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A2 Bio: Chapter 14
Homeostasis
 Homeostasis
 Maintenance of constant internal environment
 Physiological factors controlled:
 Body temp
 Metabolic wastes (CO2, urea)
 Blood pH
 Blood glucose concentration
 Water potential of blood
 Concentrations of CO2 and O2
Internal Environment
 Influence of tissue fluid
 Temperature
○ Low temp- slows metabolic rates
○ High temp – denatures enzymes
 Water potential
○ Decrease will cause osmosis to occur
○ Metabolic reactions – stops/slows
 Cells swell-bursts
 Concentration of glucose
○ Causes respiration to slow down
Homeostatic control
 Negative feedback
 Around set point
 Aided by
 Nervous system
 Endocrine system
 Control of body temperature
 Thermoregulation
 Involves both coordination systems
 Vasoconstriction/ vasodilation
 Shivering/ sweating
 Raising / Lowering body hairs
 Decreasing/Increasing production of sweat
 Increasing/Decreasing secretion of adrenaline
 Increasing/Decreasing the secretion of Thyroxine
EXCRETION
 Removal of metabolic wastes
 Carbon dioxide
 Aerobically by respiring cells
 Diffuses from blood into alveoli
 Urea
 Liver
 From excess amino acids
 Transported from liver to the kidney
 Kidney remove urea from blood, excreted as
urine
Deamination
 Removal of excess amino acid
 Avoids wastage
 In liver
 Amino acid removed with H atom
 Form ammonia
 Keto acid
 Enter Krebs cycle for respiration
 Converted to glucose
 Stored as glycogen or fat
Deamination
 Ammonia
 Soluble, toxic
 Prevents damage by converting into
 Urea – less soluble & toxic
○ Main nitrogenous excretory product
○ Removed in urine from kidney
 Other nitrogenous product
 Creatinine
○ Made in liver from aa
 Used in muscles as Creatine phosphate
○ Excreted as creatinine
 Uric acid
○ Breakdown of purines (nucleotides)
Structure of kidney
 Cortex
 Medulla
 Pelvis
Your name:
 A ___________
 B ___________
 C ___________
 D ___________
 E ___________
 F ___________
 G ___________
 H ___________
 I ____________
 J ____________
Labeling
ULTRAFILTRATION
 Filters small molecules out of blood into
Bowman’s capsule
 Blood separated by 2 cell layers
 Endothelium
○ Cell has holes
○ Basement membrane
 collagen & glycoproteins
 Epithelial cells
○ Inner lining of Bowman’s capsule
○ Has finger-like projections - podocytes
ULTRAFILTRATION
 Holes in endothelium, gaps between
podocytes
 Substances pass through
 Some substance cannot pass
 Protein with mass 69,000 +
 RBCs, WBCs
 Basement membrane acts as a filter
 Glomerular filtrate identical to blood plasma
 No plasma proteins
Factors affecting glomerular
filtration rate
 Rate at which fluid filters from the blood
 In a human, the rate is about 125 cm3 min−1
 Determined by
1. Differences in water potential between capillaries &
Bowman’s capsule
2. Difference in solute concentration
“the effect of differences in pressure outweighs the
effect of the differences in solute concentration”
Reabsorption in the PCT
 Cuboidal epithelial cells adapted by
 Microvilli
 Increase SA
 Tight junction
 Do not allow fluid to pass between cells
 Many mitochondria
 Energy for Na+-K+ pump proteins
- Outer membrane
 Co-transporter protein
 Sodium ions, glucose, amino acid
- Membrane facing lumen
Loop of Henle
 Counter current multiplier
 2 limbs – fluid flowing down
in one & up the other
 Enables maximum conc of
solutes both inside & outside
 Cells of AL & collecting
duct– permeable to urea
Reabsorption in DCT & CD
 Na+ pumped out
into tissue fluid
into blood
 K+ pumped into
tubule
 Rate of exchange
(Na+ & K+)
regulate conc of
these ions in blood
Control of water content
 Osmoregulation – control of water
potential of body fluids
 Involves the hypothalamus
(Osmoreceptors), posterior pituitary gland &
kidneys and Anti-diuretic Hormone(ADH)
 Water potential in blood monitored by
osmoreceptors
OSMORECEPTORS
 Sensory receptor primarily found in the
hypothalamus
 Detects decrease in water
 Sense change in osmotic pressure
 Nerve impulses sent along the neurons
 Stimulates the release of ADH
Summary of osmoregulation
 Dehydration
○ Decrease in blood water
○ Pituitary gland secrete ADH
○ Makes kidney reabsorb water
○ = concentrated urine
 Water-logged
○ Too much water in blood
○ Less ADH (or none) secreted by Posterior Pituitary
Gland(PPG)
○ Less water reabsorbed by kidney
○ = Dilute urine
ADH
 A peptide hormone
 Made of 9 amino acids
 ADH enter capillaries and carried
around body
 Key effect:
 Reduce loss of water in the urine
 By reabsorption
 Diuresis – production of diluted urine
ADH
 Target cells – collecting duct cells
 ADH acts on the cell surface membrane
of CDC
 Makes them more permeable to water
 By increasing no. of water-permeable
channels – aquaporins
 Bind to receptor proteins
 Activates enzymes in cells with vesicles
 Activated vesicles move to CSM & fuse
 Secretion of ADH increases
reabsorption of water into blood
ADH
 Enough water in body
 Increase in water potential
 Osmoreceptors no longer stimulated
 Neurons stop secreting ADH
 Makes aquaporins move out of CSM of collecting
ducts to cytoplasm
 Makes CD less permeable to water
 Dilute urine
 Takes 15-20 min for ADH to be broken down
 Once ADH stops arriving at the CD cells,
takes 10-15 for aquaporins to be removed
Control of glucose
 Every 100 cm3 of blood: 80-120 mg of
glucose
 Conc. below this = not enough for
respiration
 Especially for brain cells
 Very high conc = upsets normal cell
function
 Homeostatic control by 2 hormones by
endocrine tissue in pancreas
 α cells – glucagon
 ß cells - insulin
Control of high blood glucose conc
 α and β cells detect the increase
○ α cells stop secretion of glucagon
○ β cells secrete insulin
 How?
 Signaling molecule, cannot pass through
○ Binds to a receptor on cell surface membrane
 Affects through intracellular messengers
 Vesicles with GLUT proteins move to surface
○ Muscle cells = GLUT4
○ Brain cells = GLUT1
○ Liver cells = GLUT 2
 Also stimulates activation of glucokinase,
phosphofructokinase and glycogen synthase
Decrease in blood glucose conc
 α and β cells detect the decrease
 α secrete glucagon , β stop insulin production
 Glucagon binds to different receptor on liver
cells
 This activates a G protein
 This activates enzyme that catalyzes conversion
of ATP to AMP
 AMP+ Kinase enzyme = amplifies signal from
glucagon
 Glycogen phosphorylase – end of cascade
 Breakdown of glycogen  glucose
Decrease in blood glucose
conc
 Two sources of glucose:
 Enzyme cascade
1. Gluconeogenesis
○ From amino acids & lipids
 Glucagon in liver – increases glucose
 Muscle – no receptors for glucagon
2. Adrenaline
○ increases conc of glucose
○ breakdown of glycogen stores in muscle
Diabetes mellitus
 Type I diabetes
 due to a deficiency in the gene that codes for the
production of insulin
 Type II diabetes
 Liver & and muscle cells do not respond to insulin
 Symptoms
 the kidney cannot reabsorb all the glucose
 some passes out in the urine
 extra water and salts accompany this glucose
 feels extremely hungry and thirsty
Urine analysis
 Presence of glucose & ketones - diabetes
 Presence of proteins – problem with kidney
 Most proteins – too large
 Some filtered through
 Reabsorbed by endocytosis in PCT
 Broken down, amino acids absorbed into blood
 Dipsticks & biosensors
 Dipsticks has glucose oxidase & peroxidase
 Biosensors measure conc of glucose
Homeostasis in plants
 Stomata – the hole between the guard cells
 Opening during the day
 Diffusion of gases
 diffusion of water vapor in transpiration
 Closure of stomata at night
 abscisic acid (ABA)
 Stomata respond to
 increasing light intensity
 low carbon dioxide concentrations in the air spaces
within the leaf.
Opening & Closing of stoma
 Guard cells lose/gain water by osmosis
 Decrease in water potential by
 ATP-powered proton pumps transport H+
 Decrease of H+ in cells causes K+ to move
in
 Electrochemical gradient
 Extra K+ lower WP inside
 Osmosis occur
 Increases turgor of cells, stoma opens
 Bundles of microfibrils arranged lengthwise
Opening & Closing of stoma
 Stomata close when
 H+ pump proteins stop
 K+ leave guard cells
 enter other cells
 Effects
 Reduces uptake of CO2
 Reduces rate of transpiration
 Abscisic acid – stimulate closure

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Homeostais- maintenance of balance in the human body

  • 2. Homeostasis  Homeostasis  Maintenance of constant internal environment  Physiological factors controlled:  Body temp  Metabolic wastes (CO2, urea)  Blood pH  Blood glucose concentration  Water potential of blood  Concentrations of CO2 and O2
  • 3. Internal Environment  Influence of tissue fluid  Temperature ○ Low temp- slows metabolic rates ○ High temp – denatures enzymes  Water potential ○ Decrease will cause osmosis to occur ○ Metabolic reactions – stops/slows  Cells swell-bursts  Concentration of glucose ○ Causes respiration to slow down
  • 4. Homeostatic control  Negative feedback  Around set point  Aided by  Nervous system  Endocrine system  Control of body temperature  Thermoregulation  Involves both coordination systems  Vasoconstriction/ vasodilation  Shivering/ sweating  Raising / Lowering body hairs  Decreasing/Increasing production of sweat  Increasing/Decreasing secretion of adrenaline  Increasing/Decreasing the secretion of Thyroxine
  • 5.
  • 6. EXCRETION  Removal of metabolic wastes  Carbon dioxide  Aerobically by respiring cells  Diffuses from blood into alveoli  Urea  Liver  From excess amino acids  Transported from liver to the kidney  Kidney remove urea from blood, excreted as urine
  • 7. Deamination  Removal of excess amino acid  Avoids wastage  In liver  Amino acid removed with H atom  Form ammonia  Keto acid  Enter Krebs cycle for respiration  Converted to glucose  Stored as glycogen or fat
  • 8. Deamination  Ammonia  Soluble, toxic  Prevents damage by converting into  Urea – less soluble & toxic ○ Main nitrogenous excretory product ○ Removed in urine from kidney  Other nitrogenous product  Creatinine ○ Made in liver from aa  Used in muscles as Creatine phosphate ○ Excreted as creatinine  Uric acid ○ Breakdown of purines (nucleotides)
  • 9. Structure of kidney  Cortex  Medulla  Pelvis
  • 10.
  • 11. Your name:  A ___________  B ___________  C ___________  D ___________  E ___________  F ___________  G ___________  H ___________  I ____________  J ____________ Labeling
  • 12. ULTRAFILTRATION  Filters small molecules out of blood into Bowman’s capsule  Blood separated by 2 cell layers  Endothelium ○ Cell has holes ○ Basement membrane  collagen & glycoproteins  Epithelial cells ○ Inner lining of Bowman’s capsule ○ Has finger-like projections - podocytes
  • 13. ULTRAFILTRATION  Holes in endothelium, gaps between podocytes  Substances pass through  Some substance cannot pass  Protein with mass 69,000 +  RBCs, WBCs  Basement membrane acts as a filter  Glomerular filtrate identical to blood plasma  No plasma proteins
  • 14. Factors affecting glomerular filtration rate  Rate at which fluid filters from the blood  In a human, the rate is about 125 cm3 min−1  Determined by 1. Differences in water potential between capillaries & Bowman’s capsule 2. Difference in solute concentration “the effect of differences in pressure outweighs the effect of the differences in solute concentration”
  • 15. Reabsorption in the PCT  Cuboidal epithelial cells adapted by  Microvilli  Increase SA  Tight junction  Do not allow fluid to pass between cells  Many mitochondria  Energy for Na+-K+ pump proteins - Outer membrane  Co-transporter protein  Sodium ions, glucose, amino acid - Membrane facing lumen
  • 16.
  • 17.
  • 18.
  • 19.
  • 20.
  • 21. Loop of Henle  Counter current multiplier  2 limbs – fluid flowing down in one & up the other  Enables maximum conc of solutes both inside & outside  Cells of AL & collecting duct– permeable to urea
  • 22. Reabsorption in DCT & CD  Na+ pumped out into tissue fluid into blood  K+ pumped into tubule  Rate of exchange (Na+ & K+) regulate conc of these ions in blood
  • 23. Control of water content  Osmoregulation – control of water potential of body fluids  Involves the hypothalamus (Osmoreceptors), posterior pituitary gland & kidneys and Anti-diuretic Hormone(ADH)  Water potential in blood monitored by osmoreceptors
  • 24. OSMORECEPTORS  Sensory receptor primarily found in the hypothalamus  Detects decrease in water  Sense change in osmotic pressure  Nerve impulses sent along the neurons  Stimulates the release of ADH
  • 25. Summary of osmoregulation  Dehydration ○ Decrease in blood water ○ Pituitary gland secrete ADH ○ Makes kidney reabsorb water ○ = concentrated urine  Water-logged ○ Too much water in blood ○ Less ADH (or none) secreted by Posterior Pituitary Gland(PPG) ○ Less water reabsorbed by kidney ○ = Dilute urine
  • 26.
  • 27. ADH  A peptide hormone  Made of 9 amino acids  ADH enter capillaries and carried around body  Key effect:  Reduce loss of water in the urine  By reabsorption  Diuresis – production of diluted urine
  • 28.
  • 29. ADH  Target cells – collecting duct cells  ADH acts on the cell surface membrane of CDC  Makes them more permeable to water  By increasing no. of water-permeable channels – aquaporins  Bind to receptor proteins  Activates enzymes in cells with vesicles  Activated vesicles move to CSM & fuse  Secretion of ADH increases reabsorption of water into blood
  • 30.
  • 31.
  • 32. ADH  Enough water in body  Increase in water potential  Osmoreceptors no longer stimulated  Neurons stop secreting ADH  Makes aquaporins move out of CSM of collecting ducts to cytoplasm  Makes CD less permeable to water  Dilute urine  Takes 15-20 min for ADH to be broken down  Once ADH stops arriving at the CD cells, takes 10-15 for aquaporins to be removed
  • 33. Control of glucose  Every 100 cm3 of blood: 80-120 mg of glucose  Conc. below this = not enough for respiration  Especially for brain cells  Very high conc = upsets normal cell function  Homeostatic control by 2 hormones by endocrine tissue in pancreas  α cells – glucagon  ß cells - insulin
  • 34.
  • 35.
  • 36. Control of high blood glucose conc  α and β cells detect the increase ○ α cells stop secretion of glucagon ○ β cells secrete insulin  How?  Signaling molecule, cannot pass through ○ Binds to a receptor on cell surface membrane  Affects through intracellular messengers  Vesicles with GLUT proteins move to surface ○ Muscle cells = GLUT4 ○ Brain cells = GLUT1 ○ Liver cells = GLUT 2  Also stimulates activation of glucokinase, phosphofructokinase and glycogen synthase
  • 37.
  • 38. Decrease in blood glucose conc  α and β cells detect the decrease  α secrete glucagon , β stop insulin production  Glucagon binds to different receptor on liver cells  This activates a G protein  This activates enzyme that catalyzes conversion of ATP to AMP  AMP+ Kinase enzyme = amplifies signal from glucagon  Glycogen phosphorylase – end of cascade  Breakdown of glycogen  glucose
  • 39.
  • 40. Decrease in blood glucose conc  Two sources of glucose:  Enzyme cascade 1. Gluconeogenesis ○ From amino acids & lipids  Glucagon in liver – increases glucose  Muscle – no receptors for glucagon 2. Adrenaline ○ increases conc of glucose ○ breakdown of glycogen stores in muscle
  • 41.
  • 42. Diabetes mellitus  Type I diabetes  due to a deficiency in the gene that codes for the production of insulin  Type II diabetes  Liver & and muscle cells do not respond to insulin  Symptoms  the kidney cannot reabsorb all the glucose  some passes out in the urine  extra water and salts accompany this glucose  feels extremely hungry and thirsty
  • 43. Urine analysis  Presence of glucose & ketones - diabetes  Presence of proteins – problem with kidney  Most proteins – too large  Some filtered through  Reabsorbed by endocytosis in PCT  Broken down, amino acids absorbed into blood  Dipsticks & biosensors  Dipsticks has glucose oxidase & peroxidase  Biosensors measure conc of glucose
  • 44.
  • 45.
  • 46.
  • 47. Homeostasis in plants  Stomata – the hole between the guard cells  Opening during the day  Diffusion of gases  diffusion of water vapor in transpiration  Closure of stomata at night  abscisic acid (ABA)  Stomata respond to  increasing light intensity  low carbon dioxide concentrations in the air spaces within the leaf.
  • 48.
  • 49. Opening & Closing of stoma  Guard cells lose/gain water by osmosis  Decrease in water potential by  ATP-powered proton pumps transport H+  Decrease of H+ in cells causes K+ to move in  Electrochemical gradient  Extra K+ lower WP inside  Osmosis occur  Increases turgor of cells, stoma opens  Bundles of microfibrils arranged lengthwise
  • 50. Opening & Closing of stoma  Stomata close when  H+ pump proteins stop  K+ leave guard cells  enter other cells  Effects  Reduces uptake of CO2  Reduces rate of transpiration  Abscisic acid – stimulate closure

Editor's Notes

  1. Creatinine and Uric Acid
  2. Beer (diuretic) – makes blood conc/ urine diluted Hangover caused by conc blood in brain
  3. -glucokinase: Glucose  Glucose-6-phosphate -phosphofructokinase: fructose-6-phosphate  fructose-1,6-biphosphate
  4. A level between 100 and 125 mg/dl indicates prediabetes, while a level between 70 and 99 mg/dl is considered “normal.” [https://www.diabetesselfmanagement.com/about-diabetes/diabetes-basics/understanding-your-lab-test-results/]