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Sulphurous Mineral Waters: New Applications for Health.

1. Introduction

Hydrogen sulphide ([H.sub.2]S), the active molecule in sulphurous mineral waters, is currently attracting the attention of scientists due to its potential therapeutic applications [1]. These past few years have witnessed a growing body of knowledge regarding the potent role of hydrogen sulphide as a signalling molecule and protein sulfhydration [2] in numerous cytoprotective biochemical reactions of the body. Besides supporting the known properties of sulphurous mineral waters, these new data are starting to unveil new therapeutic applications for these waters.

Being a gas, [H.sub.2]S can be absorbed by numerous routes. It is able to penetrate the skin and mucosae and can therefore act at the cell level both in the skin and in internal organs of our organism. This means that the topical application of sulphurous mineral waters rich in hydrogen sulphite has the potential to treat disorders of the internal organs such as high blood pressure, ischemia, and conditions affecting the kidneys or nervous system. Further, if sulphurous mineral water is applied to the skin in the form of a matured mud, or peloid, its effects may be potentiated. Many authors have examined the mechanisms of action of medicinal waters and their therapeutic effects, and certain inorganic components have been linked to the effects of curing baths [3-7] and muds [8-11].

Several studies have also assessed the properties of mineral water as a whole, although the different constituents of waters may act in an antagonistic manner [12]. Similarly, peloids have often been considered as equivalent despite their different origins conferring them very different properties [13].

In this paper, we revisit the chemical properties of [H.sub.2]S in sulphurous mineral waters and describe how environmental factors such as pH, temperature, and the presence of oxygen can affect its concentrations and thus the final activity of the waters or their products. Finally, we review the impacts of [H.sub.2]S on mammalian cells and organs, with special attention paid to the new therapeutic possibilities of sulphurous mineral waters and their peloids.

2. Hydrogen Sulphide Chemistry

Hydrogen sulphide is a colourless gas and, being a weak acid, is highly soluble in water. It is heavier than air, very poisonous, flammable, and corrosive. Above a certain concentration, its toxic effects are comparable to those of carbon dioxide and cyanide. Its stability depends on the pH, temperature, and the oxygen concentration of the environment.

Sulphur forms change at two critical pHs, pKa = 7.04 and pKa = 11.96. At physiological pH, the ratio of hydrogen sulphide to bisulphide ([HS.sup.-]) is 1:3. Thus, two identical solutions of [H.sub.2]S show different concentrations at different ambient temperature and the presence of oxygen will promote the reduction of hydrogen sulphide to hydrogen sulphate.

At acidic pH, [H.sub.2]S is the only form of sulphur. At a pH of 7.04, sulphur salts occur at a 50% concentration and when the pH is around 9.5 only bisulphide will exist ([HS.sup.-]). Beyond pH 9.5, sulphides ([S.sup.2-]) start to form and as pH increases, this anion is the only viable form of sulphur (Figure 1).

At physiological pH (7.2-7.4), only a third of sulphur is found as [H.sub.2]S, although, at skin pH (4.5-6.5), virtually all sulphur occurs as [H.sub.2]S.

The composition of sulphurous mineral water has been well-established. However, regardless of accompanying salts, for this mineral water to exert its beneficial effects, it must contain a reasonable amount of [H.sub.2]S or [HS.sup.-] and thus have a relatively acidic pH. In contrast, [S.sup.2-] usually found in alkaline waters are inert or do not exert the same activity [14].

Another factor to consider is that although [H.sub.2]S is a gas, [HS.sup.-] and [S.sup.2-] are salts. This means that [H.sub.2]S will be more easily absorbed through the skin and mucosa than its soluble salts. Further, given that the reactivity of dissociated [HS.sup.-] is greater than that of [H.sub.2]S, it may be assumed that [15] (1) both the gas and anions coexist in vivo; (2) dissociated bisulphide is more reactive than [H.sub.2]S and peaks at pH 11 [16]; and (3) the presence of oxygen could diminish the reduction force. This means that [H.sub.2]S molecules will more actively penetrate the skin rather than remaining on the surface.

Hydrogen sulphide derivatives will act depending on their molecular state too, that is, their degree of reduction or oxidation, which is usually determined by the external environment. Oxidation causes the transformation of [H.sub.2]S (valence -2) to sulphur (S valence: 0), which is in turn oxidized to hyposulphites ([H.sub.2][S.sub.2][O.sub.3]: valence +2) and then to sulphites ([H.sub.2]S[O.sub.3]: valence +4) and sulphates ([H.sub.2]S[O.sub.4]: valence +6). Conversely, reduction leads to the reverse order of formation [17].

In nature, [H.sub.2]S is generated by the decomposition of organic matter, whereby it is aerobically oxidized to elemental sulphur and then transformed to sulphates through the activity of bacteria and other microorganisms. Likewise, sulphates can be anaerobically reduced to [H.sub.2]S through their assimilation by living organisms or their decomposition by microorganisms, thus closing the sulphur cycle [18]. Thus, in simple terms, anaerobically reduced sulphates give rise to [H.sub.2]S, which is aerobically oxidized to sulphate.

In balneology, medicinal muds (peloids) can be generated through these reactions [9]. This mud has similar properties to water [19] and matures over time improving their properties of granulometry, specific heat, caloric retentivity, inertia time, relaxation time, hardness, adhesiveness, cohesion, and springiness [20, 21]. Mud treatments have been used for wounds produced by trauma. In this application, water remains in contact with the skin surface for a long time and absorption of the active principle is enhanced due to occlusion and ion exchange at temperatures slightly above physiological [22]. For this purpose, the use of peloids produced from sulphurous mineral waters is common. These peloids have their own peculiar characteristics [11].

According to the data available so far, balneotherapy using thermal-mineral waters and peloids has proved to be an effective remedy for lower back pain and knee and hand osteoarthritis [23-26].

3. Hydrogen Sulphide and Body Physiology

Recently, [H.sub.2]S and nitric oxide (NO) have been described as gasotransmitters that contribute to many physiological and pathophysiological functions as signalling molecules with potent cytoprotective actions [27].

Hydrogen sulphide is an endogenous gas with important physiological functions [28]. Endogenous hydrogen sulphide has been reported to function as a neuromodulator in the brain [29] and within the vasculature; the main functions of [H.sub.2]S are vasodilation and promoting new vessel growth.

The proangiogenic effects of hydrogen sulphide have been associated with increased vascular endothelial growth factor (VEGF) expression and activation of its receptor. Hydrogen sulphide-based therapies have therapeutic potential in diseases such as renal ischemia-reperfusion disorders, hypertension, and hypertensive-associated heart disease. Thus, several compounds releasing [H.sub.2]S have been described as candidates for the treatment of vascular disease [30] and decreasing platelet-leukocyte aggregation and improving endogenous thrombolysis [31]. Hydrogen sulphide and oestrogen have been shown to inhibit the development of atherosclerosis [32] through upregulating protein S-nitrosylation [33].

Hydrogen sulphide and nitric oxide play a fundamental role as gasotransmitters in the urinary tract, both lower tract and higher tract [34]. In addition, hydrogen sulphide regulates fundamental renal processes such as glomerular filtration and sodium reabsorption, both in the healthy organ and in different pathologies and ischemia [35].

In mammals, the gas is produced from L-cysteine by the three enzymes cystathionine-[gamma]-lyase (CSE or CGL), cystathionine b-synthase (CBS), and 3-mercaptopyruvate sulphur transferase (MST) [36, 37].

Hydrogen sulphide-induced relaxation ofvascular tissues can be partially reduced by the removal of the vascular endothelium and/or the presence of L-NAME (an inhibitor of NO synthase) [38]. New microvessel formation or angiogenesis occurs as a consequence ofthese mechanisms and we propose that [H.sub.2]S absorbed through the skin can potentiate this effect [39] (Figure 2).

Hydrogen sulphide acts on the migration and survival of endothelial cells to form a network of vessels. This is done through the two genes mitogen-activated protein- (MAP-) kinase-1, an ERK gene (extracellular signal-regulated kinase), and p38, a gene with effects on chaperone heat shock protein 27 (Hsp27) that promotes VEGF secretion. In turn, VEGF inhibits apoptosis, regulating cell development, differentiation, and cell function [40].

There are also three nonenzymatic ways to produce [H.sub.2]S: through sulphurous proteins, sulphite, or thiosulphate. Conversely, there are five ways of removing [H.sub.2]S in the organism: by its conversion into thiocyanate via rhodanese; by its transformation into sulphurous proteins; through thiol molecules; by converting haemoglobin into sulfhaemoglobin; and by its transformation into methanethiol.

Some human bacteria are able to transform [H.sub.2]S into its sulphur derivatives [41]. Thus, Pseudomonas spp. transform [H.sub.2]S into sulphur ([S.sub.0]), [S.sub.2][O.sub.6.sup.2-], and [S.sub.4][O.sub.6.sup.2-], Acinetobacter spp. into [S.sub.0] and [S.sub.2][O.sub.6.sup.2-], and Alcaligenes spp. and Ochrobactrum spp. into [S.sub.2][O.sub.6.sup.2-] and [S.sub.4][O.sub.6.sup.2-].

The following factors have been implicated in the storage and release of [H.sub.2]S [15]:

(1) pH and the conversion of [H.sub.2]S into [HS.sup.-] and/or [S.sup.2-].

(2) Oxidation/reduction in the presence of oxygen and its conversion into hydrogen thioperoxide and sulphenic, sulphinic, and sulphonic acids, where coenzyme Q-10 plays an important role [42].

(3) Hydrogenation and alkalization and transformation in acid labile sulphur (iron-sulphur clusters) and bound sulphane sulphur (persulphite, polysulphite, thiosulphate, etc.).

(4) Reduction by microorganisms like sulphate reducing bacteria (SRB) through sulphite reductase a-subunit (CysJ), anaerobic sulphide reductase A (AsrA).

(5) Enzymatic synthesis from L-cysteine through the above-described enzymes CSE, CBS, and MST.

Jin et al. [43] described [H.sub.2]S as a messenger that acts like a cell signalling molecule on the regulation of blood flow through and with NO and CO; on the protection of organs through phosphoinositide 3-kinase (PI3K), MAP kinase (MAPK), extracellular-signal-regulated kinase (Erk), glycogen synthase kinase 3 beta (GSK3[beta]), and protein kinase C (PKC); on inflammation through nuclear factor kappa beta (NF-k[beta]); in cellular defences through NF-E2 p45-related factor 2 (Nrf2); as an antiapoptotic factor in growing Bcl-2 cells (B-cell lymphoma 2) and reducing apoptosis by regulating BAX (bcl-2-like protein 4) and caspase-3, influencing cell metabolism in a dose dependent manner and promoting mitochondrial ATP synthesis at low concentrations and inhibition of cytochrome C oxidase at high concentrations; on ion channels producing vasorelaxation via [K.sub.ATP] channels, inflammation through transient receptor potential cation channel subfamily V member 1 (TRPV-1), TRPV-4 [44] and on calcium channels; and through its antioxidation properties acting as a reactive oxygen species (ROS) scavenger and increasing levels of superoxide dismutase (SOD) and glutathione (GSH) [45].

Recently, Beltowski and Jamroz-Wisniewska [46] showed that experimentally induced short-term obesity in rats increased endogenous production of hydrogen sulphide in perivascular adipose tissue, while long-term obesity had the opposite effect. These authors also observed that hyperglycaemia suppressed the CSE-[H.sub.2]S pathway in adipose tissue and proposed that hydrogen sulphide deficiency could play a role in adipose tissue inflammatoryprocesses associated with obesity or metabolic syndrome.

4. Skin Absorption

Sulphurous mineral water may be absorbed through the skin causing vasodilation, analgesia, immune response inhibition, and keratolytic effects that reduce skin desquamation [47]. It is also known that the topical application of [H.sub.2]S will also have an effect on the internal organs [48].

The therapeutic action of sulphurous mineral waters is related mainly to sulphur's keratolytic, or peeling, effect. Sulphurous mineral water exerts beneficial anti-inflammatory, keratoplastic, and antipruritic effects [49]. Its bactericidal and antifungal properties have determined its use for the treatment of infected leg ulcers, tinea versicolor, tinea corporis, and tinea capitis [50]. Further, within the epidermis, [H.sub.2]S is transformed into sulphur, which may also interact with oxygen radicals in the deeper layers of the epidermis. Here, sulphur maybe converted into pentathionic acid ([H.sub.2][S.sub.5][O.sub.6]), which could explain the antibacterial and antifungal properties of sulphurous mineral waters [51].

As mentioned above, the pH of sulphurous mineral waters is essential and responsible for its therapeutic effects. Whether effects are superficial or deep depends on the formation of [H.sub.2]S on the surface or deep within the skin. Hence, colloidal sulphur acts on the skin surface, [HS.sup.-] is able to penetrate deeper, and [H.sub.2]S can either penetrate or be absorbed through the skin reaching the dermis.

5. Topical Transformations and Hazards

Skin treatments based on mineral water or muds derived from mineral waters have been traditionally used in Europe [52]. Some of the cutaneous activity of sulphurous mineral waters is based on the formation of colloidal sulphur inside the skin via chemical reactions or microbial metabolism, where it then acts as a keratolytic agent. Accordingly, sulphur eliminates disulphide cystine bonds between corneocytes. This gives rise to two cysteine molecules, promoting desquamation of the stratum corneum (Figure 3). The keratolytic or keratoplastic properties of sulphurous mineral waters are support by the following observations:

(1) On the skin, [H.sub.2]S is converted into sulphur [53].

(2) Sulphur may also interact with oxygen radicals in the deeper layers of the epidermis and may in turn be transformed into pentathionic acid or produce [H.sub.2]S. This phenomenon was first described in 1913 by McMurtry, who reported that pentathionic acid is a product of oxidized sulphur only when oxygen and water are present. Pentathionic acid is a peptizing agent for sulphur generated by the reaction of [H.sub.2]S and sulphur dioxide (S[O.sub.2]) [54].

(3) In certain conditions, two cysteine molecules may be oxidized to form a new cystine bond [55] and return to their original state [56]. Cysteine residues are also responsible for the quenching of ROS, both within cell protein structures and in the keratinized outer layers of epithelial corneocytes. This quenching leads to the formation of intermolecular and intramolecular S-S bonds in the proteins [57].

In parallel, another study has shown that [H.sub.2]S speeds up wound healing in rats with diabetes. The authors related this effect to granulation tissue formation, anti-inflammation, and antioxidant effects, along with increased levels of VEGF [58].

Sulphurous spa baths have been used successfully for immunomediated conditions such as contact dermatitis, psoriasis, and atopic dermatitis, and it has been recently suggested that the active principles of sulphurous mineral waters could play a role in immune regulation in the skin [59].

Sulphurous mineral water inhalations and irrigations have been traditionally used to treat airway diseases [60-63]. According to Keller et al. [64],

compared to isotonic saline solution, sulphurous mineral water shows benefits and should be investigated further. It has also demonstrated endogenous production of hydrogen sulphide in human gingival tissue [65] and recent studies suggest that hydrogen sulphide may act as an inhibitory transmitter in esophagus tract [66].

The inhalation of sulphurous mineral waters has been shown to improve the health state of patients with chronic obstructive pulmonary disease (COPD) [67]. The mechanism of these observed effects is thought to be via the antielastase activity of thiol groups which could help control the inflammation associated with upper and lower airway diseases [68].

Topically administered [H.sub.2]S plays both physiological and toxicological roles in biological systems. Acute exposure to high levels of [H.sub.2]S is life-threatening, while long-term exposure to environmental levels has detrimental effects on human health. As an example, concentrations higher than 25ppm in the environment have been linked to eye damage and chronic exposure to hydrogen sulphide has been attributed to severe effects on health [69]. The acute inhalation of [H.sub.2]S at levels above 50-100 ppm is considered harmful and breathing problems arise when exposure is chronic at 10-20 ppm [70].

Emergency hospital visits for heart disease often accompanied by respiratory disease or stroke have been linked to same-day hydrogen sulphide concentrations exceeding 7.00 [micro]g/[m.sup.3]. This correlation was more pronounced among males and those 73 years and older than among females and younger individuals [71].

Long-term exposure to even low levels of [H.sub.2]S at the workplace has been reported to raise mean methaemoglobin and sulfhaemoglobin levels [72].

The topical use of [H.sub.2]S is not free of complications. The use of concentrated sulphurous mineral water and especially bathing in hot springs can produce skin conditions ranging from irritative dermatitis to chemical burns.

Lee and Wu [73] described the case of a 65-year-old man with no history of dermatologic disease, who suddenly developed painful, confluent round ulcers on his legs after bathing in a hot sulphurous spring, which had been a regular habit for the past 10 years. In a skin biopsy, these lesions were attributed to epidermal necrosis accompanied by numerous neutrophils typical of a chemical burn.

In contrast, Ferreira et al. [74] described that some sulphurous mineral waters are anti-irritants and may help relieve skin irritation. In dermatologic formulations, they may also improve the tolerability of the products.

6. Cell and Immunological Messengers

In mammalian cells, [H.sub.2]S passes through the cell membrane and its salts pass through bisulphide channels, where they are exchanged for [Cl.sup.-] (by anion exchange protein AE1). In the extracellular matrix, under physiological conditions of pH 7.4 and 37[degrees]C, only approximately 20% [H.sub.2]S exists as a gas. [H.sub.2]S dissociates to [HS.sup.-] with a trace amount of [S.sup.2-]. This means it is mostly absorbed as bisulphide (Figure 4).

Hydrogen sulphide is released from the cell and then dissociates in the extracellular environment where the pH is slightly higher than inside the cell. The reaction balance is mainly in this direction.

In bacteria, the extracellular environment pH is slightly lower than inside the cell. While [H.sub.2]S enters cells through the plasma membrane, [HS.sup.-] is released through bisulphide channels to the extracellular environment. This time, the reaction occurs in the opposite direction [75].

However, within the epidermis, the extracellular environmental pH is much lower than inside the cell (4.5-6.5) and the temperature is also slightly lower (35[degrees]C). Thus, [H.sub.2]S is the main molecule involved in the absorption and release of sulphur.

Merighi et al. [76] conducted a study in which it was shown for the first time that [H.sub.2]S significantly increases NO levels in a protein kinase B (Akt) gene-dependent manner. Inside keratinocytes, NO is synthesized from arginine at low concentrations of [H.sub.2]S by constitutive nitric oxide synthases (NOS) and at higher concentrations by inducible nitric oxide synthases (iNOS). Hence any increase in NO concentration reduces ERK1/2 activation with the consequence of diminished VEGF release [77] (Figure 5). According to these authors, the proliferation of keratinocytes is enhanced by their exposure to low [H.sub.2]S concentrations, while high concentrations of [H.sub.2]S lead to considerably increased NO concentrations, exerting a cytostatic effect on these cells. Other authors have observed that, in psoriasis, despite apparently elevated iNOS, the levels of NO produced were inadequate to induce cell differentiation, although sufficient to promote proliferation. Increasing the concentrations of NO in the epidermis will promote keratinocyte differentiation rather than proliferation [43].

These observations suggest promising therapeutic applications of [H.sub.2]S releasing agents for chronic inflammatory disorders of the skin such as psoriasis owing to its NO donor and anti-VEGF properties. However, such compounds still need to be assessed in a clinical setting.

According to Jin et al. [43], [H.sub.2]S shows dual behaviour depending on its concentration outside the cell. At low concentrations, it stimulates keratinocyte proliferation (antiapoptotic) and has provasodilation and proangiogenesis properties, while, at high concentrations, it promotes keratinocyte differentiation (proapoptotic) and shows antivasodilation and antiangiogenesis properties.

Yang et al. [78] reported that the newly synthesized [H.sub.2]S donor is capable of protecting human skin keratinocytes from methylglyoxal-induced injury and dysfunction. Thus, it could be that [H.sub.2]S-releasing molecules will improve wound healing in patients with diabetes mellitus. Suzuki et al. [79] have found differences in plasma levels of hydrogen sulphide in diabetic patients.

Under appropriate conditions, [H.sub.2]S reduces clonal growth, cell proliferation, and the adhesion of mature human keratinocytes by limiting the keratinocyte stem cell subpopulation in culture [80].

Some mineral waters have effects on the immune system. Different mineral waters seem to exert some immunomodulation activity and to increase levels of beta-endorphins in human skin. Unfortunately, these "miraculous" effects are still poorly documented and the lack of double-blinded studies precludes any generalizations about mineral waters as cutaneous prescriptions [81].

Hydrogen sulphide inhibits IL-8 expression in human keratinocytes via MAP kinase signalling. Along with its known anti-inflammatory activity, this could help explain some of the biological effects of sulphurous mineral water therapy [82] including Langerhans cell migration [83].

Mirandola et al. [84] reported that mitogen-activated protein is able to diminish the IL-2 production and cell cytotoxic response shown by peripheral blood lymphocytes and therefore mitigates local inflammatory responses and cell toxicity as characteristic anti-inflammatory effects of sulphur compounds.

Rinaldi et al. [85] assessed the in vitro effects of [H.sub.2]S on the survival capacity and bactericidal actions of human neutrophils. These authors proposed the following:

(1) Bisulphide ions favour the survival of granulocytes cultured in serum-free medium but not the survival of lymphocytes or eosinophils.

(2) This prosurvival effect is mediated through caspase-3 cleavage inhibition and p38 MAP-kinase phosphorylation.

(3) The bactericidal actions of neutrophils are not modified by [H.sub.2]S. They concluded that bisulphide promotes the short-term survival of neutrophils and that this could speed up the resolution of inflammation and prevent further inflammation.

Inflammation is a response to traumatic, infectious, postischemic, toxic, or autoimmune damage. However, uncontrolled inflammation can lead to disease, and inflammation is now believed to be responsible for several disease conditions.

Bhatia [86] reported that [H.sub.2]S acts as a novel mediator of inflammation. Soria et al. [87] determined that sulphurous mineral water intake improves haematological and biochemical markers of muscle damage produced in response to endurance exercise in well-trained athletes and thus may protect from exercise-induced muscle damage.

Sulphurous mineral waters may help manage chronic inflammatory and age-related disorders through their combined anti-inflammatory and antioxidant properties [88].

Transient receptor potential ankyrin 1 (TRPA1), activated by [H.sub.2]S, plays an important role in chronic arthritis/osteoarthritis and related pain behaviours in the mouse. This receptor may therefore be a promising target for novel analgesic/anti-inflammatory drugs [89]. The interaction of hydrogen sulphide on T-Type [Ca.sup.2+] channels can serve as a therapeutic target for the treatment of intractable pain and neuronal lesions [90].

Hydrogen sulphide decreases IL-1[beta]-induced activation of fibroblast-like synoviocytes obtained from patients with osteoarthritis [91] and is thought to delay cartilage destruction in part by reducing activation of the nuclear factor NFkB [92].

Finally, Benedetti et al. [93] suggested that, to ensure long-lasting chondroprotective effects of sulphur-based therapies, standard mud bath treatments should be associated with hydropinotherapy to keep reduced oxidative, inflammatory, and degradative stimuli for longer.

7. Discussion

[H.sub.2]S induces a wide range of physiological responses such as blood pressure modulation, protection against ischemic reperfusion injury, and anti-inflammatory reactions.

It is well documented that [H.sub.2]S is the main factor responsible for capillary vasodilation. Accordingly, the exogenous administration of [H.sub.2]S elicits vascular relaxation in animal preparations both in vitro and in vivo [94]. Exogenous [H.sub.2]S could protect arterial endothelial cells [95]. Mancini et al. [96] described additional benefits of balneokinetic treatment with sulphurous mineral water over elastic compression in patients with symptomatic varices. According to these authors, the improvement in the venoarteriolar reflex observed could support these subjective benefits.

Sulphurous mineral water-based balneotherapy significantly reduces limb spasticity and pain and can help in the treatment of poststroke patients [97]. These observations are compatible with the regeneration and anti-inflammatory activity of sulphurous mineral waters [98] and may be essential for Schwann cell responses to peripheral nerve injury [99].

Observations so far strongly suggest that [H.sub.2]S modulation could have therapeutic benefits. Hence, sulphurous mineral waters are not only useful research tools but also show promise as therapeutic agents [100].

Intriguingly too, [H.sub.2]S has been reported to regulate cell cycle and survival in healthy cells which suggests that it may regulate cell fate and hence the ageing process [101].

Intense research effort is also being devoted to addressing the use of [H.sub.2]S-donor drugs capable of the controlled release of [H.sub.2]S into the bloodstream. Notwithstanding, according to Haouzi [102], the levels of [H.sub.2]S tested in vitro are toxic and the low levels that will need to be administered in vivo to avoid any toxic effects are unlikely to give rise to adequate [H.sub.2]S concentrations in tissues.

Pharmacological molecules that release [H.sub.2]S too quickly do not adequately mimic the physiological effects of the gas. Hence, slow-releasing [H.sub.2]S donors are a more appropriate source of hydrogen sulphide than even a sulphur salt solution. In addition, the beneficial effects of [H.sub.2]S on inflammation are concentration and time-dependent and may involve bell-shaped dose-response curves.

The therapeutic properties of mineral-medicinal waters are determined by their inherent properties. This means they cannot be chemically modified but can be modified discretely by simple physical means. Sulphurous mineral water springs used in balneotherapy tend to have low sulphide concentrations. In Spain, such sulphide concentrations are 45 mg/l maximum and are therefore not considered toxic.

Besides an attenuating effect of slow skin absorption, the topical application of sulphurous mineral waters in well-ventilated and controlled environments such as spas can be considered safe. In these environments, treatment duration and chronicity can be modulated in addition to the active concentrations of sulphurous mineral water. In this manner, sulphide release by sulphurous mineral waters can be to a certain extent controlled.

In a review of studies assessing the clinical use of [H.sub.2]S, Beltowski [103] describes clinical applications of the gas in the following conditions: pulmonary hypertension, arterial hypertension, atherosclerosis, ischemia-reperfusion injury, heart failure, peptic ulcer, acute and chronic inflammatory diseases, Parkinson's disease, Alzheimer's disease, erectile dysfunction, and skin diseases.

In conclusion, several new lines of evidence indicating a role of hydrogen sulphide as a cell messenger with cytoprotective effects anticipate promising perspectives for treatments with sulphurous mineral waters [104].

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this paper.


This work was funded by the Research Group UCM-911757 (Universidad Complutense de Madrid, Medical Hydrology).


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Jose Manuel Carbajo (1) and Francisco Maraver (1,2)

(1) Professional School of Medical Hydrology, Faculty of Medicine, Universidad Complutense de Madrid, 28040 Madrid, Spain

(2) Department of Physical Medicine and Rehabilitation, Medical Hydrology, Faculty of Medicine, Universidad Complutense de Madrid, 28040 Madrid, Spain

Correspondence should be addressed to Francisco Maraver;

Received 31 January 2017; Revised 17 March 2017; Accepted 28 March 2017; Published 6 April 2017

Academic Editor: Marisa Colone

Caption: Figure 1: Hydrogen sulphide concentrations versus pH. According to the pH (7.04 or 11.96), sulphurous derivatives occur in saline ([HS.sup.-] and [S.sp.2-]) orgaseous ([H.sub.2]S) solution. On the skin (pH < 6), hydrogen sulphide is mainly present as gas ([H.sub.2]S), whereas, at physiological pH, (7.2-7.4) only one-third exists as gas ([H.sub.2]S) and it is mainly found in saline solution ([HS.sup.-]).

Caption: Figure 2: Mechanism of endothelial cell proliferation through hydrogen sulphide activity and NO production by the [H.sub.2]S pathway. An increase in vessel formation is produced that is significantly attenuated through NO production blockade by nitro-L-arginine methyl ester (L-NAME).

Caption: Figure 3: Mechanisms of action of hydrogen sulphide on bonds between corneocytes. Sulphur can be transformed into pentathionic acid and/or produce [H.sub.2]S, transforming cystine into cysteine (keratolytic effect). In some situations, hydrogen sulphide can convert cysteine into cystine (keratoplastic effect).

Caption: Figure 4: Cellular uptake of hydrogen sulphide according to pH and temperature. In cells, sulphur is mostly absorbed as bisulphide salt, while, on skin, hydrogen sulphide is the main molecule involved in the absorption and release of sulphur.

Caption: Figure 5: Hydrogen sulphide has a dual effect on keratinocytes: at low concentrations, it induces their proliferation, while, at high concentrations, it exerts a cytostatic effect on these cells and reduces VEGF release via the ERK pathway.
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Author:Carbajo, Jose Manuel; Maraver, Francisco
Publication:Evidence - Based Complementary and Alternative Medicine
Date:Jan 1, 2017
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