thiamine

Biochemistry for medics 1

Thiamine- Chemistry, functions and clinical significance

Biochemistry for Medicshttp://www.namrata.co/

http://www.namrata.co/




Thiamine- Introductionalso known as vitamin B1, anti beriberi factor or anti-neuritic vitamin is an important water-soluble vitamin is involved in carbohydrate, fat, amino acid, glucose, and alcohol metabolism. is required as a coenzyme in enzymatic reactions that involve the transfer of an aldehyde group. is essentially nontoxic.


Thiamine - Structure

Thiamine contains a substituted pyrimidine ring (dimethyl 6-amino pyrimidine) connected to a substituted thiazole ring (Methyl hydroxy ethyl thiazole) by means of Methylene bridge.


Thiamine- SynthesisThiamine can be synthesized by plants and some microorganisms, but not usually by animals. Human beings require thiamine from diet, though small amounts may be obtained from synthesis by intestinal bacteria. Whole wheat flour, unpolished rice, beans, nuts and yeast are the good sources of thiamineIt is also present in liver, meat and eggs.The body can only store up to 30 mg of thiamine in its tissues.


Thiamine-Occurrence

It is present in large amounts in skeletal muscle, heart, liver, kidney, and brain. It has a widespread distribution in foods, but there can be a substantial loss of thiamine during cooking above 100°C (212°F). The half-life of thiamine is 9-18 days. It is excreted by the kidney.


Activation of Thiamine

The active form of the coenzyme, thiamine pyrophosphate (thiamine diphosphate, TPP), is synthesized by an enzymatic transfer of a pyrophosphate group from ATP to thiamine).


Recommended daily Allowance of thiamineDepends on calorie intake (0.5 mg/1000 cals) RDA is 1-1.5 mg/day Requirement increases with-o increased carbohydrate intakeo Pregnancyo Lactationo Smokingo Alcoholismo Prolonged antibiotic intakeo Serious or prolonged illness


Metabolic role of ThiamineThiamine has a central role in energy-yielding metabolism, and especially the metabolism of carbohydrates Thiamine pyrophosphate is an essential cofactor for enzymes that catalyze the oxidative decarboxylation of α-keto acids to form an acylated coenzyme A (acyl CoA).These include pyruvate dehydrogenase , α -keto glutarate dehydrogenase and branched-chain α-keto acid dehydrogenase. These three enzymes operate by a similar catalytic mechanism.


Role of TPP in Pyruvate dehydrogenase complexThe pyruvate dehydrogenase complex is a large, highly

integrated complex of three kinds of enzymes; Pyruvate

dehydrogenase, dihydrolipoyl transacetylase and Dihydrolipoyl

dehydrogenase.

At least two additional enzymes regulate the activity of the

complex and five coenzymes: thiamine pyrophosphate (TPP), lipoic acid, CoASH, FAD and NAD+ participate in the overall

reaction.


PDH Complex and role of TPP

Pyruvate is decarboxylated by the pyruvate dehydrogenase component of the enzyme complex to a hydroxyethyl derivative of the thiazole ring of enzyme-bound thiamine diphosphate, which in turn reacts with oxidized lipoamide, the prosthetic group of dihydrolipoyl transacetylase, to form acetyl lipoamide. In thiamine deficiency, glucose metabolism is impaired, and there is significant (and potentially life-threatening) lactic and pyruvic acidosis.


Role of TPP in α-Keto Glutarate dehydrogenase complex

The enzyme complex is similar to that involved in the oxidative decarboxylation of pyruvate. The α-ketoglutarate dehydrogenase complex requires the same cofactors as the pyruvate dehydrogenase complex—thiamine diphosphate, lipoate, NAD+, FAD, and CoA—and results in the formation of succinyl-CoA.


Role of TPP in branched-chain α-keto acid dehydrogenase complex

Reaction 2 is catalyzed by α-keto acid dehydrogenase complex


Role of TPP in branched-chain α-keto acid dehydrogenase complexFollowing transamination, all three -keto acids of branched chain amino acids undergo oxidative decarboxylation catalyzed by mitochondrial branched-chain α-keto acid dehydrogenase. This multimeric enzyme complex of a decarboxylase, a transacylase, and a dihydrolipoyl dehydrogenase closely resembles pyruvate dehydrogenase and α-keto glutarate dehydrogenase complex.


Role of TPP in Transketolase reactionThiamine pyrophosphate is also an important cofactor for the Transketolase reactions in the pentose phosphate pathway of carbohydrate metabolism. These reactions are important in the reversible transformation of pentoses into the glycolytic intermediates fructose 6-phosphate and glyceraldehyde 3-phosphate. Transketolase transfers the two-carbon unit comprising carbons 1 and 2 of a ketose onto the aldehyde carbon of an aldose sugar. It therefore effects the conversion of a ketose sugar into an aldose with two carbons less and an aldose sugar into a ketose with two carbons more. The reaction requires Mg2+ and thiamine diphosphate (vitamin B1) as coenzyme.


Role of TPP in Transketolase reaction


Role of TPP in Tryptophan Metabolism

Thiamine is also required for the metabolism of Tryptophan( As a coenzyme for Tryptophan pyrrolase)

Tryptophan oxygenase (tryptophan pyrrolase) opens the indole ring, incorporates molecular oxygen, and forms N-formyl kynurenine.


Role of TPP in nerve conductionThiamine pyrophosphate has a role in nerve conduction; It phosphorylates, and so activates, a chloride channel in the nerve membrane.Thiamine appears to have a role in axonal conduction particularly in acetyl cholinergic and serotoninergic neurons.


Thiamine deficiency and impaired reactionsA deficiency in thiamine will decrease the efficiency of the enzymes for which TPP is required as a cofactor. Thus, the rate of conversion of pyruvate to acetyl-CoA and the flow of acetyl-CoA through the tricarboxylic acid cycle will be depressed as a result of the inefficiency of the TPP-requiring enzymes pyruvate dehydrogenase and α-keto glutarate dehydrogenase.


Thiamine deficiency and impaired reactions (Contd.)The production of the reduced electron carrier, NADH, and the ATP produced from it via oxidative phosphorylation is also decreased as a consequence. Because nervous tissue and heart use at high rates ATP synthesized from the oxidation of NADH produced from pyruvate conversion to acetyl-CoA and from the TCA cycle, these tissues are most affected by a deficiency in thiamine.When deficient in thiamine, the brain can no longer efficiently metabolize pyruvate through the TCA cycle to produce ATP and thus must convert it to lactate to produce ATP.


Thiamine deficiency and impaired reactions (Contd.)A deficiency in thiamine also adversely affects the flux of glucose metabolized by the pentose phosphate pathway. When these reactions cannot proceed, precursor metabolites build up, and the flow through the pathway is decreased. This results in a decreased production of NADPH and decreased conversion of glucose to pentose, including ribose. This can lead to decreased regeneration of reduced glutathione and susceptibility to oxidative stress.


Thiamine deficiency(Beri-Beri)

Beriberi is observed in developed nations in- persons with alcoholism, people on fad diets, persons on long-term peritoneal dialysis without thiamine replacement, persons undergoing long-term starvation,or persons receiving intravenous fluids with high glucose concentration.


Pathophysiology of Thiamine deficiency (Beri-Beri)Deficiency causes degeneration of peripheral nerves, thalamus, mammillary bodies, and cerebellum. Cerebral blood flow is markedly reduced, and vascular resistance is increased.The heart may become dilated; muscle fibers become swollen, fragmented, and vacuolized, with interstitial spaces dilated by fluid.Vasodilation occurs and can result in edema in the feet and legs. Arteriovenous shunting of blood increases. Eventually, high-output heart failure may occur.


Classification of Beri-Beri Dry BeriberiCardiovascular(Wet Beriberi)Infantile BeriberiShoshin BeriberiWernicke-Korsakoff syndrome


Dry Beriberi

Nervous system involvement is termed dry beriberi.

The neurologic findings can be peripheral neuropathy characterized by symmetric impairment of sensory, motor, and reflex functions of the extremitiesThese deficits are bilateral and roughly symmetric, occurring in a stocking-glove distribution.


Dry Beriberi (Contd.)They affect predominantly the lower extremities, beginning with paresthesias in the toes, burning in the feet (particularly severe at night), muscle cramps in the calves, pains in the legs, and plantar dysesthesias. Calf muscle tenderness, difficulty rising from a squatting position, and decreased vibratory sensation in the toes are early signsContinued deficiency worsens polyneuropathy, which can eventually affect the arms.


Dry Beriberi

Deficiency causes degeneration of peripheral nerves, thalamus, mammillary bodies, and cerebellum.


Cardiovascular (wet) beriberi

Wet beriberi is the term used for the cardiovascular involvement of thiamine deficiency.The first effects are vasodilatation, tachycardia, a wide pulse pressure, sweating, warm skin, and lactic acidosis. Later, heart failure develops, causing orthopnea and pulmonary and peripheral edema. Vasodilatation can continue, sometimes resulting in shock.


Cardiovascular (wet) beriberi

"Pedal edema before and after the application of pressure to the shin."


Infantile beriberiInfantile beriberi occurs in infants (usually by age 3 to 4 wk) who are breastfed by thiamine-deficient mothers.Heart failure (which may occur suddenly), aphonia, and absent deep tendon reflexes are characteristic.


Shoshin beriberiShoshin beriberi A more rapid form of wet beriberi is termed acute fulminant cardiovascular beriberi, or Shoshin beriberi. The predominant injury is to the heart, and rapid deterioration follows the inability of the heart muscle to satisfy the body's demands because of its own injury. In this case, edema may not be present.Instead, cyanosis of the hands and feet, tachycardia, distended neck veins, restlessness, and anxiety occur.


Wernicke-Korsakoff syndromeWernicke-Korsakoff syndrome, which combines Wernicke's encephalopathy and Korsakoff's psychosis occurs in some alcoholics who do not consume foods fortified with thiamine.Wernicke's encephalopathy consists of psychomotor slowing or apathy, nystagmus, ataxia, ophthalmoplegia, impaired consciousness, and, if untreated, coma and death.

Biochemistry for medics

Korsakoff psychosis

Korsakoff psychosis consists of mental confusion, dysphonia, and confabulation with impaired memory of recent events. It probably results from chronic deficiency and may develop after repeated episodes of Wernicke's encephalopathy.

32


Causes of thiamine deficiency

Lack of thiamine intakeFood containing a high level of thiaminase, including milled rice, raw freshwater fish, raw shellfish, and fernsFood high in anti-thiamine factor, such as tea, coffee, and betel nutsProcessed food with a content high in sulfite, which destroys thiamineAlcoholic stateStarvation state


Causes of thiamine deficiency ( contd.)Increased consumption statesDiets high in carbohydrate or saturated fat intakePregnancyHyperthyroidism LactationFever - severe infectionIncreased physical exercise


Causes of thiamine deficiency(contd.)Increased depletionDiarrheaDiuretic therapiesPeritoneal dialysisHemodialysisHyperemesis gravidarum


Causes of thiamine deficiency(contd.)Decreased absorptionChronic intestinal diseaseAlcoholismMalnutritionGastric bypass surgeryMalabsorption syndrome - Celiac and tropical sprue


Laboratory Studies in thiamine deficiency

Diagnosis is usually based on a favorable response to treatment with thiamine in a patient with symptoms or signs of deficiency. Electrolytes, including Mg, should be measured to exclude other causes. For confirmation in equivocal cases, erythrocyte Transketolase activity and 24-h urinary thiamine excretion may be measured. Diagnosis of cardiovascular beriberi can be difficult if other disorders that cause heart failure are present.


Treatment of Thiamine deficiency

Supplemental thiamine, with dose based on clinical manifestationsFor mild polyneuropathy, thiamine 10 to 20 mg once/day is given for 2 wk. For moderate or advanced neuropathy, the dose is 20 to 30 mg/day; it should be continued for several weeks after symptoms disappear. For edema and congestion due to cardiovascular beriberi, thiamine 100 mg IV once/day is given for several days.


Prognosis of Beriberi

The prognosis for beriberi is usually good, unless patients have established Korsakoff syndrome. When patients have progressed to this stage, the degree of damage is only minimally reversible.


Summary BeriberiThiamine deficiency (causing beriberi) is most common among people subsisting on white rice or highly refined carbohydrates in developing countries and among alcoholics. Symptoms include diffuse polyneuropathy, high-output heart failure, and Wernicke-Korsakoff syndrome.Diagnosis is usually based on a favorable response to treatment with thiamine in a patient with symptoms or signs of deficiency. For confirmation in equivocal cases, erythrocyte transketolase activity and 24-h urinary thiamin excretion may be measured.Because thiamine deficiency often occurs with other B vitamin deficiencies, multiple water-soluble vitamins are usually given for several weeks


Therapeutic uses of Thiamine

Thiamine deficiencyThiamine is also used for digestive problems including

poor appetite, ulcerative colitis, and ongoing diarrhea.also used for AIDS and boosting the immune system,

diabetic pain, heart disease, alcoholism, aging, vision problems such as cataracts and glaucoma, motion sickness, and improving athletic performance.

Other uses include preventing cervical cancer and progression of kidney disease in patients with type 2 diabetes.

thiamine

Education

thiamine synthesis thiamine

thiamine structure thiamine

thiamine chemistry

thiamine deficiency

activation of thiamine

thiamine introduction

halflife of thiamine

thiamine pyrophosphate