ENDOCRINOLOGY Flashcards
Network of ductless glands that secrete hormones directly into the blood
Considered to be the regulatory system of the body
Regulated by means of control of hormone synthesis rather than by degradation
Endocrine System
Chemical signals produced by specilized cells, secreted into the blood stream and carried to a target tissues
Hormones
An increased in the product results to elevation of the activity of the system and the production rate
Ex: Gonadal, Thyroidal and Adrenocortical hormone
Positive Feedback System
An increased in the product results to decreased activity of the system and the production rate
Ex: Leutenizing Hormone
Negative Feedback system
Secreted in one location and release into blood circulation; binds to specific receptor to elicit physiological response
Endocrine
Secreted in endocrine cells and released into interstitial space; binds to specific receptor in adjacent cell and affects its dunction
Paracrine
Secreted in endocrine cells and released into interstitial space; binds to specific receptor in adjacent cell and affects its function
Paracrine Hormones
Secreted in edocrine cells and sometimes released into interstitial space; binds to specific receptor on cell of origin resulting to self-regulation of its function
Autocrine
Secreted in endocrine cells and remains in relation to plasma membrane; acts on immediately adjacent cell by direct cell-to-cell contact
Juxtacrine Hormone
Secreted in endocrine cells and remained as well as function inside the synthesis of origin
Intracrine hormone
Secreted in endocrine cells and released into lumen of gut; affects their function
Exocrine Hormone
Secreted in neurons and released into extracellular space; binds to receptor in nearby cell and affects its funciton
Neurocrine Hormone
Synthesized and stored within the cell in the form of secretory granules and are cleaved as needed
Cannot cross the cell membrane due to their large molecular size and thus; produce their effects on the outer surface of the cell
Peptides and Proteins
Follicle-Stimulating Hormone
HCG
Thyroid Stimulating Hormone
Erythropoietin
Glycoprotein
ACTH
ADH
GH
Angiotensin
Calcitonin
Cholecystokinin
Gastrin
Glucagon
Insulin
Melanocyte-Stimulating Hormone
Oxytocin
PTH
Prolactin
Somatostatin
Polypeptide
Lipid molecules that have cholesterol as a common precurosi
Produced by adrenal glands, ovaries, testes and placenta
Water insoluble (hydrophobic) and circulate bound to a carrier protein
Steroids
Derived from an amino acid & they are intermediary between steroid and protein hormones
Ex: Epinephrine, Norepinephrine, Triiodothyronine, Thyroxine
Amines
Portion of the brain located in the walls and floor of the third ventricle
Link between the nervous system and the endocrine system
Hypothalamus
Hormone
TRH
Gn-RH
GH-IH
GH-RH
PIF
Hormones produced in the Hypothalamus
Attached to the midbrain
Secretes melatonin that decreases the pigmentation of the skin
Secretions are controlled by nerve stimuli
Pineal Gland
“Master Gland”
Located in a small cavity in the sphenoid bone of the skull called the sella turcica or Turkish saddle
Connected by the infundibular stalk to the median eminence of the hypothalamus
All pituitary hormones have circadian rhythms
Pituitary Gland
Hypophysis
“True Endocrine Gland”
Regulates the released and production of hormones
Hormones are either peptides or glycoproteins
Adenohypophysis
Anterior Pituitary Gland
Secrete growth hormone
Immunochemical Test
Somatotrophs
Secrete prolactin
Immunochemical Test
Lactotrophs
Mammotrophs
Secrete TSH
Immunochemical Test
Thyrotrophs
Secrete Proopiomelandcortin produce ACTH, B-endorphin, & B-lipotropin
Immunochemical Test
Corticotrophs
Secrete LH & FSH
Immunochemical Test
Gonadotrophs
Most abundant of all pituitary hormones
Major stimulus: Deep sleep
Secretion is erratic and occurts in short burst
Growth Hormone (GH) Somatotropin
Reference Value:
(< 7 ng/mL)
Most common cause of GH deficiency in children
Children with pituitary dwarfism, normal proportions are retained and show no intellectual abnormalities
Idiopathic Growth Hormone Deficiency
Most common etiology in adult-onset GH deficiency
Pituitary Adenoma
Due to Overproduction of GH
Acromegaly
Patient preparation for Growth Hormone measurement
Rest 30 minutes before blood collection
Screening Test for measurement of GH
Result: Elevated Serum GH
Physical Activity Test
Exercise test
Confirmatory test:
GOLD STANDARD for measurement of GH
Insulin Tolerance Test
2nd Confirmatory Test for GH
It is a 24-hour or nighttime monitoring of GH
Confirmed GH deficiency: Failure of GH to rise >5ng/mL in adults & >10ng/mL in children
Arginine Stimulation Test
Screening test for detection of Acromegaly
Insulin-like Growth Factor 1 (IGF-1)
Confirmatory test for the detection of Acromegaly
Blood is collected every after 30 minutes for 2 hours
Fasting sample is required
Glucose Suppression Test
Important markers in diagnosing fertility and menstrual cycle disorders
Present in the blood of both male and female at all ages
Gonadotropins
FSH & LH
Aids in spermatogenesis in male (Sertoli cells)
Aids in follicular growth in female
Follicle-Stimulating Hormone
Helps Leydig cells to produce testosterone and is necessary for ovulation and final follicular growth in female
Luteinizing Hormone
Acts on Thecal cells to cause the synthesis of androgens, estrogens and progesterone
Luteinizing Hormone
Elevation of FSH is a clue in the diagnosis of
Premature menopause
Also known as Thyrotropin
Main stimulus for the uptake of iodide by the thyroid gland
Acts to increase the number & size of follicular cells; stimulates thyroid hormone synthesis
Thyroid Stimulating Hormone (TSH)
Single-chain peptide without disulfide bonds
Produced in response to low serum cortisol, regulator of adrenal androgen synthesis
Adrenocorticotrophic Hormone (ACTH)
Deficiency of ACTH will lead to atrophy of the _____
Zona Glomerulosa
Zona Reticularis
Highest levels of ACTH is between
6:00 - 8:00
Lowest level of ACTH is between
6:00 pm - 11:00 pm
ACTH is increased in:
Addison’s Disease
Ectopic Tumors
Protein-rich meals
Best time to collect specimen for ACTH
8:00 am - 10:00 am
Pituitary lactogenic hormone; Stress hormone; Direct effector hormone
Functions in the initiation and maintenance of lactation
Acts in conjunction with estrogen & progesterone to promote breast tissue development
Prolactin
Major inhibitor of Prolactin:
Dopamine
Highest levels of prolactin during:
4:00 am - 8:00 am
8:00 pm - 10:00 pm
Reference Value of Prolactin
Male: 1-20 ng/mL
Female: 1-25 ng/mL
Capable of releasing the hormones: Oxytocin & Vasopressin but not capable of producing it
Release is in response to serum osmolality and by suckling
Neurohypophysis
Posterior Pituitary Gland
Secreted in association with a carrier protein
Stimulates contractions of the gravid uterus at term “Fergusson Reflex”
Released in response to neural stimulation of receptors in birth canal & uterus, and of touch receptors in breast
Oxytocin
Nonapeptide that acts on the distal convoluted and collecting tubules of the kidneys
Maintains Osmotic homeostatis by regulating Water balance
Decreases production of Urine by promoting reabsorption of water by the renal tubules
Increases blood pressure
Promotes Factor VII release from hepatocytes & factor VIII
Anti-Diuretic Hormone
Arginine Vasopressin (AVP)
Reference Value of Vasopressin/ ADH
0.5 - 2 pg/uL
Principal regulator of ADH secretion
Increased plasma osmolality
Deficiency of ADH; Results in severe Polyuria (>3L of urine/day)
Diabetes insipidus
Clinical picture of Diabetes insipidus
- Normoglycemia
- Polyuria with low specific gravity
- Polydipsia
- Polyphagia
Deficiency of ADH with normal ADH receptor
Due to failure of the pituitary gland to secrete ADH
Large volume of urine excreted (3-20L/day)
True Diabetes Insipidus
Neurogenic DI
Characterized by having normal ADH but abnormal ADH receptor
Due to failure of the kidneys to respond to normal or elevated ADH levels
Nephrogenic Diabetes Insipidus
Diagnostic Test for Diabetes Insipidus
Fasting: 10:00 pm onwards
After 8-12 hours without fluid intake, urine osmolality does not rise above 300 mOsm/kg
Overnight Water Deprivation Test
Concentration Test
Overnight Water Deprivation Test
ADH: LOW
Kidneys rapidly acts to conserve water in response to Exogenous ADH administration
Neurogenic DI
Overnight Water Deprivation Test
ADH: N/High
Administration of additional ADH has little or no effect on renal water reabsorption
Nephrogenic DI
Refers to the sustained production of ADH in the absence of a known stimuli
Characterized by decreased urine volume, low plasma osmolality and normal or elevated urine sodium levels
Syndrome of Inappropriate Antidiuretic Hormone Secretion (SIADH)
Also known as the butterfly-shaped gland
Consist of two lobes located in the lower part of the neck
Thyroid Gland
Fundamental structural unit of the thyroid gland
Follicles
Two types of cells in Thyroid Gland
Follicular cells (T3 & T4)
Parafollicular Cells (Calcitonin)
Glycoprotein that acts as a preformed matrix containing tyrosyl groups
Stored in the follicular colloi of the thyroid gland
Thyroglobulin
Most important element in the biosynthesis of thyroid hormone
Iodine
Neuroendocrine system that regulates the production and secretion of thyroid hormones
Hypothalamic-Pituitary-Thyroid Axis (HPTA)
Most active thyroid hormonal activity
75-80% is produced from the tissue deiodination of T4
Better indicator of recovery from hyperthyroidism as well as the recognition of recurrence of hyperthyroidism
Triiodothyronine
T3
Reference Value for T3
Adult: 60-160 ug/dL
Child: 105-245 ng/dL
Principal Secretory product
Major fraction of organic iodine in the circulation
Prohormone for T3 production
Amount of serum T4 is a good indicator of the thyroid secretory rate
Tetraiodothyronine
T4
Transports majority of T3 (affinity for T3 is lower than T4)
Transports 70-75% of total T4
Thyroxine-Binding Globulin
TBG
Transports 15-20% of total T4
T3 has NO affinity for prealbumin
Thyroxine-Binding Prealbumin (Transthyretin)
Transports T3 and 10% of T4
Thyroxine-Binding Albumin
Thyroid autoantibodies responsible for autoimmune thyroid disorders:
- Thyroperoxidase (TPO)
- Thyroglobulin
- TSH Receptor
Autoantibody involved in Hashimoto’s disease
Thyroperoxidase
Autoantibody involved in Grave’s disease
TSH Receptor
Excess of circulating thyroid hormone
Hyperthyroidism
Elevated T3 and T4
Decreased TSH
Primary hyperthyroidism
Increased FT4 and TSH
Secondary Hyperthyroidism
Signs and Symptoms:
1. Tachycardia
2. Tremors
3. Weight LOSS
4. HEAT intolerance
5. Emotional ability
6. Menstrual changes
Hyperthyroidism
Group of syndromes caused by high levels of free thyroid hormone in the circulation
Thyrotoxicosis
FT3 increased
FT4 Normal
TSH Low
T3 Thyrotoxicosis
Plummer’s Disease
T3 Normal or Low
T4 Increased
TSH Low
T4 Thyrotoxicosis
Most commonc cause of Thyrotoxicosis
Antibodies are produced that activate the TSH receptor
Occurs 6x more commonly in women
Features: Exophthalmos & pritibial myxedema
Graves’ Disease
Diffuse Toxic Goiter
Thyroid turns into a wooy or stony hard mass
Riedel’s Thyroiditis
Shows no clinical symptoms but
TSH Low
FT3 FT4 Normal
Subclinical Hyperthyroidism
Associated with neck pain, low-grade fever and swings in thyroid function tests
Thyroidal peroxidase (TPO) antibodies are absent
De Quervain’s Thyroiditis
Subacute Granulomatous Thyroiditis
Insufficient amounts of thyroid hormone are available to tissues
Treated with thyroid hormone replacement therapy
Hypothyroidism
Signs & Symptoms:
1. Bradycardia
2. Weight GAIN
3. Coarsened skin
4. COLD intolerance
5. Mental Dullness
Hypothyroidism
Primarily due to deficiency of elemental ioding
Caused by destruction or ablation of thyroid gland
Primary Hypothyroidism
Most common cause of Primary Hypothyroidism
Characterized by a thyroid replaced by a nest of lymphoid tissue causing cell lysis and inflammatory reaction
TSH High
TPO Antibody POSITIVE
Hashimoto’s Disease
Peculial nonpitting swelling of the skin
Skin becomes infiltrated by mucopolysaccharides
Myxedema
Severe form of Primary Hypothyroidism
Myxedema Coma
Due to pituitary destruction or pituitary adenoma
T3 T4 Low
TSH Low
Secondary Hypothyroidism
Due to hypothalamic disease
T3 T4 low
TSH Low
Tertiary hypothyroidism
Defect in the development or function of the fland
Screening: T4 Low
Confirmatory: TSH High
Congenital Hypothyroidism
Cretinism
TSH Value <10mIU/L
No further test
TSH value 10-12mIU/L
Repeat test in 2-6 weeks
TSH >20mIU/L
For Endocrinologic evaluation to diagnose hypothyroidism
T3 T4 Normal
TSH S. High
Subclinical Hypothyroidism
Measures the relationship between TRH & TSH secretions
Used to differentiate euthyroid and hyperthyroid patients who had undetectable TSH levels
TRH Stimulation Test
Most important thyroid function test
Best method for detecting clinically significvant thyroid dysfunction
Most clinically sensitive assay for the detection of primary thyroid disorders
Helps in early detection of hypothyroidism
Differentiates primary from secondary hypothyroidism
TSH Test
Smallest endocrine gland in the body
Parathyroid Gland
Most common cause of hypercalcemia
Due to presence of a functioning parathyroid adenoma
Accompanied with phosphaturia
Lab:
1. PTH High
2. Ionized Ca High
3. Ca in Urine High
4. Phosphate Low
Primary Hyperparathyroidism
Develops in response to decrease serum calcium
Diffuse hyperplasia of all 4 glands
Patient develops severe bone disease
Secondary Hyperparathyroidism
Occurs with Secondary hyperparathyroidism
Phosphate Normal to High
Tertiary Hyperparathyrodism
Due to accidental injury to the parathyroid gland during surgery
Hypoparathyroidism
Has pyramid-like shape located above the kidneys
Composed of distinct but conjoined glands, the outer adrenal cortex and inner adrenal medulla
Adrenal Gland
Outer Region of the Adrenal gland secreting the Steroid hormone
Major site of steroid hormone production
Yellow
Adrenal Cortext
3 Layers of Adrenal Cortex
- Zona glomerulosa - Mineralocorticoid
- Zona fasiculata - Glucocorticoid
- Zona reticularis - Androstenedione & Dehydroepiandrosterone
Principal Glucocorticoid
Synthesis is regulated by ACTH
Mostly bound to glycoprotein, transcortin
Stimulates Gluconeogenesis
Cortisol
Urinary Metabolite of Cortisol:
- 17-hydroxycorticosteroid
- 17-Ketogenic steroids
Method to detect 17-hydroxycorticosteroid
Porter-Silber Method (Yellow)
Phenyl hydrazine in H2SO4 + Alcohol
Method used to detect 17-Ketogenic Steroids
Method: Zimmermann Reaction (Reddish Purple)
Meta-Dinitrobenzene
Norymberski (Oxidation procedure)
Excessive production of CORTISOL & ACTH, but decreased Aldosterone & renin
Hypercortisolism
Cushing’s Syndrome
Due to decreased Cortisol production - 90% destruction of the adrenal cortex
Aldosterone deficiency
ACTH release
Disorder: Addison’s Disease
Primary Hypocorticolism
Primary Adrenal Insufficiency
due to hypothalamic-pituitary insufficiency with loss of ACTH
Secondary Hypocorticolism
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