the study of bioligcal rhtyms is call chronbiology - i t si bruilogcal rthyms are regualtiflcuation in any lviivng process - there is the circadian rhty that is about 24 hours
the ultradian rhtyemp repeast more than ocnea. day which is sleep and pappetiete
infradian rhtyms rpease less thant onca. day
the circadian rhtym uses light dark cycles in order to use th retinosomething pathway to
in mamamls some retinaal ganglion cells make the re
in mamamls the reginaol ganglion clel makes the retiohypothalamic pathway and accires light from the eye to the SCN.
so light enteres the eye and ganglian cells will take the light through the rentionhypothaalmic pathways to send to the SCN which is in the hhyptholamsu
THe SCN is located in the hypothalamus above tht eoptic chiasm the SCN is in the hypthalaism above the opic chaism -
cutting the scn will stop circadian rthyms drink oand hormone rhtym
so the clock -
the protein clocl and cucle will bind together to make a dimer,
the clock and cycle will bind to the DNA the enahcne trancriptiono fth egenes per and cry.
clock and cycle will bind and then go into the neuclus and then bind to the dna to make cry and per. then cry and per will leave . and then they will bind together to form a compex that stop s the clock and cycle dimer slowing trnacirption of the per and cry genes and slow produciton of the per and cry genes. then per and cry will break down and release clock and cy and the cycel starts all over again this is a 24 ohuor cycle of protien formation and degration.
the retinal ganglion cells will teect light wiht a melaospin and their axons will go into the retinohyptohalmic tract and relase glutatmute into the neuons of the SCNthe gluatmate will incrase tracnription of per and synchronize the moelcular colcl
olkie so clock and cycle will bind go into the nucleus and bind to dna to make per and cry and then per and cry will be made and then they will bind and stop clock and cycle from going and then they drgade an the cycle starts all over again. But then there are gnaglian cells that detect light and send singals through the hyppothalamic pathway and then relase gluatamate into the SCN and then glitatme wil spead up per gene.
per is elevated when light is experience. SCN will als o synchroinze the rithyms of the liver and kidney
so sleep conserve erngy - muslc tnetion heart rate blood pressure and tempeateu and reat of repriiton are reduced. sa
slepp leads to growth hormones realesed during SWS
propersleep is for imune funciton and insomia is assocated ith risk of moralith
hormones growth hormones are released during slow wave sleep.
sleep during the inveral between learning and recall improve
leanring of perceptual skill sis improved by a perof of REM consoliadion of dlecative mamroy and complicated mootor skill is in SWS REM sleep is not abosluncety necessary for elarning
SLLLEEEEP STAGE -
stage 1 - smaller ampliteude waves - heart slows muscles relay eyes role
stage 2 - burst of sleep spindles sharp EEG
stage 3 - LArge ampliateu slwo waves
REM - small amplutudes high frequencey eyes dark rapidly under closed lids
stage 3 is the slow waves
narcolepsy - intense sleep attack lasting 5-30 minues anyttime of the day for severla times every 90 mins -
they don go through slow wave sleep befor erem and sho cataplex a sudden loss of muscl eto ne a n collpasing. 90% of htie rorexin neursons
alterness drugs for managin narcoplesy - modafinil
soltriom
okie whatever back to the fucking EATINGGG -
so the VMH and the LH
VMH is assocuated with satisfhying hunger this is assocaited with POMC
and LH is with increase pappteit and this is assocated with NPY
then there is leptin that will either increase POMC or decrease NPY
so leptin wil inccrease POMC which is satisfy hunger and decrease NPY
anyways this take place in arcurate nucleus
soo what happens is the the arcuate neruosn will active the brainstem the LH and paraventricular nuclue PVN. so high leptin levels will activate the brian stemp the LH and the PVN
acruate the BS LH and VMP will increase body temp decrease feaeding and increase metabolims so basically the POMPC
okie again so leptin comes from the adipose and will increase POMC decrease NPY neuron in the acurate which activates BS VPN and LH
ghrelin andd PYY acts on the NPY hunger neruons
Ghrelin sitmualtes PYY so it increases hunger
and PYY will decrease hunger
ghrelin is in the tummy and it increases hunger so therefore NPY
PYY is in the intestince and isnt hungry so it reduces hunger so it reduces NPY
insuline reduces appetite by acitvating POMC and NPY
so leptin and insuline will reduce hinger
Ghrelin will make hunder and PYY will reduce it
Ghrelin drops after eating
PYY 3-36 increases after eating
GLP -1 increases after eating
leptin comes from the adipose tissues
insulin from the pancrease
ghrelin from the stomcahe and glp and PYY from the intestine
reduce hunger - leptin , insuline, GLP CCK
Makes hunger - PYY, Ghrelin, Cannabinoids.
So CCK is released by the gut like ghrelin and instead it will reduce hunger with the vagus nerve to inhibit pattetide. I twill convey gastri distention infor
So CCK will actt on the vagus nerve to stop hunger.
So CCK is in the tummy and will send out signals to stop hunger to the vagus nerv
GLp will also stop hunger
stops hunger - GLP, CCK, leptin. insulin POMCP
makes hunger - cannacboids - ghrelin - PYY
orexin targets the mesolimbocortial dopami increases consumption of high palatable foods