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Introduction 
ArginineVasopression plasma (AVP) 
Calcitonin 
Catecholamines 
Epinephrines 
Metanephrines 
Vanillylmandelic acid 
Glucagon plasma 
Gonadal function test 
Gonadal steroids 
Androstenedione 
Estradiol 
Progesterone 
Testosterone
Arginine vasopressin (AVP), also known 
as vasopressin, argipressin or antidiuretic hormone (ADH), is 
a hormone found in most mammals , including humans. 
Vasopressin is a peptide hormone that controls the reabsorption of 
molecules in the tubules of the kidneys by affecting the tissue's 
permeability. 
It also increases peripheral vascular resistance , which in turn 
increases arterial blood pressure. 
It plays a key role in homeostasis, and the regulation of water, 
glucose, and salts in the blood. 
It is synthesized in the hypothalamus and stored in vesicles at the 
posterior pituitary. Most of it is stored in the posterior pituitary to be 
released into the bloodstream, however, some AVP is also released 
directly into the brain.
One of the most important roles of AVP is to 
regulate the body's retention of water. it is 
released when the body is dehydrated and 
causes the kidneys to conserve water, thus 
concentrating the urine, and reducing urine 
volume. In high concentrations, it also raises 
blood pressure by inducing 
moderate vasoconstriction.
In Kidney 
Vasopressin has two effects by which it contributes to 
increased urine osmolality (increased concentration) 
and decreased water excretion. 
Cardiovascular system 
Vasopressin increases peripheral vascular resistance 
and thus increases arterial blood pressure. This effect 
appears small in healthy individuals,however it 
becomes an important compensatory mechanism for 
restoring blood pressure in hypovolemic shock such as 
that which occurs during hemorrhage.
Decreased vasopressin release or decreased renal 
sensitivity to AVP leads to diabetes insipidus, a condition 
featuring hypernatremia(increased blood sodium 
concentration), polyuria (excess urine production), 
and polydipsia (thirst). 
High levels of AVP secretion (syndrome of inappropriate 
antidiuretic hormone, SIADH) and 
resultant hyponatremia (low blood sodium levels) occurs 
in brain diseases and conditions of the lungs(Small cell 
lung carcinoma). In the perioperative period, the effects of 
surgical stress and some commonly used medications 
(e.g., opiates, syntocinon, anti-emetics) lead to a similar 
state of excess vasopressin secretion. This may cause mild 
hyponatremia for several days.
Alcohol Consumption 
Upon excessive alcohol consumption, the 
vasopressin production is reduced 
significantly. The inability to store water in 
the kidneys will prove fatal to those who 
participate in heavy consumption of alcohol, 
due to the dehydration caused by 
dilute urine and vomit. 
Random intake of AVP: 1.5-5.6pmol/L(1.5- 
6ng/ml)
Calcitonin is a hypocalcemnic peptide hormone that in many ways acts as the 
physiologic antagonist to parathyroid hormone. 
Calcitonin is a hormone known to participate in calcium and phosphorus 
metabolism. In mammals, the major source of calcitonin is from the parafollicular 
or C cells in the thyroid gland, but it is also synthesized in a wide variety of other 
tissues, including the lung and intestinal tract. 
The thyroid is the major source of the hormone & the cells involved in calcitonin 
synthesis arise from neural crest tissue. 
The naturally occuring calcitonins consist of a peptide chain of 32 amino acids. 
In humans, calcitonin has at best a minor role in regulating blood concentrations 
of calcium. One interesting piece of evidence to support this statement is that 
humans with chronically increased (medullary thyroid cancer) or decreased 
(surgical removal of the thyroid gland) levels of calcitonin in blood usually do not 
show alterations from normal in serum calcium concentration.
A large and diverse set of effects has been attributed to calcitonin, but in 
many cases, these were seen in response to pharmacologic doses of the 
hormone, and their physiologic relevance is suspect. It seems clear 
however, that calcitonin plays a role in calcium and phosphorus 
metabolism. In particular, calcitonin has the ability to decrease blood 
calcium levels at least in part by effects on two well-studied target organs: 
Bone: Calcitonin suppresses resorption of bone by inhibiting the activity of 
osteoclasts, a cell type that "digests" bone matrix, releasing calcium and 
phosphorus into blood. 
Kidney: Calcium and phosphorus are prevented from being lost in urine by 
reabsorption in the kidney tubules. Calcitonin inhibits tubular reabsorption 
of these two ions, leading to increased rates of their loss in urine. 
It seems clear that there are species differences in the importance of 
calcitonin as a factor affecting calcium homeostasis.
The secretin of calcitonin is under the direct control of blood calcium: 
As increase in calcium causes an increase & decrease in calcium causes a 
decrease in calcitonin levels. 
Once secreted calcitonin disappears from the circulation with a half life of 
2 to 15 mins. 
A large number of diseases are associated with abnormally increased or 
decreased levels of calcitonin. 
There are several therapeutic uses for calcitonin. It is used to treat 
hypercalcemia resulting from a number of causes, and has been a valuable 
therapy for Paget disease, which is a disorder in bone remodeling. 
Calcitonin also appears to be a valuable aid in the management of certain 
types of osteoporosis. 
Calcitonin, plasma: <50 ng/L (<50 pg/mL).
Catecholamines are small molecules made by nerve 
tissue (including the brain) and the adrenal gland. 
The major catecholamines 
are dopamine, norepinephrine, and epinephrine. 
These substances break down into other compounds, 
which leave our body through our urine. 
A urine test can be done to measure the level of 
catecholamines in our body. 
Catecholamines can also be measured with a blood 
test.
A listing of some major effects mediated by epinephrine and norepinephrine are: 
Increased rate and force of contraction of the heart muscle: this is predominantly an 
effect of epinephrine acting through beta receptors. 
Constriction of blood vessels: norepinephrine, in particular, causes widespread 
vasoconstriction, resulting in increased resistance and hence arterial blood 
pressure. 
Dilation of bronchioles: assists in pulmonary ventilation. 
Stimulation of lipolysis in fat cells: this provides fatty acids for energy production in 
many tissues and aids in conservation of dwindling reserves of blood glucose. 
Increased metabolic rate: oxygen consumption and heat production increase 
throughout the body in response to epinephrine. Medullary hormones also 
promote breakdown of glycogen in skeletal muscle to provide glucose for energy 
production. 
Dilation of the pupils: particularly important in situations where you are 
surrounded by velociraptors under conditions of low ambient light. 
Inhibition of certain "non-essential" processes: an example is inhibition of 
gastrointestinal secretion and motor activity. 
Common stimuli for secretion of adrenomedullary hormones include exercise, 
hypoglycemia, hemorrhage and emotional distress.
Elevated levels of urinary catecholamines may 
indicate: 
Acute anxiety 
Ganglioblastoma (very rare) 
Ganglioneuroma(very rare) 
Neuroblastoma (rare) 
Pheochromocytoma (rare) 
Severe stress 
Additional conditions under which the test may be 
performed: 
Multiple endocrine neoplasia (MEN)
Epinephrine (also known as adrenaline) is 
a hormone and neurotransmitter. 
It increases heart rate, contracts blood vessels, 
dilates air passages and participates in the fight-or-flight 
response of the sympathetic nervous system. 
As a hormone, epinephrine acts on nearly all body 
tissues. Its actions vary by tissue type and tissue 
expression of adrenergic receptors. For example, 
epinephrine causes smooth muscle relaxation in the 
airways, but causes contraction of the smooth 
muscle that lines mostarterioles.
Measurement in biological fluids 
1. Epinephrine may be quantitated in blood, plasma or 
serum as a diagnostic aid, to monitor therapeutic 
administration or to identify the causative agent in a 
potential poisoning victim. 
2. Endogenous plasma epinephrine concentrations in 
resting adults are normally less than 10 ng/L, but may 
increase by 10-fold during exercise and by 50-fold or 
more during times of stress. 
3. Pheochromocytoma patients often have plasma 
epinephrine levels of 1000-10,000 ng/L. 
4. Parenteral administration of epinephrine to acute-care 
cardiac patients can produce plasma concentrations of 
10,000 to 100,000 ng/L.

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Biochemical components

  • 1. SUBMITTED TO SUBMITTED BY KIRAN SIR PRIYANKA DAS
  • 2. Introduction ArginineVasopression plasma (AVP) Calcitonin Catecholamines Epinephrines Metanephrines Vanillylmandelic acid Glucagon plasma Gonadal function test Gonadal steroids Androstenedione Estradiol Progesterone Testosterone
  • 3. Arginine vasopressin (AVP), also known as vasopressin, argipressin or antidiuretic hormone (ADH), is a hormone found in most mammals , including humans. Vasopressin is a peptide hormone that controls the reabsorption of molecules in the tubules of the kidneys by affecting the tissue's permeability. It also increases peripheral vascular resistance , which in turn increases arterial blood pressure. It plays a key role in homeostasis, and the regulation of water, glucose, and salts in the blood. It is synthesized in the hypothalamus and stored in vesicles at the posterior pituitary. Most of it is stored in the posterior pituitary to be released into the bloodstream, however, some AVP is also released directly into the brain.
  • 4. One of the most important roles of AVP is to regulate the body's retention of water. it is released when the body is dehydrated and causes the kidneys to conserve water, thus concentrating the urine, and reducing urine volume. In high concentrations, it also raises blood pressure by inducing moderate vasoconstriction.
  • 5. In Kidney Vasopressin has two effects by which it contributes to increased urine osmolality (increased concentration) and decreased water excretion. Cardiovascular system Vasopressin increases peripheral vascular resistance and thus increases arterial blood pressure. This effect appears small in healthy individuals,however it becomes an important compensatory mechanism for restoring blood pressure in hypovolemic shock such as that which occurs during hemorrhage.
  • 6. Decreased vasopressin release or decreased renal sensitivity to AVP leads to diabetes insipidus, a condition featuring hypernatremia(increased blood sodium concentration), polyuria (excess urine production), and polydipsia (thirst). High levels of AVP secretion (syndrome of inappropriate antidiuretic hormone, SIADH) and resultant hyponatremia (low blood sodium levels) occurs in brain diseases and conditions of the lungs(Small cell lung carcinoma). In the perioperative period, the effects of surgical stress and some commonly used medications (e.g., opiates, syntocinon, anti-emetics) lead to a similar state of excess vasopressin secretion. This may cause mild hyponatremia for several days.
  • 7. Alcohol Consumption Upon excessive alcohol consumption, the vasopressin production is reduced significantly. The inability to store water in the kidneys will prove fatal to those who participate in heavy consumption of alcohol, due to the dehydration caused by dilute urine and vomit. Random intake of AVP: 1.5-5.6pmol/L(1.5- 6ng/ml)
  • 8. Calcitonin is a hypocalcemnic peptide hormone that in many ways acts as the physiologic antagonist to parathyroid hormone. Calcitonin is a hormone known to participate in calcium and phosphorus metabolism. In mammals, the major source of calcitonin is from the parafollicular or C cells in the thyroid gland, but it is also synthesized in a wide variety of other tissues, including the lung and intestinal tract. The thyroid is the major source of the hormone & the cells involved in calcitonin synthesis arise from neural crest tissue. The naturally occuring calcitonins consist of a peptide chain of 32 amino acids. In humans, calcitonin has at best a minor role in regulating blood concentrations of calcium. One interesting piece of evidence to support this statement is that humans with chronically increased (medullary thyroid cancer) or decreased (surgical removal of the thyroid gland) levels of calcitonin in blood usually do not show alterations from normal in serum calcium concentration.
  • 9. A large and diverse set of effects has been attributed to calcitonin, but in many cases, these were seen in response to pharmacologic doses of the hormone, and their physiologic relevance is suspect. It seems clear however, that calcitonin plays a role in calcium and phosphorus metabolism. In particular, calcitonin has the ability to decrease blood calcium levels at least in part by effects on two well-studied target organs: Bone: Calcitonin suppresses resorption of bone by inhibiting the activity of osteoclasts, a cell type that "digests" bone matrix, releasing calcium and phosphorus into blood. Kidney: Calcium and phosphorus are prevented from being lost in urine by reabsorption in the kidney tubules. Calcitonin inhibits tubular reabsorption of these two ions, leading to increased rates of their loss in urine. It seems clear that there are species differences in the importance of calcitonin as a factor affecting calcium homeostasis.
  • 10. The secretin of calcitonin is under the direct control of blood calcium: As increase in calcium causes an increase & decrease in calcium causes a decrease in calcitonin levels. Once secreted calcitonin disappears from the circulation with a half life of 2 to 15 mins. A large number of diseases are associated with abnormally increased or decreased levels of calcitonin. There are several therapeutic uses for calcitonin. It is used to treat hypercalcemia resulting from a number of causes, and has been a valuable therapy for Paget disease, which is a disorder in bone remodeling. Calcitonin also appears to be a valuable aid in the management of certain types of osteoporosis. Calcitonin, plasma: <50 ng/L (<50 pg/mL).
  • 11. Catecholamines are small molecules made by nerve tissue (including the brain) and the adrenal gland. The major catecholamines are dopamine, norepinephrine, and epinephrine. These substances break down into other compounds, which leave our body through our urine. A urine test can be done to measure the level of catecholamines in our body. Catecholamines can also be measured with a blood test.
  • 12. A listing of some major effects mediated by epinephrine and norepinephrine are: Increased rate and force of contraction of the heart muscle: this is predominantly an effect of epinephrine acting through beta receptors. Constriction of blood vessels: norepinephrine, in particular, causes widespread vasoconstriction, resulting in increased resistance and hence arterial blood pressure. Dilation of bronchioles: assists in pulmonary ventilation. Stimulation of lipolysis in fat cells: this provides fatty acids for energy production in many tissues and aids in conservation of dwindling reserves of blood glucose. Increased metabolic rate: oxygen consumption and heat production increase throughout the body in response to epinephrine. Medullary hormones also promote breakdown of glycogen in skeletal muscle to provide glucose for energy production. Dilation of the pupils: particularly important in situations where you are surrounded by velociraptors under conditions of low ambient light. Inhibition of certain "non-essential" processes: an example is inhibition of gastrointestinal secretion and motor activity. Common stimuli for secretion of adrenomedullary hormones include exercise, hypoglycemia, hemorrhage and emotional distress.
  • 13. Elevated levels of urinary catecholamines may indicate: Acute anxiety Ganglioblastoma (very rare) Ganglioneuroma(very rare) Neuroblastoma (rare) Pheochromocytoma (rare) Severe stress Additional conditions under which the test may be performed: Multiple endocrine neoplasia (MEN)
  • 14. Epinephrine (also known as adrenaline) is a hormone and neurotransmitter. It increases heart rate, contracts blood vessels, dilates air passages and participates in the fight-or-flight response of the sympathetic nervous system. As a hormone, epinephrine acts on nearly all body tissues. Its actions vary by tissue type and tissue expression of adrenergic receptors. For example, epinephrine causes smooth muscle relaxation in the airways, but causes contraction of the smooth muscle that lines mostarterioles.
  • 15. Measurement in biological fluids 1. Epinephrine may be quantitated in blood, plasma or serum as a diagnostic aid, to monitor therapeutic administration or to identify the causative agent in a potential poisoning victim. 2. Endogenous plasma epinephrine concentrations in resting adults are normally less than 10 ng/L, but may increase by 10-fold during exercise and by 50-fold or more during times of stress. 3. Pheochromocytoma patients often have plasma epinephrine levels of 1000-10,000 ng/L. 4. Parenteral administration of epinephrine to acute-care cardiac patients can produce plasma concentrations of 10,000 to 100,000 ng/L.