The Alcohols

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The Alcohols By S. Bohlooli, Ph.D

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The Alcohols. By S. Bohlooli, Ph.D. History. The alcohol had important place in humankind for at least 8000 years The diluted alcoholic beverages were preferred over water, In western countries Today, 75% of US adult population drinks alcohol regularly - PowerPoint PPT Presentation

Transcript of The Alcohols

Page 1: The Alcohols

The Alcohols

By

S. Bohlooli, Ph.D

Page 2: The Alcohols

History

• The alcohol had important place in humankind for at least 8000 years

• The diluted alcoholic beverages were preferred over water, In western countries

• Today, 75% of US adult population drinks alcohol regularly

• About 10% of the general population in the US are alcohol abuser.

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Basic Pharmacology ofEthanol

• Pharmacokinetics– Ethanol is a small water soluble molecule– Presence of food delays absorption– Vd approximates total body water– Over 90% of alcohol consumed is oxidized in

the liver.– Rate of oxidation follows zero order kinetics.

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Metabolism of ethanol

• Alcohol Dehydrogenase pathway

• Microsomal ethanol oxidizing system (MEOS).

• Acetaldehyde metabolism

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Alcohol Dehydrogenase (ADH) pathway

NAD+

EthanolCH3CH2OH

NADHAcetaldehyde

CH3CHO

AcetateCH3COO-

NADPH + O2

NADP+

NAD+

NADH

Alcohol Dehydrogenase(ADH)

MEOS

AldehydeDehydrogenase

Fomepizole

ΘDisulfiram

Θ

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Microsomal Ethanol Oxidizing System (MEOS)

• At concentration below 100 mg/dl the MEOS has little contribution to the ethanol metabolism.

• During chronic consumption there is an induction in enzyme activity

• Enzyme inducing drugs like phenobarbital may increase activity of MEOS.

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Acetaldehyde metabolism

• It seems several enzymes are responsible for acetaldehyde metabolism

• The primary enzyme system is aldehyde dehydrogenase

• The product is acetate• Oxidation of acetaldehyde is inhibited by

disulfiram.• Co-cosumption of ethanol and disulfiram leads

to acetaldeyde accumulation.• Facial flushing, nausea, dizziness and headache

are the main unpleasant reaction.

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Pharmacodynamics of acute ethanol consumption

• Central nervous system– Sedation, relief of anxiety,– Slurred speech, impaired judgment,

disinhibited behavior– Condition called “intoxication” or

“drunkenness”– There is too different between tolerant and

nontolerant individuals– At higher blood concentration:

• Coma, respiratory depression and death.

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Ethanol Mechanism of action

• Enhances the action of GABA at GABAA

• Inhibits the action of Glutamate at NMDA

• Disruption of biological membranes through reduction in lipid viscosity (fluidization)

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Effect on Heart

• Depression of myocardial contractility (blood concentration > 100 mg/dl)

• It seems that acetaldehyde is responsible for ultra structural changes

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Effect on Smooth Muscle

• Vasodilator– Depression of vasomotor center– Direct effect

• Relaxes Uterus

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Consequences of Chronic Alcohol Consumption

• Liver and gastrointestinal tract• Nervous system

– Tolerance and physical dependence– Neurotoxicity

• Cardiovascular system• Blood• Endocrine system and electrolyte balance• Fetal alcohol syndrome• Immune system• Increased risk of cancer

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Liver and gastrointestinal tract

• About 15-30% chronic heavy drinkers develop sever liver disease:– Alcoholic fatty liver– Alcoholic hepatitis– Cirrhosis and liver failure

• Increased ratio of NADH/NAD+reduced gluconeogenesis, hypoglycemiaa nd ketoacidosis

• Excess of Acetaldehyde (very reactive compound)• Decreased level of Glutathione• Hormonal factors• Increased gastric and pancreatic secretion.• Altered mucosal barriers• Malabsorption of water soluble vitamines

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Nervous system

• Tolerance and physical dependence– Metabolic tolerant– Neurotransmitters, receptors, ion channels,

enzymes that participate in signal transduction pathway

– Acute increase in local concentration of serotonin, opioids, and dopamine

– Withdrawal syndrome• Hyperexcitability, convulsion, toxic psychosis

– Dose, rate and duration of alcohol consumption

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Nervous system

• Neurotoxicity– Generalized symmetric peripheral nerve injury– Gait disturbance and ataxia – Wernicke-Korsakoff syndrome

• Thiamine deficiency

– Impaired visual acuity

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Cardiovascular system

• Heavy alcohol consumption dilated cardiomyopathy – Depressed function of mitochondria and sarcoplasmic

reticulum, intracellular accumulation of fatty acids and phospholipids up regulation of voltage dependent calcium channels.

– Arrhythmias

• Arrhythmias Seizure, syncope and sudden death during alcohol withdrawal

• Hypertension• Low coronary heart disease high HDL

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Blood

• Mild anemia alcohol related folic acid deficiency

• Hemolytic syndromes

• Abnormalities in platelets and leukocytes

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Endocrine system and electrolyte balance

• Gynecomastia and testicular atrophy

• Alcoholic with chronic liver diseases ascites, edema and effusions.

• Low potassium

• Hypoglycemia, ketosis

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Fetal alcohol syndrome

• Heavy drinking in first trimester– Retard body growth– Microcephaly– Poor coordination– Underdevelopment of mild facial region

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Immune system

• Alteration in: – Chemotaxis of Granulocytes– Lymphocyte response to mitogens– T cell numbers– Natural killer cell activity– Level of tumor necrosis factor

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Increased risk of cancer

• Increased risk for cancer of:– The mouth, pharynx, larynx, esophagus and

liver– Breast

• Alcoholic beverages may carry potential carcinogens

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Alcohol – Drug interactions

• Pharmacokinetics– Chronic intake:

• Alcohol induced increase drug metabolism• Increased level of Acetaminophen toxicity

– Acute intake:• Drug metabolism inhibition

• Pharmacodynamics– Additive central nervous system depression

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Management of acute alcohol intoxication

• Degree of intoxication depends on:– The blood ethanol concentration– The rapidity of the rise of the alcohol level – The time during which the blood level

maintained.

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Management of alcohol withdrawal syndrome

• The major objective of drug therapy is prevention of:– Seizure– Delirium– Arrhythmias

• Potassium, magnesium and phosphate balance• Thiamine therapy• Replacement therapy with long acting sedative-

hypnotic drugs

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Pharmacotherapy of alcoholism

• Disulfiram– slow elimination rate– Inhibitor of other drug’s metabolism (phenytion, isoniazide)– Compliance is low– Some drugs have Disulfiram like effect : metronidazole,

sulfonylurea hypoglycemic drugs

• Naltrexone– Decreased rate of relapse– Reduced alcohol craving

• Acamprosate– Weak NMDA receptor antagonist– GABAA Activator– Reduce replapse

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Pharmacology of other alcohols

• Methanol• Ethylene Glycol• Drug therapy: ethanol, fomepizole