Psoriasis is a common skin disease, with chronic inflammation and a complex etiology. It has long been recognized that chronic skin conditions and mental health disorders are often co-morbid. Thus, the concept of the gut–brain–skin axis emphasized in mental health disorders may also regulate the health of skin.
Results
The gut microbiota has been found to be the bridge between the immune system and nervous system. By leveraging clinical cases and animal models of psoriasis, an important communication pathway has been identified along the gut–brain–skin axis that is associated with the modulation of neurotransmitters from the microbiota. Furthermore, mammalian neurotransmitters, including dopamine, serotonin, or γ-aminobutyric acid (GABA), can be produced and/or consumed by several types of bacteria. Other studies suggest that manipulating these neurotransmitters by bacteria may have an effect on host physiology, and the levels of neurotransmitter can be altered by microbiota-based interventions.
Conclusions
Nonetheless, it is unknown whether or not the manipulation of neurotransmitter levels by bacteria can affect the occurrence and development of psoriasis. Notably, preliminary experiments found that oral consumption of probiotics improves the clinical symptoms in patients with psoriasis, perhaps correlated with the gut microbiome-mediated crosstalk between the immune system and the nervous system by secreting neurotransmitters in psoriasis. In this review, the communication along the gut–brain–skin axis is discussed.
Hinweise
Guang Chen and Zai-ming Chen contributed equally to this work.
Key Summary Points
It has long been recognized that chronic skin conditions and mental health disorders are often co-morbid.
The concept of the gut–brain–skin axis emphasized in mental health disorders may also regulate the health of skin.
Notably, preliminary experiments found that oral consumption of probiotics improves the clinical symptoms in patients with psoriasis, perhaps by altering the composition of intestinal flora leading to changes in neurotransmitter levels.
The gut microbiome can mediate crosstalk between the immune system and the nervous system by secreting neurotransmitters in psoriasis.
Digital Features
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Introduction
Psoriasis is a common skin disease, with chronic inflammation and a complex etiology. The World Health Organization reported that psoriasis affects almost 100 million individuals worldwide [1]. The current view emphasizes an imbalance among environmental, genetic, and immunological factors in psoriasis [2]. For genetic factors, HLA-Cw6 and HLA-Cw7 act as histocompatibility complexes, and bacterial or viral infections, trauma, and stress act as environmental factors, which contribute to the occurrence of skin pathological injury in patients with psoriasis, including erythematous and inflamed and thickened skin [3]. Notably, the pathogenesis of psoriasis, similar to other immune-associated skin diseases, is based on close interactions between components of the adaptive and the innate immune systems [4‐9]. The activation of T lymphocytes (Th1 and Th17) is involved in the production of several pro-inflammatory cytokines, including interleukins (IL-1, IL-6, IL-17, IL-27, IL-18, IL-22, IL-23, and IL-33) [10, 11], tumor necrosis factor alpha (TNFα), and interferon gamma (IFNγ) [12, 13].
At present, immunologists accept the concept that the immune system and the nervous system could crosstalk with each other. Although it has taken a long time, researchers finally confirmed that the immune system has modes of regulation other than self-regulation [14‐17]. For example, at the local level of organization, immune factors are produced and used by the central nervous system (CNS); in turn, neuroendocrine mediators are produced and used by the immune system [18]. In addition, researchers found that intestinal commensals are also capable of producing neuroactive molecules and neurotransmitters that can affect the function of the vagus nerve. The observations that intestinal dysbiosis is associated with different diseases of the nervous system suggest that crosstalk occurs amongst the gut, the nervous system, and the immune system [17].
Firstly, researchers considered that communication from the nervous system to the immune system happens exclusively and is associated with circulating hormones and neurotransmitters. The hormones are secreted by the neuroendocrine system, including cortisol, growth hormone, and prolactin. Neurotransmitters, including epinephrine and norepinephrine, are released by nerve endings of immune cells in primary and secondary lymphoid organs. However, the immune system can also self-regulate, where neuroendocrine factors and neuromediators are produced and released by immune cells, which mediate a shift in the communication pathways from long-range to short-range [18].
In addition, studies have found that mammalian neurotransmitters, including dopamine, serotonin, or γ-aminobutyric acid (GABA), can be produced and/or consumed by several types of bacteria. The manipulation of these neurotransmitters by bacteria may impact host physiology in animal experiments, and it was found that microbiota-based interventions can also alter neurotransmitter levels in preliminary human studies [19]. In other words, intestinal flora regulates the production of neurotransmitters, and neurotransmitters mediate the communication between the nervous system and the immune system. This review emphasizes the different regulatory functions of intestinal neurotransmitters, the current understanding of their pathological role, and the potential mechanisms associated with psoriasis. Moreover, this review proposes a potential therapeutic target aiming at intestinal neurotransmitters for the management of psoriasis and associated diseases.
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This article is based on previously conducted studies and does not contain any new studies with human participants or animals performed by any of the authors.
Gut Microbial Composition in Patients with Psoriasis
Recently, some studies investigated the effect of the gut microbiome on certain dermatological diseases, such as psoriasis, atopic dermatitis, acne, and atopic eczema. The microbiome of feces from 52 patients with psoriasis was analyzed using 16S rRNA and detected an average of 85,000 sequences per sample. The data demonstrated a defined microbial structure and notably different gut microbial composition, defined as the “psoriasis microbiome”, in patients with psoriasis compared with the healthy population. Furthermore, another study found that change of microbial composition was correlated with bacterial translocation [20]. In addition, Tan et al. recruited healthy controls (n = 14) and patients with vulgaris psoriasis (n = 14), and analyzed the microbial composition in psoriasis using a 16S rDNA sequencing platform. The results showed that the abundance of Akkermansia muciniphila was notably decreased in patients with psoriasis [21]. Accumulating evidence considered A. muciniphila as a type of beneficial microbe that is inversely associated with obesity, diabetes, cardiometabolic diseases, and low-grade inflammation, and is a promising candidate for future drug development [22]. In addition, compared with controls, the abundances of the Firmicutes and Actinobacteria phyla were significantly increased in patients with psoriasis. At the species level, the relative proportions of Ruminoccocus gnavus, Dorea formicigenerans, and Collinsella aerofaciens were significantly increased, while Prevotella copri and Parabacteroides distasonis were notably decreased in patients with psoriasis [23]. Recently studies found that the relative abundances of Firmicutes and Bacteroidetes were inverted at the phylum level, and 16 kinds of phylotype at the genus level were found with significant difference [24]. Hidalgo-Cantabrana et al. observed severe dysbiosis in the patients with psoriasis, with lower diversity and altered relative abundance for certain bacterial taxa [25]. Thus, studies suggest that psoriasis alters the characteristics and functions of gut microbiota in patients with psoriasis, which provides a new insight into the association between the intestinal flora and the pathogenesis of psoriasis.
Gut Microbial and Skin–Gut Axis in Psoriasis
The adult intestine hosts a number of diverse bacterial species, collectively referred to as the microbiome, that reside mainly in the lower gut, where they maintain a symbiotic relationship with their host. Psoriasis, like many other systemic inflammatory diseases, likely involves inappropriate activation of various immune pathways leading to elevations in pro-inflammatory cytokines [26]. The gut microbiome is believed to be involved in the development of pro-inflammatory Th17 cells, allowing it to modulate inflammation in diseases such as inflammatory bowel disease and obesity [21]. Like the skin microbiota, the composition of the gut microbiota and its association with psoriasis are unclear. Tan et al. compared the gut microbiota in patients with psoriasis with those without the disease and found that those with psoriasis had a significant decrease in A. muciniphila, a species believed to strengthen the integrity of the gut epithelium and protect against systemic inflammatory diseases, such as inflammatory bowel disease, obesity, and atherosclerosis [21, 27‐30]. Scher et al. found that the diversity and abundance of the gut microbiota were altered in patients with psoriasis and arthritis compared with healthy controls; microbial diversity was decreased, with the main characteristic of reduced relative abundance of Akkermansia, Ruminococcus, and Pseudobutyrivibrio [31]. Conversely, psoriatic exacerbation was deemed to be associated with increased colonization of Staphylococcus aureus, Candida albicans, and Malassezia in the skin and gut [32]. Thus, the association between the gut and skin is strong and bidirectional, and gastrointestinal health is associated with skin homeostasis and allostasis [33, 34].
An imbalanced gut microbiome, a pathological state named intestinal dysbiosis, has a negative impact on skin function and integrity [35, 36]. O’Neill et al. found that the gut microbiome can influence skin homeostasis via regulating the coordinate epidermal differentiation and immune system, although the mechanism is not yet fully elucidated [33]. Furthermore, studies provide new evidence to clarify the effect of the gut microbiome on dermatologic physiology, pathology, and immune response, which rely on the dissemination of intestinal microbiota and their metabolites from the gut to the skin [33, 37]. Certain pathogenic bacteria can produce certain metabolites, such as phenol and p-cresol. These metabolites can disrupt the skin barrier integrity and epidermal differentiation, reduce skin hydration, and impair keratinization, which are associated with entry into the bloodstream and accumulation in the skin [38, 39]. In fact, except for skin health, gut microbial metabolite production can significantly impact the health and disease states of the host. This is demonstrated in the examples of short-chain fatty acid and trimethylamine production via bacterial metabolism of dietary complex carbohydrates and choline, respectively. In addition to its role in cardiovascular disease and chronic kidney disease, the gut microbiota impacts the development of inflammatory bowel disease (IBD) and so on [40]. Furthermore, certain gut microbes may recruit regulatory T cells and lymphocytes to promote anti-inflammatory response by certain metabolites, such as retinoic acid and polysaccharide A [41]. Short-chain fatty acids (SCFAs), a type of metabolite, are involved in the activation and apoptosis of immune cells. Accumulating evidence in animals showed that chronic systemic inflammation is the main consequence of intestinal dysbiosis, due to the imbalance between increased epithelial permeability and the activated effector T cells, resulting from the secretion of pro-inflammatory cytokines; this leads to a vicious circle of chronic systemic inflammation [33, 42]. This may be one of numerous mechanisms by which the gut microbiome induces skin impairment.
The “skin–gut axis” concept provides a new insight to investigate the association between the intestinal flora and the skin. Modulated aberration of gut microbes leads to a wide variety of inflammatory dermatologic disorders, such as acne vulgaris, seborrhoeic dermatitis, and psoriasis. Increasing evidence shows the existence of the gut–skin axis, and that an imbalanced gut microbiome can induce inflammatory skin diseases [43]. This offers a feasible approach for improving skin conditions, by the modulation of the gut microbiota [43]. On the basis of these findings, the treatment of skin inflammation by oral probiotics is favored, since its therapeutic management is simple, safe, and cheap [43].
Gut Microbial and Gut–Brain–Skin Axis In Psoriasis
The concept of the brain–gut–microbiome (BGM) was supported by preclinical studies published during the past decade. The microbiome can regulate the CNS by neuroimmune and neuroendocrine systems primarily, often involving the vagus nerve [44‐47], and the mechanism of this communication is associated with several microbial metabolites, including SCFAs, secondary bile acids, and tryptophan metabolites [45, 48, 49]. In addition, the activation of the endogenous CNS signaling by microbial metabolites involves a number of neuroactive molecules, including GABA [50, 51], 5-hydroxytryptamine (5-HT) [52, 53], norepinephrine [53, 54], and dopamine [52‐54] produced by the microbiota. However, how these metabolites elicit a host response is unknown; perhaps via relevant receptors or reaching sufficient levels.
Stokes and Pillsbury (1930) first proposed the gut–brain–skin axis concept, based on various experimental evidence and clinical anecdotes, suggesting that gastrointestinal regulation mediates the influence of emotional and nervous states on the skin. The authors considered that the function and microbiota of the gastrointestinal tract can be altered by emotional states, such as depression and anxiety, which promote local and systemic inflammation [55, 56]. Furthermore, studies also found that an important connection between emotional states and inflammatory skin conditions can be regulated by bacteria of the gastrointestinal tract [55, 56]. Recently, many recent studies have provided evidence that supports the gut–brain–skin theory. It is obvious that gut microbes could affect the condition of skin (such as the severity of acne), which is consistent with their ability to regulate systemic inflammation, oxidative stress, and emotional changes. Furthermore, these aforementioned data can be confirmed by oral probiotics [56].
It has long been recognized that chronic skin inflammation and mental health disorders are often co-morbid, following neuro-dermatology and psycho-dermatology discovered in recent years [57‐60]. However, through literature review, it was demonstrated that bacteria in the gut can produce many types of neurotransmitters, which regulate the function of immune cells in the host via the nervous system. However, it is believed that the nervous system does not contribute to tissue repair and combating pathogens via the activated immune system. Indeed, numerous observations and discoveries support the notion of the nervous system as an immunoregulatory system involved in immune responses [61].
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At present, although there are no any reports that neurotransmitters can treat psoriasis by regulating the immune response, it is postulated that neurotransmitters, especially from the gut, as a new immunoregulator, can be clinically applied for psoriasis. This hypothesis is based on (1) gut microbes can secrete neurotransmitters; (2) psoriasis is also a common and frequently occurring disease, which endangers people’s physical and mental health; and (3) psoriasis is mainly characterized by the imbalance of immunologic factors.
Gut Microbial and Neurotransmitters in Psoriasis
Regarding the crosstalk between the microbiota and the nervous system, studies suggest that host neurotransmitters and/or related pathways have a key role during the process of communication (Fig. 1). Indeed, Strandwitz reported that bacteria have the capability to produce a range of major neurotransmitters (Table 1) [19]. Consistently, Valles-Colomer et al. also considered that microbial metabolism, including neurotransmitters (e.g., serotonin and GABA), affected microbiota–gut–brain communication [62]. Notably, studies revealed that antidepressants have beneficial effects in common inflammatory skin disorders; the mechanism may be associated with the immunoregulatory capacities of these agents [63]. Moreover, in animal models, it was found that antidepressants have anti-inflammatory or immunomodulatory effects [64, 65]. Furthermore, new-generation antidepressants usually introduced selective neurotransmitters reuptake inhibitors [66]. The results indicated that neurotransmitters may be a key regulator of communication in the gut–brain–skin axis. Subsequently, several types of neurotransmitters secreted by gut microbes were selected to investigate their potential function in psoriasis.
Fig. 1
Gut microbiome-mediated crosstalk between the immune system and the nervous system by secreting neurotransmitter in psoriasis
A number of bacteria have been reported to be able to produce a range of mammalian neurotransmitters. This table was curated to include only one organism per species, and the strain is indicated in parentheses when available. Much of the information listed here was adopted from Strandwitz [19]; please consult that article for reference details
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Dopamine
Dopamine is an important neurotransmitter in the CNS and locomotive control, cognition, emotion, immunology, and neuroendocrine secretion [67]. Many studies reported that about 11 bacteria can produce dopamine. Dopamine and norepinephrine can promote the growth of pathogenic Escherichia coli O157:H7 (EHEC) [68], and norepinephrine also exhibits the ability to increase motility, biofilm formation, and virulence [69]. Consistently, in vitro norepinephrine improved the growth of EHEC and the pathogens K. pneumoniae, Pseudomonas aeruginosa, Enterobacter cloacae, Shigella sonnei, and S. aureus which may be associated with its effect on iron acquisition [70]. Regarding the association between dopamine and psoriasis, there are three key points. Firstly, in psoriasis, crosstalk between the immune system and the nervous system, via neurotransmitters such as dopamine, modulates immune responses by influencing the local tissue environment and can, for example, influence the activation status and migration of T cells. Immune cells also use neurotransmitters to communicate with each other, targeting tissue-specific inflammation of psoriasis [71]. Secondly, evidence shows that in 31–88% of cases, patients reported stress as a trigger for their psoriasis. In addition, stress is also a consequence of psoriasis outbreaks [72]. Thus, all stress hormones, including dopamine, should be a vital regulator in psoriasis. Thirdly, dopamine can increase the activity of keratinocytes, which play a role in the release of cytokines and chemokines. A study by Mori et al. in a mouse animal model (in vitro) showed that the intervention of a dopamine 1 (D1) receptor antagonist (SCH 23390) decreases the expression of IL-4 and IFNγ within 3 h (rapid-phase immunological reactions) and 24 h (slow-phase immune reaction) in rat skin [73]. Keren et al. reported that dopamine can inhibit activated T cells and has the potential for modulating this communication to target T cell-mediated inflammation in psoriasis [74]. In addition, dopamine can induce keratinocytes to release cytokines [75], and an increase of dopamine levels in patients with psoriasis [76]. Dopamine causes rapid depolarization of both resting and activated T cells via dopamine receptors, and targeting D1-like receptors in activated T cells and inflamed human skin could be a new therapeutic option [71, 74].
Serotonin
Serotonin is a signaling molecule that regulates numerous physiological processes, including the immune [77], gastrointestinal [78], and nervous [79] systems, via paracrine, endocrine, and juxtacrine regulation. Furthermore, the majority of 5-HT (more than 90%) is synthesized by gastrointestinal enterochromaffin cells (ECs) and 5% of 5-HT is synthesized in myenteric neurons and some in the brain [80]. Many studies have reported that about seven bacteria can produce serotonin (Table 1). It was found that host serotonin levels may facilitate ECs to produce serotonin, with the aid of tryptophan hydroxylase, by the secretion of small molecules (such as SCFAs) [48]. In the 1980s, 5-HT was defined as an immunomodulator [81], due to its ability to inhibit inflammation, including in psoriasis [71]. Although the effects of 5-HT on the immune system were not fully elucidated, it is certain that 5-HT altered immune responses in patients with dysregulated serotonergic systems. In these cases, 5-HT receptor antagonist treatment provides beneficial immunomodulatory effects in animal experiments [82].
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GABA
GABA is widely present in microorganisms, plants, and vertebrates as a main inhibitory neurotransmitter of the CNS [83]. GABA has a broad biological activity, including modulating synaptic transmission, promoting neuronal development and relaxation, and preventing sleeplessness and depression [84‐88]. Accumulating evidence clarified that GABA can be consumed and/or produced by bacteria. Many related articles reported that about 13 bacteria can produce GABA (Table 1). Lactic acid bacteria and Bifidobacterium are the main source of GABA [89, 90]. Importantly, fecal microbiome transplant from lean to obese individuals increased GABA levels in the plasma in a recent human study, which reveals that the levels of GABA production can be manipulated by the microbiome [91].
Notably, researchers found various biological activities of GABA, such as anti-hypertension, anti-diabetes, anticancer, antioxidant, anti-inflammation, antimicrobial, and anti-allergy effects [92]. Han et al. also found that GABA can inhibit the levels of iNOS, IL-1, and TNFα production to exert the anti-inflammatory activity [93]. In addition, GABA also inhibits IFNγ and IL-17 production and the function of antigen-presenting cells by the expression of MHCII and CD80. On the other hand, GABA displayed the strongest stimulatory effects on the expression of Foxp3+, IL-10, TGFβ, CTLA4, and SIRP-α immunoregulatory molecule [94]. Patients with psoriasis generally have pruritus, which may be associated with the GABA system. Experimental studies reported the expression of GABA ligand and the GABAA receptor to be increased in the psoriatic skin, suggesting their potential as a key target in the pathogenesis and pruritus associated with psoriasis [95]. Therefore, GABA may be considered as a potential alternative therapeutic for the prevention and treatment of psoriasis.
Future Prospects
The treatment of psoriasis, similar to other immune-mediated complex diseases, is limited to improving the symptoms, due to the lack of effective therapy [96]. Nevertheless, accumulated evidence suggests that the gut microbiota may mediate the crosstalk between the nervous system and the immunity system, via secreting neurotransmitters (Fig. 1). Fecal microbiota transplantation (FMT) is a method to directly change the recipient’s gut microbiota to normalize the composition and gain a therapeutic benefit [97]. Moreover, accumulated studies found that FMT could be a novel therapy for psoriasis [98, 99]. Further clinical trials are needed to provide solid evidence. Further studies are also required to validate the potential mechanisms. The gut–brain–skin axis is a likely communication route involved in neurotransmission modulation. However, this theory needs to be validated by experiments, which combine bacteria-based intervention with neurotransmitter receptor antagonists or investigate the change in the composition of bacteria that produce neurotransmitters. On the basis of the gut–brain–skin axis theory, by understanding these communication routes and their associations with disease characteristics, microbiome-mediated interventions could be designed to manipulate these targets for the treatment of psoriasis.
Acknowledgements
Funding
The authors gratefully acknowledge funding from the Fund for Taizhou science and technology planning project (20ywa57, 1902ky31, 1701ky29); outstanding youth program of Taizhou University (Z 2020080). Taizhou University Hospital funded the journal’s rapid service fee.
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Authorship
All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this article, take responsibility for the integrity of the work as a whole, and have given their approval for this version to be published.
Disclosures
Guang Chen, Zai-ming Chen, Xiao-yan Fan, Yue-lei Jin, Xin Li, Shi-ren Wu, Wei-wei Ge, Cao-hua Lv, Yao-kun Wang and Jin-guang Chen have nothing to disclose.
Compliance with Ethics Guidelines
This article is based on previously conducted studies and does not contain any new studies with human participants or animals performed by any of the authors.
Data Availability
Data sharing is not applicable to this article as no datasets were generated or analyzed during the current study.
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