Since it was proposed in 2007, molecular hydrogen therapy has been widely concerned and researched. Many animal experiments were carried out in a variety of disease fields, such as cerebral infarction, ischemia reperfusion injury, Parkinson syndrome, type 2 diabetes mellitus, metabolic syndrome, chronic kidney disease, radiation injury, chronic hepatitis, rheumatoid arthritis, stress ulcer, acute sports injuries, mitochondrial and inflammatory disease, and acute erythema skin disease and other pathological processes or diseases. Molecular hydrogen therapy is pointed out as there is protective effect for sepsis patients, too. The impact of molecular hydrogen therapy against sepsis is shown from the aspects of basic vital signs, organ functions (brain, lung, liver, kidney, small intestine, etc.), survival rate, and so forth. Molecular hydrogen therapy is able to significantly reduce the release of inflammatory factors and oxidative stress injury. Thereby it can reduce damage of various organ functions from sepsis and improve survival rate. Molecular hydrogen therapy is a prospective method against sepsis.
Sepsis is a systematic inflammatory response to infection. It is one of the most serious diseases in ICU, which is a worldwide challenge. Although comprehensive therapy has been developed for it, sepsis is still associated with high morbidity and mortality and costs a lot for hospitalization. In the United States, severe sepsis affects 750,000 people per year, which costs $16.7 billion annually and increases in its incidence over time of 8.7% [
Sepsis leads to abnormal blood pressure, heart rate, and PaO2. It also influences different organs and even leads to multiple organ dysfunction syndromes (MODS). The main clinical characteristics of brain include delirium, coma, disorientation, the slowing of mental processes, and cognitive dysfunction. Sepsis leads to acute lung injury and acute respiratory distress syndrome (ARDS), whose mortality rate is as high as 30% to 50% in critically ill patients. In liver, disruption of protein synthetic function manifests as progressive disruption of blood clotting and disruption of metabolic functions leads to impaired bilirubin metabolism. The incidence of acute kidney injury is nearly 65% in critically ill patients and is able to aggravate the condition of patients with septic shock. Sepsis also decreases the blood flow of the gastrointestinal tract, which might induce severe ischemia, hypoxia, and reperfusion injury.
Recent research suggests that molecular hydrogen works as a therapeutic antioxidant activity by selectively reducing hydroxyl radicals and protects against organ damage effectively. In 2007, inhalation of hydrogen gas was found to suppress brain injury by buffering the effects of oxidative stress in an acute focal ischemia and reperfusion rat mode [
There are 3 main methods of molecular hydrogen therapy: inhalation of hydrogen (H2), oral intake of hydrogen-rich water (HRS), and injection of hydrogen-saturated saline (HRS). Molecular hydrogen therapy also can be combined with other therapy such as resuscitation and oxygen therapy.
Autoimmune injury occurs in sepsis, and the pathogenesis is very complicated, in which oxidative stress plays an important role.
The immunocyte is activated and the respiratory burst creates amount of reactive oxygen species (ROS). Oxidative stress induced by ROS can change the permeability of epithelial cells by destroying the cell membrane. The imbalance of antioxidant defense systems against oxidative stress also can damage the epithelial cells [
Molecular hydrogen is a scavenger of the hydroxyl radical. H2 can selectively reduce ROS in vitro; it will react with only the strongest oxidants, which means the use of H2 is mild enough having no serious side effects [
Molecular hydrogen can suppress the release of cell adhesion molecules, as well as proinflammatory cytokines. H2 could elevate anti-inflammatory cytokine levels. H2 enhanced HO-1 expression and activity, which suggest that H2 could suppress excessive inflammatory responses and endothelial injury via an Nrf2 (nuclear factor erythroid 2 p45 related factor 2)/HO-1 pathway [
Possible mechanisms of molecular hydrogen. Possible pathways for molecular hydrogen. It has been proposed that molecular hydrogen has the capabilities to affect the pathways mentioned and to directly or indirectly assist in the gene regulation or protein expression of the following: MPO, MCP, Caspase-3, Caspase-12, TNF, interleukins, Bcl-2, Bax, and Cox-2.
In animal experiments, sepsis alters general condition of mice, such as mean artery pressure (MAP) decreasing and PaO2 declining.
In Liu et al.’s study, MAP decreased in 20 minutes after LPS (Lipopolysaccharide) injection. There was no significant difference in resuscitation group and resuscitation+H2 group, while the fluid volume and usage of norepinephrine were less used in resuscitation+H2 group [
Many studies showed that sepsis makes PaO2 and PaO2/FiO2 decline, and molecular hydrogen therapy can alleviate this change. Xie et al. stated that PaO2/FiO2 ratio declined significantly in cecal ligation and puncture (CLP) group. Inhalation of H2 can remit the change [
Generally, sepsis decreased MAP, PaO2, and PaO2/FiO2. Traditional resuscitation can alleviate these changes. It works better while combined with molecular hydrogen therapy. Molecular hydrogen therapy makes it possible for using less fluid and the vasoactive agent to reach the target MAP level. Molecular hydrogen therapy also significantly improves PaO2 and PaO2/FiO2 in sepsis.
The impact of molecular hydrogen on changes of the biochemistry indicator level in different organs was summarized in Table
The impact of changes of the biochemistry indicator level.
Brain | Lung | Liver | Kidney | Intestine | |
---|---|---|---|---|---|
Capase-3 | HRS |
HRS |
/ | / | / |
SOD | HRS |
HRS |
H2
|
H2
|
H2
|
ROS | H2
|
/ | / | / | / |
MPA | H2
|
HRS |
/ | H2
|
H2
|
CAT | HRS |
HRS |
H2
|
H2
|
/ |
8-iso-PGF2 |
H2
|
HRS |
H2
|
H2
|
/ |
Nrf2 | H2
|
/ | / | / | / |
TNF- |
H2
|
HRS |
H2
|
H2
|
H2
|
IL-1 |
H2
|
HRS |
/ | / | / |
IL-6 | / | HRS |
/ | H2
|
/ |
IL-8 | / | HRS |
/ | H2
|
/ |
HMGB1 | H2
|
HRS |
H2
|
/ | H2
|
IL-10 | H2
|
HRS |
H2
|
H2
|
/ |
MPO | / | HRS |
/ | / | / |
Others | Cognitive impairment: HRS is less than sepsis group; HRS is similar to sham group | ( |
ALT, ACT: H2
|
BUN, Cr: H2
|
DAO: H2
|
References | [ |
[ |
[ |
[ |
[ |
HRS: hydrogen-rich water injection or oral-taken group.
H2: H2 inhalation group.
SOD: superoxide dismutase.
CAT: catalase.
HMGB1: high mobility group box 1.
IL: interleukin.
W/D: wet/dry.
BALF: bronchoalveolar lavage fluid.
ALT: alanine aminotransferase.
Brain is one of the organs to be affected during early sepsis. It is strongly associated with higher mortality and lower quality of life.
Morphologic changes can be detected by pathologic examination. Brain sections were stained with H&E (hematoxylin-eosin staining). In normal condition, the hippocampal CA1 region shows tightly arranged nerve cell bodies with clear structures; cytoplasm in cells is plentiful. However, animal experiments found that most neurons in CLP-challenged mice were shrunken and stained dark; the intracellular space was enlarged. With HRS injection, the cells with eumorphism were significantly preserved. Total normal cell count in sham group was
Both immunohistochemical staining of cleaved Caspase-3 and western blot of cleaved Caspase-3 expression in hippocampus indicate a great increase in CLP group. With HRS therapy Caspase-3 was dramatically reduced after the CLP event. The number of cleaved Caspase-3-positive cells was
H2 treatment can attenuate blood-brain barrier disruption. Evans blue (EB) is a dye binding to serum albumin, which can seldom go through the Blood Brain Barrier (BBB). But in CLP group, obvious rise of EB quantification was observed compared with sham group; H2 treatment group showed less EB quantification compared with CLP group (
HRS treatment and H2 treatment prevented the abnormal changes of oxidation and antioxidation. Septic mice had lower levels of SOD and higher levels of ROS and MDA (Malondialdehyde); both HRS treatment and H2 treatment can prevent those changes. There was also a dose-response relationship showed in studies [
H2 inhalation can significantly decrease the levels of proinflammatory cytokines (TNF-
Researchers measured the cognitive function of CLP-challenged mice with several methods. In
In conclusion, sepsis can destroy the structure of brain especially hippocampus CA1 region through stimulating oxidative stress reaction and inflammatory response, which lead to impairment of cognition. However, molecular hydrogen therapy was proved to attenuate the disruption.
Acute lung injury/acute respiratory distress syndrome (ALI/ARDS) are common syndromes in sepsis. When ALI occurs, the oxygenation index, lung MPO activity, lung W/D weight ratio, BAL (bronchoalveolar lavage) and total protein, lung’s histology, antioxidant enzymatic activity, and inflammatory cytokines are all different from normal conditions.
The normal lung structure has no hyperemia, neutrophil infiltration. But in sepsis, there can be found disordered alveolar structures, collapse of alveoli, incomplete alveolar wall, severe neutrophil infiltration, alveolar capillary congestion, and thickened alveolar wall by edema. Resuscitation only can reduce neutrophil accumulation and the alveolar-capillary exudate but cannot alleviate alveolar edema. When combined with H2 inhalation, the therapy significantly decreased in alveolar damage and alveolar edema as well [
Moreover, effects of H2 treatment on pulmonary cell apoptosis were investigated. Numerous lung cells were positive for TUNEL (TdT-mediated dUTP Nick-End Labeling) staining which identified apoptotic cells in LPS group. In the samples of H2 treatment group, a few of positive cells were observed. Caspase-3 detection showed the same tendency in those groups. Those data revealed LPS-induced septic stimulated pulmonary cell apoptosis and H2 therapy would prevent this process [
Lung W/D weight ratio is an indicator of the magnitude of pulmonary edema. Septic lung showed higher W/D ratios in all studies. Resuscitation+H2 group showed a significant decrease in the lung W/D value compared with resuscitation group, which indicates that H2 inhalation was benefit to relieve edema [
Examination of cell counts and protein concentration in BALF is a particular technique to evaluate lung effusion and its character. Animals studies mentioned that CLP or LPS increased the cell counts and protein in BALF, which could be remitted with H2 inhalation [
Antioxidant enzymatic activity in lung (SOD and CAT) was suppressed and level of oxidative products (MDA and 8-iso-PGF2
Inflammatory cytokines (TNF-
Liu et al. [
Generally speaking, lung structure was damaged by sepsis. Lung W/D ratios, cell counts and protein concentration in BALF, level of oxidative products, and inflammatory cytokines were found increased, while antioxidative enzyme activity and anti-inflammatory cytokines were found decreased. Although there still were controversies [
Liver is one of the most important organs, but also one of the first organs to be affected during sepsis. Except for degree of oxidative stress reaction and inflammatory reaction, ALT and AST (aspartate aminotransferase) can also reveal hepatic function.
Histopathological changes in liver were shown in sepsis. Animal study shows liver histologic scores significantly increased in CLP group; O2 inhalation group and H2 inhalation group both showed much lower scores, which even had no difference to sham group [
In addition, CLP mice developed significant liver injury, which was assessed by ALT and AST increase. H2 inhalation and HRS injection both could attenuate these abnormal changes [
Oxidative stress reaction and inflammatory reaction of liver were similar with lung. Inflammatory cytokines like TNF-
Studies about liver damage and hepatic function in sepsis with molecular hydrogen therapy were in a small number. Even so, these results revealed a dramatic effect of molecular hydrogen therapy. It may indicate that molecular hydrogen therapy is much more efficacious in liver protection. More research is needed in this area.
Acute kidney injury (AKI) is a common disease in septic patients and can aggravate the condition of septic shock patients, resulting in higher mortality. Except for degree of oxidative stress reaction and inflammatory reaction, blood urea nitrogen (BUN) and creatinine (Cr) can also reveal hepatic function.
H&E staining of kidney tissues exhibited edema in renal tubular epithelial, damaged brush border, and interstitial edema with hemorrhage in septic mice. Tubular epithelial cell damage was ameliorated in H2 inhalation group. The similar result showed in transmission electron microscopic analysis of glomerular filtration membrane [
Serum BUN and Cr were much higher in LPS or CLP group than in sham group. H2 inhalation group had significant reductions of serum BUN and Cr [
Oxidative stress reaction and inflammatory reaction of kidney were similar with lung and liver. Inflammatory cytokines (TNF-
In spite of some dispute, molecular hydrogen therapy was considered as a useful method to alleviate structure damage of kidney, protect renal function, and resist inflammatory reaction and oxidative reaction.
Sepsis leads to significant decrease in blood flow of the gastrointestinal tract. Hyperperfusion induces severe ischemia, hypoxia, and reperfusion injury. Researchers also work at molecular hydrogen therapy alleviating septic damage in intestine.
In animal study, after LPS manipulating, the structure of the small intestinal mucosa was damaged. Glands of the small intestine were destroyed. Edema of mucosal villi, neutrophil infiltration, and even intestinal ulceration was also commonly observed in sepsis. Resuscitation therapy worsened the damage mentioned above while H2 inhalation reduced the damage. The histologic score of LPS group was significantly higher than sham group, but the score of H2 inhalation group was significantly decreased compared with LPS group [
The serum diamine oxidase (DAO) activity reflects degree of intestinal mucosa epithelium cell impaired. Levels of DAO in sham group, LPS group, and H2 group were
Oxidative stress reaction and inflammatory reaction of intestine were similar with lung, liver, and kidney. Inflammatory cytokines (TNF-
The effect of molecular hydrogen therapy of intestinal damage in sepsis curing with molecular hydrogen therapy needs more research. According to the only literature of study, molecular hydrogen therapy protected intestine from sepsis.
All the research indicated molecular hydrogen therapy can improve survival rate of septic animal whatever the method of drug administration and sepsis inducing.
Zhang et al. compared 3 different ways to induce sepsis and the survival rate, respectively. The survival rates of LPS-induced septic mice at 24, 48, and 72 hr were 88.89%, 66.67%, and 66.67%. With HRS treatment, the survival rate increased to 100% (
As mentioned before, there are 3 methods of molecular hydrogen therapy: inhalation of hydrogen (H2), oral intake of hydrogen-rich water, and injection of hydrogen-saturated saline. In low concentration (4.1% in pure oxygen or 4.6% in the air), hydrogen is neither explosive nor dangerous. Others thought it is safer to dissolve hydrogen into water and administrate the HRS by oral or by injection. However, the best way of molecular hydrogen therapy, the appropriated dosage, and the safety concerns are still to be discussed.
Molecular hydrogen therapy has a protective effect on sepsis, which has been proved by pathological biopsy, level of inflammatory factors/anti-inflammatory factors, oxidative stress reaction, behavioral experiment, and other related indicators of organ function. Although there is a dispute of affections of molecular hydrogen therapy in liver and kidney, the mainstream view shows molecular hydrogen therapy is benefit to organs, such as brain, lung, liver, kidney, and small intestine.
Molecular hydrogen therapy combining with oxygen therapy or fluid resuscitation can reduce oxygen free radical damage, the amount of fluid and vasoactive drugs, and the overload of liquid. As a result, molecular hydrogen therapy may reduce the complications of oxygen therapy and fluid resuscitation.
However, most of the study conclusion came from animal experiment while reports of clinical research were rare. Much more clinical evidence is still demanded.
In conclusion, molecular hydrogen therapy is a promising method to alleviate organ damage, improve outcome, and reduce mortality rate in sepsis.
The authors declare that they have no competing interests.