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Endocrine System Biology 211: Anatomy & Physiology 1

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Presentation on theme: "Endocrine System Biology 211: Anatomy & Physiology 1"— Presentation transcript:

1 Endocrine System Biology 211: Anatomy & Physiology 1
Tony Serino, Ph.D. Biology Department Misericordia University

2 Endocrine System Controls and modifies the internal environment by releasing chemicals (hormones) into the blood Slower response time but longer duration of action compared to nervous system

3 Chemical Messengers (hormones)
Hormone –secreted by cell into blood and acts on another cell some distance away Neurohormone –secreted by neuron into blood to affect a target cell some distance away Local hormones –secreted by cell into interstitial fluid to affects cells nearby Paracrines –affect neighboring cells Autocrines –affect the secreting cell Pheromones –secreted by cell onto body surface to affect cells of another individual

4 Hormones Chemical Classification
Amines –single or few amino acids, most water soluble Epinephrine, Thyroxine (but water insoluble), Melatonin Proteins –short to long chains of amino acids; water soluble GH, FSH, LH, Insulin, Glucagon, ADH, etc. Steroids –derivatives of cholesterol; water insoluble Estrogen, Testosterone, Progesterone, Cortisol, Aldosterone

5 Steroid Hormones

6 Characteristics Common to all Hormones
Must have target cell with appropriate receptor molecules Receptor-hormone complex must trigger events in target cell that changes its physiology Mechanisms for deactivating the hormone response must be present

7 Controlling Hormone Response
Half-life of the hormone Physiological range Modifying target cell response Up and down regulation Turning off secretion Negative feedback Control by other hormones, neurons and metabolites

8 Control of Hormone Secretion

9 Mechanisms of Hormone Action
2nd messengers Water Soluble Water Insoluble Carrier protein

10 2nd Messengers: cAMP

11 2nd Messengers: IP3 and Ca++-Calmodulin

12 Steroid Hormone Transduction

13 Different Styles of Secretion
Prohormone –a hormone that is made as a larger (inactive form) that must be changed prior to secretion (allows for storage of hormone in secreting cell) Ex.: proinsulin, pro-opiomelanocortin Prehormone –a hormone that is secreted in an inactive form that must be changed near or in the target cell Ex.: Thyroxine, Angiotensinogen

14 Proinsulin

15 Types of Endocrine Disorders
Hypersecretion Too much secretion of the hormone Hyposecretion Too little secretion of hormone Hyporesponsiveness Normal secretion, but little to no response by target cells

16 Endocrine Glands

17 Hypothalamus Control of Pituitary

18 Posterior Pituitary

19 Anterior Pituitary

20 Control of Growth Growth periods: prenatal and postnatal (consists of pre-puberal (especially the first 2 years –infancy) and puberty Several factors influence growth: genetics, diet, health, and hormonal balance Prenatal growth dominated by insulin secretion, post-natal dominated by GH, thyroxine, and sex hormones

21 GH secretion and effects
GH secretion stimulated by exercise, fasting, sleep (diurnal rhythm), stress, decreased plasma glucose, increased plasma AA (such as after a high protein meal) Increase protein synthesis Increase differentiation (increase mitosis)

22 GH interactions with other Hormones
Thyroxine: essential and permissive for GH Needed to maintain energy levels for growth Increases sensitivity of target cells to GH effects Insulin: essential for GH effects Dominant hormone for pre-natal growth Estrogen and Testosterone: surge at puberty stimulates GH release, synergistic with GH anabolism; also trigger epiphyseal closure Cortisol: anti-growth effects; decrease GH secretion, cell division, and increase catabolism

23 GH pathologies Hypersecretion:
Gigantism –in children with responsive epiphyseal plates Acromegaly –in adults, with closed epiphyseal plates

24 GH pathologies Hypofunction: Dwarfism –in children
Pituitary –decreased GH secretion Laron –decreased responsiveness due to lack of GH receptors 28 yo woman with pituitary dwarfism; 45” tall Achondroplastic Dwarfism (genetic dwarf) due to failure of cartilage to form in epiphyseal plate

25 Thyroid Location

26 Thyroid Follicle Parafollicular cells  calcitonin
(follicular cells  thyroxine) Parafollicular cells  calcitonin

27 T3 & T4 Formation and Secretion

28 T3 & T4

29 Control of Thyroxine Secretion
Short loop Long loop

30 Thyroid Malfunction Hypothyroidism
Endemic goiters –due to iodine deffeicency Cretinism –i thyroxine in child results in igrowth (dwarf) and severe mental retardation Myxedema –i thyroxine in adult, leads to swelling of tissues plus other symptoms

31 Cretinism

32 Thyroid Malfunction Hyperthyroidism
Toxic goiters (Graves disease) –Ab may stimulate thyroid without negative feedback control Exophthalmos –symptom present in many hyperthyroid patients

33 Parathyroid Location

34 Parathyroid

35 PTH Actions Stimulates resorption of bone  hCa+ and PO4- in blood
Stimulates Ca+ absorption in intestine (active Vit. D3 necessary for Ca+ absorption) Stimulates Ca+ reabsorption and PO4- excretion in kidney Stimulates Vit. D3 formation (skin) and activation (kidney) Vital for life

36 Adrenal Location and Structure

37 Adrenal Layers (Epinephrine (adrenalin)) (Androgens)
(Glucocorticoids (cortisol)) (Mineralocorticoids, (Aldosterone))

38 GAS (General Adaptation Syndrome)

39 Adrenal Malfunction Hypersecretion
Cushing’s syndrome –increase in glucocorticoids Usually due to over secretion of ACTH by pituitary or from adrenal cortex tumors stimulating an increase in glucocorticoids. Characteristic obesity of trunk only and development of “buffalo hump” (a fat pad behind the shoulders). Will develop hypertension, atherosclerosis, muscular weakness and fatigue. Conn’s syndrome –excess amount of aldosterone Salt imbalance, water retention, hBP, muscle weakness Adrenogenital syndrome –too much androgen Premature sexual development in children or masculinization in women

40 Cushings (buffalo hump) Obesity of trunk

41 Adrenogenital syndrome
A 15 yo girl, note typical masculine build, under developed breasts, and excessive body hair

42 Adrenal Cortex Malfunction
Hyposecretion –Addison’s disease Due to decrease amounts of mineral and glucocorticoids Can be due to over use of steroids or an autoimmune mechanism resulting in destruction of the gland Dehydration, K+ loss, iBP, fatigue, pigmentation deepening (bronzing of skin) may be symptom of loss of negative feedback

43 Pineal Gland Plays a major role in circadian rhythm control through its sympathetic connection to the hypothalamus Melatonin increases at night and decreases during daylight Implicated in the control of major life changes (such as the onset of puberty and adulthood

44 Thymus Gland Bilobed organ that is largest in children, but begins to regress sharply at the onset of puberty (around age 11) It is the site of T-cell lymphocyte production and produces hormones (such as, thymosin) that modifies their physiology


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