Endocrine Flashcards

1
Q

Hypothalamus

A

Part of diencephalon that connects to pituitary gland through the infundibular or pituitary stalk. Regulates ANS (body temp, appetite, sweating, thirst, sexual behavior, rage, fear, blood pressure, sleep) and other endocrine glands through impact on pituitary gland.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Pituitary gland

A

Releases hormones that regulate several other endocrine glands. Influenced by seasonal changes or emotional stress. Secretes endorphins and reduces sensitivity to pain. Controls ovulation and production of sex hormones.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Thyroid gland

A

Controls rate at which cells burn the fuel from food. Increase in thyroid hormones will increase the rate of chemical reactions within body.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Parathyroid glands

A

Maintains normal blood levels of calcium and phosphate. Parathyroid hormone increases reabsorption of calcium and phosphate from bones to blood. Clotting, neuromuscular excitability, and cell membrane permeability are dependent on normal calcium levels.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Adrenal glands

A

Located on top of each kidney. Adrenal cortex produces corticosteroids that regulate water and sodium balance, response to stress, immune system, sexual development and function, and metabolism. Adrenal medulla produces epinepherine that increases heart rate and blood pressure with increased stress.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Pancreas

A

In upper left quadrant of abdomen. Produces glucagon and insulin. Ensure consistent level of glucose in blood stream and maintain stores of energy in body.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Ovaries

A

Secretes estrogen and progesterone.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Testes

A

Secretes androgens (testosterone)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Steroid hormones

A

E.g. prostaglandins
Do not circulate in blood and only exert effects where produced.
Related to inflammation, pain mechanisms, vasodilation, vasoconstriction, nutrient metabolism, and blood clotting.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Amine hormones

A

E.g. catecholamines (epinephrine, norepinephrine, and dopamine).
Produced in adrenal medulla. Sympathetic nervous system stimulation releases the catecholamines into the blood stream, playing a role in flight or fight response. Increases cardiac contraction, constricts blood vessels, activates glycogen breakdown, blocks insulin secretion, increases metabolic rate, and dilates airways within lungs.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Peptide hormones

A

E.g. insulin

Insulin released when there is elevation in the level of blood glucose, increasing uptake of glucose for metabolism.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Hypopituitarism

A

Rare disorders with symptoms that may include dwarfism, delayed growth and puberty, sexual and reproductive disorders, and diabetes insipidus.
Orthostatic hypotension. Bilateral hemianopsia.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Hyperpituitarism

A

Symptoms include gigantism or acromegaly, galactorrhea (abnormal lactation in males or females), amenorrhea, infertility, and impotence.
Bilateral carpal tunnel syndrome, arthritis, osteophyte formation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Addison’s Disease

A

Hypofunction of adrenal cortex.
Etiology: Decreased production of cortisol and aldosterone.
Signs/symptoms: Hypotension, weakness, anorexia, weight loss, altered pigmentation, if untreated shock and death.
Treatment: Corticosteroids and mineralcorticoids

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Cushing’s Syndrome

A

Hyperfunction of adrenal gland.
Etiology: Excessive cortisol production.
Sings/symptoms: Hyperglycemia, growth failure, truncal obesity, purple abdominal striae, moon shaped face, buffalo hump, weakness, acne, hypertension, depression, poor concentration, and memory loss.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Hypothyroidism

A

Slows metabolic processes. Symptoms include fatigue, weakness, decreased HR, weight gain, constipation, delayed puberty, and retarded growth/development.

17
Q

Hyperthyroidism

A

Symptoms include increase in nervousness, excessive sweating, weight loss, increase in BP, exophthalmos, myopathy, chronic periarthritis, and enlarged thyroid gland.

18
Q

Grave’s disease

A

Most specific cause of hyperthyroidism. Most common in women over age 20.
Etiology: Autoimmune disease in which antibodies produced by immune system overstimulate thyroid gland.
Signs/symptoms: enlarged thyroid gland, heat intolerance, nervousness, weight loss, tremor, and palpitations.
Treatment: Pharmacological intervention and/or removal of thyroid glad using radiation or surgery.

19
Q

Hypoparathyroidism

A

Symptoms include hypocalcemia, neurological symptoms like seizures, cognitive defects, short stature, tetany, muscle pain, and cramps.
Treatment includes rapid elevation in serum calcium levels through IV. Long term treatment includes pharmacological management and dietary modifications.

20
Q

Hyperparathyroidism

A

Symptoms include renal stones and kidney damage, depression, memory loss, muscle wasting, bone deformity, and myopathy.
Acute treatment includes pharmacological intervention that lowers serum calcium using diuretics or antiresorptive meds. Surgical intervention required to remove disease parathyroid gland.

21
Q

Type I Diabetes Mellitus

A

Pancreas fails to produce enough or any insulin. Normally diagnosed in childhood but can occur at any age. Known as insulin-dependent or juvenile diabetes.
Etiology: Genetic predisposition in combination with viral or environmental trigger may cause immune response that damages pancreas.
Signs/symptoms: Rapid onset of symptoms, polyphagia, weight loss, ketoacidosis, polyuria, polydipsia, blurred vision, dehydration, and fatigue.
Treatment: Insulin injections, exercise, and nutritional management.

22
Q

Type II Diabetes Mellitus

A

Usually occurs over the age of 45 but can occur in children. Usually can produce some insulin but resistant to insulin receptor sites.
Etiology: Hyperglycemia, obesity.
Signs/symptoms: Same as type 1 DM but ketoacidosis does not occur. Gradual onset.
Treatment: Blood glucose control through diet, exercise, oral medication, or insulin injections.

23
Q

Gestational Diabetes

A

Increase in insulin resistance during pregnancy, usually in last trimester. Believed that hormones that assist the fetus to grow may lead to insulin resistance. Usually return to normal glucose metabolism after pregnancy. Babies at risk for increase glucose levels and increased size. Baby may have breathing difficulties, jaundice, and hypoglycemia after birth.

24
Q

Diabetes Testing

A

Fasting plasma glucose: > 125 mg/dL is positive
Oral glucose tolerance test: blood glucose test 2 hours after sugary drink. > 200 mg/dL is positive
A1c testing: based on attachment of glucose to hemoglobin over past 2-3 months. > 6.5% is positive

25
Q

Male hypogonadism

A

Deficiency of testosterone due to failure of testes to respond to FSH and LH. Most common cause is Klinefelter’s syndrome. Secondary hypogonadism occurs when there is a failure of the hypothalamus or pituitary to produce hormones that stimulate testosterone production.
If present before puberty, symptoms include decrease body hair, underdeveloped skeletal muscles, long arms/legs secondary to delay in closure of epiphyseal growth plates.
If onset in adulthood, symptoms include decrease libido, erectile dysfunction, infertility, decreased cognitive skills, mood changes, and sleep disturbances.
Treatment includes hormone replacement.

26
Q

Female hypogonadism

A

Primary hypogonadism results if gonad does not produce sufficient sex steroid to suppress secretion of LH and FSH at normal levels. Most common primary cause is Turner syndrome. Secondary occurs if there is failure of hypothalamus or pituitary to produce hormones that stimulate production of estrogen.
If onset prior to puberty, symptoms will include gonadal dysgenesis, short stature, failure to progress through puberty, amenorrhea, premature gonadal failure.
If onset after puberty, amenorrhea occurs.
Treatment includes hormone replacement.

27
Q

Bone Mineral Regulating Agents

A

Action: Enhance and maximize bone mass and prevent bone loss/rate of reabsorption. Typical agents include estrogen, calcium and vitamin D, biphosphonates, calcitonin, and anabolic agents.
Indications: Paget’s disease, osteoporosis, hyperparathyroidism, rickets, hypoparathyroidism, and osteomalacia
Side effects: GI distress, dyspepsia, dysphagia, anorexia, bone pain, cardiac arrhythmias

28
Q

Hormone Replacement Agents

A

Action: Restore normal endocrine function
Indications: decrease in endogenous hormone secretion
Side effects: Vary by hormone replacement type

29
Q

Hyperfunction Agents

A

Action: Manage hyperactive endocrine function to inhibit hormone function.
Indications: Hyperactive or excessive endocrine function, excessive hormone levels.
Side effects: Vary