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Physiology of Hypothalamus by Dr. Mudassar Ali Roomi

Apr 14, 2018

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    PHYSIOLOGY

    of

    HYPOTHALAMUS

    BY

    DR. MUDASSAR ALI ROOMI (MBBS, M. PHIL)

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    HYPOTHALAUMS

    it is the part ofdiencephalon which isbelow the hypothalamicsulcus.

    Hypothalamus is the Major

    Control Headquarters for theLimbic System

    It forms the anteroinferiorwall and the floor of thethird ventricle.

    It extends from optic

    chiasma to mamillary body

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    Nuclei of

    hypothalamus

    Three groups of nuclei:

    1. Anteriotr or Preoptic group : lateral and

    medial preoptic nuclei, suproptic nucleus,

    suprachiasmatic nucleus, paraventricular

    nucleus and anterior nucleus.

    2. Middle or Tuberal: Ventromedial,

    dorsomedial, arcuate or tuberal nucleus,posterior and lateral nuclei.

    3. Posterior or Mammillary:

    supramammillary, premammillary, medial

    and lateral mammillary nuclei.

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    AFFERENTS TO THE HYPOTHALAMUS ARE FROM

    1. Amygdala

    2. Hippocampus

    3. Reticular formation of brainstem

    4. Nucleus of tractus solitarius

    5. Locus ceruleus: these secrete norepinehrine at the nerve endings

    6. Raphe magnus nucleus: these secrete serotonin at their nerve endings7. Afferents from the sensory pathways

    8. retina

    9. Thalamic nuclei

    10. Hippocampus

    11. Frontal cortex12. Globus pallidus

    13. Lentiform nucleus

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    EFFERENTS FROM THE HYPOTHALAMUS GO TO

    1. Amygdala

    2. Hippocampus

    3. Frontal cortex

    4. Nucleus of tractus solitarius

    5. mid brain

    6. Reticular formation of brainstem

    7. Spinal cord8. Nervous connections with posterior pituitary and vascular

    connections with the anterior pituiatory:

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    Nervous connections with posterior pituitary and

    vascular connections with the anterior pituiatory:

    Supraoptic and paraventricularnuclei of hypothalamus secreteADH and oxytocin. Thesehormones are transported alongwith their carrier proteins alongthe nerve fibers to the posterior

    pituitary where they are stored.These are the hormones ofhypothalamoneurohypophysealsystem.

    In the median eminence andinfundibulum of the

    hypothalamus, there aresinusoids. Blood from thesesinusoids pass through thehypophyseal portal blood vesselsand these pass through the orcommunicate with the capillaryplexus in the anterior pituitary.

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    FUNCTIONS OF HYPOTHALAMUS

    1. Secretion of posterior pituiatry hormones (paraventricular andsupraoptic nucleus)

    2. Control of anterior pituitary (discrete areas)

    3. Control of adrenal cortex (paraventricular nucleus)

    4. Regulation of heart rate and blood pressure (posterior, lateral and

    anterior hypothalamus)5. Regulation of sleep and wakefulness (ant. Hypothalamus and mamillary

    body)

    6. Role in behaviour and emotional changes (ventromedial, post and lateralnuclei)

    1. Reward centre: in ventromedial nucleus

    2. Punishment centre: Post. And lateral nuclei3. Rage centre: Post. And lateral nuclei.

    7. Regulation of response to smell (post. hypothalamus)

    8. Role of circadian rhythm (supraoptic and ant. nuclei)

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    9. Control of autonomic nervous system

    stimulation ofposterior and lateral hypothalamus resultsinto sympathetic responses such as increase in the heart

    rate and blood pressure, pupillary dilatation,

    piloerection, secretion of catecholamines from adrenal

    medulla and hyperglycemia. Stimulation ofanterior hypothalamus (preoptic area)

    results into parasympathetic responses such as slowing

    of heart rate and fall in blood pressure, papillary

    constriction, contraction of urinary bladder, GIT motilityand secretions.

    in addition hypothalamus is also a relay station in the

    pathway of sympathetic cholinergic nerves which

    produce vasodilatation in skeletal muscle and sweating.

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    10. Control of water balance of the body

    water balance is maintained through the control of water intakeand excretion through the kidney.

    When the thirst centre in lateral hypothalamus is stimulated,

    there is conscious desire to take water and fluids.

    Thirst centre is stimulated when there is increased osmolarity ofECF, Hypovolemia and also by angiotensin II.

    In the anterior hypothalamus, there are osmoreceptors which

    are specialized neurons which respond to changes in osmolarity.

    Water excretion is controlled by ADH. Stimuli which secrete ADH

    may be osmotic or volume.

    If there is hyperosmolarity or Hypovolemia, there is secretion of

    ADH. These stimuli will act on hypothalamus and ADH is

    released which acts on the distal parts of renal tubules to

    reabsorb water.

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    11. Control of uterine contraction and milk

    ejection

    oxytocin is synthesized in hypothalamus, mainly the

    paraventricular nuclei.

    Oxytocin causes uterine contraction to help in the child birth.

    In the second stage of labor there are high levels of oxytocin.

    In milk ejection (milk letdown) there is role of oxytocin. The

    baby suckles breast of the mother, impulses from the receptor

    around nipples go to the hypothalamus and then there is

    release of oxytocin from post. pituitary. Oxytocin causes contraction of myo-epithelial cells as a result

    of which milk is ejected from the breast. This is a neuro-

    endocrinal reflex. Afferent part is nervous and efferent is

    endocrine.

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    12. Control of food intake or hunger

    inthe lateral hypothalamus, there is a feedingcentre or hunger centre. When this centre isstimulated there is desire to take food and there

    is hunger. Activity of the feeding centre is controlled by a

    satiety centre in the ventromedial nucleus of thehypothalamus.

    When satiety centre is active, feeding centre isinhibited. When satiety centre is inactive, feedingcentre is activated.

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    12. Control of food intake or hunger

    (cont)

    Glucostat mechanism: In the satiety centre, neurons arecalled glucostat cells. Glucose uptake in the glucostat cellsdepends upon the presence of adequate concentration ofinsulin. In almost all brain cells glucose uptake dont requireinsulin except glucostat cells in satiety centre. In

    uncontrolled diabetes mellitus, there is polyphagia andincreased appetite because of inactivity of satiety centrebecause there is less insulin as result of which there isoveractivity of feeding centre resulting in polyphagia.

    Lipostatic mechanism: through leptin.

    Mammillary bodies in the hypothalamus control feedingreflexes such as swallowing and licking of the lips.

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    13. Regulation of body temperature

    Heat loss centre: in the preoptic nucleus of ant.hypothalamus there is a centre which regulate thetemperature. When temperature of the body increaseswith respect to thermostat in the hypothalamus,

    various temperature decreasing mechanisms areinitiated which include cutaneous vasodilatation andsweating.

    Heat gain centre: When body temperature decreaseswith respect to thermostat, various temperature

    increasing mechanisms are initiated and these includecutaneous vasoconstriction, shivering and later onthere is chemical thermogenesis. Shivering centre islocated in posterior hypothalamus.

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    DISORDERS OF HYPOTHALAMUS:

    1. Central Diabetes insipidus: may be because of

    tumor or damage to hypothalamus.

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    Laurence-Moon-Beidl Syndrome

    moon face, obesity,

    polydactylism, mental

    retardation,

    hypogentalism.

    http://www.claro-search.com/imageres.php?iu=http://www.mlmorris.com/lmbbs/ashleysmiles.jpg&ir=http://www.lmbbs.org/&ig=http://t0.gstatic.com/images?q=tbn:ANd9GcSOid7r-NzRtoKYwE6dcsT7pQaL1msLA7jXcpbAerXaVJpyYZ6PU_FmZQ&h=209&w=236&q=Laurence-Moon-Beidl+Syndrome&babsrc=HP_ss
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    Dystrophia adipogentalis (Frohlichs syndrome):

    obesity, sexual infantalism, dwarfism.

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    Narcolepsy: sudden uncontrollable desire for sleep

    during daytime.

    Cataplexy: sudden uncontroled outburts of emotions

    associated with narcolepsy.