FUNCTION/DYSFUNCTION OF ENDOCRINE PANCREAS

Diabetes

Anatomy of the pancreas: Both an exocrine and endocrine organ Cells with exocrine function release an alkaline fluid containing sodium bicarbonate and enzymes pancreatic duct small intestine Pancreatic juice aids in breakdown and digestion of food in the small intestine Pancreatic exocrine cells = acinar cells

Endocrine Function : Cells of the Islet of Langerhans synthesize and release hormones into the circulation. Hormones travel through the bloodstream to target tissues (especially liver and muscle) At the target cells, hormones bind specific receptors and cause cell changes that control metabolism

Pancreatic endocrine cells regulate carbohydrate, fat, protein metabolism: Alpha cells secrete the hormone glucagon Beta cells secrete the hormones insulin and amylin Delta cells secrete the hormones gastrin and somatostatin F cells - secrete hormone pancreatic polypeptide
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Beta Cells
Synthesize pre-proinsulin, a protein This is cleaved by enzymes proinsulin, then cleaved again insulin

Insulin is the biologically active hormone that is released into the bloodstream

Insulin secretion is controlled through several mechanisms:

Chemically high levels of glucose and amino acids in the blood Hormonally beta cells are sensitive to several hormones that may inhibit or cause insulin secretion Neurally stimulation of the parasympathetic nervous system causes insulin to be secreted.
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Insulin secretion is decreased by:

Decreased blood glucose concentration Increased blood insulin concentration Sympathetic stimulation

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Insulin
Transported through the blood to target tissues where it binds to specific receptors The binding of insulin to target cells: Acts as a biochemical signal to the inside of the cell Overall, cell metabolism is stimulated There is increased glucose uptake into the cell Regulation of glucose breakdown within the cell Regulation of protein and lipid breakdown within the cell

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 Blood glucose is decreased because insulin causes glucose to leave the bloodstream and enter the metabolizing cells. With the exception of brain, liver and erythrocytes, tissues require membrane glucose carriers.

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Disorder - Diabetes mellitus

The single most common endocrine disorder group of glucose intolerance disorders Incidence is estimated at 1-2% of the North American population Many of these cases are undiagnosed

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Diabetes mellitus
Historically - distinguished by weight loss, excessive urination, thirst, hunger Excessive urination = polyuria Excessive thirst = polydipsia Excessive hunger = polyphagia

Modern characterization is by hyperglycemia and other metabolic disorders

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Modern classifications (Table17.7) Type 1 or IDDM - Insulin Dependent Diabetes Mellitus

Type 2 or NIDDM - Non-Insulin Dependent Diabetes Mellitus Other Types of Diabetes Mellitus GDM - Gestational Diabetes Mellitus
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Type 1 or IDDM
Accounts for 10% all DM in the Western world ~10-15% have parent or sibling with the disease Peak age of diagnosis = 12 years

Genetic/environmental/autoimmune factors destroy beta cells Believed abrupt onset now immunomarkers and preclinical symptoms have been discovered
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Disequilibrium of hormones produced by islets of Lagerhans : low insulin and high glucagon

Ratio insulin/glucagons apparently controls metabolism of glucose and fats.

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Clinical Manifestations:
Glucose in urine- Because when insulin is not present, glucose is not taken up out of the blood at the target cells. So blood glucose is very highly increased increased glucose filtered and excreted in the urine (exceeds transport maximum)

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Clinical Manifestations:
Weight loss - Patient eats, but nutrients are not taken up by the cells and/or are not metabolized properly
Osmotic diuresis results in fluid loss

Loss of body tissue by metabolism of fats and proteins

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Polyuria, polydipsia, pholyphagia Ketoacidosis Fats and proteins are metabolized excessively, and byproducts known as ketone bodies are produced. These are released to the bloodstream and cause: Decreased pH (so increased acidity) Compensations for metabolic acidosis Acetone given off in breath

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Treatment
1. Administer insulin May be of animal or human origin Cannot be given orally Patient must monitor their blood glucose concentration and administer insulin with the correct timing

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2. Control diet Carbohydrates should make up about 55-60% of patients total calories Fats should make up <30% of patients total calories Proteins should make up about 15-20% of patients total calories

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3. Monitor exercise Remember: muscles are a target tissue of insulin, and metabolize much glucose for energy Sometimes exercise irregular blood glucose levels So diabetic patients should be monitored when they are exercising

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Other: Pancreatic transplant so far not successful Experimental therapies not as successful as hoped

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Type 2 or NIDDM
More common than IDDM, often undiagnosed It has a slow onset Most common in those > 40 years, though children are being diagnosed more regularly May be genetic Obesity is the greatest risk factor for this disease And is related to increased incidence in children
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NIDDM insulin resistance in target cells See decreased cell responsiveness Decreased insulin secreted by cells Also abnormal amount of glucagon secreted

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These effects may be due to: 1.Abnormally functioning cells 2. Decreased cell mass, or a combination of the two 3. Target cell resistance to insulin Due to: Decreased number of insulin receptors Postreceptor events may be responsible Cells burn out and become insensitive

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Clinical manifestations
Overweight, hyperlipidemia common (but these are precursors, not symptoms) Recurrent infections Visual changes, paresthesias, fatigue

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Treatment
1. Weight loss

2. Appropriate diet (see IDDM above) 3. Sulfonyl ureas stimulate cells to increase insulin secretion Works only when cells are still functioning An enhancement of insulins effect at target cells 4. Exercise - promotes weight loss
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Gestational Diabetes
Due to increased hormone secretion during pregnancy Seen if patient has predisposition If previous or potential glucose intolerance has been noted Important - increased mortality risk for mother, child

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Complications of Diabetes Mellitus

Acute: Hypoglycemia = rapid decrease in plasma glucose = insulin shock Neurogenic responses probably due to decreased glucose to hypothalamus. Symptoms include: Tachycardia, palpitations, tremor, pallor Headache, dizziness, confusion Visual changes

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Treatment : provide glucose (I.V. or subcutaneous if unconscious) Observe for relapse

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Ketoacidosis involves a precipitating event: Increased hormones released w/ trauma increased glucose produced by the bodys cells This antagonizes the effects of any glucose present Increased ketones in blood Acid/base imbalance Polyuria, dehydration Electrolyte disturbances Hyperventilation (Kussmaul deep, gasping) CNS effects Acetone on breath
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Treatment: - low dose insulin Also, administer fluids, electrolytes

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Chronic Complications of DM Neuropathies = nerve dysfunctions slowing of nerve conduction. In these patients, see: Degeneration of neurons Sensory, motor deficits Muscle atrophy, paresthesias Depression G.I. problems, as muscle motility decreased Sexual dysfunction
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Microvascular disease chronic diabetes w/ improper glucose metabolism thickening of the basement membrane of capillaries, particularly in the eye and the kidney. As the capillary changes in this way, Decreased tissue perfusion So ischemia hypoxia

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In the eye the retina is metabolically quite active, so hypoxia here is a big problem So see: Retinal ischemia Formation of microaneurisms, hemorrhage, tissue infarct, formation of new vessels, retinal detachment

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In the kidney diabetes is the most common cause of end-stage renal disease Injured glomeruli (glomerulosclerosis) In these patients, see: Proteinuria (protein is excreted into the urine) Generalized body edema, hypertension

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Macrovascular disease atherosclerosis Plaque formation increases Increased risk of coronary artery disease, so increased risk of myocardial infarction Increased risk of congestive heart failure Stroke Peripheral vascular disease why diabetic patients face problems with their lower legs and feet Increased risk of infections

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