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Endocrine System: Overview
• Acts with the nervous system to coordinate and integrate the activity of body cells
• Influences metabolic activities by means of hormones transported in the blood
• Responses occur more slowly but tend to last longer than those of the nervous system
• Endocrine glands: pituitary, thyroid, parathyroid, adrenal, and pineal glands
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Endocrine System: Overview
• Some organs produce both hormones and exocrine products (e.g., pancreas and gonads)
• The hypothalamus has both neural and endocrine functions
• Other tissues and organs that produce hormones include adipose cells, thymus, cells in the walls of the small intestine, stomach, kidneys, and heart
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Figure 16.1
Pineal glandHypothalamus
Pituitary gland
Parathyroid glands(on dorsal aspectof thyroid gland)Thymus
Thyroid gland
Adrenal glands
Pancreas
Ovary (female)
Testis (male)
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Chemical Messengers
• Hormones: long-distance chemical signals that travel in the blood or lymph
• Autocrines: chemicals that exert effects on the same cells that secrete them
• Paracrines: locally acting chemicals that affect cells other than those that secrete them
• Autocrines and paracrines are local chemical messengers and will not be considered part of the endocrine system
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Chemistry of Hormones
• Two main classes
1.Amino acid-based hormones
• Amines, thyroxine, peptides, and proteins
2.Steroids
• Synthesized from cholesterol
• Gonadal and adrenocortical hormones
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Mechanisms of Hormone Action
• Hormone action on target cells
1. Alter plasma membrane permeability of membrane potential by opening or closing ion channels
2. Stimulate synthesis of proteins or regulatory molecules
3. Activate or deactivate enzyme systems
4. Induce secretory activity
5. Stimulate mitosis
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Mechanisms of Hormone Action
• Two mechanisms, depending on their chemical nature
1. Water-soluble hormones (all amino acid–based hormones except thyroid hormone)
• Cannot enter the target cells
• Act on plasma membrane receptors
• Coupled by G proteins to intracellular second messengers that mediate the target cell’s response
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Mechanisms of Hormone Action
2. Lipid-soluble hormones (steroid and thyroid hormones)
• Act on intracellular receptors that directly activate genes
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Plasma Membrane Receptors and Second-Messenger Systems
• cAMP signaling mechanism
1.Hormone (first messenger) binds to receptor
2.Receptor activates G protein
3.G protein activates adenylate cyclase
4.Adenylate cyclase converts ATP to cAMP (second messenger)
5. cAMP activates protein kinases
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Plasma Membrane Receptors and Second-Messenger Systems
• cAMP signaling mechanism
• Activated kinases phosphorylate various proteins, activating some and inactivating others
• cAMP is rapidly degraded by the enzyme phosphodiesterase
• Intracellular enzymatic cascades have a huge amplification effect
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Figure 16.2
Hormone (1st messenger)binds receptor.
Receptoractivates Gprotein (GS).
G proteinactivatesadenylatecyclase.
cAMP acti-vates proteinkinases.
Adenylatecyclaseconverts ATPto cAMP (2ndmessenger).
Receptor
G protein (GS)
Adenylate cyclase
Triggers responses oftarget cell (activatesenzymes, stimulatescellular secretion,opens ion channel,etc.)
Hormones thatact via cAMPmechanisms:
EpinephrineACTHFSHLH
Inactiveprotein kinase
Extracellular fluid
Cytoplasm
Activeproteinkinase
GDP
GlucagonPTHTSHCalcitonin
1
2 3 4
5
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Figure 16.2, step 1
Hormone (1st messenger)binds receptor.
Receptor
Hormones thatact via cAMPmechanisms:
EpinephrineACTHFSHLH
Extracellular fluid
Cytoplasm
GlucagonPTHTSHCalcitonin
1
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Figure 16.2, step 2
Hormone (1st messenger)binds receptor.
Receptoractivates Gprotein (GS).
Receptor
G protein (GS)
Hormones thatact via cAMPmechanisms:
EpinephrineACTHFSHLH
Extracellular fluid
Cytoplasm
GDP
GlucagonPTHTSHCalcitonin
1
2
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Figure 16.2, step 3
Hormone (1st messenger)binds receptor.
Receptoractivates Gprotein (GS).
G proteinactivatesadenylatecyclase.
Receptor
G protein (GS)
Adenylate cyclase
Hormones thatact via cAMPmechanisms:
EpinephrineACTHFSHLH
Extracellular fluid
Cytoplasm
GDP
GlucagonPTHTSHCalcitonin
1
2 3
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Figure 16.2, step 4
Hormone (1st messenger)binds receptor.
Receptoractivates Gprotein (GS).
G proteinactivatesadenylatecyclase.
Adenylatecyclaseconverts ATPto cAMP (2ndmessenger).
Receptor
G protein (GS)
Adenylate cyclase
Hormones thatact via cAMPmechanisms:
EpinephrineACTHFSHLH
Extracellular fluid
Cytoplasm
GDP
GlucagonPTHTSHCalcitonin
1
2 3 4
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Figure 16.2, step 5
Hormone (1st messenger)binds receptor.
Receptoractivates Gprotein (GS).
G proteinactivatesadenylatecyclase.
cAMP acti-vates proteinkinases.
Adenylatecyclaseconverts ATPto cAMP (2ndmessenger).
Receptor
G protein (GS)
Adenylate cyclase
Triggers responses oftarget cell (activatesenzymes, stimulatescellular secretion,opens ion channel,etc.)
Hormones thatact via cAMPmechanisms:
EpinephrineACTHFSHLH
Inactiveprotein kinase
Extracellular fluid
Cytoplasm
Activeproteinkinase
GDP
GlucagonPTHTSHCalcitonin
1
2 3 4
5
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Plasma Membrane Receptors and Second-Messenger Systems
• PIP2-calcium signaling mechanism
• Used by some amino acid–based hormones in some tissues
• Involves a G protein
• G protein activates phospholipase C enzyme
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Plasma Membrane Receptors and Second-Messenger Systems
• Phospholipase splits membrane phospholipid PIP2 into two second messengers: diacylglycerol (DAG) and IP3
• DAG activates protein kinases; IP3 triggers release of Ca2+
• Ca2+ alters enzymes or channels or binds to the regulatory protein calmodulin
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Intracellular Receptors and Direct Gene Activation
• Steroid hormones and thyroid hormone
1.Diffuse into their target cells and bind with intracellular receptors
2.Receptor-hormone complex enters the nucleus
3.Receptor-hormone complex binds to a specific region of DNA
4.This prompts DNA transcription to produce mRNA
5.The mRNA directs protein synthesis
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Figure 16.3
mRNA
New protein
DNA
Hormoneresponseelements
Receptor-hormonecomplex
Receptorprotein
Cytoplasm
Nucleus
Extracellular fluid
Steroidhormone
The steroid hormonediffuses through the plasmamembrane and binds anintracellular receptor.
The receptor-hormone complex entersthe nucleus.
The receptor- hormonecomplex binds a hormoneresponse element (aspecific DNA sequence).
Binding initiatestranscription of thegene to mRNA.
The mRNA directsprotein synthesis.
Plasmamembrane
1
2
3
4
5
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Figure 16.3, step 1
Receptor-hormonecomplex
Receptorprotein
Cytoplasm
Nucleus
Extracellular fluid
Steroidhormone
The steroid hormonediffuses through the plasmamembrane and binds anintracellular receptor.
Plasmamembrane
1
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Figure 16.3, step 2
Receptor-hormonecomplex
Receptorprotein
Cytoplasm
Nucleus
Extracellular fluid
Steroidhormone
The steroid hormonediffuses through the plasmamembrane and binds anintracellular receptor.
The receptor-hormone complex entersthe nucleus.
Plasmamembrane
1
2
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Figure 16.3, step 3
DNA
Hormoneresponseelements
Receptor-hormonecomplex
Receptorprotein
Cytoplasm
Nucleus
Extracellular fluid
Steroidhormone
The steroid hormonediffuses through the plasmamembrane and binds anintracellular receptor.
The receptor-hormone complex entersthe nucleus.
The receptor- hormonecomplex binds a hormoneresponse element (aspecific DNA sequence).
Plasmamembrane
1
2
3
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Figure 16.3, step 4
mRNA
DNA
Hormoneresponseelements
Receptor-hormonecomplex
Receptorprotein
Cytoplasm
Nucleus
Extracellular fluid
Steroidhormone
The steroid hormonediffuses through the plasmamembrane and binds anintracellular receptor.
The receptor-hormone complex entersthe nucleus.
The receptor- hormonecomplex binds a hormoneresponse element (aspecific DNA sequence).
Binding initiatestranscription of thegene to mRNA.
Plasmamembrane
1
2
3
4
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Figure 16.3, step 5
mRNA
New protein
DNA
Hormoneresponseelements
Receptor-hormonecomplex
Receptorprotein
Cytoplasm
Nucleus
Extracellular fluid
Steroidhormone
The steroid hormonediffuses through the plasmamembrane and binds anintracellular receptor.
The receptor-hormone complex entersthe nucleus.
The receptor- hormonecomplex binds a hormoneresponse element (aspecific DNA sequence).
Binding initiatestranscription of thegene to mRNA.
The mRNA directsprotein synthesis.
Plasmamembrane
1
2
3
4
5
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Target Cell Specificity
• Target cells must have specific receptors to which the hormone binds
• ACTH receptors are only found on certain cells of the adrenal cortex
• Thyroxin receptors are found on nearly all cells of the body
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Target Cell Activation
• Target cell activation depends on three factors
1. Blood levels of the hormone
2. Relative number of receptors on or in the target cell
3. Affinity of binding between receptor and hormone
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Target Cell Activation
• Hormones influence the number of their receptors
• Up-regulation—target cells form more receptors in response to the hormone
• Down-regulation—target cells lose receptors in response to the hormone
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Hormones in the Blood
• Hormones circulate in the blood either free or bound
• Steroids and thyroid hormone are attached to plasma proteins
• All others circulate without carriers
• The concentration of a circulating hormone reflects:
• Rate of release
• Speed of inactivation and removal from the body
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Hormones in the Blood
• Hormones are removed from the blood by
• Degrading enzymes
• Kidneys
• Liver
• Half-life—the time required for a hormone’s blood level to decrease by half
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Interaction of Hormones at Target Cells
• Multiple hormones may interact in several ways
• Permissiveness: one hormone cannot exert its effects without another hormone being present
• Synergism: more than one hormone produces the same effects on a target cell
• Antagonism: one or more hormones opposes the action of another hormone
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Control of Hormone Release
• Blood levels of hormones
• Are controlled by negative feedback systems
• Vary only within a narrow desirable range
• Hormones are synthesized and released in response to
1. Humoral stimuli
2. Neural stimuli
3. Hormonal stimuli
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Humoral Stimuli
• Changing blood levels of ions and nutrients directly stimulates secretion of hormones
• Example: Ca2+ in the blood
• Declining blood Ca2+ concentration stimulates the parathyroid glands to secrete PTH (parathyroid hormone)
• PTH causes Ca2+ concentrations to rise and the stimulus is removed
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Figure 16.4a
(a) Humoral Stimulus
Capillary (lowCa2+ in blood)
Parathyroidglands
Thyroid gland(posterior view)
PTH
Parathyroidglands
1 Capillary blood containslow concentration of Ca2+,which stimulates…
2 …secretion ofparathyroid hormone (PTH)by parathyroid glands*
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Chemical classes of hormonesAmino acid derivatives: polar-water soluble
Tyrosine
Catecholamines: epinephrine and norepinephrine
thyroxine
Induce fight or flight response- increase sympathetic nervous targets
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Chemical classes of hormones
Tryptophane based - Melatonin
Resets body clock.
Water soluble
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Chemical classes of hormones
Peptide hormones: - chains of amino acids Water soluble
Glycoproteins: TSH, FSH, LH, EPO
ADH, ACTH, GH, ANP, Insulin, Calcitonin, leptin
Less than 200 aa.
2 chain- insulin
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Chemical classes of hormones
Lipid derivatives- nonpolar (often require carriers)
Steroids
testosterone
cholesterol
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Steroids make it hard to know when to quit
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Chemical classes of hormones
Eicosanoids: leukotrienes, prostaglandins,
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Figure 16.14
Primary regulators Other factors
Blood volumeand/or blood
pressure
Angiotensin II
Blood pressureand/or blood
volume
K+ in blood
DirectstimulatingeffectRenin
Initiatescascadethatproduces
Kidney
Hypo-thalamus
Heart
CRH
Anteriorpituitary
Zona glomerulosaof adrenal cortex
Enhancedsecretionof aldosterone
Targetskidney tubules
Absorption of Na+ andwater; increased K+ excretion
Blood volumeand/or blood pressure
Inhibitoryeffect
Stress
ACTH Atrial natriureticpeptide (ANP)
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Homeostatic Imbalances of Aldosterone
• Aldosteronism—hypersecretion due to adrenal tumors
• Hypertension and edema due to excessive Na+
• Excretion of K+ leading to abnormal function of neurons and muscle
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Glucocorticoids (Cortisol)
• Keep blood sugar levels relatively constant
• Maintain blood pressure by increasing the action of vasoconstrictors
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Glucocorticoids (Cortisol)
• Cortisol is the most significant glucocorticoid
• Released in response to ACTH, patterns of eating and activity, and stress
• Prime metabolic effect is gluconeogenesis—formation of glucose from fats and proteins
• Promotes rises in blood glucose, fatty acids, and amino acids
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Homeostatic Imbalances of Glucocorticoids
• Hypersecretion—Cushing’s syndrome
• Depresses cartilage and bone formation
• Inhibits inflammation
• Depresses the immune system
• Promotes changes in cardiovascular, neural, and gastrointestinal function
• Hyposecretion—Addison’s disease
• Also involves deficits in mineralocorticoids
• Decrease in glucose and Na+ levels
• Weight loss, severe dehydration, and hypotension
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Figure 16.15
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Gonadocorticoids (Sex Hormones)
• Most are androgens (male sex hormones) that are converted to testosterone in tissue cells or estrogens in females
• May contribute to
• The onset of puberty
• The appearance of secondary sex characteristics
• Sex drive
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Adrenal Medulla
• Chromaffin cells secrete epinephrine (80%) and norepinephrine (20%)
• These hormones cause
• Blood glucose levels to rise
• Blood vessels to constrict
• The heart to beat faster
• Blood to be diverted to the brain, heart, and skeletal muscle
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Adrenal Medulla
• Epinephrine stimulates metabolic activities, bronchial dilation, and blood flow to skeletal muscles and the heart
• Norepinephrine influences peripheral vasoconstriction and blood pressure
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Figure 16.16
Short-term stress More prolonged stress
Stress
Hypothalamus
CRH (corticotropin-releasing hormone)
Corticotroph cellsof anterior pituitary
To target in blood
Adrenal cortex(secretes steroidhormones)
GlucocorticoidsMineralocorticoids
ACTH
Catecholamines(epinephrine andnorepinephrine)
Short-term stress response
1. Increased heart rate2. Increased blood pressure3. Liver converts glycogen to glucose and releases glucose to blood4. Dilation of bronchioles5. Changes in blood flow patterns leading to decreased digestive system activity and reduced urine output6. Increased metabolic rate
Long-term stress response
1. Retention of sodium and water by kidneys2. Increased blood volume and blood pressure
1. Proteins and fats converted to glucose or broken down for energy2. Increased blood glucose3. Suppression of immune system
Adrenal medulla(secretes amino acid-based hormones)
Preganglionicsympatheticfibers
Spinal cord
Nerve impulses
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Pineal Gland
• Small gland hanging from the roof of the third ventricle
• Pinealocytes secrete melatonin, derived from serotonin
• Melatonin may affect
• Timing of sexual maturation and puberty
• Day/night cycles
• Physiological processes that show rhythmic variations (body temperature, sleep, appetite)
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Pancreas
• Triangular gland behind the stomach
• Has both exocrine and endocrine cells
• Acinar cells (exocrine) produce an enzyme-rich juice for digestion
• Pancreatic islets (islets of Langerhans) contain endocrine cells
• Alpha () cells produce glucagon (a hyperglycemic hormone)
• Beta () cells produce insulin (a hypoglycemic hormone)
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Figure 16.17
Pancreaticislet (ofLangerhans)
• (Glucagon- producing) cells
• (Insulin- producing) cells
Pancreaticacinarcells (exocrine)
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Glucagon
• Major target is the liver, where it promotes
• Glycogenolysis—breakdown of glycogen to glucose
• Gluconeogenesis—synthesis of glucose from lactic acid and noncarbohydrates
• Release of glucose to the blood
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Insulin
• Effects of insulin
• Lowers blood glucose levels
• Enhances membrane transport of glucose into fat and muscle cells
• Participates in neuronal development and learning and memory
• Inhibits glycogenolysis and gluconeogenesis
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Insulin Action on Cells
• Activates a tyrosine kinase enzyme receptor
• Cascade leads to increased glucose uptake and enzymatic activities that
• Catalyze the oxidation of glucose for ATP production
• Polymerize glucose to form glycogen
• Convert glucose to fat (particularly in adipose tissue)
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Figure 16.18
Liver
Liver
Tissue cells
Stimulates glucose uptake by cells
StimulatesglycogenformationPancreas
Pancreas
Insulin
Bloodglucosefalls tonormalrange.
Stimulatesglycogenbreakdown
Bloodglucoserises tonormalrange.
Glucagon
Stimulus Bloodglucose level
Stimulus Bloodglucose level
GlycogenGlucose
GlycogenGlucose
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Homeostatic Imbalances of Insulin
• Diabetes mellitus (DM)
• Due to hyposecretion or hypoactivity of insulin
• Three cardinal signs of DM
• Polyuria—huge urine output
• Polydipsia—excessive thirst
• Polyphagia—excessive hunger and food consumption
• Hyperinsulinism:
• Excessive insulin secretion; results in hypoglycemia, disorientation, unconsciousness
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Table 16.4
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Ovaries and Placenta
• Gonads produce steroid sex hormones
• Ovaries produce estrogens and progesterone responsible for:
• Maturation of female reproductive organs
• Appearance of female secondary sexual characteristics
• Breast development and cyclic changes in the uterine mucosa
• The placenta secretes estrogens, progesterone, and human chorionic gonadotropin (hCG)
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Testes
• Testes produce testosterone that
• Initiates maturation of male reproductive organs
• Causes appearance of male secondary sexual characteristics and sex drive
• Is necessary for normal sperm production
• Maintains reproductive organs in their functional state
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Other Hormone-Producing Structures
• Heart
• Atrial natriuretic peptide (ANP) reduces blood pressure, blood volume, and blood Na+ concentration
• Gastrointestinal tract enteroendocrine cells
• Gastrin stimulates release of HCl
• Secretin stimulates liver and pancreas
• Cholecystokinin stimulates pancreas, gallbladder, and hepatopancreatic sphincter
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Other Hormone-Producing Structures
• Kidneys
• Erythropoietin signals production of red blood cells
• Renin initiates the renin-angiotensin mechanism
• Skin
• Cholecalciferol, the precursor of vitamin D
• Adipose tissue
• Leptin is involved in appetite control, and stimulates increased energy expenditure
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Other Hormone-Producing Structures
• Skeleton (osteoblasts)
• Osteocalcin prods pancreatic beta cells to divide and secrete more insulin, improving glucose handling and reducing body fat
• Thymus
• Thymulin, thymopoietins, and thymosins are involved in normal the development of the T lymphocytes in the immune response
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Developmental Aspects
• Hormone-producing glands arise from all three germ layers
• Exposure to pesticides, industrial chemicals, arsenic, dioxin, and soil and water pollutants disrupts hormone function
• Sex hormones, thyroid hormone, and glucocorticoids are vulnerable to the effects of pollutants
• Interference with glucocorticoids may help explain high cancer rates in certain areas
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Developmental Aspects
• Ovaries undergo significant changes with age and become unresponsive to gonadotropins; problems associated with estrogen deficiency begin to occur
• Testosterone also diminishes with age, but effect is not usually seen until very old age
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Developmental Aspects
• GH levels decline with age and this accounts for muscle atrophy with age
• TH declines with age, contributing to lower basal metabolic rates
• PTH levels remain fairly constant with age, but lack of estrogen in older women makes them more vulnerable to bone-demineralizing effects of PTH