Module 3: Hypothalamus & Monogenic Obesity Flashcards
Where is leptin synthesized?
Subcutaneous adipose tissue
Where is leptin regulated
Regulated at level of gene expression and protein secretion
Signals associated with positive energy balance and how do they affect leptin express.
Insulin, glucocorticoids (cortisol), glucose, branched chain A.A
= increase leptin expression
Signals associated with “starvation” and how do they affect leptin express.
Catecholamines (epinephrine), tumor necrosis factor (TNF-a)
=decrease leptin expression
Association between leptin and body weight
Obesity associated with a leptin RESISTANCE
-blood leptin levels strongly/positively correlated with body fat
Leptin loss-of-function mutation in humans symptoms (6)
-little to no serum leptin
-severe early onset obesity
-hyperphagic (increased drive to eat)
-delayed puberty
-thyroid dysfunction
-50% body fat
SEEN IN OB/OB MOUSE
Leptin mutation type of disorder
Autosomal RECESSIVE disorder
Examples of loss-of-function mutations (leptin) that have been identified
1.frameshift mutation
(leptin stuck in adipose tissue, unsecreted)
2.missense mutation
(changes conformation of leptin protein, prevents interaction w receptor)
Affects of leptin therapy in humans (6)
-BMI and % body fat drop
-Blood triglyceride level normalized
-Increased HDL-C
-normalized insulin
-improved thyroid function
-improved immunity
POMC/CART neuron
-activated by leptin after binding to leptin receptor
-inhibit food intake, increase energy expenditure
NPY/AgRP neuron
-inhibited by leptin after binding to leptin receptor
-stimulate food intake, decrease energy expenditure
Leptin receptor (LEPR) mutation characteristics
-severe early onset obesity, continue through adolescence
-no developmental delays
-normal leptin levels
How many isoforms of LEPR exist and which is expressed in hypothalmic neurons
-6 isoforms
-LEPRb –> has intracellular domains to activate JAK/SKAT signal pathway (necessary for appetite regulation)
Leptin pathway
-leptin binds to LEPRb
-LEPRb activates Jak2 kinase, allows for STAT3 to be activated
–> activates POMC
–> inhibits NPY/AgRP
POMC mutation characteristics
(5)
-severe early onset obesity
-hyperphagia (excessive eating)
-normal birth weight, rapid gain
-RED HAIR
-cant produce ACTH (produces cortisol) = adrenal insufficiency = hypocortisolism