Physio: Regulation of Feeding Flashcards
2 hypothalamic nuclei involved in stimulating appetite and feeding.
Lateral and Medial Pre-optic Nuclei
Hypothalamic nucleus involved in satiety (inhibition of appetite and feeding).
Ventromedial Nucleus
What will a lesion in the amygdala and prefrontal cortex cause in regards to feeding regulation?
Hyperphagia
Name 4 chemical mediators that limit food intake in the short term.
- cholecystokinin (CCK)
- Peptide Tyrosine Tyrosine (PYY)
- Oral Receptors (located in mouth to tell brain we are eating)
- GLP-1
Name 2 long term chemical mediators that inhibit feeding.
- Leptin
2. Insulin
Chemical mediator that is released when the stomach is empty to stimulate feeding.
Ghrelin (pronounced: “grlnrnnrn”)
Neurons in the arcuate nucleus of the hypothalamus that is stimulated by Ghrelin and release NT into the paraventricular nucleus to increase food intake, decrease energy expenditure and increase parasympathetics.
Class 1 neurons: NPY
–> releases neuropeptide Y
Neurons in the arcuate nucleus of the hypothalamus that is stimulated by leptin, insulin and CCK and release NT into the lateral thalamic area to decrease food intake, increase energy expenditure, and increase sympathetics.
Class 2 neurons: POMC
–> releases alpha-MSH
What does the arcutate nucleus of the hypothalamus project out to the brain stem and spinal cord during feeding?
Sends signals to regulate the ANS to increase or decrease GI motility.
Explain the theory on how glucose regulates feeding long term.
Glucose is thought to increase firing in the paraventricular and ventromedial nuclei resulting in satiety.
It is also thought to decrease firing in the lateral areas of the hypothalamus which also leads to satiety.
Where does leptin come from and how does it decrease feeding?
Leptin comes from growing white adipose tissue.
It stimulates POMC and inhibits NPY centers and also increases cortiosl release which increase energy expenditure.
Anorexigenic drugs that lead to loss of appetite similar to the action of the POMC neurons.
Cocaine and Amphetamines - regulated transcript
CART
Receptor that can become mutated and lead to obesity, first observed in mice.
MCR4
-mice never think they are full