Target type: biologicalprocess
Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a hydrogen sulfide stimulus. [GO_REF:0000071, GOC:TermGenie, PMID:24012591]
Hydrogen sulfide (H2S) is a colorless gas with a characteristic rotten egg odor. While it is toxic in high concentrations, H2S also plays a crucial role in various physiological processes in living organisms. H2S is produced endogenously by enzymes like cystathionine β-synthase (CBS), cystathionine γ-lyase (CSE), and 3-mercaptopyruvate sulfurtransferase (3MST). It acts as a signaling molecule, influencing a wide range of cellular processes, including:
- **Vasodilation:** H2S relaxes smooth muscle cells, leading to vasodilation (widening of blood vessels). This effect contributes to the regulation of blood pressure and blood flow.
- **Anti-inflammatory effects:** H2S has been shown to suppress inflammation by inhibiting the production of pro-inflammatory cytokines like TNF-α and IL-1β.
- **Neuroprotection:** H2S protects neurons from damage caused by oxidative stress, excitotoxicity, and other insults. It also plays a role in synaptic plasticity and learning.
- **Mitochondrial function:** H2S modulates mitochondrial respiration and oxidative phosphorylation, influencing energy production and cell survival.
- **Cardioprotection:** H2S has been implicated in protecting the heart from ischemic injury and promoting cardiac function.
- **Antioxidant activity:** H2S scavenges reactive oxygen species (ROS), contributing to the cellular defense against oxidative stress.
The response to H2S involves various signaling pathways and mechanisms, including:
- **Activation of KATP channels:** H2S opens potassium channels (KATP) in smooth muscle cells, leading to hyperpolarization and relaxation.
- **Inhibition of mitochondrial cytochrome c oxidase:** H2S binds to cytochrome c oxidase, a key enzyme in the electron transport chain, inhibiting mitochondrial respiration.
- **Activation of Nrf2 pathway:** H2S activates the Nrf2 pathway, a transcription factor that regulates the expression of antioxidant and cytoprotective genes.
- **Regulation of gene expression:** H2S can directly or indirectly influence gene expression, modulating cellular responses to various stimuli.
The cellular response to H2S is highly complex and involves interactions with various cellular components and signaling pathways. Further research is ongoing to fully elucidate the intricate mechanisms of H2S signaling and its implications for human health.'
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Protein | Definition | Taxonomy |
---|---|---|
NAD | An NAD(P)H dehydrogenase [quinone] 1 that is encoded in the genome of human. [PRO:DNx, UniProtKB:P15559] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
4'-bromoflavone | 4'-bromoflavone: structure in first source | ||
beta-naphthoflavone | beta-naphthoflavone : An extended flavonoid resulting from the formal fusion of a benzene ring with the f side of flavone. beta-Naphthoflavone: A polyaromatic hydrocarbon inducer of P4501A1 and P4501A2 cytochromes. (Proc Soc Exp Biol Med 1994 Dec:207(3):302-308) | extended flavonoid; naphtho-gamma-pyrone; organic heterotricyclic compound | aryl hydrocarbon receptor agonist |
beta-lapachone | beta-lapachone : A benzochromenone that is 3,4-dihydro-2H-benzo[h]chromene-5,6-dione substituted by geminal methyl groups at position 2. Isolated from Tabebuia avellanedae, it exhibits antineoplastic and anti-inflammatory activities. beta-lapachone: antineoplastic inhibitor of reverse transcriptase, DNA topoisomerase, and DNA polymerase | benzochromenone; orthoquinones | anti-inflammatory agent; antineoplastic agent; plant metabolite |
vitamin k 3 | Vitamin K 3: A synthetic naphthoquinone without the isoprenoid side chain and biological activity, but can be converted to active vitamin K2, menaquinone, after alkylation in vivo. | 1,4-naphthoquinones; vitamin K | angiogenesis inhibitor; antineoplastic agent; EC 3.4.22.69 (SARS coronavirus main proteinase) inhibitor; human urinary metabolite; nutraceutical |
sulforaphane | sulforaphane : An isothiocyanate having a 4-(methylsulfinyl)butyl group attached to the nitrogen. sulforaphane: from Cardaria draba L. | isothiocyanate; sulfoxide | antineoplastic agent; antioxidant; EC 3.5.1.98 (histone deacetylase) inhibitor; plant metabolite |
c 1303 | C 1303: DNa-binding drug; structure given indicates that the cpd should be the dimethylamino cpd, but it is named as the diethylamino cpd | ||
nsc 366140 | NSC 366140: a 9-methoxypyrazoloacridine; structure given in first source | ||
5-methoxy-1,2-dimethyl-3-((4-nitrophenoxy)methyl)indole-4,7-dione | 5-methoxy-1,2-dimethyl-3-((4-nitrophenoxy)methyl)indole-4,7-dione: structure in first source | ||
bisantrene | |||
4,3',5'-tri-o-methylpiceatannol | |||
memoquin | memoquin: structure in first source | ||
dicumarol | Dicumarol: An oral anticoagulant that interferes with the metabolism of vitamin K. It is also used in biochemical experiments as an inhibitor of reductases. | hydroxycoumarin | anticoagulant; EC 1.6.5.2 [NAD(P)H dehydrogenase (quinone)] inhibitor; Hsp90 inhibitor; vitamin K antagonist |
ethyl biscoumacetate | Ethyl Biscoumacetate: A coumarin that is used as an anticoagulant. It has actions similar to those of WARFARIN. (From Martindale, The Extra Pharmacopoeia, 30th ed, p226) | hydroxycoumarin | |
nsc 158393 | NSC 158393: structure given in first source |