Chapter 4-Adrenal Glands

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Chapter 4-Adrenal Glands. Ch. 4-- Study Guide . Critically read (1) pages pp. 61-69 before postsecretory metabolism of adrenal cortical hormones section; (2) pp. 71-76 (physiology of the mineralocorticoids) before Effects on water balance subsection. - PowerPoint PPT Presentation

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Chapter 4-Adrenal Glands

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Ch. 4-- Study Guide 1. Critically read (1) pages pp. 61-69 before

postsecretory metabolism of adrenal cortical hormones section; (2) pp. 71-76 (physiology of the mineralocorticoids) before Effects on water balance subsection.

2. Comprehend Terminology (the text in bold/italic)

3. Study and understand the text and corresponding figures.

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4.1. Introduction

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§ Introduction1. Adrenal hormones:

– required for maintenance of life– Without them, deranged

electrolyte or CHO metabolism, hypoglycemic coma, and death

– Outer cortex– three steroid hormones: mineralocorticoids, glucocorticoids, and androgens

– Inner medulla—a component of the sympathetic nervous system

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4.2. Morphology

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§ Morphology (1)– Fig. x + 4.11. Location— right above the kidneys2. Gross Anatomy and Histology–

A. Outer cortex-- > 3/4 of adrenal mass– Divided into 3 zones and produces

steroids;– Zona glomerulosa– aldosterone– Zona fasciculata– cortisol and androgens– Zona reticularis– cortisol and androgensB. Inner medulla -- @ 1/4 – A modified sympathetic ganglion, releases

epinephrine and norepinephrine4-6

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4.3. Adrenal cortex

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§ Adrenal Cortex1. Adrenal cortex is essential for maintenance of

life. 2. Addison’s disease– pathological destruction or

surgical removal of the adrenal cortex– death within 1-2 weeks

3. Why? 3 categories of hormones: Fig. 4.2– ALL come from cholesterol

– Mineralocorticoids– essential to maintain sodium and potassium balance– Aldosterone + deoxycorticosterone (DOC)

– Glucocorticoids– include cortisol and corticosterone– maintain CHO reserves

– Androgens– on puberty and fetal life4-10

The principal adrenal steroid hormones

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4.3A. Adrenocortical hormones

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§ adrenocortical hormones1. All the adrenal steroids are from

cholesterol– same as other steroids including . . .

2. Naming steroids—– Fully saturated 21-carbon molecule is

called pregnane– Delta– location of double bond(s) and

-ane changes to -ene or to –diene– Presence of a hydroxyl group (-ol)– Presence of a keto group (-one)– Fig. 4.3

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All three reactions are catalyzed by a single enzyme, cytochrome P450SCC. Pregnenolone– an important molecule for other adrenal hormones

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§ Adrenal Cortex (1)1. Pregnenolone and progesterone (21

Carbons) is the common precursor of all steroid hormones produced by the adrenals or the gonads (Fig. 4.4)

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Z. glomerulosa

Z. fasciculata

Z. reticularis; 19 carbons

Z. glomerulosa & reticularis Biosynthesis of adrenal cortical H.

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§ Adrenal Cortex (2)2. A hydroxyl group at carbon 11 is found in

all glucocorticoids–that is corticosterone and cortisol

3. Corticosterone is the major glucocorticoid in the rat but is of only secondary importance in humans

4. Cortisol is the most potent of the naturally occurring glucocorticoids in humans

5. Corticosterone is a precursor of aldosterone (a major mineralocorticoid)

Fig. 4.44-17

Z. glomerulosa

Z. fasciculata

Z. reticularis; 19 carbons

Z. glomerulosa & reticularis Biosynthesis of adrenal cortical H.

Glucocorticoids

A major mineralocorticoid4-18

§ Adrenal Cortex (3)6. Male hormones--Steroids in the 19-carbon

series usually have androgenic (male hormone) activity)

7. Locations--This above reaction normally occurs only after puberty, and is confined to the cells of the zona reticularis (Fig. 4.4)

8. Female hormones--19-carbon steroids are precursors of the estrogens (female hormones; 18-carbon)—unsaturated A ring due to aromatization (loss of the methyl carbon at position 19). This reaction happens in ovary and placenta normally.

Fig. 4.5 4-19

Z. glomerulosa

Z. fasciculata

Z. reticularis; 19 carbons– Male steroid hormones

Z. glomerulosa & reticularis Biosynthesis of adrenal cortical H.

Glucocorticoids

A major mineralocorticoid4-20

Principal 18-carbon estrogens

A

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4.3B. Control of adrenal cortical hormone synthesis

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§ Effects of ACTH1. ACTH has impact on z. fasciculata and

reticularis but not glomerulosa2. Through G-protein-coupled mem receptor3. Increases cholesterol availability– in the cell

and specifically also in mitochondria4. (specifically on androgens)--ACTH is the only

hormone known to control synthesis of the adrenal androgens (dehydroepiandrosterone sulfate; DHEAS)

5. Adrenarche– Beginning of increased secretion of adrenal hormones at puberty (another similar term: menarche)

Fig. 4.6 + 4.7 4-23

Steroid synthesis by ACTH in Z. Fasciculata

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§ control of aldosterone synthesis1. Location– in zona glomerulosa2. ACTH is NOT an important regulator of

aldosterone production in most species3. Angiotensin II (from Angiotensinogen, from

liver) regulates the production of aldosteroneHow?4. (first messenger-receptor)—Angiotensin II

binds with specific G-protein-coupled receptor5. (second messengers)– IP3 and calcium to

promote the formation of pregnenolone from cholesterol

Fig. x + 4.84-26

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Angiotensin II

§ control of aldosterone synthesis• Impact by three ions--6. (K+)-- Cells of the zona glomerulosa are

very sensitive to changes in potassium in the ECF; increased K+ (ECF) stimulates production of aldosterone

7. (Na+)-- Aldosterone is the principal regulator of body sodium content

8. (Ca+2)-- Intracellular calcium also stimulates the synthesis of aldosterone.

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4.3C. Adrenal steroid hormones in blood

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§ plasma binding proteins1. CBG, corticosteroid binding globulin (or

called transcortin), and albumin2. Both are produced in the liver3. CBG has a single steroid hormone

binding site whose affinity for cortisol is 20 times higher than for aldosterone

4. About 95% of the cortisol and about 60% of the aldosterone in blood are bound to protein

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4.4A. Physiology of the mineralocorticoids (Mainly aldosterone & deoxycorticosterone, also others; See Fig. 4.2)

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The principal adrenal steroid hormones

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§ Introduction1. Aldosterone is the most important

mineralocorticoid2. Aldosterone’s physiology and life-threatening

changes: A. Reabsorption of sodium is decreased and fall

of sodium in blood (hyponatremia)B. An accompanying loss of waterC. Resulting decrease in blood volume called

hypovolemia.D. Locations of these effects– the kidney is the

most important; also in the sweat glands, the colon, and the salivary glands

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§ Aldosterone on the kidney-A1. Increased potassium excretion2. Sodium retention (decrease in urinary

sodium)– The above two ions are not tightly coupled and sodium is not simply exchanged for potassium

3. Increase in body weight due to fluid retention

Fig. 4.13

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§ Aldosterone on the kidney-B1. Aldosterone sensitive cells called

principal cells found in the nephrons– specifically in the connecting tubule and the cortical portion of the collecting duct

2. Details—– Sodium (two-step transfer)– (A) enters the

principal cells via sodium channels; (B) and is pumped out by sodium-potassium ATPase

– Potassium– ROMK (renal outer medullary K+) channels on both sides of principal cells

– Fig. 9.2; Fig. 4.144-37

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In principal cells of cortical

colleting duct

lumenInterstitium

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§ Aldosterone on the kidney-C1. On principal cells–

A. after 30 minutes– resulting in prolonged half-life of ENaC

B. Later effects--Mainly by increasing the expression of proteins associated of sodium transport

– Fig. 4.14B & 4.14C

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In principal cells—aldosterone effects after 30

min. delay

SGK1– serum glucocorticoid dependent kinase 1ENaC--Epithelial sodium channel

Mainly by prolonging the half-life of ENaC

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In principal cells– later effects of

aldosterone

Mainly by increasing the expression of proteins associated of sodium transport.

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§ Aldosterone on the kidney-D1. Aldosterone also targets intercalated

cells found in the nephrons– specifically in the distal nephron and collecting duct

– Fig. 9.2; Fig. 4.14D

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Mainly by promoting the secretion of protons (hydrogenions) in luminal membranes

AR– Aldosterone receptors on the cell surface

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4.4B– Regulation of aldosterone secretion

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§ Aldosterone secretion and function1. Stimuli for aldosterone secretion:

– Primary-- Angiotensin II– Also by ACTH and high conc. of potassium

2. Angiotensin II is regulated by renin from the kidney (glomerular arterioles)

– Principal stimulus for renin secretion is a decrease in the blood (or vascular) volume

3. Principal physiology of aldosterone:– Defend the blood volume by reabsorbing

sodium & water from the kidney– X + Fig. 4.15

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Monitored variables– A--blood volume B--plasma potassium conc.

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4.5– Physiology of the glucocorticoids

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§ Glucocorticoids1. Physiology roles can be summarized as

“Coping with adversity”2. Major role-- in maintaining carbohydrate

reserves3. Do have many other functions (Table

4.2); every tissue of the body is affected by glucocorticoids

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§ Major effects on energy metabolism by the glucocorticoids (cortisol etc.)

1. CHO—A. Decrease utilization of glucoseB. Promote hepatic gluconeogenesis (produce sugar from

nonglucose precursors)C. Defend against hypoglycemiaD. Promote glycogen storage in liver and muscle

2. Proteins--Inhibit protein synthesis and promote proteolysis (rapid breakdown of stored protein in muscle tissues etc.)

3. Lipids-- Increase lipolysis in adipose tissue

Fig. 4.16 4-52

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