Carbohydrate metabolism is the process by which carbohydrates are broken down and the products are used for energy.
Glycolysis is the metabolic pathway that breaks down glucose into pyruvate.
The metabolic fate of pyruvate involves its conversion into acetyl-CoA, which is then used in the citric acid cycle.
Gluconeogenesis is the process by which glucose is synthesized from non-carbohydrate sources.
The pentose phosphate pathway is a metabolic pathway that converts glucose into ribose.
Glycogen metabolism involves the storage and breakdown of glycogen.
Monosaccharides are metabolized through a process called glycolysis.
Blood glucose is regulated through a process called glycolysis.
The citric acid cycle is a metabolic pathway that converts acetyl-CoA into CO2.
Glycogen metabolism involves the synthesis and degradation of glycogen.
The structure of glycogen involves the presence of glucose, glucose 1 phosphate, UTP, and uridine phosphate.
Glycogen synthesis involves the activation of glucose, primer, Glycogen with glucose 10 residues, Glycogenin, elongation, a - 1,4 bond formation, Glycogen synthase (rate limiting enzyme), branching, a - 1,6 bond formation, branching enzyme.
Glycogen degradation involves trimming, phosphorolysis of a 1,4 glycosidic bonds, Glycogen phosphorylase (rate limiting enzyme), debranching, transfer of trisaccharides from branch point (Glucan transferase), and hydrolysis of single glucose from branch point (Debranching enzyme).
Glycogen metabolism involves the regulation of blood glucose.
Glucose is the precursor of milk sugar, lactose (breastfeeding).
Below critical level (hypoglycemia), there is brain dysfunction resulting in coma & death.
GLUTs (Facilitative bidirectional transporters) include GLUT 1&3 for basal glucose uptake in organs such as brain, kidney, colon, red blood cells, and placenta; GLUT 2 for rapid uptake in liver and pancreas; GLUT4 for insulin dependent skeletal muscle and adipose tissue uptake; and GLUT5 for glucose absorption in small intestine.
Normal blood glucose level is 80 - 100 mg/dl or 4.5 - 5.5 mmol/L post absorptive (4 - 6 hours after last meal), 120 - 130 mg/dl or 6.5 - 7.2 mmol/L after carbohydrate meal, and 60 - 70 mg/dl or 3.3 - 3.9 mmol/L during fasting.
The kidney is a Glucostat organ that regulates hypoglycemia.
Sources of blood glucose include diet, glucogenic compounds, glucogenic amino acids, glycerol, lactate, propionic acid (in ruminants), and liver glycogen.
All cells require a basal, minimum requirement for glucose.
The liver is a Glucostat organ that regulates hyperglycemia.
The brain is a Glucostat organ that regulates satiety.
GLUTs are freely permeable to glucose (GLUT 2, Insulin independent) and include Glucokinase; High Km (low affinity) & High Vmax (efficient).
Insulin plays an important role in regulating blood glucose level and is the only hypoglycemic hormone.
Brain and nervous tissues depend solely on blood glucose as a source of energy.
Stimulate release of glucocorticoids (11 - oxy steroids)
Galactose metabolism in liver
Promotegluconeogenesis
After birth lactalbumin synthesis is stimulated by Prolactin.