Endocrine System Flashcards

1
Q

Define homeostasis and allostasis.

A

The bodies ability to regulate fluids and temeperature to optimise its function.
Allostasis is the idea that the body predicts effects before they happen and adjusts accordingly.

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2
Q

Discuss what regulates body temperature and possible problems with this.

A

Humans are able to maintain a steady core temperature despite changes to external environments. The volume of the core can expand in warm conditions and shrink in cool conditons. Heat is produced by metabolic processes in the body.

  • Thermoreceptors in the tissues record changes in temperature and send sensory afferents to the hypothalamusn (2 centres for cold and hot response). Acts on multiple effector systems.
  • Change in muscle activity: shivering, adrenergic pathway with hypothalamus (non-voluntary somatic).
  • Brown fat metabolism: important in newborns, an increase in epinephrine and thyroid hormones causes metabolism of brown adipose.
  • behavioural
  • blood flow to skin (constriction and dilation): adrenergic efferents from the hypothalamus. Can override the medulla.
  • Not enough in extreme temperatures
  • Fever- Pyrogens from microorgansim reset hypothalamus set point by the activation of prostglandins. Can trick the body into producing excessive heat, Aspirin blocks.
  • Hyperthermia can be induced by exercise
  • Excess thyroid hormones or epinephrine can cause hyperthermia.
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3
Q

Discuss the role for the hypothalamus in homeostasis.

A

The hypothalamus acts as a controll centre for homeostasis. It produces several hormones which are important for regulation of temperature and fluid retention. An example would be its action on the pituitary gland. ADH is released from the posterior pituitary (neurohormone acts on kidneys to increase fluid retention in the kidneys. Recruits aquapores that insert into the kidney tubules). On the posterior pituitary there is no portal system connecting the two (neurons whos bodies are in the hypothalamus), signals the release of neurohormones
It controls the anterior pituitary through releasing and inhibiting hormones that reach the pituitary via a capillary network. The anterior pituitary releases hormones such as TSH (TRH from hyp), GH (GNRH from hyp), (GnRH)LH, FSH, Prolactin (PIH, PRH).

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4
Q

Explain the anatomy of the kidneys and adrenal glands including their location within the abdomen.

A

Kidneys are located in the posterior portion of the abdominal cavity. They are bilateral bean shaped organs. They are paired structures which sit retroperitoneally in the abdomin. Kidneys sit roughly in the region of T12- L3 but right kidney sits slightly lower due to the liver. The kidneys are incased in several layers of fat and fascia. The innermost layer is the renal capsule. The kidneys can be split functionally between the outer cortex and the inner medulla. The cortex extends into the medulla via triangular structures known as renal pyramids. The apex of the pyramid is known as the renal papilla. The renal papillae are associated with structures known as minor calyx which lead into major calyx. The calices collect urine from the pyramids to be transported to the ureter via the renal pelvis. Pyramids contain functional units known as nephrons. Blood supply via the renal arteries and drainage by the renal veins. (renal helum, interlobar arteries> arcuate arteries> interlobular). Pelvic Kidney- In utero, the kidneys develop in the pelvic region, and ascend into the abdomen. Occasionally, one of the kidneys can fail to ascend, and remains in the pelvis, at the level of the common iliac artery.
The adrenal glands sit directly inferior to the kidneys in the renal fascia. Contain outer capsule> cortex (embryonic mesodemr)> medulla (ectodermal neural crest cell).

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5
Q

Compare the renal and endocrine anatomy between males and females.

A

The ureter transports urine to the bladder which exits as the urethra through the penis in males and the perineum in females. The main difference in endocrine anatomy between males and females lies in the sex organs. Women contain ovaries which produce oestrogen and progesterone and also utilise oxytocin and prolactin for breast development and lactation. The male sex organs are the testies which produce testosterone.

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6
Q

Describe the anatomy of the key endocrine organs including the hypothalamus, pituitary, thyroid and pancreas.

A

The hypothalamus is a subcortical brain structure located anterioposteriorly from the thalamus.
The pituitary consists of 2 lobes which suspend from the base of the brain via a pituitary stock. It sits in small indentations in the sphenoid bone known as the sella turcica.
The thyroid gland is located posterior to the sternothyroid and sternohyoid muscles in the neck. It consists of 2 lobes joined by an isthmus which wraps around the cricoid cartilage. Vasculature- superior and inferior thyroid arteries. Some individuals also have thyroide ima artery. Drainage via a venus plexus which leads into the internal jugular veins.
Pancreas- Located posteriorly to the stomach, duedonem lies anteriorly and laterally, Transverse mesocolon – Attaches to the anterior surface of the pancreas
Common bile duct – Descends behind the head of the pancreas before opening into the second part of the duodenum alongside the major pancreatic duct through the major duodenal papilla
Spleen – located posteriorly and laterally. The lienorenal ligament is formed from peritoneum and connects the spleen to the tail of the pancreas. The pancreatic duct runs the length of the pancreas and unites with the common bile duct, forming the hepatopancreatic ampulla of Vater. This structure then opens into the duodenum via the major duodenal papilla.

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7
Q

Discuss the function of the key endocrine organs.

A

Hypothalamus- hormone secretion which acts on various systems
Pituitary- also hormone synthesis- controlled by hypothalamus
Thyroid- secretes thyroid hormones
Pancreas- secretes insulin and glucagon

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8
Q

Define the componants of an endocrine system and understand how they interact to cause physiological effects.

A

An endocrine system consists of cells which secrete hormones which are released into the blood stream and have an action on cells elewhere in the body. They consist of endocrine cells, their hormones/ neurotransmitters and the tissues that the act upon. Hormones can bind to surface receptors on cells or bind to receptors on the nuclear membrane. They normally cause a change in gene expression (production of proteins).

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9
Q

Define hormones on the basis of structure.

A

Peptides: Polypeptide chains which are normally synthesised in the rough endoplasmic reticulum as preprohormones which require the removal of subunits in order to be in their active state (insulin). Stored in vessicles.
Tyrosine derivatives: derived from tyrosine groups (thyroid hormones). They can be both hydrophobic and hydrophilic and therefor have different mechanisms.
Steroids: large hydrophobic proteins that are derived from cholesterol. They are important for growth, sexual characteristics and stress response. Can freely diffuse through the cellular membrane and bind to nuclear receptors. They are released upon their production attatched to carrier proteins.

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10
Q

Discuss the simple principles of feedback mechanisms in the control of hormone secretion using the HPA- axis as an example.

A

Feedback mechanisms involve a control centre, an effector, a controlled mechanism and a feedback to the control centre. An example would be the HPA axis. The hypothalamus acts as a control centre. Hypothalamus sends CRH to the anterior pituitary> Anterior pituitary (effector) sends ACTH to the Adrenal cortex> Adrenal cortex releases cortisol (response). The increase in cortisol is detected which feeds back to both the pituitary and hypothalamus to decrease the release of effector hormones.

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11
Q

Discuss insulin production and action.

A

Insulin is produced in the B islet cells of the liver. Its primary function is to reduce glucose levels in the blood. Insulin binds to membrane-bound receptors on target tissues and causes proteins in the membrane to become phosphorelated. Inreases the number of transport proteins for glucose and amino- acids. Insulin and receptor then enters the cell by endocytosis. It causes the conversion of excess glucose into glycogen for storage in the liver and other tissues or converted into lipids in adipose tissues.

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12
Q

Explain ATP synthesis and glycolosis.

A

Carbohydrate metabolism
Glycolysis- Phosphorylation of ATP forms a glucose intermediate. This is rearanged to form a fructose intermediate. A second ATP then phosphorelates the fructose intermediate forming a biphosphate intermediate. The sugar is cleaved into 2 3C molecules. 2x NADH is produced by the oxidation of the molecules by NAD+. 2 ATP molecules are produced in the final step per molecule creating a net gain of 2 ATP. The molecules are converted to pyruvate in this step which can travel on to the citric acid cycle or be converted into lactic acid in the absence of O2.

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13
Q

Describe carbohydrate/ glucose homeostasis.

A

High glucose levels leeds to the production of insulin from B islet cells and in cases of low insulin glucagon is relased from a- islet cells. Insulin works primarily on the liver

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14
Q

Describe what diabetes mellitus is.

A

It is either the result of inadequate production of insulin (type 1) or the inadequate response to insulin (type 2).
Type 1 is the result of autoimmune response towards pancreatic islet cells. Type 2 usually develops in older individuals with high sugar diets. The over stimulation of insulin receptors results in lower sensitivity (reduced numbers of receptors) which makes tissue response to insulin considerably lower. This in turn can cause an increase in blood glucose.

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15
Q

Discuss how diabetes effects the body.

A

An increase of glucose in the blood which causes it to be converted into lipids for storage (impaired), increased urine production and thirst is common and can lead to hyperosmolity of blood and dehydration of cells. Lethargy, fatigue and periods of irritability. Type 1 tend to undergo sudden spikes and drops in blood glucose due to reduced control hormones.

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16
Q

Discuss how treatments of diabetes work

A

Type 2 diabetes is often treated with dietary changes, however, some individuals may require insulin.
Insulin injection is a common treatment for type 1 diabetes. By closely measuring dietary habits individuals can calculate how much insulin they need after meals and measure blood sugar frequently. There is research currently going into using insulin pumps which automatically calculate glucose levels.

17
Q

Describe the main principles of circadian rhythms under different environmental conditions.

A

There are different kinds of circadian rhythms: Ultradian: cycles lasts shorter than a day
- milliseconds it takes for a neuron to fire
- 90 minutes sleep cycle (REM and NON REM sleep)
- hunger
Infradian: cycles lasts longer than a day
- monthly menstrual cycle
- hibernation in animals
- bird migration
Circadian rhythms are cyclical processes that happen over the course of a day. For instance core temperature fluxes under normal conditions at different times of the day being lower at night an peeking in the evenings.
- These can be effected by sleep wake patterns and exposure to abnormal light- dark patterns.

18
Q

Discuss the physiological structures and the molecular and genetic basis that govern the function of the biological clock

A

Environmental cues determine the biological clock: day and night, meal times, social interaction.
Siprachiasmic nucleus: involved in setting the cloch- located at optic chiasm.

19
Q

Discuss the physiological structures and the molecular and genetic basis that govern the function of the biological clock

A

Environmental cues determine the biological clock: day and night, meal times, social interaction.
Siprachiasmic nucleus: involved in setting the cloch- located at optic chiasm.
Different species express different cycles (some longer and some shorter).

20
Q

Describe the development of the pronephros, mesenephros and metenephros.

A

Derived from embryonic intermediate mesoderm: begins as urogenital ridge.
- Forms either side of the dorsal aorta.
- forms along full length of embryo
- Initially gives rise to 3 pairs of kidneys
- Pronephros, mesenephros and metenephros (form cranio-caudally and cronologically)
- Early week 4 embryonic mesoderm forms a small duct at C5-C7 level.
- Forms through MET, grows caudally (initially a rod but canalises at day 26 to form mesonephric or wolffian duct.)
- Intermediate mesoderm adjacent to the duct condenses and reorganises to form a series of epithelial buds which become hollow and form the pronephros (these arent functional in humans and disapear around day 25.
- Pronephroi are succeeded by mesenephroi (thoracic- lumbar region)
- As the mesonephric ducts extend caudally, induce formation of ~40 mesonephric buds/tubules.
- As caudal ones dev, cranial regress. Leaves ~20 pairs of tubules. Functional tubules develop into nephrons. Connect with and drain into ducts. Functional in weeks 6-10 and then regress.
- d28 a pair of uteric buds sprout from the distal mesenephric ducts= collecting tubes, minor and major calices and ureter..
- Buds induce overlying intermediate mesoderm to form the metanephros
= definitive kidneys
Development of metanephros involves: Epithelial tube formation & elongation, Tubular branching, MET, Angiogenesis, Diffn of specialized cells, FGF2 & BMP7 stimulate prolif of mesoderm to form
metanephros
- Ureteric buds induce overlying intermediate mesoderm (= metanephric
blastema) to form metanephroi
• Tips of ureteric buds induce mesoderm to condense
– MET to form nephric vesicle = nephron
• Regulated by Pax2 & Wnt4
– Requires several hours of direct contact
– This in turn induces ureteric bud to grow & branch to form the
collecting ducts
- unilateral renal agenisis (failure 1 to develop), bilateral (failure of both- fatal)

21
Q

Discuss the link between the developing urinary tract and reproductive systems.

A

Both the developing urinary tract and reproductive systems originate in the inermediate mesoderm (urogenital ridge). Systems are linked in males (ureter and penis).

22
Q

Describe endocrine response to stress.

A

One of the key endocrine systems involved in the response to stress is the HPA axis involving the adrenal cortex and the release of cortisol. Long term stress leads to the release of cortisol. It is classified as a glucocorticoid, a hormone that plays a role in glucose, or blood sugar, metabolism.It helps regulate blood pressure, blood sugar, and insulin levels.
It aids fat, carbohydrate, and protein metabolism. When you get stressed, cortisol levels spike to give you the energy and strength you need to fight or flee. It’s a survival mechanism. It suppresses the onset of acute inflammation. Blood pressure rises as vessels constrict.
Gastric acid production increases in the stomach. Insulin cannot do its job of regulating blood sugar.
Blood sugar levels rise. You crave carbohydrates and more food. The immune system is suppressed. The release of the DHEA hormone is curtailed (important for cell repair). It inhibits collagen formation.

23
Q

Discuss the normal and diseased anatomy of Cushings syndrome and congenital adrenal hyperplasia.

A

Cushings syndrome
- prolonged exposure to the hormone cortisol
- production of too much cortisol due to adrenal dysfunction, or caused by excessive intake of cortisol-containing medications
- Normally the adrenal glands become stimulated by ACTH released from the pituitary glands, resulting in the secretion of cortisol. ACTH is released in response to corticotropin-releasing hormone (CRH) from the hypothalamus. Cushing’s syndrome can be classified as ACTH dependant or independant. ACTH-dependant can be a cause of a tumor of the pituitary, whereas ACTH-dependant is the overproduction of adrenal cortisol. - When the cortisol levels are very high, due to the dysfunction of the adrenal glands, negative feedback is exerted on the CRH, decreasing the amount of ACTH released from the pituitary glands.
Congenital adrenal hyperplasia
- CAH involves a genetically conditioned defect of the enzymes regulating the synthesis of steroid hormones in the adrenal cortex. The result of these enzyme defects is the increased formation of male sexual hormones (androgens) with virilization of the outer female genitals.
- Due to the defect in 21-hydroxylase, cortisol is not produced or is only produced to some extent. Thus, the disease may vary in phenotypic presentation depending on the amount of secreted hormone. The deficiency triggers an increased release of ACTH from the pituitary due to a lack of negative feedback in the superior hormone centers. The ACTH stimulates the adrenal cortex, and it results in a hyperplasia.
The result is an increased production of androgens and an accumulation of intermediate products which are, in turn, used for the androgenic synthesis.
The patients have the karyotype 46, XX and female inner genitals which are normally formed. The outer genitals, however, experience masculinization (virilization), which can be pronounced to different extents, depending on the excess synthesis of androgens. The forms of masculinization reach from sole hypertrophy of the clitoris to a merging of the labioscrotal folds and formation of a male urethra.

24
Q

Specifically describe the role of the vagus nerve, Hering’s nerve, splanchnic nerve and adrenoreceptors in regulating blood pressure.

A

The vagus nerve carries information from the baroreceptors in the aorctic arc to the NTS nucleus in the medulla (afferent) and carries parasympathetic impulses to the SAN (efferent). Causes a decrease in blood pressure.
The Hering’s nerve is a branch of the glossopharyngeal nerve which carries information from carotid sinus baroreceptors to the NTS (afferent)
The splanchnic nerves carry sympathetic efferent signals to the SAN causing an increase in blood pressure.
Adrenoreceptors are G-protein coupled receptors found in vascular smooth muscle.

25
Q

Explain the histology and physiology of a nephron.

A

Nephrons are the functional units of the kidneys. They consist of a renal corpuscle which contains a glomerulus (bundle of capillaries) and a bowmans capsule which collects filtrate from the glomerulus. The glomerulus filters out small molecules and waste products (larger molecules such as proteins cannot pass through). The bowmans capsule collects the filtrate and carries it to the proximal conveluted tubule which leads into the loop of henle which extends into the medulla. Electrolyte gradients are established which allow for the reabsorption of useful elecotrolytes and water. This is a process which is tightly regulated. The loop of henle ascends and leads into the distal conveluted tubule which leads into the collecting ducts which lead to the minor calices.

26
Q

Discuss hormonal control of the kidneys.

A

Aldosterone
– increased reabsorption of sodium and water
– increased potassium secretion into urine
– Ion exchange
ADH (posterior pituitary)
– increased water reabsorption
– increased recruitment of aquaporins

27
Q

Outline the multiple roles of the urinary system in maintaining homeostasis.

A

Excretion of wastes (e.g. from breakdown of proteins; drugs etc.)
• Regulation of blood pH (acidity).
• Regulation of electrolyte balance (blood ionic composition;
blood osmolarity)
• Regulation of blood volume and blood pressure
• Regulation of blood glucose level (gluconeogenesis)
• Production of hormones (e.g. calcitriol – vit. D & erythropoietin)

28
Q

Explain urine production in relation to nephron structureand the process of filtration, selective reabsorption and tubular secretion.

A

Tubule reabsorption is highly selective.
Primary active transport (ATP hydrolysis)
• Secondary active transport (using ion electrochemical
gradient) drives another substance across a membrane using SYMPORTERS and ANTIPORTERS
• 90% of Water is absorbed with solutes (obligatory
reabsorption) via osmosis (in PCT & Descending limb
of loop)
• Remaining 10% = facultative reabsorption- regulated
by ADH (collecting ducts mainly)

29
Q

Explain how diuretics work

A

Diuretics- Act on the kidney (nephron) to increase urine
production (diuresis). This reduces blood volume which
reduces BP.