Title: Endocrinology 2
1Endocrinology 2
2Adrenal Glands
- We have 2 adrenal glands located above the
kidneys. - The adrenal gland is divided into 3 portions, the
adrenal cortex the adrenal medulla. - The adrenal cortex is further divided into 3
layers - Zona glomerulosa ? releases aldosteron
- Zona fasciculata ? releases cortisol
- Zona reticularis ? releases sex steroids
3Adrenal Medulla
- Adrenal medulla cells secrete catecholamines
(epinephrine norepinephrine, 4 1 ratio , more
epinephrine secretion) - It is innervated by sympathetic nerve fibers,
activated by stress, meaning that it will support
the sympathetic nervous system - Secretion is initiated by stimulation of
preganglionic sympathetic neurons
4Adrenal Medulla
- Effects are very similar to those caused by
stimulation of sympathetic nervous system, they
last 10 times longer. - Activation of adrenal medulla along with the
sympathetic nervous system prepares the body for
greater physical performance (fight-or-flight)
5Effects of Fight-or-Flight
- Increase heart rate
- Vasoconstricts arterioles to most tissues
- Vasodilates arterioles to muscles, lungs and
heart - Dilate pupils so more light reaches retina
- Stimulates ventilation
- Increases glycogenolysis in the liver to provide
energy - Stimulate glucagon ? increases blood glucose
level - Inhibits insulin ? prevent the uptake of glucose
from blood - Increases lipolysis in adipose tissue to provide
energy - Increases efficiency of muscle contraction
- Increases sweating ? heat loss
6Adrenal Cortex
- Secrets steroid hormones called corticosteroids
including - Mineralocorticoids (aldosterone)
- Glucocortecoids (cortisol)
- Sex steroids (estrogens, androgens)
7Adrenal Cortex
- Mineralocorticoids (aldosterone)
- Zona glomerulosa ? aldosterone ? kidneys ?
regulates Na and K balance in body fluids - Glucocortecoids (cortisol? catabolic hormone)
- ACTH stimulates the zona fasciculata ? cortisol
is released ? acts on liver, muscle adipose
tissue to regulate carbohydrate, prootein and fat
metabolism? leading to - Increase in serum glucose
- Increase in serum fatty acid
- Increase in serum amino acid
- Sex steroids (estrogens, androgens)
- Weak andorgens secreted by different zones of
adrenal cortex (Zona reticularis) - Not the main sex steroids, the main sex steroids
are provided by the gonads, these are supplement
of sex steroids secreted by gonads.
8Adrenal Cortex Secretion Abnormalities
- Cushings Disease
- Cause hypersecretion of corticosteroids
(cortisol) as a result of - Tumor of adrenal cortex (Cushing's syndrome)
- Oversecretion of ACTH from anterior pituitary (
Cushing's disease)
9Important!Cushings Disease is Different From
Cushings Syndrome
- Cushings Syndrom
- One cause for Cushings syndrome is exogenous
glucocorticoids. Meaning that a person take
corisol exogenously by injections or tablets to
treat various diseases. - Another cause for Cushings syndrome is a tumor
of the adrenal gland, the patient will have high
production of cortisol ? it will inhibit ACTH
through negative feedback mechanism. - In these two cases the person is said to have
Cushings syndrome
10Important!Cushings Disease is Different From
Cushings Syndrome
- Cushings Disease
- A patient has high secretion of ACTH from the
anterior pituitary ? high ACTH will stimulate the
adrenal gland to produce cortisol
11Important!Cushings Disease is Different From
Cushings Syndrome
- If you take a serum sample from a Cushings
Disease patient he will have - High levels of ACTH High level of cortisol
- If you take a serum sample from a Cushings
Syndrom patient he will have - Low levels of ACTH High level of cortisol
-
12Important!Cushings Disease is Different From
Cushings Syndrome
- Changes in the body are the same in the two cases
EXCEPT - The hyperpigmentation in Cushings Disease
patients because of excess ACTH - ACTH is a melanocyte stimulating hormone, it
stimulates the melanocyte , so the patient will
have a darker skin -
13Cushings Disease and Cushings Syndrome
- Characterized by
- Hyperglycemia because cortisol is a catabolic
hormone?it will cause the breakdown of
carbohydrates ? increase level if glucose in the
circulation - Hypertension because cortisol can stimulate Na
and water retention - Muscular weakness due to the breakdown of
protiens - Thin arms and legs
14Cushings Disease and Cushings Syndrome
- Those patients will also have red cheeks because
cortisol stimulates erythropoietin which is the
hormone that causes the production of red blood
cells from the bone marrow. - The patients also have purple abdominal striae,
the look like stretch marks but they are wider
and purple in color - Hirsutism a side effect of the stimulation of
ACTH is the stimulation of the androgens
production, and thats why growth of excessive
hair happens
15Addisons Disease
- Cause
- Inadequate secretion of cortisol and aldosterone
- Characterized by
- Hypoglycemia because of low cortisol.
- Na loss and K retention because of low
aldosterone. - Dehydration because of Na and water loss.
- Hypotension because of Na and water loss.
- Rapid wieght loss because cortisol is one of the
hormones that stimulates the appetite. - Generalized weakness.
- High ACTH causes hyperpigmentation.
- May lead to death if not treated with
corticosteroids.
16Adrenogenital Syndrome
- Cause
- Hypersecretion of adrenal sex hormones,
particularly androgens - In young children ? premature puberty and
enlarged genitals - In mature women ? growth of beard (Hirsutism)
boldness (similar to male boldness)
17Thyroid Gland
- Thyroid gland does not have a certain tissue to
act on it acts all over the body - It secretes
- Thyroxine (T4)
- Triiodothyronine (T3)
- Calcitonin ? responsible for phosphate and Ca
metabolism.
18Hypothyroidism
- 1- Iodine-deficiency (endemic goitre, meaning it
happens in a certain geographic area) - A form of hypothyroidism, caused by the lack of
adequate iodine in the died
19Hypothyroidism
- 2- Cretinism
- New born infants born in areas of low iodine
intake and endemic goitre. - Symptoms include mental retardation, short
stature, puffy face and hands, deaf mutism, etc.
20Hypothyroidism
- 2- Cretinism
- Happens becase the mother doesnt provide enough
thyroid hormone to the fetus during the first 3
months. - Thyroid hormone is important for the development
of CNS - During the first 3 months the fetus can not
produce thyroid hormone but depends on the mother - After the first 3 month the baby is able to
produce thyroid hormone on its own - But, if the baby was deprived from thyroid
hormone during the first 3 months, he will still
develop cretinism because the damage is done
21Hypothyroidism
- 3- Infantile hypothyroidism
- Occurs during childhood
- Symptoms include
- Retarded growth because thyroid hormone is needed
for the action of growth hormone. - Abnormal bone development.
- General lethargy.
- Low body temperature because of low BMR .
22Hypothyroidism
- 4- Hashimoto thyroditis
- Form of hypothyroidism .
- Characterized by a goitre, high concentration of
antibodies, which are directed against
thyroglobulin and thyroid peroxidase. - The progressive destruction of thyroid follicular
tissue results in hypothyroidism.
23Hypothyroidism
- 5- Myxoedema
- Hypothyroidism in adulthood
- Symptoms include
- Edema
- Low basal metabolic rate
- Cold intolerance
- Lethargy
- Weight gain tendency
24Whats Happening in The Case of Iodine-deficiency
Hypothyroidism?
- We have TRH stimulating the pituitary.
- TSH is secreted stimulating the thyroid gland.
- The thyroid glad is trying to produce T3 T4 but
it cant because of inadequate iodine (We need
iodine for the formation of T3 T4). - We will have low levels of T3 T4.
- Low negative feedback will lead to high TSH.
- TSH will act on the thyroid gland causing it
hypertrophy (become bigger in size) producing a
goitre.
25Goitres can occur in both hypothyroidism and
hyperthyroidism
26HyperthyroidismGraves Disease (Toxic Goitre)
- It is an autoimmune disease caused by antibodies
that are similar in structure to TSH, so they act
like causing the growth of the thyroid associated
with hypersecretion of thyroxine. - The antibodies will bind to the TSH receptors on
the thyroid gland - Then they will stimulate thyroid hormone
production the growth of the gland.
27HyperthyroidismGraves Disease (Toxic Goitre)
- Clinical symptoms include
- High metabolic rate
- High heart rate
- Wight loss
- Excessive sweating
- Heat intolerance
- Exopthalamus (bulging of the eyes because of
edema in tissues of eye sochet)
28Regulation of Calcium Phosphate
- Ca phosphate concentration in plasma is
affected by - Bone resorption taking Ca and phosphate out of
the bone into the circulation. - Bone absorption taking Ca and phosphate into
the bone. - intestinal absorption
- Urinary excretion
29Regulation of Calcium Phosphate
- Regulation of plasma calcium and phosphate by
- Parathyroid hormone
- Calcitriol (Dihydroxyvitamin D3)
- Calcitonin
30Parathyroid Hormone (PTH)
- Usually 4 parathyroid glands
- PTH is secreted by the parathyroid gland whenever
the plasma concentration of Ca begins to fall - PTH promotes a rise in blood calcium levels by
acting on - The bones ( causing bone resorption)
- kidneys ( causing reabsorption)
- Intestines (indirectly)
31Parathyroid Hormone (PTH)
- The stimulus of PTH secretion is low Ca.
- PTH will be released.
- It will act on the bone causing an increase in
bone resorption. - Ca will go from the bone to blood circulation.
- It will also cause an increase in Ca
reabsorption from the kidney. - It will promote formation of 1,25
dihydroxyvitamin D3 by acting on the kidney.
32Calcitriol (1,25 Dihydroxyvitamin D3)
- Production starts in the skin where Vitamin D3
(prehormone) is produced from precursor molecule
7-dehydrocholestrol under influence of sunlight. - Actions
- Activity stimulated by PTH
- Helps to raise plasma concentration of Ca and
phosphate by stimulating - Intestinal absorption of Ca and phosphate (main
function) - Resorption of bones
- Renal reabsorption of calcium and phosphate
33Calcitonin
- Calcium lowering hormone
- Secreted by the parafollicular cell in the
thyroid gland - It antagonizes the hypercalcemic effect of
calcitriol and PTH - Is stimulated by high plasma Ca and phosphate
levels and acts to lower Ca levels by - Inhibitong bone resorption ( cause bone
absorption) - Stimulating the urinary excretion of Ca and
phosphate by inhibiting their reabsorption by the
kidneys
34Rickets
- A disease in which the Bones become weaker
35Action of Insulin
- After approximately ½ an hour of having a meal we
have the peak of glucose level. - This will stimulate the secretion of insulin.
- Insulin will cause the glucose to be converted
into glycogen (glycogenesis) in the muscles. - Insulin will stimulate the uptake of glucose in
the liver to convert it into glycogen and also
into triglycerides (lipogesesis). - Glucose is also taken into the adipose tissue and
converted into triglycerides.
36Action of Glucagon
- When we have low levels of glucose in the
circulation glucagon is secreted. - It will act in the muscle causing the breakdown
of protein into amino acids. - It will act on adipose tissue to cause the
breakdown of triglycerides into fatty acids. - Amino acids fatty acids will be converted in
the liver into glucose. - Glucagon will also aid in the breakdown of
glycogen into glucose. - In the end youll have higher glucose level in
the circulation
37Abnormalities
- Diabetes Mellitus is characterized by
- Fasting hyperglycemia
- Glucose in the urine
- Types of Diabetes Mellitus
- Type 1 diabetes
- 10 of cases
- Also known as insulin dependent diabetes mellitus
- Caused by lack of insulin secretion as a result
of destruction of the beta cells - Also known as juvenile-onset diabetes
38Abnormalities
- Types of Diabetes Mellitus
- Type 2 diabetes
- 90 of cases
- Patients are usually over weight
- Also known as insulin independent diabetes
mellitus - Large amount of insulin secretion however,
decreased tissue sensitivity to insulin secreted - Also known as maturity-onset diabetes
39Long Term Complications of Diabetes Mellitus
- Strokes
- Retinopathy
- Blindness
- Hypertension
- Renal failure
- Impotence (in males)
- Skin infections that might lead to Gangrene
- Vascular diseases
40End of The Second Lecture