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Endocrinology Hangman

 
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Question Answer
endocrine glands  anterior pituitary, posterior pituitary, thyroid, parathyroid pancreas, adrenal cortex, adrenal medulla, ovaries, testes  
receptor  integral membrane protein that receives hormones  
target cell has how many receptors for a particular hormone?  2000-100,000  
down-regulation  when a hormone is present in excess the number of target cell receptors may decrease  
steroids  lipids that are derived from cholesterol. These are lipid soluble and will thus cross the plasma membrane and enter cells rapidly. Estrogens, progesterone, testosterone, aldosterone, cortisol  
biogenic amines  synthesized by modifying amino acids; T3 and T4, epinephrine, histamine, serotonin  
peptides and proteins  these hormones consist of chains of 3 to 200 amino acids. Oxytocin, ADH, Insulin, parathyroid hormone, calcitonin, CCK and gastrin  
how are most hormones transported in the blood?  carrier proteins  
master gland  anterior pituitary, now known to be controlled by the hypothalamus. has structure of an endocrine gland  
seven hormones of anterior pituitary  growth hormone GH, Adrenocorticotripic hormone ACTH, Thyroid stimulating hormone TSH, prolactin PRL, follicle stimulating hormone FSH, luteinizing hormone LH, melanocyte stimulating hormone MSH  
two hormones of posterior pituitary  antidiuretic hormone ADH, oxytocin  
the hypothalamus makes hormones for which pituitary  posterior  
the hypothalamus transports hormones down the axons of the neurosecretory cells for which pituitary  posterior  
which pituitary is controlled by substances made in the hypothalamus  anterior  
releasing or inhibitory hormones  hypothalamic substances which regulate the anterior pituitary; CRH stimulates ACTH; TRH stimulates TSH and a little prolactin; GnRH or LHRH stimulates FSH and LH; GIH or somatostatin inhibits GH  
Growth Hormone  GH or somatotropin; stimulates the uptake of amino acids into cells; stims growth of long bones and soft tissues; closure of epiphyseal cartilage stops growth of long bones-puberty (sex hormones)  
pituitary adenoma causes  acromegaly and gigantism  
gigantism & acromegaly  gigantism-excess GH before puberty; acromegaly-excess GH in adults  
symptoms of acromegaly/gigantism  overgrowth of bone, particularly of the skull and mandible; nose thickened and puffy, large ears, large tongue, large hands, increased sweating, fatigue, and weight gain  
Pituitary Dwarfism  lack of GH or GRH before puberty; may also be caused by hypothalamic-pituitary tumor; symptoms-small body, normal proportions; mild obesity w/ lack of appetite  
How to diagnose pituitary dwarfism  inadequate rise in serum GH after provocative stimulus such as Arginine infusion, oral levodopa, or clonidine  
Prolactin  stimulates the production of milk; promotes breast development in pregnancy  
Thyroid stimulating hormone- TSH  promotes and maintains growth and development of the thyroid gland and stimulates it to secrete thyroxine (T4) and triidothyronine (T3)  
Follicle Stimulating Hormone FSH  stimulates growth and develpment of the follicle to maturity, stims the follicle to secrete estrogens, stimulates testicular growth, enhances production of androgen-binding protein in the Sertoli cells (this increases the conentratino of testosterone near  
Luteinizing hormone LH  acts with FSH in the development of the follicle, promotes ovulation, responsible for the formation of the corpus luteum, stims corpus luteum to produce estrogen and progesterone, stims production of testosterone by the interstitial cells in males  
Adrenocorticotropin ACTH or corticotropin  Promotes and maintains normal growth and development of the adrenal cortex and stims the secretion of the glucocorticoids (cortisol); also affects the secretion of the androgens and the mineralcorticoids (aldosterone). ACTH is a polypeptide that is 39 a  
osteoblast activity  stimulated by GH  
epiphyseal cartilage  stimulates by GH; makes space for bone formation  
somatomedins  GH exerts growth-promoting effects indirectly by stimulating somatomedins; somatomedin IGF is an insulin-like growth factor  
GH does not act directly on its target cells to bring about  cell division, enhanced protein sythesis, or bone growth  
where is IGF-I made  liver mostly  
production of IGF-I is controlled by  nutritional status, age, and tissue specific factors  
what closes the epiphyseal plate?  sex hormones among other things  
hormones of the posterior pituitary  oxytocin and ADH (vasopressin)  
where are posterior pituitary hormones synthesized  in the hypothalamus and then transported intracellularly to the posterior pituitary from which they are released  
oxytocin functions  stimulate milk secretion and strong uterine contractions  
milk secretion physiology  oxytocin causes contraction of myoepithelial cells surrounding mammary alveoli (women not secreting enough milk are given an oxytocin nasal spray)  
uterine contraction physiology  oxytocin alters transmembrane ionic currents in myometrial smooth muscle cells to produce sustained uterine contractions. Sensitivity to oxytocin of uterine muscle increases during pregnancy.  
diabetes insipidus  lack of ADH (often due to damage to the pituitary or the hypothalamus. loss of 75% of ADH secretory neurons is necessary before polyuria is evident)  
Alcohol's effect on ADH  decrease release of  
Narcotics effect on ADH  increase release of  
symptoms of lack of ADH  polyuria, polydipsia, dehydration, fever, dry tongue, delirium  
where are catecholamine hormones secreted  adrenal medulla; these are epinephrine and norepinephrine (these supplement the action of the sympathetic nervous system)  
what does the adrenal cortex secrete in general  corticosteroids  
chromaffin cells do what  secrete catecholamines in the adrenal medulla  
corticosteroid hormones of the adrenal cortex  mineralocorticoids, glucocorticoids, and gonadocorticoids  
three zones of adrenal cortex  zona glomerulosa, zona fasciculata, zona reticularis  
other name for mineralcorticoids  aldosterone  
other name for glucocorticoids  cortisol (hydrocortisone)  
other name for gonadocorticoids  sex hormones  
action of mineralcorticoids (aldosterone)  regulate the concentration of extracellular electrolytes, especially sodium and potassium, water balance  
regulation of mineralcorticoids (aldosterone)  renin-angiotensin system (angiotensin II)  
action of glucocorticoids (cortisol)  influence the metabolism of carbohydrates, proteins, and fats; promote vasoconstriction; anti-inflammatory; decrease antibody production  
regulation of glucocorticoids (cortisol)  ACTH from the adenohypophysis of the pituitary gland in response to stress  
action of gonadocorticoids (sex hormones)  supplement the sex hormones from the gonads  
addison's disease  inadequte secretion of glucocorticoids and mineralcorticoids which results in hypoglycemia, na+ and K+ impalance, dehydration, hypotension, weight loss, and general weakness  
cushing syndrome  hypersecretion of corticosteroids generally caused by a tumor of the adrenal cortex or by oversecretion of ACTH by the pituitary. Symptoms are puffy face, hyperglycemia, hypertension, decreased antibodies, and muscle weakness  
adrenogenital syndrome  alteration of enzymes required to produce mineralcorticoids and glucocorticoids, results in an increase in the production of sex hormones. symptoms: masculinization of females, facial and body hair, acne, paleness, increased muscularity, atrophy of breas  
what does the thyroid gland produce  thyroxine (T4) and triiodothyronine (T3), and calcitonin  
physical structure of thyroid  two laterla lobes interconnected by an isthmus (neck area)  
histological structure of thyroid  spherical sacs called thyroid follicles. Humans have about one million follicles. Each follicle is lined with principal cells which synthesize T3 and T4 and contain a protein-rich fluid called colloid. Between the follicles are perifollicular cells whi  
action of triiodothyronine and thyroxine  regulate metabolism; increase rate of protein synthesis; increase rate of energy release from carbs; regulate growth; stimulate maturity of nervous system; regulate body temp  
regulation of T3 and T4  hypothalamus and release of TSH from adenohypophysis of the pituitary gland  
Action of Calcitonin (thyrocalcitonin)  lowers blood calcium by inhibiting the release of calcium from bone tissue  
regulation of calcitonin  calcium levels in the blood  
cretinism  insufficient secretion of T4 and T3 in infants and children. Stunted growth, thickened facial features, large protruding tongue, abnormal bone growth, mental retardation, decreased metabolic rate, general lethargy. Treat with T3 and T4  
myxedema  insufficient secretion of T4 and T3 in adults. Weight gain, slow pulse, dry brittle hair, decreased basal metabolic rate, lack of energy, sensation of coldness, diminished perspiration, weakness. treat with T3 and T4  
goiter  a pathological enlargment of the thyroid gland due to insufficient iodine intake. Take iodine.  
graves' disease (thyroxicosis)  excessive secretion of T4 and T3. Loss of weight, rapid pulse, warm, moist skin, increased appetite, increased basal metabolic rate, tremor, goiter, exophthalmos (bulging eyes); muscular weakness. Treatment: surgical removal of a portion of thyroid gland,  
what percent of calcium is in crystalline form  99%  
lf the non crystalline calcium, what percent is in cells and what percent is in extracellular fluid  of 1%, .9% is inside the cells and .01% is in the extracellular fluid  
parafollicular or C cells  produce calcitonin in the thyroid gland; lower the blood calcium and phosphates by: 1. decreasing bone resorption by inhibiting the activity of osteoclasts 2. stimulating urinary excretion of calcium and phosphate by inhibiting their reabsorption in the k  
parathyroid glands  four small glands attached to the posterior surface of the thyroid glands. Principal or chief cells in the parathyroid glands secrete parathyroid hormone (PTH) or parathormone.  
what happens in the absence of PTH  death in a few days from hypocalcemia  
functions of PTH (parthormone)  stimulates the activity of osteoclasts to reabsorb bone (remove Ca++ from bones), stims the kidneys to reabsorb ca++ from the filtrate, promotes the formation of 1,25 dihydroxyvitamin D3  
1, 25 dihydroxyvitamin D3 function  helps raise the plasma calcium and phosphate levels by stimulating 1. intestinal absorption of Ca++ and Phosphate 2. reabsorption of Ca++ from bones 3. renal absorption of ca++ and phosphate so that less is excreted in the urine  
hyperparathyroidism  usually caused by a tumor in one of the parathyroid glands. Is characterized by hypercalcemia- muscle weakness, neurological disorders, decreased alertness, poor memory  
hypoparathyroidism  used to be caused by removal of parathyroids during thyroid surgury. Could lead to death. Other symptoms- hypocalcemia, increased neuromuscular excitability  
endocrine gland in the pancreas  islets of langerhans (clusters of cells); alpha cells secrete glucogon, beta cells secrete insulin  
Glucogon  elevates blood glucose by stimulating glycogenolysis in the liver, this helps the body maintain sufficient blood glucose levels during fasting and starvation  
Insulin  promotes the cells to take up glucose; some tissue do not require insulin for glucose uptake (brain, kidney, intestinal, and red blood cells); stimulates glycolysis; lowers blood glucose levels  
diabetes mellitus  insulin deficiency  
genetic factors in diabetes mellitus  predisposition of diabetes is inherited, the genetic factors are complex (on chromosome 6), over 20% of the relatives of diabetic patients have abnormal glucose tolerance curves  
other possible causes (not hereditary) of diabetes mellitus  environmental chemicals and drugs, infectious agents (mumps virus, rubella, pancreatitis), autoimmune events (antibodies damage the beta cells, anti-insulin receptor antibodies  
two types of diabetes mellitus  type I-insulin-dependent (juvenile onset), type II-noninsulin-dependent (maturity onset)  
type I insulin-dependent (juvenile onset) diabetes mellitus  requires insulin injections (there is no insulin being secreted), often severe and complicated by ketoacidosis, onset usualy in youth but may occur at any age  
type II noninsulin-dependent (maturity onset) diabetes mellitus  90-95% of diabetes, injections not required, patient usually obese, may use oral hypoglycemic drugs to stimulate insulin release from beta cells, insulin resistance is a factor for 60-80% of patients with type II diabetes  
how to diagnose diabetes mellitus  oral glucose tolerance test; oral administration of 1.75 g/Kg of glucose after at least 3 days on a 300 g carbohydrate diet  
symptoms of diabetes mellitus  glycosuria, polyuria (glucose acts as an osmotic diuretic), polydipsia, hyperglycemia, weakness, loss of weight, acetone breath (ketoacidosis), acetone in the urine  
increased risk of infection due to diabetes mellitus  factors that increase infection 1. pathogens proliferate rapidly b/c of excess glucose 2. hypoxia-glycosylated hemoglobin in RBC's impedes the release of O2 3. decreased blood flow to infected area b/c of vascular damage 4. white blood cells have impaired  
insulin excess results in  insulin shock (hyperinsulinism)  
gestational diabetes mellitus (GDM)  refers to diabetes that occurs during pregnancy (in 1 to 14% of pregnancies) and then disappears following delivery  
GLUT4  transporter that moves glucose across the membrane