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 vitamin B1 stimulus. [GOC:pz]
Vitamin B1, also known as thiamine, is an essential nutrient that plays a crucial role in carbohydrate metabolism and various other cellular processes. The body cannot synthesize thiamine and must obtain it from dietary sources. Thiamine deficiency, also known as beriberi, can lead to severe neurological and cardiovascular complications.
Upon ingestion, thiamine is absorbed in the small intestine and transported to various tissues throughout the body. The primary active form of thiamine is thiamine pyrophosphate (TPP), which is a coenzyme for several key enzymes involved in carbohydrate metabolism. These enzymes include pyruvate dehydrogenase (PDH), alpha-ketoglutarate dehydrogenase (α-KGDH), and transketolase.
**PDH** catalyzes the conversion of pyruvate to acetyl-CoA, a key step in the breakdown of glucose for energy production. This reaction is essential for the citric acid cycle and oxidative phosphorylation, the primary pathways for ATP generation.
**α-KGDH** is another crucial enzyme involved in the citric acid cycle, catalyzing the oxidative decarboxylation of α-ketoglutarate. This step is crucial for the efficient production of ATP and the generation of reducing equivalents (NADH) for electron transport.
**Transketolase** is a key enzyme in the pentose phosphate pathway, a metabolic pathway that generates NADPH and the precursor for nucleotide biosynthesis. Thiamine deficiency can lead to impaired activity of transketolase, resulting in a decrease in NADPH production and impaired nucleotide biosynthesis.
**Cellular response to thiamine:**
1. **Thiamine uptake:** Cells take up thiamine through specific transporters. Once inside the cell, thiamine is phosphorylated to thiamine monophosphate (TMP) by thiamine pyrophosphokinase.
2. **TPP synthesis:** TMP is further phosphorylated to TPP by thiamine pyrophosphokinase. TPP is the active coenzyme form of thiamine.
3. **Enzymatic activity:** TPP is required for the activity of several key enzymes involved in carbohydrate metabolism, including PDH, α-KGDH, and transketolase.
4. **Metabolic regulation:** The activity of these enzymes is tightly regulated, ensuring adequate energy production and biosynthesis pathways.
5. **Cellular signaling:** Thiamine deficiency can trigger cellular signaling pathways that contribute to the pathogenesis of beriberi.
**Clinical implications:**
Thiamine deficiency can lead to beriberi, characterized by neurological and cardiovascular complications. Neurological symptoms include peripheral neuropathy, Wernicke's encephalopathy, and Korsakoff's syndrome. Cardiovascular symptoms include tachycardia, arrhythmias, and heart failure.
**Dietary sources:**
Rich sources of thiamine include whole grains, legumes, nuts, seeds, and pork. Supplementation with thiamine is recommended in individuals with a high risk of deficiency, such as alcoholics and individuals with malabsorption disorders.
**Summary:**
Thiamine is an essential nutrient that plays a crucial role in carbohydrate metabolism. It is a coenzyme for several key enzymes involved in energy production and biosynthesis. Thiamine deficiency can lead to beriberi, characterized by neurological and cardiovascular complications. Ensuring adequate thiamine intake is essential for maintaining optimal health.'
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Protein | Definition | Taxonomy |
---|---|---|
Translocator protein | [no definition available] | Homo sapiens (human) |
Delta-aminolevulinic acid dehydratase | A delta-aminolevulinic acid dehydratase that is encoded in the genome of human. [PRO:DNx, UniProtKB:P13716] | Homo sapiens (human) |
Compound | Definition | Classes | Roles |
---|---|---|---|
pk 11195 | PK-11195 : A monocarboxylic acid amide obtained by formal condensation of the carboxy group of 1-(2-chlorophenyl)isoquinoline-3-carboxylic acid with the amino group of sec-butylmethylamine | aromatic amide; isoquinolines; monocarboxylic acid amide; monochlorobenzenes | antineoplastic agent |
ro 5-4864 | 4'-chlorodiazepam: selectively binds peripheral benzodiazepine receptor | ||
clonazepam | clonazepam : 1,3-Dihydro-2H-1,4-benzodiazepin-2-one in which the hydrogens at positions 5 and 7 are substituted by 2-chlorophenyl and nitro groups, respectively. It is used in the treatment of all types of epilepsy and seizures, as well as myoclonus and associated abnormal movements, and panic disorders. However, its use can be limited by the development of tolerance and by sedation. Clonazepam: An anticonvulsant used for several types of seizures, including myotonic or atonic seizures, photosensitive epilepsy, and absence seizures, although tolerance may develop. It is seldom effective in generalized tonic-clonic or partial seizures. The mechanism of action appears to involve the enhancement of GAMMA-AMINOBUTYRIC ACID receptor responses. | 1,4-benzodiazepinone; monochlorobenzenes | anticonvulsant; anxiolytic drug; GABA modulator |
nordazepam | nordazepam : A 1,4-benzodiazepinone having phenyl and chloro substituents at positions 5 and 7 respectively; it has anticonvulsant, anxiolytic, muscle relaxant and sedative properties but is used primarily in the treatment of anxiety. Nordazepam: An intermediate in the metabolism of DIAZEPAM to OXAZEPAM. It may have actions similar to those of diazepam. | 1,4-benzodiazepinone; organochlorine compound | anticonvulsant; anxiolytic drug; GABA modulator; human metabolite; sedative |
diazepam | diazepam : A 1,4-benzodiazepinone that is 1,3-dihydro-2H-1,4-benzodiazepin-2-one substituted by a chloro group at position 7, a methyl group at position 1 and a phenyl group at position 5. Diazepam: A benzodiazepine with anticonvulsant, anxiolytic, sedative, muscle relaxant, and amnesic properties and a long duration of action. Its actions are mediated by enhancement of GAMMA-AMINOBUTYRIC ACID activity. | 1,4-benzodiazepinone; organochlorine compound | anticonvulsant; anxiolytic drug; environmental contaminant; sedative; xenobiotic |
flunitrazepam | flunitrazepam : A 1,4-benzodiazepinone that is nitrazepam substituted by a methyl group at position 1 and by a fluoro group at position 2'. It is a potent hypnotic, sedative, and amnestic drug used to treat chronic insomnia. Flunitrazepam: A benzodiazepine with pharmacologic actions similar to those of DIAZEPAM that can cause ANTEROGRADE AMNESIA. Some reports indicate that it is used as a date rape drug and suggest that it may precipitate violent behavior. The United States Government has banned the importation of this drug. | 1,4-benzodiazepinone; C-nitro compound; monofluorobenzenes | anxiolytic drug; GABAA receptor agonist; sedative |
lorazepam | Lorazepam: A benzodiazepine used as an anti-anxiety agent with few side effects. It also has hypnotic, anticonvulsant, and considerable sedative properties and has been proposed as a preanesthetic agent. | benzodiazepine | |
nitrazepam | nitrazepam : A 1,4-benzodiazepinone that is 1,3-dihydro-2H-1,4-benzodiazepin-2-one which is substituted at positions 5 and 7 by phenyl and nitro groups, respectively. It is used as a hypnotic for the short-term management of insomnia and for the treatment of epileptic spasms in infants (West's syndrome). Nitrazepam: A benzodiazepine derivative used as an anticonvulsant and hypnotic. | 1,4-benzodiazepinone; C-nitro compound | anticonvulsant; antispasmodic drug; drug metabolite; GABA modulator; sedative |
cm 7116 | norflutoprazepam: structure | benzodiazepine | |
oxazepam | oxazepam : A 1,4-benzodiazepinone that is 1,3-dihydro-2H-1,4-benzodiazepin-2-one substituted by a chloro group at position 7, a hydroxy group at position 3 and phenyl group at position 5. Oxazepam: A benzodiazepine used in the treatment of anxiety, alcohol withdrawal, and insomnia. | 1,4-benzodiazepinone; organochlorine compound | anxiolytic drug; environmental contaminant; xenobiotic |
temazepam | Temazepam: A benzodiazepine that acts as a GAMMA-AMINOBUTYRIC ACID modulator and anti-anxiety agent. | benzodiazepine | |
chlordesmethyldiazepam | benzodiazepine | ||
halazepam | halazepam: structure | organic molecular entity | |
alpidem | imidazoles | ||
n-desmethylflunitrazepam | |||
7-aminonitrazepam | 7-aminonitrazepam: urinary metabolite of nitrazepam | benzodiazepine | |
ro 20-1815 | 7-aminoflunitrazepam: flunitrazepam metabolite; structure given in first source | benzodiazepine | |
dx 9065 | |||
ro 11-6893 | Ro 11-6893: RN given refers to (R)-isomer | ||
n,n-di-n-hexyl-2-(4-fluorophenyl)indole-3-acetamide | N,N-di-n-hexyl-2-(4-fluorophenyl)indole-3-acetamide: binds with high affinity to glial mitochondrial diazepam binding inhibitor receptors & increases mitochondrial steroidogenesis | phenylindole | |
7-aminoclonazepam | benzodiazepine | ||
ro 5-3438 | Ro 5-3438: structure | ||
5-benzimidazolecarboxylic acid | 5-benzimidazolecarboxylic acid: structure in first source | ||
n-desmethylflunitrazepam | N-desmethylflunitrazepam: metabolite of flunitrazepam | ||
ro 05-4082 | ID 690: methyl deriv of clonazepam; structure | ||
ac-5216 | |||
cb 34 | CB 34: ligand for peripheral benzodiazepine receptors; structure in first source | ||
n-(2-methoxybenzyl)-n-(4-phenoxypyridin-3-yl)acetamide | N-(2-methoxybenzyl)-N-(4-phenoxypyridin-3-yl)acetamide: for imaging brain peripheral benzodiazepine receptors; structure in first source | ||
ssr180575 | SSR180575: structure in first source | ||
daa 1106 | |||
naluzotan | naluzotan: an antidepressant and anti-anxiety agent; structure in first source | ||
dpa-713 | |||
a 803467 | A 803467: an Nav1.8 sodium channel blocker; structure in first source | ||
n-fluoroacetyl-n-(2,5-dimethoxybenzyl)-2-phenoxyaniline | N-fluoroacetyl-N-(2,5-dimethoxybenzyl)-2-phenoxyaniline: a peripheral benzodiazepine receptor PET ligand; structure in first source | ||
MS-417 | MS-417 : A member of the class of thienotriazolodiazepines that is the methyl ester of [(6S)-4-(4-chlorophenyl)-2,3,9-trimethyl-6H-thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepin-6-yl]acetic acid. A bromodomain and extra-terminal domain (BET)-specific inhibitor that belongs to a group of thienodiazepine-based compounds | methyl ester; monochlorobenzenes; thienotriazolodiazepine |