Lecture Outline

Lecture Outline - Chapter 26


 

Chapter Twenty-Six - Nutrition and Metabolism

 

I. Nutrition (p. 931)

A. Body Weight and Energy Balance (p. 931)

1. Weight is determined by the body's energy balance - if our energy intake and output are equal, our weight is stable. We gain weight if intake exceeds output and lose it if output exceeds intake.

2. Weight tends to remain stable over the long term and people seem to have a homeostatic set point. The set point varies greatly from one person to the next, dependent on hereditary and environmental influences.

a. It appears that 30% of the variation in weight among people is due to variation in environmental influences, and 70% is due to hereditary variation.

B. Appetite (p. 931; Fig. 26.1)

1. In the 1940s, it was discovered that a region in the lateral hypothalamus triggers the desire for food, called a feeding center. The ventromedial hypothalamus has a satiety center; damage here causes hyperphagia and extreme obesity.

a. The satiety center has neurons called glucostats that rapidly absorb blood glucose after a meal. One hypothesis on hunger is that glucose uptake causes the satiety center to send inhibitory signals to the hunger center and thus suppresses the appetite.

2. Hunger and satiety are regulated by a complex interaction of multiple brain centers, hormones, and sensory and motor pathways.

3. Hunger is stimulated partly by gastric peristalsis. Mild hunger contractions begin soon after the stomach is emptied and increase in intensity over a period of hours.

4. Hormones also play a role in appetite regulation. Cholecystokinin, secreted by the duodenum in response to amino acids and fatty acids in the chyme, is a well-known appetite suppressant. Also, evidence suggests that adipocytes secrete appetite-stimulating hormones when their lipid stores decline.

C. Calories (p. 932)

1. One calorie is the amount of heat that will raise the temperature of 1 g of water 1oC. One thousand calories is a kilocalorie (kcal) or Calorie (C). the relevance of calories to physiology is that they are a measure of the capacity to do biological work.

2. Nearly all dietary calories come from carbohydrates (4 kcal/g), proteins (4 kcal/g), and fats (9 kcal/g).

D. Nutrients (p. 933; Table 26.1)

1. A nutrient is any ingested chemical that is used for growth, repair, or maintenance of the body. Nutrients fall into six major classes: water, carbohydrates, lipids, proteins, minerals, and vitamins.

2. Nutrients needed in comparatively large quantities are called macronutrients, including water, proteins, carbohydrates, and lipids.

3. Nutrients needed in comparatively small quantities are called micronutrients, including the vitamins and minerals.

4. Recommended daily allowances (RDAs) were first developed in the 1940s and are safe estimates of the daily intake that would meet the nutritional needs of most healthy people.

5. Essential nutrients are those that must be included in the diet and cannot be synthesized by the body.

E. Carbohydrates (p. 933)

1. Carbohydrates serve a wide variety of functions in the body, but most of the body's carbohydrate serves as an energy source and is concentrated in muscle glycogen, liver glycogen, and blood glucose.

a. Some cells, such as neurons and erythrocytes, must have energy in the form of glucose, thus blood glucose levels are carefully maintained by insulin and glucagon.

2. Carbohydrate intake also influences the metabolism of other nutrients.

2. Requirements (p. 934)

a. Because carbohydrates are rapidly oxidized, they are required in greater amounts than any other nutrient. The RDA is 125 to 175 g. The brain alone consumes about 120 g of glucose per day.

b. Carbohydrate consumption in the United States has become quite excessive over the past century due to a combination of fondness for sweets, increased use of sugar in processed foods, and reduced levels of physical activity.

c. Dietary carbohydrates come in three principal forms: monosaccharides, disaccharides, and polysaccharides. The only nutritionally significant polysaccharide is starch.

d. The three disaccharides are sucrose, lactose, and maltose. The monosaccharides - glucose, galactose, and fructose - arise mainly from the digestion of starch and disaccharides.

e. Outside of the hepatic portal system, glucose is the only monosaccharides present in the blood in any quantity, and is thus known as blood sugar.

3. Dietary Sources (p. 934)

a. Nearly all dietary carbohydrates come from plants - grains, legumes, fruits, and root vegetables.

4. Fiber (p. 934)

a. Dietary fiber refers to all fibrous materials of plant and animal origin that resist digestion. Most fiber is from cellulose, pectin, gums, and lignin, all derived from plant matter. Fiber is an essential component of the diet.

b. Fiber in the intestines absorbs water and increases its bulk by 40% to 100%. It binds and carries away toxins and other undesirable chemicals, thus reducing the risk of colon cancer.

c. Fiber is categorized as water- soluble or insoluble.

d. Water-soluble fiber found in oats, beans, peas, carrots, brown rice, and fruits reduces blood cholesterol and low-density lipoprotein levels.

e. Cellulose, hemicellulose, and lignin are water-insoluble fibers and aid digestion.

F. Lipids (p. 935)

1. By weight, the adult males averages 15% fat, and the adult females 25% fat. Fat accounts for most of the body's stored energy.

a. Fat has glucose-sparing and protein-sparing effects as long as there is enough fat available to meet the energy needs of tissues.

b. Vitamins A, D, E, and K are fat-soluble vitamins, which depend on dietary fat for their absorption by the intestine.

c. Phospholipids and cholesterol are major structural components of plasma membranes and myelin. Cholesterol is also important as a precursor of steroid hormones, bile salts, and vitamin D.

2. Requirements (p. 935)

a. The average adult needs 80-100 g of dietary fat per day. Fat should account for no more than 30% of the daily caloric intake, and no more than 10% of daily calories should come from saturated fat.

b. A typical American consumes 40-50% of calories from fat, and ingests twice as much cholesterol as the recommended limit.

c. Most fatty acids can be synthesized by the body, except for linoleic and linolenic acids, which are essential fatty acids.

3. Sources (p. 935)

a. Saturated fats are predominantly of animal origin, with the exceptions of coconut and palm oil.

b. The richest source of cholesterol is egg yolk, but it is also prevalent in milk products, shellfish, organ meats, and meat in general. Cholesterol does not occur in foods from plant origins.

c. Saturated fat intake must be controlled because it stimulates cholesterol synthesis.

4. Cholesterol and Serum Lipoproteins (p. 936; Fig. 26.2; Transp. 458; Table 26.2)

a. Lipids would stick to the insides of blood vessels if not transported as lipoproteins, structures with a core of cholesterol and triglycerides and a coating of proteins and phospholipids. The coating allows the lipids to be transported in the bloodstream and also serves as a recognition marker for cells that absorb the lipoproteins.

b. Lipoproteins are classified as chylomicrons, high-density lipoproteins (HDLs), low-density lipoproteins (LDLs), and very low-density lipoproteins (VLDLs). Lipoproteins vary not only in size and density but more importantly in composition and function.

c. Chylomicrons form in the absorptive cells of the small intestine and are transported through lacteals and lymphatic vessels before entering the bloodstream. Endothelial cells in capillaries have lipoprotein lipase that hydrolyzes triglycerides into glycerol and fatty acids. These products pass through the capillary walls into adipocytes where they are reconstructed into triglycerides and stored. The remainder of the chylomicron is removed and degraded by the liver.

d. VLDLs, produced by the liver, transport lipids to adipose tissue for long term storage. Lipoprotein lipase converts VLDLs to LDLs, which contain mostly cholesterol. Cells needing the cholesterol have membrane receptors for LDLs and absorb them by receptor-mediated endocytosis.

e. HDL production begins in the liver, which releases a protein shell that travels in the blood and picks up cholesterol and phospholipids, and thus removes excess cholesterol from the body.

f. It is necessary to maintain serum cholesterol within limits, and most authorities agree that it should not exceed 200 mg/dL. High HDL levels are seen as protective because cholesterol is removed from circulation and transported to the liver for disposal.

G. Proteins (p. 937)

1. Protein constitutes 12-15% of the body's mass; 65% of it is in the skeletal muscles. No other class of biomolecules has such a broad variety of functions.

2. Requirements (p. 937)

a. For persons of average weight, the RDA of protein is 44-60 g, depending on age and sex. A higher intake is recommended under conditions of stress, infection, injury, and pregnancy. Infants and children also require more protein relative to body weight.

b. Essential amino acids are those, which the body cannot synthesize. The nutritional value of a protein depends on whether it is a complete protein (with all the necessary essential amino acids), or an incomplete protein (lacking one or more essential amino acids). Meats and dairy products are complete proteins; plant sources are incomplete proteins but can be used in a complimentary fashion to provide complete proteins.

c. Protein quality is also determined by net protein utilization, which is the percent of amino acids in a protein that the human body uses.

3. Dietary Sources (p. 938)

a. The animal proteins of meat, eggs, and dairy products closely match human proteins in amino acid composition, thus animal proteins are complete proteins.

b. An exclusive vegetarian diet cannot meet all of your nutritional needs unless supplemented with vitamin B12 and essential amino acids.

c. Proteins are our chief dietary source of nitrogen. Nitrogen balance is the state in which nitrogen ingestion equals rate of excretion (as waste material mostly).

d. Someone in positive nitrogen balance is in a period of growth, like a child or pregnant woman. Negative nitrogen balance means that body proteins are being broken down and used as fuel. This condition may occur is carbohydrate and fat intake are insufficient to meet the need for energy.

e. Nitrogen balance is affected by growth hormone and sex hormones that promote protein synthesis. Glucocorticoids promote protein catabolism during times of stress.

H. Minerals and Vitamins (p. 938)

1. Minerals are inorganic elements and vitamins are small organic compounds. Neither is used as fuel, but both are essential to our ability to use other nutrients. Minerals and vitamins cannot be synthesized by the body, and are required only in minute amounts. Indeed, excessive amounts are toxic and potentially lethal.

2. Minerals (p. 939; Table 26.3)

a. Minerals constitute about 4% of the body mass, with three-quarters of this being the calcium and phosphorus in bones and teeth.

b. Table 26.3, p. 939, summarizes adult mineral requirements and dietary sources. Broadly speaking, the best sources of minerals are vegetables, legumes, milk, eggs, fish, shellfish, and some meats.

3. Vitamins (p. 940; Table 26.4)

a. Vitamins were originally named with letters in the order of their discovery, but also have chemically descriptive names. Most of the vitamins must be obtained from the diet but the body synthesizes some of them from precursors called provitamins. Vitamin K, pantothenic acid, and folic acid are also produced by bacterial flora in the large intestine.

b. Vitamins, their requirements, and some dietary sources are listed in Table 26.4, p. 940.

c. Vitamins are classified as water-soluble or fat-soluble. The water-soluble vitamins include the B vitamins and vitamin C. In general, these vitamins are not stored by the body to any great extent, and excesses are excreted in the urine. They seldom accumulate to excess.

d. The fat-soluble vitamins are vitamins A, D, E, and K. They can be stored in the body and are more likely to reach toxic levels if ingested in excess. However, deficiency in vitamin A is the world's most common vitamin deficiency.

II. Carbohydrate Metabolism (p. 941)

A. Glucose Catabolism (p. 941)

1. The purpose of glucose catabolism is to transfer energy from glucose to ATP. In the body, this process is carried out by a series of small, enzyme-catalyzed steps. Energy is released in small, manageable amounts, and some is transferred to ATP. The rest is lost as heat.

2. The three major pathways of glucose metabolism are as follows.

a. Glycolysis involves splitting a glucose molecule into two molecules of pyruvic acid.

b. Anaerobic fermentation, which occurs in the absence of oxygen, reduces pyruvate to lactic acid.

c. Aerobic respiration occurs in the mitochondria in the presence of oxygen and oxidizes pyruvic acid to carbon dioxide and water.

3. Coenzymes are vitally important to these reactions. Enzymes remove electrons, transfer the hydrogen atoms to coenzymes, and the coenzymes donate them to other compounds later in one of the reaction pathways.

a. The two coenzymes of special importance to glucose catabolism are NAD+ (nicotimamide adenine dinucleotide) and FAD (flavin adenine dinucleotide). Both are derived from B vitamins: NAD+ from niacin and FAD from riboflavin.

4. Coenzymes become the temporary carriers of the energy extracted from glucose metabolites.

B. Glycolysis (p. 942; Fig. 26.3; Transp. 459)

1. Upon entering a cell, glucose begins a series of conversions called glycolysis.

2. Fig. 26.3 (Transp. 459) shows the numbered steps, and corresponding discussion in the text (p. 942-943) of the steps of glycolysis.

3. The end products of glycolysis are 2 pyruvic acid, 2 NADH, 2 H+, and 2 ATP. Note that 4 ATP are actually produced but 2 ATP were consumed to initiate glycolysis, so the net gain is 2 ATP per glucose.

4. Some of the energy originally in the glucose is contained in this ATP, some is in the NADH, and some is lost as heat. Most of the energy, however, remains in the pyruvic acid at this point.

C. Anaerobic Fermentation (p. 943)

1. The fate of pyruvic acid depends on whether or not oxygen is available. In an exercising muscle, the demand for ATP may exceed the supply of oxygen, and the only ATP the cells can make under these circumstances is the 2 ATP produced by glycolysis. Cells that lack mitochondria, such as erythrocytes, are also restricted to making ATP by this method.

2. Glycolysis would quickly come to a halt because NAD+ must be replenished. In the absence of oxygen, a cell resorts to a one-step reaction called anaerobic fermentation. In this pathway, NADH donates a pair of electrons to pyruvic acid, reducing it to lactic acid and regenerating NAD+.

3. Lactic acid leaves the cells that generate it and travels by way of the bloodstream to the liver. When oxygen becomes available again, the liver oxidizes lactic acid back to pyruvic acid. The oxygen required to do this is part of the oxygen debt created by exercising skeletal muscles.

4. Anaerobic fermentation does have its drawbacks. One is that it is wasteful, because most of the energy of glucose is still in the lactic acid and has contributed no useful work. The other is that lactic acid is toxic and contributes to muscle fatigue.

D. Aerobic Respiration (p. 943)

1. Most ATP is generated in the mitochondria, which require oxygen as the final electron acceptor. In the presence of oxygen, pyruvic acid enters the mitochondria and is oxidized by aerobic respiration. This occurs in two principal steps: the matrix reactions and the membrane reactions.

2. The Matrix Reactions (p. 944; Fig. 26.4; Transp. 460)

a. The matrix reactions are shown in Fig. 26.4, p. 944 (Transp. 460), where the reaction steps are numbered to correspond with text descriptions on p. 944-945.

b. After the matrix reactions, there is nothing left of the organic matter of the glucose; its carbon atoms have all been carried away as CO2 and exhaled.

c. The citric acid cycle not only oxidizes glucose metabolites but is also a pathway and a source of intermediates for the synthesis of fats and nonessential amino acids.

3. The Membrane Reactions (p. 945; Figs. 26.5, 26.6; Transps. 461, 462)

a. The membrane reactions have two purposes: (1) to further oxidize NADH and FADH2 and (2) to regenerate NAD+ and FADH and make them available again to earlier reaction steps.

b. The membrane reactions are carried out by a series of compounds called the electron-transport chain. Most members of the chain are bound to the inner mitochondrial membrane. The members of the chain are flavin mononucleotide, iron-sulfur centers, coenzyme Q, copper ions, and several cytochromes.

c. Fig. 26.5, p. 945 (Transp. 461), shows the order in which electrons are passed along the chain.

d. Hydrogen atoms are split apart as they are transferred from coenzymes to the chain. The protons are released to the mitochondrial matrix. Each electron carrier in the chain becomes reduced when it receives an electron pair and oxidized again when it passes the electrons along to the next carrier. Energy is liberated at each transfer.

e. The final electron acceptor in the chain is oxygen. Each oxygen atom accepts two electrons from cytochrome a3 and two protons from the mitochondrial matrix. The result is a molecule of water, the body's primary source of metabolic water.

f. As electrons are passed along the electron transport chain, some of the energy is used to drive proton pumps that remove H+ from the mitochondrial matrix and pump it into the space between the inner and outer mitochondrial membranes. This creates a steep electrochemical gradient across the inner mitochondrial membrane.

g. The inner membrane is permeable to H+ only through specific channel proteins called ATP synthase. As H+ flows through these channels, it creates an electrical current. ATP synthase harnesses the energy of this current to drive ATP synthesis. This process is called the chemiosmotic mechanism.

E. Overview of ATP Production (p. 947; Fig. 26.7; Transp. 463; Table 26.5)

1. For each glucose molecule, there are 30 ATP generated by NADH, 4 ATP generated by FADH2, plus 2 ATP generated by glycolysis and 2 ATP from the matrix reactions for a total of 38 ATP generated per molecule of glucose.

2. Aerobic respiration has an efficiency of 40%. The other 60% is body heat.

F. Glycogen Metabolism (p. 947; Fig. 26.8; Transp. 464; Table 26.6)

1. ATP is quickly used after it is synthesized. It is an energy transfer molecule, not one that stores energy.

2. Glycogen is a short-term store for glucose; fat is long-term energy storage.

a. When glucose is in excess, the liver stores glucose as glycogen through the process of glycogenesis.

b. When glucose in the blood declines, glycogen can be converted back to glucose through glycogenolysis.

c. Gluconeogenesis is the synthesis of glucose from noncarbohydrates such as fats and amino acids.

3. The conversions between glucose and its storage forms are shown in Fig. 26.8, p. 948; Transp. 464.

G. Functions of the Liver (p. 948; Fig. 26.7; Transp. 463)

1. The numerous functions of the liver are listed in Table 26.7, p. 949. Except for phagocytosis, all of these are carried out by the cuboidal hepatocytes.

III. Lipid and Protein Metabolism (p. 949)

A. Lipids (p. 950)

1. Triglycerides are stored in the body's adipocytes, where they remain for 2-3 weeks. There is a continual turnover as lipids are released.

2. Lipogenesis (p. 950; Fig. 26.9; Transp. 465)

a. Lipogenesis refers to the synthesizing of triglycerides from other molecules. These pathways are summarized in Fig. 26.9, p. 950; Transp. 465.

3. Lipolysis (p. 950)

a. Breaking down fat to be used as fuel is lipolysis. These pathways are also summarized in Fig. 26.9, p. 950.

b. Inadequate carbohydrate intake interferes with the complete oxidation of fat. Under such circumstances, fat oxidation leads to ketogenesis and potentially to ketoacidosis.

B. Proteins (p. 950)

1. About 100 g of tissue breaks down each day into free amino acids. These combine with the amino acids from the diet to form an amino acid pool that cells can draw upon to make new proteins.

a. Some amino acids in the pool can be converted to others. Free amino acids also can be converted to glucose and fat or directly used as fuel. Such conversions involve either deamination, amination, or transamination.

2. Use as Fuel (p. 951; Fig. 26.10; Transp. 466)

a. The first step in using amino acids as fuel is to deaminate them. After removal of the -NH2 group, the remainder of the molecule is called a keto acid. Depending on which amino acid is involved, the resulting keto acid may be converted to pyruvic acid, acetyl CoA, or one the acids of the citric acid cycle.

3. Transamination, Ammonia, and Urea (p. 951; Fig. 26.11; Transp. 467)

a. When deamination reactions occur, the -NH2 becomes ammonia, NH3, which is extremely toxic to cells and cannot be allowed to accumulate. The liver quickly converts the ammonia to its less toxic form, urea, by a pathway known as the ornithine cycle. Urea is then excreted in the urine.

4. Protein Synthesis (p. 951)

a. The liver can make many amino acids from other amino acids or from citric acid cycle intermediates by transamination reactions. The essential amino acids, however, must be obtained from the diet.

IV. Metabolic States and Metabolic Rate (p. 952; Table 26.8)

A. Absorptive State (p. 952)

1. Absorptive state lasts about 4 hours after a meal. During this time, blood glucose is readily available for ATP synthesis. It serves as a primary fuel and spares the body from having to draw on stored fuels.

a. Absorbed sugars are transported by the hepatic portal system to the liver. Most glucose passes through the liver and is available to body cells. Excessive glucose is stored as glycogen or body fat.

b. Fats enter lymph as chylomicrons and initially bypass the liver. Lipoprotein lipase removes fats from the chylomicrons for uptake by the tissues, especially adipose and muscular tissue.

c. Amino acids, like sugars, circulate first to the liver. Most pass through and become available for protein synthesis. Some are removed by the liver for protein synthesis and fatty acid synthesis after deamination.

2. Regulation of the Absorptive State (p. 952)

a. The absorptive state is regulated largely by insulin, which stimulates nearly all cells to absorb glucose. Neurons are an exception and absorb glucose at their own independent rate.

B. Postabsorptive State (p. 953)

1. Postabsorptive state (fasting) prevails hours after meals and overnight. The essence of this state is to regulate blood glucose levels, which is especially critical to the brain.

a. Glucose is drawn from the body's glycogen reserves or synthesized from other compounds (gluconeogenesis).

b. Adipocytes and hepatocytes hydrolyze fats and convert the glycerol to glucose. After 4 to 5 days of fasting, the brain begins to use ketone bodies as supplemental fuel.

c. If glycogen and fat reserves are depleted, the body begins to use proteins as fuel. The first to go are skeletal muscle proteins, and starvation results in wasting away of muscle mass.

2. Regulation of the Postabsorptive State (p. 953)

a. Postabsorptive metabolism is regulated mainly by the sympathetic nervous system and several hormones.

b. As blood glucose drops, the pancreas releases glucagon that promotes glycogenolysis and gluconeogenesis, raising blood glucose level. It also promotes lipolysis and a rise in FFA levels, thus making both glucose and lipids available for fuel.

c. The sympathoadrenal system richly innervates adipose tissue and can mobilize stored energy reserves as needed.

d. Growth hormone has the opposite effects of insulin and raises blood glucose concentrations.

C. Metabolic Rate (p. 953)

1. Metabolic rate (MR) means the amount of energy liberated in the body per unit of time, expressed in terms as kcal/hr or kcal/day.

2. Metabolic rate depends on physical activity, mental state, absorptive or postabsorptive state, and other factors.

3. The basal metabolic rate (BMR) is a standard of comparison that minimizes the effects of such variables. BMR is the metabolic rate while relaxed, seated, and in a room of comfortable temperature. Sleeping metabolic rate is less than BMR.

4. Total metabolic rate is the sum of BMR plus energy expended during voluntary activities.

5. The BMR of the average adult male is 2,000 kcal/day, with that of females slightly less.

6. BMR is stimulated by activity, pregnancy, anxiety, eating, and certain hormones. It is lowered by apathy, depression, and prolonged starvation.

V. Body Heat and Thermoregulation (p. 954)

A. Body Temperature (p. 954)

1. Body temperature fluctuates about 1oC in a 24-hour cycle.

2. The most important body temperature is the core temperature, which is that of the cranial, thoracic, and abdominal cavities.

3. Shell temperature is closer to the surface, especially skin and oral temperature. Adult oral temperature is normally 36.6oC to 37oC (97.9o - 98.6oF) but may be higher during strenuous exercise.

B. Heat Production and Loss (p. 954; Fig. 26.12)

1. Most body heat comes from exergonic chemical reactions such as nutrient oxidation and ATP use. At rest, skeletal muscles contribute 20-30% of the total resting heat. Increased muscle tone or exercise greatly increases heat generation in the muscles. During vigorous exercise, they produce 30-40 times as much heat as the rest of the body.

2. The body loses heat through radiation, conduction, and evaporation.

C. Thermoregulation (p. 956)

1. Thermoregulation is achieved through several negative feedback loops. Within the hypothalamus lies a hypothalamic thermostat that monitors the blood temperature and receives signals from peripheral thermoreceptors in the skin. When necessary, it sends impulses to either a heat-losing center or a heat-promoting center, both located separately within the hypothalamus.

a. When blood temperature is too high, the heat-losing center signals the dilation of dermal arterioles, conducting more heat to the body surface. If this fails, sweating is triggered.

b. When blood temperature drops too low, the heat-promoting center causes dermal vasoconstriction and the body may resort to shivering thermogenesis.

c. During colder seasons, the body raises its metabolic rate by 20-30% through nonshivering thermogenesis.

D. Disturbances of Thermoregulation (p. 956)

1. Exposure to excessive heat causes heat cramps, heat exhaustion, and heat stroke.

a. Heat cramps are painful muscle cramps that result from excessive electrolyte loss in the sweat.

b. Heat exhaustion results from more severe electrolyte loss, and is characterized by hypotension, dizziness, vomiting, and sometimes fainting.

c. During heat stroke, the body temperature can rise to as high as 43oC (110oF). Brain cells misfunction, hypothalamic mechanisms break down, and convulsions, coma, and death may suddenly occur.

2. Hypothermia can result from exposure to cold weather or immersion in icy water.

a. If the core temperature falls below 33oC (91oF), the metabolic rate drops so low that heat production cannot keep pace with heat loss, and the temperature falls further.

b. A body temperature below 24oC (75oF) is usually fatal.

CHAPTER ESSAY: Alcohol and Alcoholism (p. 957)

i. Alcohol is an addictive drug that adversely affects many of the body's systems.

ii. Alcohol is rapidly absorbed and distributed throughout the body. It crosses the blood-brain barrier. The liver enzyme, alcohol dehydrogenase, detoxifies the alcohol.

iii. Alcohol is a depressant to the nervous system; it can cause inflammation of the pancreas and liver, as well as cirrhosis of the liver; it adversely affects the cardiovascular system; it creates malnutrition; it is addictive.

 

 

 


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