Blood glucose levels are maintained
within narrow limits. In healthy individual overnight fasting glucose level is
70-90 mg/dl and post prandial level after meal do not exceed 140 mg/dl -180
mg/dl. Normoglycemia is restored within 2-4 hours. Among the hormones that
regulate glucose level, Insulin is the only hormone that lowers glucose level.
Symptoms of hypoglycemia are seen if
blood glucose is <60 mg/dl and the symptoms of hyperglycemia occurs at 215
mg/dl – 235 mg/dl.
1. Reduces
production of gluconeogenic precursors like glycerol, alanine and lactate
2. Inhibit
gluconeogenic enzymes
3. Inhibit
hepatic glycogenolysis and stimulate glycogenesis.
4. Increase
cellular glucose uptake mediated by insulin sensitive GLUT4
5. Reduces
competition for glucose oxidation by alternative fuels (Randle effect) by
inhibiting NEFA (Non-esterified fatty acid) release from adipose tissue and reducing hepatic ketogenesis.
Fig. Oral Antihyperglycemic Agents |
NORMAL GLUCOSE METABOLISM
Glucose is derived from 3 main
sources:
1. Gut: By
absorption from diet. Glucose, fructose and galactose are the principle
carbohydrates resulting from digestive process.
2. Stored
glycogen (liver).
3. Gluconeogenesis
from non carbohydrate source.
Gluconeogenesis occurs in liver
(75-90%) and kidneys (10-25%) from amino acids, glycerol, lactate and pyruvate.
Hepatic glucose output is about 2
mg/kg/min in resting postabsorptive state. Glucose is stored as glycogen (15-25%)
in liver and >50% in skeletal muscle and lesser amount in other tissues. A
70 kg man has 700-1000 g hydrated glycogen.
Glycogen in skeletal muscle provides
fuel for muscle but do not contribute to blood glucose as it lacks
G-6-phosphatase.
Glucose is the main fuel for 24
hours. During high intensity exercise and 4-6h postprandial it is the
predominant fuel of the whole body. Glucose liberates 112.2 kcal or 6 moles ATP
per mole of oxygen consumed.
Glucose is fully oxidized in liver,
muscle and brain. Brain utilizes most of the glucose in fasting state (100-124
g/24 h). During fasting or resting, state skeletal muscle takes up 10-20%
hepatic glucose output: this is converted to lactate, pyruvate, glycerol or
carbon skeletons of amino acids and then returned to liver for gluconeogenesis.
Fatty acids or their derivative ketone bodies are the prime fuel of resting muscle,
heart and liver. RBC, skin, adipose tissue and renal medulla derive energy from
anaerobic glycolysis to produce lactate and pyruvate even in resting state.
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