Carbohydrates Metabolism (Part 1) Flashcards
Carbohydrates …. of food
2/3 - (65-70%)
Monosaccharide
Glucose
Ribose
Fructose
Disaccharide
Lactose (Milk)
Sucrose (White sugar)
Maltose (Barley)
Polysaccharide
Starch (Bread - Rice)
Glycogen (Liver - meat)
Cellulose
Metabolism
All the chemical reactions that occur to the food stuff inside living cells
These substances is not metabolized
Vitamins , Minerals
Metabolism divide to
Anabolism :
- Required energy provided by cleavage of ATP into ADP or AMP
- For synthesis of PTN , CHO , lipids or their derivatives
Catabolism :
Involve oxidative processes that release energy (ATP)
CHO must be converted into …. to be absorbed
Monosaccharide
….. are chief CHO in our food
Starch, glycogen, sucrose, lactose, and cellulose
CHO hydrolyzed to ….. in GIT before they are absorbed
hexose sugar (glucose, fructose, and galactose)
Mouth enzymes
Salivary α – amylase (Ptylin)
pH : 6.7
Activation : Cl-
Stomach pH
2
Digestion action in mouth
Amylase hydrolyzes α-(1,4) glycosidic linkage
Starch , Glycogen , dextrin → Maltose , Glucose
Small intestine enzymes
Pancreatic α-amylase
pH : 7.1
Activation : Cl-
Digestion action in stomach
Stop due to its acidity inactivate salivary α – amylase
HCL → Hydrolyze dietary sucrose to glucose and
Fructose
Digestion action in small intestine
- Pancreatic α-amylase
hydrolyzes α-(1,4) glycosidic linkage - Intestinal enzymes (Disaccharidases)
Lactase : Lactose → Glucose + Galactose
Maltase : Maltose → Glucose + Glucose
Sucrase : Sucrose → Glucose + Fructose
Intestinal enzymes
Disaccharidases
Lactase : Lactose → Glucose + Galactose
Maltase : Maltose → Glucose + Glucose
Sucrase : Sucrose → Glucose + Fructose
Lactose Intolerance
Inability to digest lactose due to deficiency of lactase enzyme which remain in intestines and get fermented by bacteria (Treated by milk lactose free)
May be congenital (Rare – Birthed with) or acquired (Common – Adult)
Symptoms:
1. Bloating , Abdominal cramps and pain due to ↑ CO2 produced by bacterial fermentation
2. Diarrhea due to increasing osmotic pressure
Cellulose digestion in human
There is no β (1-4) glucosidase in human that can digest β (1-4) glycosidic bond between glucose molecules in cellulose
Congenital Lactose Intolerance
Complete absence or deficiency of enzyme
The child develop intolerance to lactose immediately after birth
Passive diffusion
Concentration gradient : Down the concentration gradient from high to low
Energy required : None
Protein carrier : Not required
Speed : Slowest
Active transport
Concentration gradient : Against concentration
gradient from low to high
Energy required : Required ATP
Protein carrier : Required
Speed : Fastest
E.g. : Glucose
Glucose transporter
Na+ dependent transporter
Na+ independent transporter
Fate of the absorbed sugar
- Glucose is delivered to liver
- All other monosaccharides are converted to glucose in the liver
Utilization by tissues
- Oxidation
- Storage
- Conversion to substances
Complete oxidation of glucose
CO2 + H2O + Energy
Oxidation Major pathways
Glycolysis , Krebs’ cycle and oxidative decarboxylation
Oxidation Minor pathways
Hexose monophosphate shunt and Uronic acid pathway
Sugar Storage
- Glycogen in the liver and muscle (Limited)
- Triacylglycerol in the adipose tissue
Conversion to substances
Galactose → Lactose , glycolipids & mucopolysaccharides synthesis
Fructose → Sperm sugar
Others : Amino sugar - Ripose - Fatty acid - Non essential a.a
Excretion of glucose in urine
Normally urine contains no glucose because the kidneys can reabsorb all the filtered glucose from the tubular fluid back into the bloodstream
When glucose blood level exceeds a certain limit (180 mg/dl) , it will pass to urine causing glucosuria
Normal range = 60 – 110 mg/dl
Glycolysis
Oxidation of glucose or glycogen to give
1. Pyruvate (in O2 presence)
2. Lactate (in O2 absence)