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1. Introduction

Insulin resistance (IR) is defined as impaired insulin function, reduced glucose uptake and increased glucose production (1), which may result in type II diabetes and metabolic syndrome (2) and may subsequently promote the development of non-alcoholic fatty liver disease (NAFLD) (3). Numerous previous studies (4-6) have reported mechanisms through which IR serves a crucial role in a variety of systemic diseases, including bone metabolic disorders (7). The etiology of IR is complex and a possible reason for the increasing incidence of IR is the aging population, as epidemiological research has reported that the prevalence of IR and type II diabetes is higher in older adults. It has also been demonstrated that aging induces IR, and in turn, hyperinsulinemia and IR may accelerate aging, promoting a vicious circle (8,9).

Adipose tissue (AT) is an active organ regulating ATP expenditure, which serves an essential role in regulating energy homeostasis of the entire body (10). Our previous studies focusing on the function of AT identified that the dysfunction of AT induced IR (11,12) and more recent studies (13,14) have also reported a crucial role for AT in IR during aging. Therefore, an improved understanding of the effects of aging on AT may prove useful in pioneering novel therapeutic strategies to target age-related diseases. The present review aimed to summarize the associative evidence between AT and age-dependent IR. Notably, the findings suggested that the browning of white AT (WAT) may be influenced to attain positive therapeutic outcomes in age-dependent IR and other metabolic complications.

2. AT characteristics

AT can be subdivided into three subtypes, namely WAT, brown AT (BAT) and beige AT, which all possess distinct characteristic features that are associated with their function, localization and composition (15). BAT develops following the stimulation of anatomical thermogenic sites corresponding with WAT in a process termed 'browning' (15,16). In mammals, BAT and WAT have opposing functions. For example, BAT expends energy, while WAT stores energy. Significant changes are known to occur over the years in the distribution and composition of AT during aging. The progressive dysfunction of AT has been proposed to be a characteristic feature of the aging process (17).

White adipocytes

The majority of AT in the human body is WAT, which is distinguishable by large unilocular lipid droplets. Functionally, WAT is subdivided into a stromal vascular fraction, which is composed of lymphocytes, progenitor and endothelial cells, preadipocytes and fibroblasts, and the adipocyte fraction, which primarily contains mature adipocytes (17,18). WAT is dispersed throughout visceral organs and the surrounding subcutaneous region of the face. Notably, despite their histological similarities, visceral AT (VAT) and subcutaneous tissue have been shown to exert distinct metabolic functions. Subcutaneous WAT has metabolic characteristics that differ from those of VAT. For example, the metabolic activity of WAT is regulated by a smaller number of insulin receptors, β-adrenoceptors (β-AR) and glucocorticoid receptors (19).

Brown adipocytes

BAT is a major source of metabolically active fat and is located in the retroperitoneal, cervical and mediastinal regions (20). BAT is named due to the brown color of the adipocytes and has a high mitochondria content and vascular supply. BAT can arise from precursor cells already present in WAT, which display identical unilocular morphology as WAT during the basal state (21). However, the morphological characteristic features of BAT are altered upon cold stimulation, eventually resulting in the expression of typical BAT proteins, and the transformation from stored fat to small lipid droplets, which are typical of BAT (22). The beta-3 adrenergic receptor (β3-AR), type 2 iodothyronine deiodinase and uncoupling protein 1 (UCP1) are highly expressed in the adipocytes of BAT (23), in which UCP1 functions as a ther- moregulator (24).

Beige adipocytes

Beige adipocytes are brown-like adipocytes that exist within WAT in adult humans and play an essential role in ATP expenditure (25), which are characterized by a mix of the features of both brown and white adipocytes (21). Inactive beige cells appear morphologically as regular white adipocytes, although upon stimulation (through adrenergic receptors), oxidative and mitochondrial biogenesis is enhanced (25). However, it has been suggested that beige adipocytes may serve a role similar to the role brown adipocytes play in the expenditure of ATP, which has been demonstrated in humans (26). Notably, beige adipocytes have also been found to be transplantable. Several studies have suggested that beige stem cells may derive from WAT cells by trans-differentiation, which is driven by bone morphogenetic protein 7 (21,27). However, there is also evidence to suggest that beige adipocytes may arise from unique precursor cells (25). For instance, Wu et al (25) reported that beige adipocytes were differentiated from myogenic factor 5 (Myf5)+ progenitor cells. Nevertheless, an ongoing debate still surrounds the anatomical location, trans-differentiation and cellular identity of the three adipocyte subtypes.

3. WAT in age-dependent IR

It has been reported that the accumulation of senescent cells was increased in the WAT of diabetic patients (28); thus, the association between WAT and aging may be of clinical significance, as numerous classical aging mechanisms have been shown to occur in WAT, which may be associated with to age-dependent IR (29).

Adipocyte self-renewal

In adults, human WAT is dynamic and can differentiate into mature lipid-storing adipocytes. In total, ~10% of adipocytes die and renew every year (30). Renewed progenitor cells were demonstrated to play a crucial role in insulin sensitivity (IS), the expansion of AT and lipid handling. Thus, the failure of progenitor cells to self-renew could lead to the exhaustion of new adipocytes, resulting in the senescence and death of adipocytes (31).

It is estimated that 15-50% of cells in WAT are preadipocytes that are continuously renewed throughout an individual's life, which results in the varying size and functional changes observed in older adults compared with younger individuals (32,33). Thus, determining the association between fat mass expansion and adipogenesis may be essential for establishing the pathophysiological role that adipocyte turnover plays in IR. Notably, the function of progenitor cells, such as those within the skeletal muscle, also decreases with age (age-related IR). Thus, the inherent characteristics of progenitor cells may contribute to the variation in WAT function with aging (34,35).

The reduced ability of adipocytes to differentiate during aging may combine with the decreased insulin responsiveness of WAT when exposed to excess nutrients during old age. Although very little is known regarding the precise age, percentage and required threshold, progenitor cells may cause physiological changes or become dysfunctional (36).

Location of AT

The location of AT is equally as essential as the absolute amount of AT during reduced IS. Fat redistribution in the elderly has been associated with an increased risk of IS (37). Subcutaneous WAT and VAT are diverse with regards to their metabolic effects; for example, subcutaneous WAT has been associated with increased IS and a lower risk of cardiovascular disease (CVD) and diabetes, while VAT has been associated with IR (38). Furthermore, pear-shaped fat distribution with more gluteal femoral AT was associated with an increased IS and lower risk of CVD and diabetes, while apple-shaped fat distribution with an increased waist circumference was associated with VAT mass and IR. Individuals with relatively higher amounts of VAT compared with WAT were also at an increased risk of developing IR (39). The loss of subcutaneous fat is a well-established feature in aging (38), as the distribution of AT primarily moves from subcutaneous fatty tissue deposition to ectopic sites, muscle and visceral deposition, including within the liver, which are all closely associated with the development of IR (40).

Increased VAT accumulation was demonstrated to result in lipotoxicity in old age (>65 years old) (41) and chronic low-grade inflammation (42). The central accumulation of VAT during aging has been closely associated with an increase of inflammatory and metabolic markers compared with peripheral fat accumulation (43). Similar to humans, the redistribution of fat in rat and mice models tended to occur with aging due to insulin-like growth factor-1 and/or growth hormone deficiencies (44). As reported by Niu et al (45), diabetes and IR was effectively reduced in aging rats by antagonizing the age-dependent accumulation of VAT.

Volume of adipocytes

Body fat mass typically increases by either hypertrophy or hyperplasia, with the former involving slower rates of adipogenesis compared with the latter. Hypertrophic adipocytes were reported to induce hypoxic conditions and have been implicated in several types of condition, including atherosclerosis, type II diabetes and IR. The development of hypoxia underpins the infiltration of macrophages, which subsequently promotes the initiation and progression of the inflammatory response in AT (46).

The migration of macrophages results in impaired insulin signaling, which is known to be central to the development of IR and metabolic syndrome (Fig. 1). In addition, during hypertrophy, adipocytes present in the senescent state and secrete a multitude of growth factors, cytokines, matrix metalloproteinases and chemokines (47). Thus, removing senescent cells in progeroid INK-ATTAC mice has been found to improve WAT IS (48,49). Free fatty acids (FFAs) are essential biomedical indicators of lipid metabolic disorders, whereby the effects of FFAs on IR are dose-dependent, which adversely affects insulin signaling pathways (45). Plasma FFA levels have been associated with aging and excess FFA accumulation was found to induce IR during aging (50).

Figure 1 Adipocyte hypertrophy results in a slower adipogenic ability and cell dysfunction compared with adipocyte hyperplasia. The average fat cell volume increases with age. Moreover, the accumulation of FFAs, TGs and DAGs in WAT induces the infiltration of macrophages, leading to impaired insulin signaling and the dysfunction of adipocytes, ultimately resulting in IR. FFAs, free fatty acids; TGs, triglycerides; DAGs, diglycerides; IR, insulin resistance; WAT, white adipose tissue.

An increase in FFAs has demonstrated to induce IR at the cellular level, while increasing very-low-density hepatic lipoprotein production (44). It has also been reported that the accumulation of FFAs, triglycerides (TGs) and diglycerides may promote adipocyte necrosis in obese mice, which resulted in the polarization of macrophages towards a standard M1 or activated phenotype in the AT.

MicroRNA (miRNA) processing

miRNAs have been identified in multiple tissues, including the skeletal muscles, AT, liver and brain (51). The number of miRNAs present in WAT was found to decrease with age, owing to the downregulation of the miRNA-processing enzyme known as Dicer15 (52). An experimental study with mice demonstrated that Dicer15 exhibited a defect in miRNA processing in AT, prevented the whitening of BAT and resulting in an inadequate response of WAT to metabolic stress, and promoted lipodystrophy, IR and inflammation (53). In addition, AT was recently reported to be an essential source of circulating exosomal miRNAs, which have been associated with glucose tolerance; thus, representing a novel target to produce therapeutics that modulate age-related metabolic diseases and various aging processes (54).

Adipokines

WAT secretes varying amounts of bioactive molecules named adipokines, which serve crucial roles in regulating diverse metabolic processes ranging from food intake to nutrient recycling, energy homeostasis and IR (55). It has been hypothesized that age-associated changes may, however, influence the impact of adipokine secretion (56).

Adiponectin

Adiponectin is an adipose-derived hormone that has been associated with an improved IS, which also inhibits the synthesis of proinflammatory cytokines (57). As adipokines secreted from WAT are involved in the regulation of glucose metabolism, it has been suggested that adiponectin may mediate IS and possess anti-inflammatory properties (58). However, the association between aging and adiponectin remains poorly understood; for example, several previous studies have reported that plasma adiponectin levels increased with age (59,60), while other studies reported the opposite results (61). Overall, the relative decrease in adiponectin secretion in VAT has been associated with an increased risk of aging (62).

In addition, lower levels of adiponectin have been associated with obesity, cigarette smoking and oxidative stress. One of the most prominent hypotheses regarding the mechanisms inducing or worsening obesity and consequently, NAFLD, is the overproduction of reactive oxygen species (ROS) (63).

Leptin

Leptin is a WAT-secreted hormone, which stimulates fatty acid oxidation and regulates insulin binding and production, by interacting with regions of the brain involved in controlling appetite (64). In addition, the availability of leptin was found to influence lipogenesis and lipolysis, and the failure of leptin to restore metabolic homeostasis is termed as a state of leptin resistance (65). Notably, aging has been associated with a decrease in leptin activity, while youth is associated with a high sensitivity of leptins; The redistribution of adipose tissue observed during old age contribute however to an increase in circulating leptin. However, leptin resistance could not be overcome by an increase in leptin levels during aging. This suggested that leptin resistance appears to be an early contributor to the development of metabolic abnormalities in old age (64,66).

Resistin

Resistin is activated during the process of IR (insulin antagonism) and is a distinctive cysteine-rich signaling molecule. In mice, resistin is produced by monocytes and AT, while in humans, resistin is produced in monocytes and macrophages, but not in AT (67). Circulating resistin levels have been reported to increase with age, and elevated levels of resistin were associated with an increased risk for coronary intervention and CVDs (68).

Inflammation

Low-grade, chronic inflammation, which is a central mechanism involved in the aging process, has been established as a precursor of aging and closely associated with IR (69). The hypotheses surrounding the WAT inflammatory capacity suggest that immune cells infiltrating WAT are the primary source of inflammation (70). Adipose resident immune cells, such as M2 macrophages, which are anti-inflammatory cells, have been reported to improve IS, whereas M1 macrophages, mast cells, natural killer cells and neutrophils, which are proinflammatory cells, promote IR during aging (71,72). Therefore, immune cells and their participation in the inflammatory response are important pathophysiological mechanisms of aging WAT (Fig. 2).

Figure 2 Chronic inflammation is closely associated with age-dependent IR. The expression levels of inflammatory factors, such as MCP-1, IL-6, IL-1, TNF-α and leptin are upregulated, while the expression levels of adiponectin are downregulated in aging WAT. Subsequently, aging WAT is infiltrated by macrophages, CD4+ T cells, CD8+ T cells and Treg cells. Excessive metabolic products flux into the mitochondria during aging, resulting in the overproduction of ROS and spin-down of electrons, which can result in oxidative stress and ultimately, damage the activation of the PI3K/AKT signaling pathway, thereby inducing IR. MCP-1, monocyte chemotactic protein 1; WAT, white adipose tissue; Treg, T regulatory; ROS, reactive oxygen species; IR, insulin resistance; IRS, insulin receptor substrate.

AT macrophages (ATMs)

ATMs are induced by aging and secrete chemokines that attract monocytes to the AT. ATMs consist of two subsets: Proinflammatory M1 ATMs (which secrete TNF-α) and anti-inflammatory M2 ATMs (which secrete arginase 1) (73). Proinflammatory ATMs also secrete their own chemokines once they migrate into the WAT, attracting additional macrophages and promoting the inflammatory processes (74).

AT T cells

T cells differentiate into proinflammatory phenotypes with elevated levels of chemokine receptors and enhanced chemotaxis potential. Notably, aging has been found to alter T cell development. T regulatory (Treg) cells, a small subset of T cells, are an essential defense mechanism of the body against inappropriate immune responses due to inflammation, autoimmunity, infection, cancer or allergies. Recently, Treg cells were identified to be involved in controlling the inflammatory state of the AT. At birth, subcutaneous AT and VAT contain low percentages of Treg cells; however, over time, the percentage of Treg cells increases in the VAT (75).

Adipose-secreted inflammatory cytokines

Aging has also been associated with higher levels of proinflammatory cytokines, which act in a paracrine or an autocrine manner to induce IR by decreasing the expression of insulin receptor substrate (IRS)-1 (76). For example, TNF-α, expressed primarily by AT macrophages, induced IR and inhibited insulin signaling in human adipocytes by affecting the expression of IRS proteins (77). A previous study has also shown that inflammatory responses disrupt normal lipid accumulation. For example, proinflammatory cytokines, such as IL-6, impaired lipid accumulation by promoting Wnt signaling (78).

Mitochondrial dysfunction

Cumulative molecular damage can result in mitochondrial impairment (78). The mitochondria are the primary origin of ROS, which are inevitable by-products of oxidative phosphorylation. Mitochondrial dysfunction and oxidative stress in WAT are important factors leading to IR during the aging process. Mitochondrial ROS were demonstrated to attenuate insulin action in adipocytes and abolish insulin-stimulated glucose transporter 4 translocation in mouse adipocytes. Notably, impaired mitochondrial function was also shown to increase endoplasmic reticulum stress (78,79). Mitochondria also serve a central role in cell death; therefore, mitochondrial dysfunction in adipocytes may trigger cell death in adipocytes to induce AT inflammation (79). Thus, the dysfunction of mitochondria highly probably a significant cause of age-dependent chronic inflammation.

Mitochondrial sirtuins (mtSIRTs) comprise three members, SIRT3, SIRT4 and SIRT5, which are all involved in regulating energy metabolism and metabolic homeostasis (80). Among the mtSIRTs, SIRT4 expression levels were found to be upregulated during senescence and were induced by different stimuli, such as DNA damage (80). SIRT4 functions as an efficient mitochondrial ADP-ribosyl transferase that inhibits mitochondrial glutamate dehydrogenase (GDH) activity. GDH is known to convert glutamate to α-ketoglutarate, which promotes ATP generation and insulin secretion in pancreatic β cells (81). In vivo experiments observed a significant increase in insulin secretion from SIRT4-deficient pancreatic β cells in response to glucose and amino acids in SIRT4-knockout (KO) mice. More recently, SIRT4 has also been shown to interact with insulin-degrading enzyme, which modulates insulin secretion, providing an alternative possible mechanism by which SIRT4 may impact insulin secretion (82).

4. BAT in age-dependent IR

BAT is a metabolically active tissue that regulates plasma glucose levels, IR, TG metabolism and hyperlipidemia (83). Notably, it has recently emerged as a potential target in the treatment of type II diabetes. BAT has the capacity to actively clear glucose from the circulation and has been suggested to serve a role in preventing age-dependent dysfunction and disease (83).

Abnormalities in BAT

A notable change in AT distribution associated with aging is due to the loss of BAT. A decline in BAT function with aging has been described in both rodents and humans (84). In one study, the proportion of BAT was >50% in younger individuals (<35 years old), but <10% in older individuals (>65 years old) (84). In addition, metabolic alterations in subcutaneous WAT harbored a subpopulation of UCP1+ brown adipocytes, thereby promoting IR (85). Indeed, a predominant consequence of aging in murine subcutaneous WAT is the loss of 'browning' subcutaneous WAT, and UCP1 expression in subcutaneous WAT was found to be increasingly downregulated with age in rodents (85). Loss of BAT in older mice was also inversely correlated with IR development (86). Furthermore, it has been suggested that BAT itself may become dysfunctional with age (86).

Mitochondrial mass in BAT

In addition to TG stores in multilocular lipid droplets, BAT has high mitochondrial density. During aging, there is a significant decline of UCP1 activity and an age-dependent accumulation of point mutations in mitochondrial DNA (87). Cumulative molecular damage was found to result in mitochondrial functional decline and impairment (88), which are both associated with an age-dependent increase in the incidence of neurodegenerative diseases and metabolic disorders (89).

Inflammation in BAT

As aforementioned, chronic inflammation increases with age. It was previously demonstrated that BAT is resistant to macrophage infiltration, as shown by the downregulated expression of immune cell-enriched genes, which indicates the anti-inflammatory properties of BAT (90). However, during the inflammatory response in mice, a novel chemokine (C-X-C chemokine ligand 14) was observed to be secreted by thermogenically activated BAT (91). In addition, several proinflammatory cytokines reduce UCP1 gene expression in BAT. For instance, TNF-α induces the apoptosis of WAT and downregulates the expression of UCP1 via Toll-like receptor activation, thereby decreasing thermogenesis in BAT (92).

Hormonal regulation of BAT function

The age-dependent decline of BAT activity has been suggested to be associated with changes in circulating levels of hormones. Ghrelin signaling is an essential thermogenic regulator during aging (93). Obestatin, which upregulates UCP1 expression, and Ghrelin, which downregulates UCP1 expression, are both derived from the same pre-proghrelin gene. During aging, following no change in plasma obestatin expression, increased growth hormone secretagogue receptor (GHS-R) expression and plasma ghrelin expression in BAT was demonstrated to promote thermogenic regulatory imbalance in middle-aged and old mice. Moreover, the knockdown of the ghrelin receptor and/or GHS-R decreased the risk of age-associated IR in Ghsr−/−mice (94). Thyroid hormones, such as triiodothyronine, were also demonstrated to be regulators of thermogenesis; therefore, a decrease in thyroid hormones may significantly contribute to the dysfunction of BAT during aging (95).

5. Beige AT in age-dependent IR

Numerous molecular mechanisms have been reported to be involved in the browning of WAT during aging. The origin of beige adipocytes may result from a white-to-brown trans-differentiation and/or the de novo differentiation of specific precursor cells. For example, progenitor cells and/or adipose stem cells of WAT may differentiate into white or beige adipocytes (96). Among them, a distinct subpopulation of WAT resident progenitors expressing CD137 and transmembrane protein 26 (TMEM26) are more able to differentiate into beige adipocytes (25). Thus, the age-related lose of beige AT may be explained by the loss of CD137/TMEM26+ progenitors. In addition, several regulators were demonstrated to serve important roles in the browning of WAT. For example, peroxisome proliferator activated receptor (PPAR)γ and PR/SET domain 16 (PRDM16) are not only be involved in the induction of BAT-associated genes, but also in the repression of WAT-associated genes. PRDM16 upregulated the expression levels of BAT-specific genes by associating with the transcriptional co-activators, PPARγ coactivator 1 (PGC)-1α and PGC-1β (97). SIRT1, an important target in adipose biology, facilitated the browning of AT via PPARγ and PRDM16 (98) and enhanced beige adipocyte differentiation ability via the senescence-associated p53/p21 signaling pathway (99), which is downregulated during aging. Irisin was also reported to upregulate the expression of UCP1 and promote the WAT browning process, which is a novel hormonal factor that converts WAT into BAT (100). Notably, irisin also induced a significant increase in total body energy expenditure (101). In conclusion, the combined effect of the aforementioned factors have been suggested to participate in the browning process.

6. Therapeutic value of beige adipocytes and acquisition of brown-like properties in WAT

In a previous study, BAT transplantation in mice improved whole-body energy expenditure and IS, suggesting a key role of WAT browning in improving whole body energy metabolism and IS (102). Thus, it may be important to shift beige adipose cells from a WAT phenotype to a BAT phenotype under specific stimuli (Fig. 3).

Figure 3 Possible mechanisms involved in the process of WAT browning. Under cold exposure, thermogenic brown and beige adipocytes produce heat by oxidizing fatty acids. Liver-derived lipid metabolites and bile acids stimulate thermogenesis in BAT. With cold exposure, the levels of bile acid were elevated. β-adrenergic receptors are activated by the release of noradrenaline, and the resultant Ca2+ influx causes AMPK-dependent SIRT1 activation, which deacetylates PPARγ and PRDM-16. A PPARγ/PRDM-16 interaction results in the browning of inguinal WAT. WAT, white adipose tissue; BAT, brown adipose tissue; AMPK, 5′AMP-activated protein kinase; SIRT1, sirtuin 1; PPARγ, peroxisome proliferator activated receptor γ; PRDM-16, PR/SET domain family-16; UCP-1, uncoupling protein 1; SIRT1, sirtuin-1.

Cold exposure

Cold exposure is a strong beige adipocyte inducer. Significant metabolism and gene expression changes in WAT were found to be induced by chronic cold exposure (103). For example, PGC-1α expression levels, a co-activator of PPARγ, were upregulated upon cold exposure. In primary human subcutaneous WAT, the overexpression of PGC-1α promoted polarization to a BAT phenotype, which was accompanied by the upregulated expression levels of fatty acid oxidation enzymes, respiratory chain proteins and UCP1 (104). In addition, chronic cold exposure was also observed to stimulate the differentiation of precursors into beige adipocytes within one week of exposure (105).

Physical exercise

Physical exercise has been reported to be associated with a reduction in lipid content, increased mitochondrial activity and the modified secretion of adipokines (106). However, the effects of physical exercise in the AT of the elderly, particularly in BAT, remain unknown. To date, the findings of previous studies investigating the effect of exercise on BAT in the elderly remain controversial. Recent studies revealed that endurance exercise training could facilitate brown-like adipocyte recruitment within WAT by activating cytokines such as irisin and IL-6 in rodents (107). Furthermore, strength and aerobic training induced an increase in BAT mitochondrial activity in old rats (108). However, another study revealed that chronic endurance exercise was not associated with the recruitment of brown and beige adipocytes (109). Thus, further studies are required to investigate the complex association between different types of exercise and exercise-induced WAT and BAT adaptations.

Diet

Previous studies have reported that several food ingredients may stimulate thermogenesis and browning of the WAT. For example, in a human model, a significant increase in insulin-induced fluorodeoxyglucose uptake in BAT was observed, suggesting that BAT may influence postprandial energy metabolism (110). In addition, capsaicin and capsinoids, which are alkaloids extracted from Capsicum genus, simulated the heat burning sensation (111). The chronic oral administration of capsinoids each day also triggered a significant increase in BAT activity (111). Fucoxanthin (FX), which was found to be present in abundance in the diatom Phaeodactylum tricornutum, significantly downregulated the expression levels and activity of lipogenic enzymes, upregulated the expression levels of AR-β3 in adipocytes and the fatty acid oxidation rate (112). In both WAT and BAT, the administration of a high-fat diet mixed with 0.2% FX upregulated the expression levels of UCP1 in mice. Carotenoids have a large spectrum of isoprenoids, such as β-carotene and retinoic acid, which regulate thermogenesis and energy expenditure in both WAT and BAT (113). β-carotene modulates the expression levels of UCP1 and retinoic acid upregulates the expression levels of catabolic and thermogenic proteins that increase mitochondrial biogenesis. Long-chain ω-3 polyunsaturated fatty acids (LCPUFAs), in particular eicosapentaenoic acid (EPA), upregulated the expression levels of mitochondrial oxidative-and thermogenic-associated genes, in addition to increasing 5′AMP-activated protein kinase (AMPK) phosphorylation and carnitine palmitoyltransferase 1 expression in mice, suggesting that the treatment with EPA may improve energy expenditure, thermogenesis and oxidation in subcutaneous adipocytes (114). Polyphenols, which are secondary metabolites of plants, were also found to recruit new brown adipocytes, and increase metabolic activity, including WAT browning (115).

Autophagy

Autophagy, a cell-protective dynamic process, rearranges subcellular membranes to segregate the cytoplasm and organelles for transmission to lysosomes, and promotes cell death via the excessive degradation of cellular constituents, which may have a role in regulating the browning of WAT. After knocking down the expression of autophagy-related 7 (ATG7) in aP2+ adipocytes to impair autophagy, a BAT phenotype was evidenced by an increased WAT and BAT mass (116). Concurrently, brown adipocyte differentiation and function were specifically disrupted by suppressing ATG7 in Myf5+ precursor cells (117). In addition, mTOR is an essential negative regulator of autophagy. Previous studies have shown that the inhibition of mTOR blocked the cold-induced browning of WAT (118). The β-AR-dependent upregulation of UCP1 expression and increase in the number of beige adipocytes in WAT were observed in mice with mTOR complex 1 impairment (119). Another previous study suggested that the tumor suppressor folliculin (FLCN) regulated WAT browning via a transcription factor binding the IGHM enhancer 3 (TFE3) and mTOR. mTOR-dependent cytoplasmic retention of TFE3 was relieved by the adipose-specific deletion of FLCN, resulting in the activation of the PGC-1α transcriptional co-activator function, suggesting that adipose browning was suppressed by mTOR (120).

7. Conclusion

As there are multiple different mechanisms to induce the WAT browning process, it is plausible that the browning process may represent a potential target to achieve efficacious therapeutic outcomes in aging-dependent IR. Numerous molecules that induce BAT activation or WAT browning may represent potential targets to treat various disease types associated with IR, including type II diabetes, metabolic syndrome and bone diseases.

Availability of data and materials

Not applicable.

Authors' contributions

RS designed the concept of the review and its structure. CW wrote and revised the manuscript. PY was involved in the writing of the review. All authors agree to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Ethics approval and consent to participate

Not applicable.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Acknowledgments

Not applicable.

Funding

The present study was supported by grants from the National Natural Science Foundation of China (grant no. 81802169) and Shanghai Sailing Program (grant no. 18YF1413900).

References