The endocrine system comprises glands located throughout the body that release specific chemical substances called hormones directly into the bloodstream. These hormones regulate varied functions of an organism, from bone growth to metabolism.
Endocrine glands secrete hormones directly into the bloodstream rather than into ducts. These chemical messengers travel through the blood to target organs and tissues, regulating essential bodily functions.
Unlike endocrine glands, exocrine glands send their chemical substances into ducts that lead to the exterior of the body. Examples include sweat glands and salivary glands.
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These hormones increase metabolism in body cells, regulating energy production and consumption throughout the organism.
This hormone lowers blood calcium levels, working in balance with parathyroid hormone to maintain proper calcium homeostasis.
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The parathyroid glands produce parathyroid hormone, which increases blood calcium levels. This hormone works opposite to calcitonin, maintaining the delicate balance of calcium in the bloodstream essential for nerve function, muscle contraction, and bone health.
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The adrenal glands sit atop the kidneys and consist of two distinct regions: the cortex (outer layer) and medulla (inner core). Each region produces different hormones with unique functions.
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Decreases blood sugar by converting glucose to glycogen for storage in the liver and muscles.
Increases blood sugar by converting stored glycogen back to glucose when energy is needed.
The pancreas plays a dual role as both an endocrine and exocrine gland. The islet cells function as the endocrine portion, regulating blood glucose levels through insulin and glucagon secretion.
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The anterior pituitary produces multiple hormones that regulate growth, metabolism, and reproduction. Often called the "master gland," it controls many other endocrine glands.
Increases bone and tissue growth throughout the body.
Stimulates thyroxine production and thyroid gland growth.
Stimulates hormone secretion from adrenal cortex, especially cortisol.
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Follicle-stimulating hormone promotes oogenesis in females and spermatogenesis in males.
Luteinising hormone promotes ovulation in females and testosterone secretion in males.
Promotes breast tissue growth and milk secretion in nursing mothers.
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Also called vasopressin, ADH stimulates reabsorption of water by kidney tubules, preventing excessive water loss and maintaining proper hydration.
Stimulates contraction of the uterus during labour and childbirth, and also plays a role in milk ejection during breastfeeding.
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Develops and maintains secondary sex characteristics in females, including breast development, body fat distribution, and regulation of the menstrual cycle.
Prepares and maintains the uterus during pregnancy, supporting the endometrial lining and preventing contractions during gestation.

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The primary male sex hormone promotes growth and maintenance of secondary sex characteristics in males, including:
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Endocrine disorders occur when glands produce too much or too little hormone, leading to various health complications. Understanding these conditions is essential for proper diagnosis and treatment.
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Overactivity of the thyroid gland resulting in excessive hormone production, increased metabolism, and symptoms like weight loss and rapid heartbeat.
Underactivity of the thyroid gland causing insufficient hormone production, decreased metabolism, and symptoms like fatigue and weight gain.
Cancer of the thyroid gland requiring surgical intervention and potentially radioactive iodine treatment.
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Excessive production of parathormone leads to elevated blood calcium levels, potentially causing kidney stones, bone weakness, and cardiovascular issues.
Deficient production of parathyroid hormone results in low blood calcium levels, causing muscle cramps, tingling sensations, and potential seizures.
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Excessive output of adrenal androgens causes masculinisation, including increased body hair, deepened voice, and altered body composition.
A group of symptoms produced by excess cortisol from the adrenal cortex, including weight gain, moon face, buffalo hump, and skin changes.
Hypofunctioning of the adrenal cortex leads to insufficient cortisol and aldosterone production, causing fatigue, weight loss, and low blood pressure.
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A tumour of the adrenal medulla where tumour cells stain a dark or dusky (phe/o) colour (chrom/o). This rare tumour causes excessive production of adrenaline and noradrenaline.
Symptoms include:
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Excess secretion of insulin causes hypoglycaemia (low blood sugar), leading to shakiness, confusion, and potential loss of consciousness.
Lack of insulin secretion or resistance to insulin prevents proper metabolism of sugar, starch, and fat in cells.
In diabetes mellitus, insulin insufficiency or ineffectiveness prevents sugar from leaving the blood (hyperglycaemia occurs) and entering body cells, where it is normally used to produce energy.
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Also called insulin-dependent diabetes mellitus (IDDM), Type I diabetes typically has onset in childhood and involves destruction of the beta islet cells of the pancreas with complete deficiency of insulin in the body.
Patients are usually thin and younger, with sudden onset of symptoms including excessive thirst, frequent urination, and unexplained weight loss.
Patients require frequent injections of insulin to maintain normal blood glucose levels. Careful monitoring and lifestyle management are essential.
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Also called non-insulin-dependent diabetes mellitus (NIDDM), Type II is a separate disease from Type I with a different inheritance pattern. Patients are usually older, and obesity is very common.
The islet cells are not destroyed. There is a relative deficiency of insulin secretion with resistance by target tissues to insulin action.
Treatment includes diet, weight reduction, exercise, and if necessary, insulin or oral hypoglycaemic agents.
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Fats are improperly burnt, leading to accumulation of ketones in the body. This dangerous condition requires immediate medical attention.
Occurs when blood sugar concentration gets too high or the patient receives insufficient insulin. Can be life-threatening without prompt treatment.
Can occur when too much insulin is taken by the patient, causing dangerously low blood sugar levels requiring immediate glucose administration.
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Long-term complications occur over many years after a patient develops diabetes. These chronic conditions result from prolonged exposure to elevated blood glucose levels.
Destruction of blood vessels in the retina causes visual loss and blindness. Regular eye examinations are crucial for early detection.
Destruction of the kidneys causes renal insufficiency, often requiring haemodialysis or renal transplantation.
Destruction of blood vessels leads to cardiovascular disease, increasing risk of heart attack and stroke.
Nerve destruction causes pain or loss of sensation, most commonly in the extremities, affecting quality of life.
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Congenital hyposecretion of growth hormone causes hypopituitary dwarfism, resulting in proportionate short stature.
Appropriate growth hormone levels during childhood and adolescence result in normal height and development.
Hyperfunctioning of the pituitary gland before puberty leads to abnormal overgrowth of the body, resulting in excessive height.
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Enlargement of the extremities (acro/o means extremities) caused by hypersecretion of growth hormone from the anterior pituitary after puberty.
Patients develop enlarged hands, feet, and facial features including prominent jaw, enlarged nose, and thickened facial features. Internal organs may also enlarge.
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All pituitary hormones are deficient, resulting in multiple endocrine deficiencies affecting growth, metabolism, reproduction, and stress response. Requires comprehensive hormone replacement therapy.
Syndrome of inappropriate ADH involves excessive secretion of antidiuretic hormone, causing water retention, diluted blood sodium, and potential neurological complications.
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Insufficient secretion of antidiuretic hormone (vasopressin) causes kidney tubules to fail to reabsorb needed water and salts.
Polyuria (excessive urination) and polydipsia (excessive thirst) are hallmark symptoms. Insipidus means tasteless, reflecting dilute urine.
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Accurate diagnosis of endocrine disorders requires comprehensive laboratory testing. These tests measure hormone levels and metabolic markers to assess gland function.
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These tests measure hormones and other substances (electrolytes and glucose) in blood and urine as indicators of endocrine function.
Measures glucose levels in fasting blood sample and in specimens taken 30 minutes, 1 hour, 2 hours, and 3 hours after ingesting 100 gm of glucose. Delayed return to normal indicates diabetes mellitus.
Measures hormone levels in plasma based on antibodies' ability to bind specifically to radioactively labelled and non-radioactively labelled hormone molecules.
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Measure levels of T4, T3, and TSH in the bloodstream to assess thyroid gland function and diagnose hyper- or hypothyroidism.
Measures the extent of eyeball protrusion as evidence in Graves' disease, an autoimmune form of hyperthyroidism.
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A radioactive compound is administered and localises in the thyroid gland. The gland is then visualised with a scanner device to detect tumours or nodules.
Radioactive iodine is administered orally, and its uptake into the thyroid gland is measured as evidence of thyroid function and metabolic activity.

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The Endocrine System