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Regulation of

Uncoupling Uncoupling proteins (UCP) in inner mitochondrial membrane of mammals  Allow some H+ leakage, bypassing ATP-synthase. Metabolic . Burn stores without generating ATP . May be important in regulating %body Pathways: . May also be important in reducing formation of dangerous Reactive Species (ROS) + – . H -leakage is activated by O2 . a summary – + 1 . O2 + 2H → H2O2 → H2O + /2O2  In brown (thermogenic) fat, UCP1 causes heat generation by burning high-caloric fuel without producing ATP

High activity tissues [] have high ATP demand. But since [ATP] would inhibit ATP synthesis — — cannot “store” excess ATP reserve. • Exchange –P of ATP to P– • Exchange back to ATP from P–Cr at myofibrils ⇑⇑ATP→ inhibits F-6-P- ∴ F-6-P → back to G-6-P Creatine → alternate pathway → G-1-P Kinase →

⇑⇑ATP→ inhibits Krebs Cycle CK CK ∴ acetyl-CoA → alternate pathway → fatty synthesis →

Cellular Cellular 1. Metabolism -6- Glucose Glucose-6-Phosphate Glucose 2.

2.

5. 3. Catabolic pathways: 6. 1. 7. 2. 3. Pyruvate Oxidation 4. Krebs Cycle 4. 5. 4. 6. ß- Oxidation = only! 7. Proteolysis

Heyer 1 Regulation of Cellular Respiration

Cellular Metabolism Cellular Metabolism 2. 1. Glucose-6-Phosphate Glucose Glucose-6-Phosphate Glucose

1. 4. 2.

6.

Anabolic pathways: 3. 5. 1. 3. 2. Glycogenesis Intermediate pathways: 3. Synthesis 1. Glucophosphatase 4. Lipogenesis 2. Pyruvate Reduction/ 5. Ketogenesis Lactate Oxidation = hepatocytes only! = hepatocytes only! 6. Translation 3. Deamination

Glycogenesis and Glycogenolysis Uses of Different Sources

• Glucose-6-phosphate cannot leak out of the . • Skeletal muscles generate glucose-6-phosphate for own glycolytic needs. • Only contains the glucose-6- phosphatase that can remove the phosphate group and produce free glucose.

Metabolic Pools Gluconeogenesis & the

4) produced by in muscle is released into the bloodstream and delivered to the liver. 7A 3 5) LDH converts lactic acid to . 7B 6 6) Gluconeogenesis: (“creating new glucose”) Pyruvic acid converted to glucose-6-phosphate: • G-6-P can be used either for 7A- liver glycogenesis or 7B- can be converted to 6 & 7B only occur in liver! free glucose and released into the bloodstream.

Heyer 2 Regulation of Cellular Respiration

Interactions of Liver, Fat & Muscle Maintenance of circulating energy substrates • Fasting or low- diet

amino glucose

lactic acid

ketone fatty acids bodies

Muscle Fuel Consumption During Exercise Oxygen Debt

1. At rest: mostly from Following anaerobic respiration, increased O2 consumption continues aerobic resp. of plama to support aerobic oxidation of lactate back to pyruvate. fatty acids. (Reverse of pyruvate reduction. — Uses same LDH enzyme.) 2. Start exercise: anaerobic Krebs Cycle resp. of plasma glucose; start muscle Lactate Lipogenesis glycogenolysis. Oxidation 3.  blood flow & O2 Gluconeogenesis delivery ➠ aerobic resp. of muscle triglycerides. 4. Gluconeogenesis  plasma glucose from Cori Cycle. 5. Lipolysis in adipose  plama fatty acids for continued aerobic resp.

Balance Between and : the primary anabolic

• The rate of deposit and withdrawal of energy substrates, and the conversion of one type of energy substrate into another; are regulated by Insert fig. 19.4 . • Antagonistic effects of insulin, , GH,

T3, , and balance anabolism and catabolism. • glycolysisATP • glycogenesis • lipogenesis

Heyer 3 Regulation of Cellular Respiration

Insulin: the primary anabolic hormone Regulation of Insulin Action • ↑Blood glucose ⇒ ↑insulin Blood amino acids ↑ • ↑Blood amino acids ⇒ ↑insulin – If high /low carb diet ⇒ ↑blood amino acids/↓blood glucose; ⇒ both ↑insulin and ↑glucagon ⇒ ↓blood amino acids without ↓blood glucose • Parasympathetic nervous system: rest-and-digest ⇒ ↑insulin • Intestinal hormones – ↑Osm of chyme⇒ ↑GIP/GLP-1/CCK ⇒ ↑insulin • “anticipates” ↑blood glucose & amino acids ↑Cellular uptake ↓Blood amino acids of amino acids • ↑insulin faster from ingested glucose than from intravenous glucose! • Adipose hormones

– Enlargement of fat cells ⇒ ↑insulin resistance factor [TNFα] Amino Acids • glycolysisATP ⇒ ↓insulin sensitivity Protein • Obesity aggravates – Atrophy of fat cells TNF insulin sensitivity • protein synthesis ⇒ ↓ α⇒ ↑ • Weight loss ⇒ more efficient lipogenesis ⇒ regain lost fat

The Catabolic Hormones Antagonistic Hormones — antagonistic to insulin action 1. Glucagon: blood glucose 2. Epinephrine: acute response – fight-or-flight 3. Cortisol [glucocorticoid]: chronic stress response – general adaptation syndrome [GAS]

i. Glucagon and Epinephrine bind to different receptors, but both receptors produce cAMP as a second messenger. Thus they activate the same catabolic enzymes producing the same response. ii. Glucocorticoids bind to an intracellular DNA-binding receptor to activate genes for a long-term response.

Regulation of Insulin and Glucagon Secretion Absorptive & Postabsorptive States

Glucagon stimulates catabolic enzymes.

Heyer 4 Regulation of Cellular Respiration

Diabetes mellitus Diabetes Mellitus: Type I: destruction of ß-islet cells ⇒ insulin deficiency Type II: inactivation of insulin receptors ⇒ insulin resistance

Type II Diabetes Mellitus Oral Glucose Tolerance Test

• Slow to develop. • Measurement of the • Genetic factors are ability of β cells to significant. secrete insulin. • Occurs most often in Insert fig. 19.12 • Ability of insulin to Insert fig. 19.8 people who are lower blood overweight. glucose. • Decreased sensitivity to insulin or an insulin • Normal person’s resistance. rise in blood – Obesity. [glucose] after • Do not usually develop drinking solution is ketoacidosis. reversed to normal • May have high blood in 2 hrs. [insulin] or normal [insulin].

Glucocorticoids work via nuclear receptors: Synopsis of metabolic hormone action change gene expression / long term effects

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