe-KB.
• Overview of all the structural information available in the PDB for UniProt: Q60994 (Mouse Adiponectin) at the PDBe-KB.