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81 Cards in this Set

  • Front
  • Back
Local Hormones
secreted and act on same organ
-Acetyl Choline -m contraction
-CCK - GB contraction
-nervous impulses +synaptic transmission
General Hormones
epi/NE
TH - works on metabolism, pancreas, testes, ovaries
GH
Endocrine Organs
Pituitary Gland
Pineal Gland
Thyroid
Parathyroid
Thymus
Adrenal
Pancreas
Ovary/testes
*placenta is endocrine organ when present
Pituitary gland
master gland
affects thyroid, para, adrenal, panc, testes, ovaries
next to optic chiasm
*can cause too tall/small, hair pattern prob, ha, visual prob
Pineal Gland
makes serotonin derivative melatonin that affects wake/sleep patterns and seasonal function
reacts to light...works on circadian rhythm
Thyroid Gland
controls how quickly body uses energy, makes proteins, controls sensitivity to hormones

makes: CALCITONIN, T3, T4
Adrenal Cortex zones
Zona glomerulosa --> aldosterone, mineralcorticoids
*conn syndrome
zona fasiculata --> cortisol, glucocorticoids
*cushing syndrome
zona reticularis --> androgens, sex hormones
When not eating what maintains glucose levels?
Glucagon
Pancreas
Endocrine - insulin, glucagon, somatostatin

Exocrine - pancreatic juice, digestive enz
steroid hormones
cortisol + aldosterone
Tyrosine derivatives are?
thyroxine
triiodothyronine
EPI/NE
Users of 2nd messenger system?
ACTH, TSH, LH, FSH, ADH, PTH, Gulcagon, catecholamines, secretin

*ACTH binds TSH --> activates cAMP --> amplify, enzyme synthesis, enhance reaction, build protein --> feedback shuts it down

*the other 2nd messenger - calmodulin
Stimuli for release of GH
starvation
protein deficiency
hypoglycemia
low FFA in blood
exercise
excitement/ trauma
deep sleep
normals
glucose = 100
NA = 125-135
Carbs = 200
TSH = .4-4
prolactin <15
GH = 1
IGF1 <300
Na = 140
Hypoglycemia due to
high insulin
high oral hypoglycemic
surgery
pentamidine, aspirin, haloperidol
age extremes
insulinoma
renal failure
adrenal insufficiency
alcohol, sepsis, heart failure
What is the driver for evaluating endocrine problems?
LAB studies

*except Empty Sella syndrome - use MRI
Obesity Dx
BMI >29
asians > 25

*obesity does accelerate atherosclerosis (more upper body obesity over lower)
2nd leading PREVENTABLE cause of death in US
obesity
Hypothalamic Hormones
Anterior Pit Hormones
Posterior Pit hormones
hypo: TRH, CRH, GHRH, somatostatin, GnRH, DA

Ant: TSH, ACTH, GH, FSH, LH, Prolactin

Post: oxytocin, ADH
Secreted at midnight? So will see in morning?
GH, ACTH

*all others are opposites
GH target
IGF1 (insulin growth factor 1)
-no diurnal variation
- half life is longer
-all around better to use then GH because is more representative of pt
Acromegaly
= pituitary tumor that makes GH
DX: IGF1 + GH
symp: big hand, feet, tongu, jaw, CHF, HTN, HA, hypersomnolence, hyperhydrosis, peripheral non pitting edema, chondroma, hyperpigment
*arthritis = most disabling syndrome
Tx: surgery - stereoscopic pituitary hypophsectomy
ACTH activator and inhibitor
activator = CRH
inhibitor = Glucocorticoids
Main Glucocorticoid
Properties of Glucocorticoid
Cortisol
Benificial: anti-inflam
Bad: enhance gluconeogenesis, antagonize glucose, cause hyperglycemia, bread down collagen
Adrenal Function Tests
1. Rapid ACTH stim test - dec. cortisol to try to stimulate it
2. dexamethasone test
Nelson Syndrome
due to: removal of adrenal from cushing
*get too much ACTH production
tx: surgery
Delphian LN
LN that contains metastatic thyroid cancer
Thyroglossal duct cyst
looks like nodule but it is a cyst on thyroid
Pemberton's sign
sizeable TG that can float into the sterna notch on hyperextension of the neck and cause asphyxiation
Riedel's struma
*thyroiditis
= rock hard thyroid gland - fibrous tissue in TG makes it firm due to long term inflammation
thyroprovic
primary defect in thyroid gland
trophoprivic
secondary defect in thyroid gland like:
sheehand syndrome, infiltrated disorders of pit or hypothal
Kocher-debre semelaingne syndrome
*Hashimoto's
in newborn m are atrophied
Hoffman's syndrome
*Hashimoto's disease
weakness, not hypertrophy of m...but deposition of mucopollysaccharide complex
DKA
Type 1 DM - emergency
triad = Hyperglycemia + ketosis + acidosis
abrupt, NV, dehydration, eyes sunken, mucous membranes dry, ab pain, KUSSMAULS BREATHING,
the acidosis is what kills + dehydration
dx: glucose >250
tx: need LOTS of insulin
Hyperosmolar Nonketotic Coma (HHNKC)
type 2 DM - emergency
VERY high glucose levels - thi sis the driver
takes a long time
tx: needs less insulin
Hypoglycemia
due to: autonomic neuropathy, DM1 on beta blcokers, not eating, too much exercise, ALCOHOL
symp:
1. adrenergic symptoms
2. neuroglycopenic symptoms
Reactive Hypoglycemia
= insulin and glucose not flowing together
- after eat carbs
Alimentary Hypoglycemia:
bowel surgery - so food absorbed too fast
Functional Hypoglycmemia:
delay of insulin by hours
Insulin Resistance contributes to?
HTN, obesity, hyperinsulin, DM, hyperTG, low HDL, high small dense LDL

all lead to atherosclerosis
Framingham risk score
=way to measure CV risk in 10 years
highest risk = 20%
Metabolic Syndrome
= looks at how at risk you are for CVS problem
5 parameters:
1. ab obesity: M >35 in F > 40 in
2. TG > 150
3. HDL: M< 40 F<50
4. BP: >130/85
5. Fasting Glucose >110
3 factors in DM/insulin resistance
1. high TG
2. low HDL
3. small dense LDL (subclass B)

all inc atherosclerosis --> inc. CVD
ATP Goals
1. highest risk LDL < 70
hear prob
2. high risk LDL <100
DM
3. moderate LDL 100-129
4. Low LDL <130
Non HDL cholesterol
= total cholesterol - HDL = apo B containing proteins

goal: LDL + 30
Tx of LDL
1. resin- dec. glucose
2. Nicotinic acid - dec. TG, inc. HDL
3. fibrates - dec. TG, inc. HDL
4. statin - dec. CHOL, dec LDL

* always tx LDL first...unless TG >500
CVS Markers
1. hs-CRP
2. Lpa
Main cause secondary hyperparathyroidism
renal insufficiency
Osteoporosis score
greater than - 2.5
Raloxifen
dec hip fractures
doesnt affect breast
Nasal calcitonin
dec. vertebral fractures only
bisphosphonates
repair osteoclastic function
dec. vertebral, nonvertebral, and hip

adr: dry socket
PTH
dec. osteoporosis
inc. bone resorption
denosumab
monoclonal ab
stops RANKL ligand binding

ADR: hypocalcemia
somatotroph makes
Prolactin + GH
papillary genes
MAP kinase - BRAF or NKT1
Follicular genes
PIC3
Medullary genes
RET
Insulinitis
MHC class 2
pheochromocytoma
SDHB
parathyroid tumor
PTHrP
Important factors determining testosterone levels
1. chornic illness
2. meds
3. obesity
Klinefelter syndrome
XXY, Barr Body
infertile, dec. sperm, gynecomastia, mental prob, high FSH/LH
Kallman's syndrome
inability to smell odors
Most common cause impotence
Diabetes
Myotonic Dystrophy
= neuromuscular failures with primary gonadal failure
premature baldness, mental retardation, Auto Dom, lenticular opacities
Noonans syndrome
karyotype is normal but look like turner's

-webbed neck, low ears, shield like chest, ptosis, pulmonic stenosis, cubitus,
testosterone replacement therapy
1. pellets
2. patch
3. IM injection
4. Gel
5. Buccal
most common cause hyperthyroid in old
toxic multinodular goiter
LADA
Latent AI DM in aultes
develops in adulthood like 2 but has pattern of 1
Double Diabetes
have 1 and fave family member with 2
Type 1 and 1/2
have 2 and develop ab and become picture of 1
MODY
maturity onset diabetes of youth
obese
mild dm
impaired glucose tolerance
pts at risk for dm
have abnormal glucose levels but not enough for dm
lined to metabolic syndrome
Dx DM
HGA1C= >7%
Fasting Glucose >126
Postprandial glucose >200
Normal levels
fasting glucose <100
Postprandial <140
Insulin Resistance
reduced ability of sugar to go into insulin sensitive cells - skel m + liver

inflam cytokines
FFA
risk: age, med, obese, inactive, gene
type 1 vs. 2
1 - beta cell function dec due to auto ab
2 - acanthosis nigricans
no phase 1
target in glycemic control
HGA1C - because linked to complications
if red to <7% you dec risk of retinopathy, nephropathy, bneuropathy
Amylin
co secreted with Insulin
from islet
will dec glucagon
long acting insulin
glargine
detmir
give 1x day
steps to DM care
1. lifestyle
2. oral agents
3. insulin
4. inc. insulin