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Hypothalamus - pituitary - Hypothalamus - pituitary - adrenal glandsadrenal glands
Magdalena Gibas-Dorna MD, PhD
Dept. of Physiology
University of Medical Sciences
Poznań, Poland
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Hypothalamus - general director of the hormone system.
At every moment, the hypothalamus analyses messages coming from: the brain and different regions of the body.
Homeostatic functions of hypothalamus include maintaining a stable body temperature, controlling food intake, controlling blood pressure, ensuring a fluid balance, and even proper sleep patterns.
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Cell bodies of neurons that produce releasing/inhibiting hormones Hypothalamus
Primary capillaries in median eminence
Arterial flow
Releasinghormones
Anteriorpituitaryhormone
LongPortalveins
Releasing/inhibiting hormones
ANTERIORPITUITARY
Secretory cells that produce anterior pituitary hormones
Anterior pituitary hormonesVenous outflow
Gonadotropic Thyroid-Proactin hormones stimulating ACTH Growth (FSH and LH) hormone hormone
HypothalamusHypothalamus releases hormones at median eminence and sends to anterior pituitary via portal veinportal vein.
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Control of pituitary hormone secretion by Control of pituitary hormone secretion by hypothalamushypothalamus
• Secretion by the anterior pituitaryanterior pituitary is controlled by hormones called hypothalamic releasing hormones and inhibitory hormones conducted to the anterior pituitary through hypothalamic - hypothalamic - hypophysial portal vesselshypophysial portal vessels . .
• Posterior pituitaryPosterior pituitary secrets two hormones, which are synthesized within cell bodies of supraoptic and paraventricular nuclei of the hypothalamus and transmitted through axonsthrough axons of these neurons.
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Function of the releasing and inhibitoryFunction of the releasing and inhibitory hypothalamic hormoneshypothalamic hormones
• Thyrotropin- releasing hormone (TRH)(TRH) - causes release of thyroid - stimulating hormone (TSH)
• Corticotropin - releasing hormone (CRH)(CRH) – causes release of ACTH
• Growth hormone releasing hormone (GHRH)(GHRH) - causes release of growth hormone, and
• Growth hormone inhibitory hormone (GHIH)(GHIH),, which is the same as the hormone somatostatinsomatostatin and which inhibits the release of growth hormone.
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Function of the releasing and inhibitoryFunction of the releasing and inhibitory hypothalamic hormoneshypothalamic hormones
• Gonadotropin - releasing hormone (GnRH) (GnRH) – causes release of the two gonadotropic hormones, LH and FSH
• Prolactin inhibitory hormone (PIH)(PIH),, - belived to be dopamine - causes inhibition of prolactin release. • PRL-releasing factor (PRF)(PRF)..
- belived to be TRH – increases prolactin release
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The location ofThe location of pituitary (hypophysis)pituitary (hypophysis) relative relative to brain and hypohalamusto brain and hypohalamus
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Hypothalamus
Pituitary stalk
Posterior lobe
Intermediate lobe
Pituitary gland
Anteriorlobe
Optic chiasm
Hypothalamic-Pituitary SystemsHypothalamic-Pituitary Systems
The pituitary is controlled largely by the hypothalamus and regulates numerous processes.
Anterior = endocrine, 6 hormones
Intermediate = minor, 1
Posterior = neuroendocrine, 2
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Six very important hormones are secreted bySix very important hormones are secreted by
anterior pituitaryanterior pituitary : • Secreted by lactotropes prolactin
(PRL)(PRL) • Secreted by thyrotropes thyroid
stimulating hormone (TSH)(TSH)• Secreted by gonadotropes follicle -
stimulating hormone FSHFSH, and luteinizing hormone LHLH
• Secreted by corticotropes adrenocorticotropin (ACTH)(ACTH)
• Secreted by somatotropes growth hormone (GH; somatotropin)(GH; somatotropin)
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HypopituitarismHypopituitarism
• deficiency of one or more anterior pituitary hormones, which results in insufficient stimulation and therefore insufficient hormonal output of the respective target glands
• Tumors• Pituitary irradiation• Pituitary apoplexy• Postpartum pituitary necrosis (Sheehan’s syndrome due to
postpartum hemorrhage and hypovolemia)
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How can pituitary tumors cause hypopituitarism?
e.g. what is the effect of prolactinoma on fertility in both sexes?
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To venous circulation
Arterial blood supply
Posterior pituitary
Supraopticnucleus
Paraventricularnucleus
Hypothalamus
Posterior pituitaryPosterior pituitary receives axons from the supraoptic ( ADH) and paraventricular nuclei ( oxytocin).
(ADH)
(oxytocin)
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Two hormones are secreted by posterior posterior pituitarypituitary::
• Antidiuretic hormone (ADH; Antidiuretic hormone (ADH; vasopressin)vasopressin)
• OxytocinOxytocin
• Intermediate - lobeIntermediate - lobe cells secretes:
• POMCPOMC (proopiomelanocortin), which is precursor of alpha-MSH (melanotropin )
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Growth hormoneGrowth hormone
(somatotropin)(somatotropin)
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Somatomedins
Liver
Growth hormone
Somatotrophs ofAnterior pituitary
Somatostatin ( - )
GHRH (+)
Portalvein
Hypothalamus
Sleep centerIn the brain
Chemicalstimuli
Stress centersIn the brain
• GHRH, somatostatin (GHIH) and ghrelin control GH release
• pancreatic somatostatin has other functions (inhibits hormone secretion by and cells)
Ghrelin from stomach (+)
(-)
(+)
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Stimuli that Stimuli that increaseincrease secretion of GH: secretion of GH:
• GHRH; Ghrelin (brain-gut peptide)
• Deficiency of energy substrate:
- Hypoglycemia
- Exercise
- Fasting
• Increase in circulating levels of certain amino acids
• Glucagon
• Stressful stimuli
• NREM stage of sleep
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Sleep
6 AMMidnight6 PMNoon
Time of day
Plasma GHconcentration(relative units)
GH is released in pulses, with a major peak GH is released in pulses, with a major peak during deep sleep before REduring deep sleep before REMM
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GhrelinGhrelin• Produced mainly by stomach
(released into blood)• Other sources: intestines;
hypothalamus• Receptors located in pituitary
(GH), hypothalamus (food intake), heart, blood vessels ( BP)
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Ghrelin causes :Ghrelin causes : GH release
food intake (appetite-stimulatory peptide) via NPY neurones in hypothalamus
fat utilization (GH-inependent mechanism)
glucose utilization
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Stimuli that Stimuli that decreasedecrease secretion of GH: secretion of GH:
• REM sleep
• High blood glucose concentration ( of ghrelin release)
• Cortisol
• FFA ( of ghrelin release)
• Growth hormone
• Somatomedins
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Physiology of growthPhysiology of growth
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GH stimulates cartilage and bone growth by:GH stimulates cartilage and bone growth by:
• increased deposition of proteindeposition of protein by the chondrocytic and osteogenic cells that cause bone growth
• increased rate of reproductionreproduction of these cells
• the specific effect of converting converting chondrocyteschondrocytes into osteogenic into osteogenic cellscells, thus causing specific deposition of new bone.
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Direct and indirect effects of GHDirect and indirect effects of GH
• Direct effects are the result of growth hormone binding its receptor on target cells
• Indirect effects are mediated primarily by an insulin-like growth insulin-like growth factor-1 factor-1 and 2 and 2 (IGF-1(IGF-1; IGF-2; IGF-2),), hormones that are secreted from the liver and other tissues in response to GH
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Somatomedins - the polypeptide growth Somatomedins - the polypeptide growth factors secreted by the liverfactors secreted by the liver (IGF-I, IGF-II)(IGF-I, IGF-II)
• IGF-IIGF-I (insulin-like growth factor) stimulates skeletal growth by increasing collagen and protein synthesis in chondrocytes. IGF-I may be also produced locally
• IGF-IIIGF-II stimulates tissue growth and increases organ size especially during fetal development (by increasing the rate of: protein synthesis, RNA synthesis, DNA synthesis)
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Distinguish between:Distinguish between:
• Somatotropin - GH• Somatostatin - GHIH• Somatomedin – polypeptide growth factor
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Physiology of growthPhysiology of growth
Growth is affected by:Growth is affected by:• thyroid hormones• androgens • estrogens • glucocorticoids • insulin• genetic factors • adequate nutrition
sex hormones
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Physiology of growth –Physiology of growth – growth periods:growth periods:
• In humans, there are 2 periods of rapid growth, the first in infancy and the second in late puberty just before growth stops
• The first period is a continuation of the fetal growth period• The second growth spurt is due to an interaction between sex sex
steroids, GH, and IGF-1steroids, GH, and IGF-1sex hormones sex hormones amplitude of the spikes of GH secretion amplitude of the spikes of GH secretion IGF-1 IGF-1 growthgrowth
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Although androgens and estrogens initially stimulate growth, they finally terminate growth by causing the epiphyses to fuse to the long bones.
Two growth periodsTwo growth periods
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1. Why pituitary dwarfs treated with testosterone first grow few inches and then stop?
2. Why people who were castrated before puberty tend to be tall?
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Physiology of growth – role ofPhysiology of growth – role of thyroid thyroid hormoneshormones:
• Thyroid hormones have a permissive action to permissive action to GHGH, possibly via potentiation of the actions of somatomedins.
• They also appear to be necessary for a completely normal rate of GH secretion
• Thyroid hormones have effects on the ossification of cartilage, the growth of teeth, the contorous of the face, and the proportions of the body
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Long bones continue to grow and elongate (lengthen) through adolescence.
This process is called ossification
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Developing heart that appears as a red nodule
While still in the embryonic stage, a baby's heart develops under the supervision of the growth hormone growth hormone
Adult heart
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Metabolic effects of GHMetabolic effects of GH
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GH plays role in promotingGH plays role in promoting protein protein depositiondeposition
• GH directly enhances transport of most amino acids through the cell membranes to the cytoplasm
• GH stimulates the transcription of DNA in the nucleus, causing formation of increased quantities of RNA. This in turn promotes more protein to be sythesized
• GH also increases rate of RNA translation, causing protein to be sythesized
• GH decreases protein and amino acides catabolism, thus acting as a “protein sparer”“protein sparer”
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GH increases fat utilization for energy:GH increases fat utilization for energy:
• It causes release of fatty acids from adipose tissue (increases the concentration of FFA in the body fluids)
• It also causes increased convertion of FFA to acetylcoenzyme A (acetyl-CoA) with subsequent utilization of this for energy (ATP)
• Excessive amounts of GH may produce excessive mobilization of fat from the adipose tissue, causing ketosis
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GH has 4 major effects on carbohydrate GH has 4 major effects on carbohydrate metabolism:metabolism:
• It decreases use of glucose for energy
• It stimulates gluconeogenesis
• It produces decreased uptake of glucose by the cells and increased blood glucose concentration
• The increase of blood glucose concentration caused by GH stimulates the beta cells of the pancreas to secrete extra insulin
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GROWTH HOMONE
MUSCLE LIVER ADIPOSE
Insulin-likeeffects of GH
Anti-insulineffects of GH
Amino aciduptake
Proteinsynthesis
Glucoseuptake
Lipolysis
Decreased adiposity
RNAsynthesis
Gluconeogenesis
Somatomedinproduction
Proteinsynthesis
Glucoseuptake
Increasedmuscle mass
Insulin-like GH effectsInsulin-like GH effects: liver and muscle protein synthesis;
AAnti-insulinnti-insulin: glucose uptake, lipolysis
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SOMATOMEDINS
CHONDROCYTES OF BONE MANY ORGANS AND TISSUES
Increased lineargrowth
Increased tissue growthIncreased organ size
Collagen synthesis
Protein synthesis
Cell proliferation
Protein synthesis
RNA synthesis
DNA synthesis
Cell size and number
IGF-IIIGF-I
IGF-IIGF-I stimulates bone growth by stimulating chondrocytes, which make cartilage.
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SOMATOMEDINS
CHONDROCYTES OF BONE MANY ORGANS AND TISSUES
Increased lineargrowth
Increased tissue growthIncreased organ size
Collagen synthesis
Protein synthesis
Cell proliferation
Protein synthesis
RNA synthesis
DNA synthesis
Cell size and number
IGF-IIIGF-I
IGF-IIIGF-II stimulates tissue growth and repair by stimulating RNA and protein synthesis
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GH GH --summarysummary
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Abnormalities of GH secretionAbnormalities of GH secretion
• Panhypopituitarism • Dwarfism (in 30% -
isolated GH)• Laron dwarfism • Gigantism • Acromegaly
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GIGANTISMGIGANTISM
• excessive production of GH before adolescence
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ACROMEGALYACROMEGALY – excessive production of GH after adolescence
Intradental separation and prognathism in a patient with acromegaly.
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AcromegalyAcromegaly
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The somatopauseThe somatopause is directly related to the decline of growth hormone
produced by the body during aging
• Clinical Signs of the Clinical Signs of the SomatopauseSomatopause::
• Weight gain • Energy Loss• Skin wrinkling• Decreasing muscle mass• Loss of bone density• Increasing body fat
(especially around the waist)
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Age-related lowering of GHAge-related lowering of GH (somatopause)(somatopause) ::• decrease in muscle mass and muscle strength
• impairment of psychical efficiency (GH contributes to the function of the hipocampushipocampus, a brain structure important for the learning and memory)
• osteoporosis; cardiac failure
• altered immune function (GH slows atrophy of thymus and controls differentiation and activity of some cells in the immune system eg. neutrophils) and many others.
• increased rate of oxidative stress and risk of cardiac mortality (cholesterol, free radicals etc.)
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GH - youth hormone?
• GH may reverse biological effects of aging
• GH is not recommended for common use in adults
• GH supplementation:- GHD- AIDS wasting syndrome- short bowel syndrome
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Other hormones of anterior pituitary: Other hormones of anterior pituitary: ACTH, TSH, FSH, LH, PRLACTH, TSH, FSH, LH, PRL
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ACTHACTH - adrenocorticotropin regulates - adrenocorticotropin regulates adrenocortical functionadrenocortical function
• It strongly stimulates cortisol production of adrenal cortex
• it also stimulates the production of other adrenocortical hormones
• ACTH also exhibits some extraadrenal effects - it has a pigmenting action (MSH activity)
• CRH, ACTHACTH and cortisol secretion exhibit circadian rhythm (high in the early morning, low in the late evening)
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TSHTSH stimulates the thyroid gland folicles:stimulates the thyroid gland folicles:
• it increases the rate of thyroglobulin synthesisthyroglobulin synthesis
• it increases the uptake of iodide ionsuptake of iodide ions from the blood by thyroid cells
• it increases T4 production and releaseT4 production and release by the thyroid gland
• the rate of TSH secretion by anterior pituitary is controlled mainly by the negative feedback effect of T4
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With the sounding of the alarm, the hypothalamushypothalamus secretes the special GnRH GnRH hormone. This hormone sends a command to the pituitary glandpituitary gland to secrete two hormones, the Follicle Stimulating Hormone (FSHFSH) and the Luteinizing Hormone (LHLH).
Because of the "hidden" clock, the brain's hypothalamus area "understands" when a person's adolescence has started
Pituitary Pituitary gonadotropinsgonadotropins
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FSHFSH functions:functions:
• FSHFSH stimulates early growth of the ovarian follicle
• FSHFSH stimulates spermatogenesis
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LHLH functions:functions:
• LHLH stimulates ovulation and luteinization
• LHLH stimulates testosterone secretion
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ProlactinProlactin
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Prolactin function – reproduction
• Lactation
• Luteal function
• Reproductive behaviora. enhances female sexual receptivity
b. parental behavior
c. oligozoospermia and decreased libido
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Prolactin function – homeostasis
• Immune response
- stimulates mitogenesis and proliferation in T lymphocytes
• Osmoregulation
- decreases the transport of Na+ and increases the transport of K+ across mammary epithelial cells
- acts on the proximal convoluted tubule of the nephron to promote Na+, K+, and water retention
• Angiogenesis
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HypothalamusHypothalamus
Prolactin Oxytocin
Anteriorpituitary
Posteriorpituitary
Alveolus
Ductalsystem
Milk synthesisMilk synthesisin alveoliin alveoli
Milk secretion from alveoliMilk secretion from alveoliinto ductal systeminto ductal system
ProlactinProlactin ↑milk synthesis and secretion into alveoli
Birth ↓ Prolactin, ↑ neural control (breast mechanorec.)
SucklingSuckling Hypothal. ↑Prolactin 1 hr ↑Milk production
Effect weakens over months
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ADHADH and oxytocin and oxytocin
- posterior pituitary hormones- posterior pituitary hormones
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Hormones of tHormones of the posterior pituitary glandhe posterior pituitary gland
• Oxytocic hormoneOxytocic hormone:: - it causes contraction especially of the uterus and to a lesser
degree other smooth muscles of the body- it stimulates myoepitelial cellsmyoepitelial cells in the breast causing milk
ejection
- it also participates in the process of sperm ejection
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"Love hormone" may also help us recognize faces
• hormone associated with trust and social bonding (including pair-bond formation, maternal behavior, sexual behavior)
• helps people recognize familiar human faces
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Risk factors for depression in new mothers
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HypothalamusHypothalamus
Prolactin Oxytocin
Anteriorpituitary
Posteriorpituitary
Alveolus
Ductalsystem
Milk synthesisMilk synthesisin alveoliin alveoli
Milk secretion from alveoliMilk secretion from alveoliinto ductal systeminto ductal system
Suckling, baby sounds hypothal ↑oxytocin (paraventricular nucleus) ↑myoepithel. contract milk
let-down
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Oxytocin central synthesis and peripheral functions
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STRESSSTRESS
NEOCORTEX
Amygdala Hipocampus
HYPOTHALAMUS HYPOTHALAMUSCRH
ACTH
Cortisol
Ant. pituitary
Adrenal cortex
INFLAMMATIONINFLAMMATION
1. neutrophil recruitment2. reactive oxygen metabolites3. pro-inflammatory cytokines
• lipid peroxidation• oxidant tissue injury
The relationship between the HPA axis,
and oxytocin
OxytocinOxytocin
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Regulation ofRegulation of oxytocinoxytocin secretion secretion (paraventricular nucleus):(paraventricular nucleus):
• suckling via stimulation of touch receptors in breast
• distension of female genital tract (during labour)
• pain
• psychological stimuli (baby’s cry, orgasm)
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Hormones of tHormones of the posterior pituitary glandhe posterior pituitary gland
• Antidiuretic hormoneAntidiuretic hormone (ADH; vasopressin): (ADH; vasopressin):- increases the permeability of the kidney collecting ducts
and tubules to water
- it allows the water to be reabsorbed, thereby conserving water in the body
- it has also vasoconstrictor and pressor effects (higher concentrations of ADH cause an increase in arterial blood pressure by vasoconstriction)
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There are special sensors in the hypothalamus area of the brain called osmoreceptors.osmoreceptors.
These sensors measure the amount of fluid in your blood at every moment you are alive.
If they determine that the amount of fluid in the blood has fallen, they immediately react and stimulate supraoptic nucleussupraoptic nucleus.
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Regulation of Regulation of ADHADH production: production:
OOsmotic regulationsmotic regulation
- when the ECF becomes too concentrated, fluid is pulled by osmosis out of the osmoreceptors, decreasing their size and initiating signals in the hypothalamus to cause additional ADH secretion
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Regulation of Regulation of ADHADH production: production:
• Hemodynamic regulationHemodynamic regulation: changes in blood volume and blood pressure affect vasopressin secretion via baroreceptors. However, stimulation of ADH release requires more than 10% blood volume decrease.
• Other stimulatorsOther stimulators for ADH secretion include: angiotensin II, nicotine, pain, increased temperature, and some emotions
• AlcoholAlcohol strongly inhibits inhibits ADH release
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Regulation of ADH Regulation of ADH secretionsecretion
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Adrenal glandsAdrenal glands
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Adrenalgland
Capsule
Medulla
Zona glomerulosa
Zonafasciculata
Zonareticularis
Cortex
Location of adrenal glandsadrenal glands
• the outer cortex cortex (80%) releases steroidssteroids;
• the inner medulla medulla (20%) releases catecholaminescatecholamines
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The adrenal cortex – three zonesThe adrenal cortex – three zones
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Adrenal gland secretionAdrenal gland secretion • Adrenal cortex secrets:Adrenal cortex secrets:- corticosterone (all 3 cortical zones)- cortisol ( z. fasciculata) - aldosterone ( z. glomerulosa)- sex hormones ( z. reticularis)
• Adrenal medulla secrets:Adrenal medulla secrets:- catecholamines (epinephrine, norepinephrine, dopamine)
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hormone (CRH)
(z. fasciculata)
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Brain
NE and E
BloodVariouseffectororgans
NE
Heart
Spinal cord
Adrenalglands Medulla
PreganglionicSympathetic neurons
Sympatheticganglia
Postganglionic sympatheticneuron
The anatomical analogy between cells of adrenal The anatomical analogy between cells of adrenal medulla and sympathetic postganglionic neuronsmedulla and sympathetic postganglionic neurons
• Postganglionic fiber has effects on one specific effector organ, such as the heart.
• The cells of adrenal The cells of adrenal medullamedulla secrete hormones to the circulation
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Adrenal catecholaminesAdrenal catecholamines
The release of AK is carried out by direct connection of nerve fibers from hypothalamus to intermediolateral
cells (IML), and then to adrenal medulla
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Tyrosine
DOPA
Dopamine
Norepinephrine
PNMT
Epinephrine
Tyrosinehydroxylase
Chromaffin cells secrete epinephrine into the blood, instead of NE at a synapse.
Tyrosine DOPA DA NENE (hydroxylation and decarboxylation of Tyrosine) PNMTPNMT (cortisol elevates) EPI EPI (methylation of norepinephrine)
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Adrenergic receptorsAdrenergic receptors
• Beta1 and 2 receptorsBeta1 and 2 receptors-- ↑cAMP → proteins phosphorylation proteins phosphorylation,
EFFECT: beta 1 – contraction, beta 2- relaxation
• Alpha 1 receptorsAlpha 1 receptors – phospholipase C activation → IP3 and DAC → proteins phospohorylation, IP3 opens channels for Ca ions.
EFFECT: muscle contraction, secretion (egzocytosis)
• Alpha 2 receptorsAlpha 2 receptors - ↓cAMP EFFECT: muscle relaxation (GI), ↓secterion (pancreas)
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Adrenergic receptors – affinity to the Adrenergic receptors – affinity to the transmittertransmitter
• Beta-1 NE and E
• Beta-2 E
• Beta-3 NE>E
• Alpha NE > > >E
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Adrenergic receptors stimulation – clinical samplesAdrenergic receptors stimulation – clinical samples
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Adrenergic receptors stimulationAdrenergic receptors stimulation – – clinical samplesclinical samples
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Adrenergic blockersAdrenergic blockers
samples• beta-1 blockers: CAD, hypertension • Alpha blockers: cardiac failure, hypertension,
CAD • Urine retention – reduction of urine bladder
tension • Headache: vasodilatation • Uterus involution after delivery
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Adrenergic receptors - summaryAdrenergic receptors - summary
Receptor Localization Affinity II messenger
α1 Most target tissues for SNS
NE>E Phospholipase C (IP3 and DAG)
α2 GI, pancreas NE>E Decrease in cAMP
β1 Heart, kidney (renin)
NE=E Increase in cAMP
β2 Selected blood vessels; smooth muscles
E >NE Increase in cAMP
β3 Adipose tissue NE>E
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The effect of catecholamines onThe effect of catecholamines on heart and heart and circulation:circulation:
• NOREPINEPHRINENOREPINEPHRINE• via receptors -
vasoconstriction,
• causes increase in systolic and diastolic blood pressure, reflex bradycardia and decrease in cardiac output per minute
• EPINEPHRINEEPINEPHRINE• via receptors -
vasoconstriction,
• via receptors - vasodilation
• widening of the pulse pressure, and increase of HR and cardiac output per minute;
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Circulatory effects of catecholaminescatecholamines
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The effects of catecholamines on smooth smooth muscles and sphinctersmuscles and sphincters:
• Epinephrine:Epinephrine:• causes dilation of the
airway, gasrtointestinal tract and urinary bladder
• Epinephrine:Epinephrine:• provokes constriction of
gastric and urinary bladder sphincters
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The metabolic effects of catecholaminesThe metabolic effects of catecholamines:
• increase in muscle glycogenolysis
• increase in liver gluconeogenesis
• increase in secretion of glucagon
• inhibition of insulin secretion (via receptors)
• increase in lipolysis
• increase in metabolic rate and calorigenic effect
blood blood glucoseglucose
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Function ofFunction of dopaminedopamine::
• vasodilation in the mesentery and kidneys
• vasoconstriction (by releasing norepinephrine?) elsewhere
• positively inotropic effect on the heart (by 1 r-ors)
• increase in systolic pressure and no change in diastolic pressureno change in diastolic pressure
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Regulation of adrenal medullary secretionRegulation of adrenal medullary secretion
• The major stimulus for catecholamine release from adrenal medulla is sympathetic nervous system activationsympathetic nervous system activation
• Stress, change in posture, low blood sugar or sodium levels are the factors that activate the sympathetic nervous system
• hemorrhagehemorrhage epinephrineepinephrine
• exerciseexercise norepinephrinenorepinephrine
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The Fight or Flight System
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Adrenergic responsesAdrenergic responses of selected tissues
Organ Receptor Effect
Heart
Blood vessels
KidneyGut
Pancreas
LiverAdipose tissueSkinBronchiolesUterus
Beta-1
AlphaBeta-2BetaAlpha, beta
Alpha
Beta
Alpha, betaBetaAlphaBeta-2Alpha, beta
Increased inotropyIncreased chronotropyVasoconstrictionVasodilationIncreased renin releaseDecreased motilityIncreased sphincter toneDecreased insulin releaseIncreased glucagon releaseIncreased insulin and glucagon releaseIncreased glycogenolysisIncreased lipolysisIncreased sweatingBronchodilationContraction, relaxation
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Liver
Lactate
Glycogenolysis
Muscle
Blood
Lactate
Glycogenolysis
Glucose
Glycerol
Lipolysis
Adiposetissue
Glucose
Fatty acids
EPIEPI raises glycogenolysis in liver/muscle and lipolysis in adipose; elevates blood glucose
Effects of epinephrine
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PPheochromocytomaheochromocytoma • High blood pressure
• Other paroxysmal symptoms are usually nonexistent, unless the person experiences pressure from the tumor, emotional stress, changes in posture, or is taking beta-blocker drugs for a heart disorder
- rapid pulse, palpitations - headache - nausea, vomiting - clammy skin; sweating
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Adrenal steroidsAdrenal steroids
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(c) 2003 Brooks/Cole - Thomson Learning
Cholesterol
Pregnenolone
Progesterone 17-OH-Pregnenolone
Dehydroepi-androsterone
Corticosterone
Aldosterone Cortisol
17-OH-Progesterone Testosterone
Estradiol
Adrenal hormones are derivatives of Adrenal hormones are derivatives of cholesterolcholesterol
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Cortisol(glucocorticoid)
Aldosterone(mineralocorticoid)
Dehydroepiandrosterone(androgen)
- Cortisol (glucocorticoid),
- Aldosterone (mineralocorticoid)
- DHEA (androgen, minor male)
Three steroids are the primary products of theThree steroids are the primary products of the adrenal cortexadrenal cortex:
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Dehydroepiandrosterone
17-OH-Pregnenolone
Pregnenolone
Cholesterol
Cortisol
17-OH-Progesterone
17-OH-Pregnenolone
Pregnenolone
Cholesterol
Aldosterone
Cholesterol
Pregnenolone
Progesterone
Corticosterone
Zona glomerulosaZona glomerulosa
Zona fasciculataZona fasciculata
Zona reticularisZona reticularis
• Cells take up and store cholesterol;
• Each cell makes steroids according to the enzymes it has.
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GlucocorticoidsGlucocorticoids
Cortisol
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Circadianrhythms
Stress
CRH
Hypothalamus
Anteriorpituitary
ACTH
Cortisol
Adrenalcortex
Corticotropes in hypothalamus CRHCRH portal pituitary ACTHACTH adrenal cortex cortisolcortisol
Hypothalamic – pituitary Hypothalamic – pituitary adrenal axisadrenal axis
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Midnight AM
Time of DayPM
Sleep
Pla
sma
Co
r tis
ol C
on
cen
tra t
ion
(arb
itra
r y u
nit
)
CRH, ACTH, cortisol show circadian sleep-wake rhythm, CRH, ACTH, cortisol show circadian sleep-wake rhythm, with peak at awakeningwith peak at awakening
Types of stress known to increase cortisol secretion:
Physical stressPhysical stress
- Hypoglycemia
- Trauma
- Heavy exercise
Psychological stressPsychological stress
- Acute anxiety (e.g. novel situations, exams, airplane flight)
- Chronic anxiety
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In times of danger, the body goes into a state of alarm by means of a link between the brain and the adrenal glands
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Resistance to stressResistance to stress
• stressor incerases ACTHACTH secretion.
• The stressors also activate the sympathetic nervoussympathetic nervous systemsystem - permissive effect of glucocorticoids on vascular reactivity to catecholamines
• GlucocorticoidsGlucocorticoids are also necessary for the catecholaminescatecholamines to facilitate their full FFA-mobilizing action (FFA are an important emergency energy supply).
• The high glucocorticoids levels caused by stress are life-saving only in the short term but over longer periods they are harmful.
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Describe changes in human body that occur during stress
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Effects of cortisol onEffects of cortisol on carbohydrates:carbohydrates:
1. Stimulation of gluconeogenesis
2. Decreased glucose utilization by the cells
3. Elevated blood glucose level and adrenal diabetes
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Plasma Liver
Cortisol
Urea
Ureacycle
Aminoacids
GlucoseGlucose
Ammonia
Gluconeogenesis
Amino acidmetabolizing
enzymes
Glycogensynthesis
Cortisol accelerates liver urea cycle and amino acid
conversion to glucoseglucose
The effects of cortisol on liver metabolism
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Effect of cortisol onEffect of cortisol on pprotein metabolismrotein metabolism:
• reduction in cellular protein
• increase of liver and plasma protein levelincrease of liver and plasma protein level
• increase of blood aa transport into the liver
• decrease of blood aa transport into the extrahepatic cells
• gluconeogenesis (formation of carbohydrates from proteins)
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Plasma
Cortisol
Aminoacids
Cortisol
Muscleprotein
The effects of cortisol on skeletal muscle
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Effect of cortisol onEffect of cortisol on fatfat metabolism metabolism::• increased mobilization of fatty acids• increased oxidation of FA in the cells• ketogenic effect• obesity – increased
fat around neck („buffalo-torso”„buffalo-torso”) and round face („moon face„moon face”)
„…the effects of glucocorticoids on lipid mobilization are still controversial. In vivo studies suggest that glucocorticoids have no effect or stimulate lipolysis, whereas other report an inhibiting effect of glucocorticoids on the lipolytic activity in vivo in man.”
Ottoson M, Lonnroth P, Bjorntorp P, Eden S. Effects of Cortisol and Growth Hormone on Lipolysis in Human Adipose Tissue. J Clin Endocrinol Metab 2000; 85(2):799.
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AntiinflammatoryAntiinflammatory effects of cortisol:effects of cortisol:
• stabilization of the lysosomal membranes
• decrease in permeability of the capilaries
• lowering of fever
• supression of the immune system (T-lymphocytes)
• inhibition of mast cells releasing histamine
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Cortisol lowers the temperature by inhibiting the production of IL-1, which activates the temperature center
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Effets of cortisol onEffets of cortisol on blood cellsblood cells:
• inincreasecreasess the number of circulating neutrophils, platelets neutrophils, platelets and red blood cellsand red blood cells
• decreaes the number of other blood cells
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Summary of effects ofSummary of effects of cortisolcortisol on on metabolism:metabolism:
LIVER:LIVER:
gluconeogenesis, and glycogen synthesis
SKELETAL MUSCLE: SKELETAL MUSCLE: protein synthesis; protein degradation; glucose uptake;
ADIPOSE TISSUEADIPOSE TISSUE:: glucose uptake; lipid mobilization
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What type of side effects may be related with What type of side effects may be related with glucocorticoid administration?glucocorticoid administration?
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CushingCushings syndromes syndrome – long lasting increase – long lasting increase in plasma corticoidsin plasma corticoids
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CushingCushings syndromes syndrome is the result of: is the result of:
• Administration of exogenous hormones• Adrenocortical tumors• Hypersecretion of ACTH• Ectopic secretion of ACTH
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CushingCushings syndromes syndrome• skin and subdermal tissues are thin, and muscles are poorly
developed • wounds heal poorly and minor trauma causes bruises and
ecchymoses • very severe osteoporosis • facial hair and acne • obesity with „buffalo torso” and „moon face”• adrenal diabetes • 80% of patients have hypertension • mental symptoms and sleep
disorders• reduced sex drive and fertility in man• irregular or stopped menstrual
cycles in women
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Obesity with Obesity with „buffalo torso„buffalo torso””
AcneAcne
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Obesity and Cushing • Cortisol acts via intracellular receptors on
transcription factors. • Exposure to glucocorticoids stimulates adipocyte
differentiation and adipogenesis via transcriptional activation of key differentiation genes (eg. lipoproteine lipase LPL, glycerol-3-phosphate dehydrogenase and leptin)
• Cortisol in the presence of insulin favors lipid accumulation by stimulation of LPL activity and by inhibition of basal and catecholamine-stimulated lipolysis
• Cortisol strongly stimulates appetite
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Cushing syndromeCushing syndrome
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Cushing Syndrome
Obesity
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Cushing Syndrome
Depression
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Explain following symptoms in Cushing’s Explain following symptoms in Cushing’s syndrome:syndrome:
• Lack of menses in women; infertility in men• Excess body hair in women and acne• Hypertension
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Mineralocorticoids Mineralocorticoids Aldosterone
(z. glomerulosa)
If the aldosterone of ten million people were pooled together, only one gram of the hormone would result.
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Aldosterone secretion
• Hyperkalemia
• Increased ECF osmolarity
• RAS
• ACTH
• Very low Na in ECF• ANP/BNP (via decreased Na reabsorption in
collecting ducts and inibition of renin)
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Liver
Lung
Angiotensin-convertingEnzyme (ACE)
ReninKidney
Angiotensinogen
Angiotensin I
Angiotensin II
Aldosterone
Zonaglomerulosa
cells
Mineralocorticoids
– RASRAS
Decreased kidney blood pressure ( ECF) renin converts angiotensinogen to angiotensin I. Lung ACE converts angiotensin I to II angiotensin II stimulates aldosterone release.
Aldosterone causes Na+ and H2O retention, increase in ECF and finally inhibition of the primary stimuli
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AII
• Vasoconstrictor
• Increases vasopressin
• Increases thirst
• Increases proxy tubule Na reabsorption
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Effects ofEffects of mineralocorticoidsmineralocorticoids::
• They cause Na+ to be conserved in the ECF, while more K+ and H+ is excreted into the urine
• They also increase the reabsorption of Na+ and the secretion of K+ by the ducts of salivary and sweat glands
• Excessive amounts of aldosterone will cause: hypokalemia, muscle weakness and mild alkalosis
Cells in the kidney channels (collecting
tubule)
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HyperaldosteronismHyperaldosteronism- Conn’s syndrome- Conn’s syndrome
Type Cause Source Effects
Primary (Conn’s syndrome)
Adrenal tumor or adrenal hyperplasia
Problem within adrenals
ECF, alkalosis, hypertension, K+ depletion
Secondary Edematous states, CHF, ascites, nephrosis
Adrenals responding to low ECF
ECF, edema, alkalosis, hypertension, K+ depletion
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Remember! - Think about Conn’s syndromeConn’s syndrome if your patient has hypertension and very low K+ level.
- Na + level is usually normal (aldosterone escape)
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Adrenal androgensAdrenal androgens
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Effects of adrenalEffects of adrenal androgens and androgens and estrogenesestrogenes
• Androgens are the hormones responsible for masculinizationmasculinization, and they also promote protein anabolism protein anabolism and growthand growth
• They cause epiphyses to fuse in the long bones, thus eventually stopping growth
• They slightly increase NaNa++, K, K++, H, H22O, O,
CaCa++++, sulfate and phosphate, sulfate and phosphate retention and they increase the size of the kidneys.
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The androgenital syndrome:The androgenital syndrome:
• typical masculine characteristics:
• much deeper voice
• occasionally baldness
• masculine distribution of hair
on the body
• masculine features
• salt loosing formsalt loosing form and
hypertensive formhypertensive form
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Deficiency of 21-beta21-beta hydroxylasehydroxylase (salt loosing form)
Deficiency of 11-beta hydroxylase11-beta hydroxylase – hypertensive form
Androgeniatal Androgeniatal syndromesyndrome
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Masculinized genitals of female baby
Genitals of male baby (4-year old boy)
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Adrenal insufficiencyAdrenal insufficiency
Loss of glucocorticoid and mineralocorticoid action – predict the
typical findings
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Addison's diseaseAddison's disease• Low plasma Na+, high plasma K+ • inability to produce concentrated
urine by the kidneys excessive urination
• Vomiting, loss of appetite, anorexia, dehydration
• Low blood pressure• Muscle weakness, fatigue• Low blood sugar• Excess pigmentation of skin in
some patients
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Addison’s disease
weakness
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The lack of all adrenocorticoidsThe lack of all adrenocorticoids - Addison's diseaseAddison's disease
Type Hormone profile
Causes Source Effects
Primary
Secondary
Corticoids ACTH
Corticoids ACTH
Idiopathic, infection, surgery, cancer
Hypothalamic-pituitary disease, Hypothalamic-pituitary inhibition (iatrogenic, ectopic steroids)
Problem in adrenals
Problem in hypothalamic-pituitary axis
Weakness, fatigue, anorexia, hypotension, weight loss, hyperpigmentation (only in primary Addison’s), fasting hypoglycemia