Carbohydrate metabolism is outlined by Assoc Prof Dr Ho Kok Lian from the Department of Pathology2.
Glycolysis is a part of carbohydrate metabolism.
The metabolic fate of pyruvate is a part of carbohydrate metabolism.
Gluconeogenesis is a part of carbohydrate metabolism.
The pentose phosphate pathway is a part of carbohydrate metabolism.
Glycogen metabolism is a part of carbohydrate metabolism.
Monosaccharides are metabolized as part of carbohydrate metabolism.
Blood glucose is regulated as part of carbohydrate metabolism.
The citric acid cycle and electron transport chain (ETC) are separate lectures in carbohydrate metabolism.
Gluconeogenesis is the synthesis of glucose from non-carbohydrate precursors, glucogenic amino acids, lactate, glycerol and propionic acid.
The liver and kidney are the main sites of gluconeogenesis, contributing 80% and 20% respectively.
Biomedical importance of gluconeogenesis includes maintaining blood glucose level during fasting and starvation, and is essential for nervous tissues and cells lacking mitochondria like RBCs.
Gluconeogenesis clears the products of metabolism, and lactate and glycerol are formed from anaerobic glycolysis.
Propionate is the major substrate for gluconeogenesis in ruminants.
In Red Blood Cells (RBCs), glutathione is reduced which removes H2O2.
The Cori cycle, also known as the Lactic acid Cycle, involves the conversion of Glucose into Lactate in the liver and RBC.
NADPH causes pathological complications in Diabetes Mellitus such as retinopathy and nephropathy, which relates to cellular redox balance and oxidative stress.
The availability of substrates, allosteric activation by Acetyl CoA, and coordinate regulation of Glycolysis and Gluconeogenesis are factors that regulate Gluconeogenesis.
In the liver, NADPH is used in the G6P pathway, converting 6 PG to NADPH + H+, and in the GS pathway, converting GS to SG, both leading to the production of glutathione and H2O2.
Gluconeogenesis is the process of creating Glucose from non-carbohydrate sources such as Pyruvate, Lactate, and Glycerol.
In the liver, NADPH is supplied for microsomal cytochrome p450.
The availability of substrates, allosteric activation
In White Blood Cells (WBCs), NADPH is used in the G6P pathway, converting 6 PG to NADPH + H+, and in the GS pathway, converting GS to SG, both leading to the production of glutathione and H2O2.
In White Blood Cells (WBCs), NADPH is generated for killing bacteria.
In Red Blood Cells (RBCs), NADPH is used in the G6P pathway, converting 6 PG to NADPH + H+, and in the GS pathway, converting GS to SG, both leading to the production of glutathione and H2O2.
In Red Blood Cells (RBCs), NADPH is used in the G6P pathway, converting 6 PG to NADPH + H+, and in the GS pathway, converting GS to SG, both