the endocrine system2

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THE ENDOCRINE SYSTEM Endocrinology – the study of the biological effects of hormones released by ENDOCRINE GLANDS and the diseases caused by their dysfunction. ENDOCRINE GLANDS – ductless glands the release chemical regulators called HORMONES directly into the extracellular fluid ( interstitial fluid and blood). What is the difference between hormones and neurotransmitters?

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Page 1: The endocrine system2

THE ENDOCRINE SYSTEM

Endocrinology – the study of the biological effects of hormones released by ENDOCRINE GLANDS and

the diseases caused by their dysfunction.

ENDOCRINE GLANDS – ductless glands the release chemical regulators called HORMONES directly into

the extracellular fluid ( interstitial fluid and blood).

What is the difference between hormones and neurotransmitters?

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Figure 16.1

The “Major” Endocrine Glands

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Release of Hormones• Hormones are released in response to

homeostatic imbalances referred to as STIMULI.

• Hormones work via NEGATIVE FEEDBACK to maintain homeostasis

• Negative Feedback Mechanism – the biological effects of hormones negate/eliminate the stimuli that caused the release of the hormones

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General Stimuli for the release of Hormones

• Humoral stimuli – changes in the levels of chemicals in the body’s humors ( bodily fluids) stimulate endocrine glands to release hormones.

• Neural stimuli – activation of the nervous system stimulates endocrine glands to release hormones

• Hormonal stimuli - released hormones stimulate endocrine glands to release other hormones

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Figure 16.5

STIMULI FOR THE RELEASE OF HORMONES

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Nomenclature• Hormones are named based on:• Organ of Origin – the endocrine gland releasing

the hormone• Ex. Parathyroid hormone

• Function – the major biological effect of the hormone

• Ex. Follicle stimulating hormone

• Chemical Structure – unique feature of the chemical structure

• Ex. Triiodothyronine(T3)

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3 Chemical Structures of Hormones• Biogenic amine hormones – hormones

derived from the amino acid TYROSINE

Biogenic hormones are generally polar chemicals

• Peptide/protein/glycoproteins hormones– hormones composed of a sequence of amino acids: attain structural complexity; protein with carbohydrate moiety attached.

These hormones are polar

• Steroid hormones – hormones derived from cholesterol.

Steroid hormones are non polar

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Target Cells/Tissues for a Hormone• Express ACCESSIBLE, FUNCTIONAL

receptors that the hormone binds to on or inside the cells.

• A cell may act as a target for several hormones.

• A target cell that possess different types of receptors may be bound to more than one hormone simultaneously.

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Hormonal Interactions – How hormones interact with their target cells

• Classical Endocrine Interaction- hormones are released into the bloodstream to reach their target cells

• Paracrine Interaction – hormones are released into interstitial fluid to reach their target cells located nearby.

• Juxtacrine Interaction – hormones bind to their target cells as they are being released from the endocrine cells which are in close contact with the target cells.

• Autocrine Interaction – the endocrine cells releasing the hormone also act as target cells for the hormone

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Hormone Receptors

• Characteristics:• All hormone receptors are Proteins (globular proteins)• Hormones bind to their cognate receptors REVERSIBLY

H + R <--------HR• Hormone receptors bind with high affinity and specificity to their

cognate (specific) hormone• Hormone receptors are located on the plasma membrane or inside

the target cells –

2 types of Hormone Receptors:

Membrane or cell surface receptors – bind polar hormones = biogenic amine hormones; peptide/protein/glycoprotein

hormones

Intracellular receptors – cytoplasmic and nuclear receptors

- bind non polar hormones = steroid hormones and the

thyroid hormones

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Figure 16.2

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Figure 16.3

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Figure 16.4

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Hormonal Interrelationships – How hormones affect the biological actions of other hormones

• Agonism – a hormone binds to the receptors of another hormone and mimics the biological effects of that hormone

• Antagonism – a hormone binds to the receptors of another hormone blocking the hormone from binding to its own receptors; No biological effects of that hormone observed

• Permissiveness – the biological effects of a hormone ( bound to its own receptors), increases the levels of another hormone and/or increases the number of receptors of that hormone resulting in the overall increase in the biological effects of that hormone

• Cooperativity – hormones work in in tandem on the same target tissue to bring about a desired biological effect.

• Synergism – a group of hormones affects a target tissue simultaneously to bring about a biological response greater than the sum of the individual hormonal effects

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Figure 16.6

HYPOTHALAMIC-PITUITARY AXIS

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Table 16.1.4

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Table 16.1.2

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Table 16.1.3

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Table 16.1.1

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Figure 16.7

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Figure 16.8

THE THYROID GLAND

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Figure 16.9

BIOSYNTHESIS OF THE THYROID HORMONES = T3 & T4

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Table 16.2.1

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Table 16.2.2

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Figure 16.10

GOITER

EXOPHTHALMOS OF GRAVES’ DISEASE

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Figure 16.11

PARATHYROID GLANDS

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Figure 16.12

THE BIOLOGICALACTIONS OF PTH

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Figure 16.13

THE ADRENAL GLANDS

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The Adrenocorticosteroids• Gluccocorticoids – CortisolFunctions: Cortisol stimulates gluconeogenesis, lipolysis,

protein catabolism

Pharmacological uses of cortisol: as anti-inflammatory drugs and as immunosuppressive drugs

Hyper function- Cushing’s syndrome

Hypofunction – Adrenocortical insufficiency

• Adrenal Androgens – DHEA and Androstenedione:

Function: substrates for testosterone• Mineralocorticoids – Aldosterone

Function: Aldosterone stimulates NaCl and water reabsorption

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Table 16.3.1

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Table 16.3.2

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Figure 16.15

Cushing’s syndrome : Buffalo hump; Moon face

Buffalohump

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Figure 16.16

THE CATECHOLAMINES = EPINEPHRINE & NOREPINEPHRINE

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Table 16.3.2

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Figure 16.1

The Major Endocrine Glands

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Figure 16.17

THE PANCREAS:

Alpha cells – produce glucagon

Beta cells – produce insulin

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Figure 16.18

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Figure 16.18 top

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Figure 16.18 bottom

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Figure 16.19

SYMPTOMS OF DIABETES MELLITUS - due to insulin deficiency or dysfunctional insulin receptors