Exam 2 Flashcards
Hormonal axis connections
Consists of a cascade of endocrine pathways that respond to specific stimuli involving the hypothalamus, anterior pituitary, and target organs/cells
Hormone half life
the time required for its concentration to decrease to half of its concentration - how long its cleared is inverse to how long its in the system
Afferent vs efferent
Related to nerves, lymph and blood vessels- afferent side takes things to, and efferent takes them away
endocrine signaling
A cell targets a distant cell through the bloodstream
Autocrine signaling
A cell targets itself (receptors on the same cell)
Paracrine signaling
A cell targets a nearby cell (adjacent cell)
Juxtacrine signaling
A ligand on a signaling cell binds to target cell receptors
Intracrine signaling
Signal is released within the cell and acts within the cell (doesn’t leave)
Hypothalamus
Especially controls homeostasis, main link of nervous and endocrine systems
Infundibulum
Stalk- portal vessels
Anterior pituitary
glandular tissue (from primitive gut tissue)
Posterior pituitary
Neural tissue, intermediate area
Anterior pituitary cell types
Acidophils, basophils, chromophobes
Acidophils
Pink with dark nuclei, protein hormones GH PRL
Basophils
Darker purple cytoplasm, glycoprotein hormones LH, FSH, ATCH, TSH
Chromophobes
Non secretory support cells
H&E stain
Hematoxylin and eosin
Lactotrophs make _ while somatotrophs make _
Prolactin, growth hormone
Oxytocin- cause neuroendocrine reflexes
Stimulate uterine contractions (receptors are low in uterus till parturition) and dilate cervix
Antidiuretic hormone
9 amino acids, from hypothalamus, stimulates water retention in the kidneys, regulates and balances water in blood
Pituitary endocrine disorders
Galactorrhea, acromegaly, cushings syndrome, gigantism, diabetes insipidus
Thyroid gland
Located in the neck where it wraps around the trachea- makes thyroid hormone. filled with colloid, follicles and iodine
Gene mutations can be either
Acquired (not hereditary) or inherited (hereditary)
Autosomal (inherited disease)
Dominant and recessive, Mutation found on chromosomes 1-22
X linked (inherited disease)
Dominant and recessive, mutation found on X chromosome
Autosomal dominant
Rare, affected person usually has only one copy of diseased gene, tend to strike adults- insufficient activity of normal gene product
Autosomal recesesive
Only apparent when two copies of the gene are present- parents with one copy are carries, higher occurrence in geographically culturally isolated populations- defects in enzymes
X- linked recessive
Expressed primarily in males, mothers and half of the sisters will be carriers
X- linked dominant
More common in females, if disease is lethal in males, then inheritance pattern changes
Chromosomal disorders
Generally involve more than one gene, may be detectable on karyotype, include translocations, deletions, and additions, can be detected prenatally
Galactorrhea
Abnormally initiated or prolonged lactation- caused by pituitary tumor- hyperprolactinemia
Acromegaly
Over production of growth hormone- hypersomatoropinsim
Cushings syndrome
Too much cortisol- pituitary produces too much ACTH
Diabetes insipidus
produce high volumes of dilute urine, excessive thirst, hyponatremia and hypernatremia (high and low blood sodium)
Central diabetes insipidus
lack ADH-injury, disease, autoimmune, genetic
Nephrogenic diabetes insipidus
ADH production ok but kidneys don’t respond- Some meds, urinary tract blockage, genetic
Dipsogenic diabetes insipidus
Problem with hypothalamus makes you thirsty (drink to much)-Injury, surgical damage, inflammation, tumor
Gestational diabetes insipidus
Placenta makes too much enzyme that breaks down ADH- rare, temporary during pregnancy, altered liver function, vasopressinase
Thyroid matrix
follicles create colloid which pools inside them and you need iodine to make this happen
hypothyroidism symptoms
Metabolism slows down, weight gain, tired/lethargic, cold, iron deficiency (autoimmune or genetic)
T4 and T3- thyroid hormones
Amine, Stimulate basal metabolic rate
Calcitonin (thyroid hormone)
Peptide, reduces blood Ca2+ levels, promotes deposition of calcium into bones, inhibits calcium reabsorption in the kidneys
Where are the parathyroid glands
Embedded in the posterior surface of the thyroid gland
How parathyroid hormone maintains blood calcium homeostasis
Increases blood calcium levels when they drop too low, and calcitonin (rom thyroid gland) decreases blood calcium levels when they become too high
Adrenal glands
Secrete epinephrine and norepinephrine, nerve synapses release hormone
Zona glomerulosa
Mineralcorticoids-,regulate mineral balance
Zona fasiculata
glucocorticoids- regulate glucose metabolism
Zona reticularis
Produces sex steroids
Receptor
Protein that binds to a ligand with high affinity and low capacity- must be saturable
target cells of a hormone
must express specific receptor for it
Hormone receptor interaction
Defined by equilibrium constant, the Kd or disassociation constant
Hormone binding proteins
Water soluble
Bound vs free hormone
Exist in equilibrium, only free can bind to receptors
Calcitonin
peptide, reduces blood Ca levels, made by parafollicular cells, stimulates osteoblasts, decreases Ca absorption from intestines and increases Ca loss from kidneys, inhibits osteoclasts
Thyroxine (T4) and triiodothyronine (T3)
Amine, stimulate basal metabolic rate, responsive to TSH levels
Thyroid hormones
T3, T4, and calcitonin
Parathyroid glands
Embedded in posterior of thyroid glands,, express calcium sensing receptor and mobilize intracellular calcium in response to CASR activation
Chief cells
main functional cells of the parathyroid glands, make and secrete PTH
PTH
Regulator of calcium, increases and decreases calcium levels by way of the kidneys and intestines, stimulates osteoclasts
Thyroid hormone function
Regulate basal metabolic rate, protein synthesis, childhood development, interact with repro hormones