Spice Up Your Life: Adipose Tissue and Inflammation

Agarwal, Anil K.

doi:https://doi.org/10.1155/2014/182575

Journal of Lipids

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Review Article | Open Access

Volume 2014 | Article ID 182575 | https://doi.org/10.1155/2014/182575

Spice Up Your Life: Adipose Tissue and Inflammation

Anil K. Agarwal¹

Academic Editor: Sampath Parthasarathy

Received16 Sept 2013

Accepted15 Jan 2014

Published20 Feb 2014

Abstract

Cells of the immune system are now recognized in the adipose tissue which, in obesity, produces proinflammatory chemokines and cytokines. Several herbs and spices have been in use since ancient times which possess anti-inflammatory properties. In this perspective, I discuss and propose the usage of these culinary delights for the benefit of human health.

1. Introduction

Up until recently, studies relating to adipose tissue were mostly neglected partly because adipose tissue (AT) was not considered to be a critical tissue, except for the fact that AT stores energy (as triglycerides) and releases it upon demand and partly because lipids are very hydrophobic in nature and are not easily soluble in aqueous solutions, further hampering biochemical analysis. Even now, most investigators still use the solvent system developed in 1950 by Bligh and Dyer, is a rapid chloroform and methanol lipid extraction method, although this extraction method is only efficient in extracting some, but not all, types of lipids.

Adipose tissue regained scientific attention in early 1980 with the rise of obesity worldwide [1]. The occurrence of obesity has continued to increase at such a pace that recently it has been classified as a disease by the American Medical Association [2]. While obesity in humans had been described in ancient literature, those who lacked AT went unnoticed. The first documented evidence of a lack of AT in humans was described by Berardinelli and Seip in 1954, who observed patients with complete loss of AT from birth [3, 4]. Since then, several investigators have identified a spectrum of the AT loss, ranging from partial to total, and has been referred to as partial lipodystrophy (PL) and congenital generalized lipodystrophy (CGL), respectively [5–7]. However, when present, AT has the potential to expand up to 50–70% of body weight causing obesity. Ironically, the clinical burden or symptoms in both of these conditions—obesity and lipodystrophy—are quite similar. Patients of both conditions suffer from hypertriglyceridemia, insulin resistance, hepatic steatosis, and development of type 2 diabetes, and in women both conditions may contribute towards polycystic ovarian syndrome (PCOS). These constellations of clinical features are also referred to as Metabolic Syndrome. Because of this, it has become apparent that AT is important for normal physiological function in the human body but may not be critical for human development and survival.

In any human population, there is a continuum of body mass, ranging from extremely lean to lean to obese and extremely obese, resulting in a bell-shaped curve (Figure 1(a)). Thus, on the extreme ends of the graph lies a set of individuals whose AT is most likely regulated by genetic alterations. Such is the case in individuals with CGL, who have germ line transmission of mutations in genes such as 1-acylglycerol 3-phosphate-O-acyltransferase 2 (AGPAT2) [8], Berardinelli Seip congenital lipodystrophy 2 (BSCL2) [9], and Caveolin 1 (CAV1) [10]. At the other end of the spectrum lies the case of extreme obesity, mostly since birth, and here again germ line transmission in genetic alterations was noted in leptin (LEP), leptin receptor (LEPR), proopiomelanocortin (POMC), prohormone convertase 1 (PCSK1), melanocortin 4 receptor (MC4R), single-minded homolog 1 (SIM1), brain-derived neurotrophic factor (BDNF), and its receptor TrkB coded by neurotrophic tyrosine kinase receptor type 2 gene (NTRK2) reviewed in [11]. Some cases of obesity, like those due to mutations in the leptin gene, can be treated with leptin replacement [12]. Others, such as those due to MC4R, which acts at the central nervous system, have been difficult. Likewise, subjects with lipodystrophy who lack leptin have also been successfully treated with leptin replacement therapy [13]. However, these extreme cases of AT loss or excess are extremely rare. It is the vast majority of the human population who fall under the bell-shaped “obesity curve” that require treatment because obesity is associated with a number of chronic diseases like fatty liver (hepatic steatosis), hyperlipidemia, hypercholesterolemia, cardiovascular diseases, and type II diabetes. Obesity in this group appears to be of polygenic nature. Numerous genomewide association studies (GWAS) have identified several single nucleotide polymorphisms (SNPs) enriched in several genes, both in the coding and noncoding regions associated with obesity. These SNPs are too numerous to mention here and are reviewed in [14]. One among them is obesity-associated gene (FTO). FTO demethylates N⁶-methyladenosine, a potential regulatory RNA modification, has recently been shown to regulate ghrelin, a hunger hormone, which predisposes to increased food intake and increases obesity [15]. It has also been observed that survivors of childhood brain cancers have a higher risk of developing obesity. A prospective study, CanDECIDE study (Canadian Study of Determinants of Endometabolic Health in CHI1DrEn) has been proposed to determine the mechanism(s) associated with inflammation, childhood brain cancer, and the development of obesity [16]. From these observations, it is clear that either losing AT or acquiring excess AT is both unacceptable strategies. Thus, maintaining an adequate amount of healthy AT seems to be a reasonable and acceptable possibility. There are several options for this group of individuals, although adopting a healthy diet and exercise program, when followed, is the most viable option.

(a)

(b)

Figure 1

Schematic of body fat in a human population and the presence of macrophages in lean and obese adipose tissue. (a) The bell-shaped curve represents the distribution of body fat in a human population. The healthy weight (within the 1 standard deviation of the healthy weight) is shown between the black dashed lines. In recent decades, this curve has shifted to the right, shown by the diagonal shaded red lines. The increase in this body weight is also associated with various single nucleotide polymorphisms found in the general population. On the extreme ends, monogenic forms of congenital generalized lipodystrophy (CGL) and obesity are shown in the circles. Various genes associated with these monogenic forms are mentioned in the text. (b) Anti-inflammatory M2 macrophages in the lean adipose tissue are converted to proinflammatory M1 macrophages in the obese adipose tissue which depends on chronic nutrition, chemokine, and cytokine signaling.

2. Adipose Tissue

In recent years, interest in AT has seen a renaissance. There have been studies which show that AT (specifically adipocytes), in addition to storing and releasing fatty acid, also secretes several proteins which act as hormones [17]. In addition, AT also secretes lipids which help to maintain systemic metabolic homeostasis [18]. However, adipocytes are not the only cell type which constitutes AT. In addition, AT also contains stromal cells, vascular cells, and cells of the immune system like macrophages [19], specifically of the M2 type, which are anti-inflammatory in lean AT. Several proteins are secreted from adipocytes, often known as adipokines, but the two most widely studied adipokines are leptin [20] and adiponectin [21]. During obesity, AT expands, attracting other cell types; the most important in recent years are the cells of the immune system.

3. Anatomical Location of Adipose Tissue

In humans and rodents, AT is found in almost all anatomical regions of the body. It is interesting to note that, unlike other organs such as the liver, heart, or lung, the AT lacks a well-defined organ boundary and thus is mainly identified by anatomical location [29]. AT found under the skin or dermis is mainly referred to as subcutaneous (sc) adipose tissue. AT can further be identified as sc abdominal or sc AT of the extremities. The AT found in the visceral cavity may be subdivided as omental, mesenteric, or perirenal [29]. Adipose tissue located behind the eyes (retroorbital), knees (periarticular), around the hip joints, or beneath the skull has not received any specific nomenclature as yet. While the white AT is distributed throughout the body, the other type of AT—the brown adipose tissue (BAT)—is more restricted in its anatomical location and is mainly found in the interscapular and cervical (neck) region. In the past, BAT was mainly recognized neonatally and in infants and was thought to recede during adulthood. In recent years, new imaging techniques have identified that BAT still exists in the adult human population. While the physiological function of subcutaneous and visceral AT is widely studied, AT found at other locations has received little attention. However, identification of adult BAT has rejuvenated studies related to the physiological function of BAT.

4. Types of Adipose Tissue

In the past, two main types of ATs were described—WAT and BAT. Regardless of WAT localization, the WAT has been implicated in maintaining lipid homeostasis. The adipocytes in WAT are insulin sensitive and, thus, in the presence of excess fatty acid, synthesize TAG. These molecules are stored as large lipid droplets in the adipocytes. WAT then releases free fatty acids as required. In contrast, BAT is mainly associated with thermogenesis. The adipocytes of BAT are rich in uncoupling protein 1 (Ucp1) which uncouples the last step in mitochondrial oxidation of fatty acid to release energy instead of generating ATP for storage. In recent years, a new type of adipocyte has been identified, referred to as a “brite” adipocyte (brown-in-white) [30]. Using lineage-tracing reporter mice, Ucp1 promoter-driven GFP for transient tracing of UCP1 expression and UCP1-CreER, ROSA-tdRFP mice to permanently label brown and brite adipocytes following tamoxifen administration, Rosenwald et al. revealed that the origin of brite adipocytes lies in the white adipocytes [31]. Furthermore, this study also revealed that this conversion of white to brite is a reversible process as well.

5. Immune Cells of Adipose Tissues

The relationship between the immune system and AT was recognized several decades ago when it was shown that neutralizing tumor necrosis factor alpha (TNFα) improved insulin resistance in rodents [19]. This observation catalyzed our thoughts towards systemic inflammation and its role in insulin resistance and obesity. Immune cells of both innate and adaptive immune systems are found in AT obtained from both lean and obese subjects [32]. These include, but are not limited to, macrophages (M1 and M2), mast cells, neutrophils, eosinophils, type 2 innate lymphoid cells (ILCs), CD4+ and CD8+ T cells, B cells, regulatory T (Treg) cells, and natural killer T cells (NKT cells) [32]. In the lean AT, the macrophages are of the M2-type which are anti-inflammatory [33]. It is upon expansion of AT that there is a significant increase in the number of proinflammatory macrophages denoted M1-type [34]. Based on cell surface markers, a new population of adipose tissue macrophage has been identified as type 3 [35], but its role in adipose tissue in relation to M1 and M2 remains to be established. The conversion of the anti-inflammatory M2-type to the proinflammatory M1-type is regulated by lipopolysaccharide and interferon γ (IFN-γ) which produce proinflammatory mediators like TNF-α, IL-6, IL-1β, nitric oxide (NO), and IL-12 (Figure 1(b)). While such events in obesity are recognized by several investigators, it is still unclear how the expanding adipose tissue in obese individuals recruits these cells of the immune system.

While the ligands for the cellular triggering of the proinflammatory immune cells can be varied, most of the signal transduction is related via the activation of nuclear factor-kappa B (NF-κB). NF-κB has many members which include REL family members RELA (p65), c-REL and RELB, NF-κB1 (p50; p105), and NF-κB2 (p52; p100). These proteins contain dimerization and DNA-binding domains and can form homo- or heterodimers. NF-κB resides in the cytoplasm and exists as a p50-p65 or p52-p65 dimer associated with the regulatory proteins inhibitor of nuclear factor κB (IκB) kinases (IKKs) [36]. This association with IKKs precludes the complex from entering the nucleus. Upon proinflammatory signals, IKK phosphorylates IkB which then dissociates itself from the p50-p65 or p52-p65 complex and is degraded via ubiquitination, while NF-κB moves into the nucleus to activate the proinflammatory gene program, reviewed in [37]. There are at least four IKKs: IKK-α, IKK-β, IKK-ε, and TANK-binding kinase 1 (TBK1). Recently, it was demonstrated that in vivo inhibition of TBK1 and IKK-ε using the small-molecule selective inhibitor amlexanox in mice fed high-fat diet improved insulin sensitivity and decreased hepatic steatosis with accompanying increased energy expenditure and weight loss [38]. This provides a rationale for the effective use of anti-inflammatory molecules for reducing inflammatory-associated obesity and its associated complications.

6. Combating Inflammation in Obesity and Metabolic Syndrome

Ever since the identification of the role of low grade inflammation in obesity and its associated complications, efforts have been underway to reduce the burden of inflammation in AT. Thus, reducing the proinflammatory response in AT should be beneficial for human health.

Several phytochemicals have been in use since prehistoric times, although the anti-inflammatory properties of these culinary herbs and spices were only recognized recently. These phytochemicals belong to several chemical groups but most belong to polyphenols, flavonoids and their analogs. When consumed in small quantities, certain plants, including plant roots themselves and their extracts, have been reported to have beneficial effects in reducing systemic inflammation and type 2 diabetes and increasing insulin sensitivity. A recent report shows that high-fat fed mice given dietary capsaicin, a component of chili pepper, showed improved glucose tolerance, reduced liver fat, and improved insulin sensitivity [39]. In another study, the topical application of capsaicin in mice saw a reduction in visceral adipose tissue resulting in decreased inflammation and increased insulin sensitivity [40]. Capsaicinoids, a group of chemicals found in chili pepper, have also been shown to have a beneficial effect on weight loss in humans [41]. This effect has been shown to be due to increased energy expenditure, increased lipid oxidation, and decrease in appetite [41]. A meta-analysis of the use of capsaicinoids further confirms their role in weight loss [42]. However, further investigations are needed to evaluate their role in long-term usage. Although it is unclear what role capsaicin plays in cancer, studies with capsaicin extract, which is a mixture of several molecules, including norhydrocapsaicin, dihydrocapsaicin, homocapsaicin, homodihydrocapsaicin, and nonivamide, have resulted in showing both the carcinogenic and anticarcinogenic activities of capsaicin (reviewed in [43]). Why capsaicin has demonstrated both activities might be due to the fact that various capsaicin extracts used in the studies do not carry the same chemical entities or might vary in the concentration of various chemical components or because of their different metabolism rates in humans and animals [43, 44].

The role of natural products in cachexia has not been fully elucidated. This is partly because there is a lack of consensus as to how to define cachexia. A recent attempt defines cancer cachexia as “…ongoing loss of skeletal muscle mass with or without loss of fat mass that cannot be reversed by conventional nutritional support and leads to progressive functional impairment” [45, 46]. In fact, both cachexia and obesity, which represent two different nutritional states, have some similarities in expression of inflammatory molecules. IL-6 and TNF are expressed in both conditions. However, in obesity, additional proinflammatory molecules IL-1β and interferon γ are also expressed. I hypothesize that the use of some of the anti-inflammatory products derived from the plant source might result in beneficial effects for these patients [47]. I have discussed genetic causes of lipodystrophy and, by itself, loss of adipose tissue does not attract cells of the immune system. However, the advent of highly active antiretroviral therapy (HAART) for the treatment of patients affected with human immunodeficiency virus (HIV) did result in partial lipodystrophy. Although lack of adipokines such as leptin or adiponectin [48] has been reported, information regarding cells of the immune system is scarce and treatment with plant derived products is yet to take hold.

I have listed in Table 1 several of these plants and roots which have been used in many cultures to enhance the food flavors. In the process, these cultures have also benefitted from their anti-inflammatory properties, which have been extensively reviewed in [22, 26, 49, 50]. This is not to say that consuming all of these spices will make the obesity-associated inflammation go away, but they will help alleviate some of its effects. A sustained but balanced diet and exercise is still required to combat obesity and associated inflammation. There are no systematic controlled clinical trials using these spices and herbs to further provide the rationale for using these spices for this purpose. This is partly because these phytochemicals are often not extracted, purified, and identified as a single chemical entity and partly because these phytochemicals vary according to the geographic location which further makes the outcome of these studies scientifically unreliable. However, these herbs and spices have been used from prehistoric times with beneficial effects. Another aspect to consider is that while one single spice might bring a small biological effect, when used in combination with a mixture of spices, they might show additive effects. Therefore, while controlled clinical trials might improve our confidence in the usage of these spices, nevertheless, their usage in crude form in our daily lives will still bring benefits.

7. Brown Adipose Tissue and Inflammation

I have discussed above the physiological function of BAT in human physiology which is to provide thermogenic activity by the uncoupling of energy which has been proposed as a mechanism to alleviate obesity. In humans, BAT was thought to be present in infants but not in adults. All this changed with the improvements in detection technology. BAT actively uptakes glucose from the blood. Thus, detecting glucose using a noninvasive technique coupled with the presence of UCP1, a molecular signature for BAT should yield the presence of BAT in adult humans. When ¹⁸F-fluorodeoxyglucose (¹⁸F-FDG) positron-emission tomographic and computed tomographic (PET-CT) scans were performed, significant depots of BAT was revealed from the anterior neck to the thorax region in human adults [51]. Therefore, activating BAT in human adults seems to be approachable now. The role of alternatively activated macrophages in the control of BAT thermogenesis was recently demonstrated in rodents by Nguyen et al. [52], suggesting for the first time the relationship between cells of the immune system and BAT. While searching for alternative ways to activate BAT, Zhu et al. [53] discovered the expression of transient receptor potential melastin 8 (TRPM8), a cold sensing ion channel, which responded to menthol in inducing BAT thermogenesis. Transient receptor potential vanilloid-4 (TRPV4) has also been found to be expressed in the BAT and is believed to be the inhibitor of the molecular function of beige adipose tissue. Thus, inhibition of TRPV4 leads to an increase in the thermogenic gene expression in WAT [54]. In addition to BAT, TRPV4 is also present in sympathetic nervous system (SNS) which could further regulate BAT. The physiological ligand for TRPV4 is still unknown but has provided new avenues for regulation BAT.

It is also interesting to note that several of the ion channels expressed in our palate are activated by compounds present in our food. The taste cells on the tongue, throat, and mouth synapse with adherent fibers that travel to the brain via the trigeminal nerve. In addition to TRPV4 and TRPM8 as found in BAT, these nerves express other ion channels such as transient receptor potential V1 (TRPV1, TRPA1, and TRPV3). These TRP-types of channels are activated by alkamides, isothiocyanates, and terpene dialdehydes found in the diet we consume. Although most spices, such as capsaicin, piperazine, chili, and rutaecarpine—found in a Chinese herb (Wu-Chu-Tu) [55], have been found to activate TRP1 in the palate, it is possible that they might activate other ion channels. Therefore, these spices might have benefits in activating BAT in addition to flavoring our food. Indeed, a recent study demonstrated the beneficial effect of capsinoids when ingested by humans for over a 6-week period, increasing energy expenditure and reducing body fat [56].

8. Characterization of Natural Products

Despite the fact that we recognize the beneficial effects of plant products, identifying the active ingredient has been challenging. First, geographic location and the prevailing climate conditions can alter the chemical composition of the active substance. In fact, such variation can be noted from season to season within the same geographic location. Second, the very extraction method employed, while this might be optimized, could also alter the chemical composition of the active substance. Third, the fact that each plant extract consists of several individual chemically distinct compounds further complicates the isolation of a single active compound.

9. Perspective

Overall, the purpose of this perspective is to advance the idea of the beneficial effect of spices used in all cultures—some more than others—including their effects in alleviating inflammation, a partner in obesity causing associated metabolic complications. A recent study demonstrated the beneficial effect of curcumin, the active substance of turmeric, as an effective treatment for inflammatory bowel disorder [57]. Salicylate, or its acetylated form, aspirin, is the oldest and most widely prescribed drug first identified in plants [58]. Its effect in lowering blood glucose was first reported by Yuan et al. [59, 60]. Salsalate’s beneficial effect was recently reported in placebo-controlled, randomized clinical trial [61, 62]. Although controlled clinical trials for many of the phytochemicals are not feasible for the reasons mentioned above, more efforts are needed to isolate and identify the chemical entity and biological activity of phytochemicals as has been demonstrated for curcumin and salsalate.

Conflict of Interests

The author declares no conflict of interest related to this work.

Acknowledgments

The author thanks Chandra Mohan, M.D., Ph.D., Division of Rheumatic Diseases and Department of Internal Medicine for reviewing this work and Katie Tunison, M.S., for copyediting the paper and generating Figure 1. The author is supported by Grants from the National Institutes of Health, R01-DK54387, by the Southwestern Medical Foundation and the Center for Human Nutrition at UT Southwestern Medical Center.

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Copyright © 2014 Anil K. Agarwal. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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