Carbohydrate metabolism is a fundamental biochemical process that ensures a constant supply of energy to living cells. The most important carbohydrate is glucose, which can be broken down via glycolysis to enter into the Krebs cycle and eventually lead to the production of ATP through oxidative phosphorylation.
Glucose transport into cells is facilitated by a family of transport proteins called GLUT (Glucose Transporters). GLUT4 is the primary glucose transporter for insulin-stimulated glucose uptake in skeletal muscle and adipocytes, while GLUT1 is responsible for basal glucose uptake in many tissues.
Once inside the cell, glucose undergoes glycolysis, a process that initially requires ATP to begin breaking down glucose into pyruvate. This process eventually generates a net gain of ATP as well as pyruvate. Pyruvate can then follow one of several pathways:
ATP Production: Pyruvate enters the mitochondria and is converted to Acetyl CoA. Acetyl CoA then enters the Krebs cycle, generating NADH and FADH2. The NADH and FADH2 molecules subsequently donate their electrons to the electron transport chain, ultimately leading to the production of ATP.
Amino Acid Synthesis: Pyruvate can be converted into alanine, a non-essential amino acid, through a process known as transamination.
Glycogen Synthesis: Glucose can be stored as glycogen in the liver and muscle cells. Liver glycogen serves as a reservoir for maintaining blood glucose levels, while muscle glycogen is primarily used for local energy needs during muscle activity.
Triglyceride Synthesis: Excess glucose can also be converted into triglycerides by the liver for long-term storage in adipose tissue.
Carbohydrate metabolism disorders are a group of metabolic conditions that affect how the body processes carbohydrates, including sugars, starches, and dietary fibers. Although dietary fibers are not fully broken down by the body, they influence carbohydrate metabolism by affecting digestion, glucose absorption, and insulin response. These disorders can lead to a variety of health problems, including hypoglycemia (low blood sugar), liver enlargement, and muscle pain.
The most common disorders of carbohydrate metabolism include glycogen storage disorders, hereditary fructose intolerance, and galactosemia. In glycogen storage disorders, the body cannot properly store or use glycogen, a polymer of glucose that stores energy for the body. Hereditary fructose intolerance is a condition in which the body cannot break down fructose (a type of sugar found in fruits, table sugar, and sorbitol), leading to a build-up of harmful substances in the liver. Galactosemia is a disorder that affects the body's ability to process galactose, a sugar commonly found in dairy products.
In normal circumstances, enzymes in your body break down most carbohydrates into glucose, a type of sugar that serves as a primary energy source for the body. However, in people with some specific carbohydrate metabolism disorders, this process may be disrupted, leading to abnormal levels of glucose in the bloodstream.
Hyperglycemia, or high blood glucose levels, is another common condition related to carbohydrate metabolism. It is often associated with diabetes, a chronic disease characterized by high blood sugar levels.
Moreover, recent studies have also shown that diabetes mellitus and metabolic syndrome can aggravate the course of COVID-19 and increase mortality rates. This highlights the importance of proper carbohydrate metabolism for overall health and disease resistance.
In terms of clinical nutrition, the effects of catabolic hormones - such as cortisol, glucagon, and catecholamines - on glucose metabolism play a significant role in stress responses ( 'fight or flight') by increasing glucose production through glycogenolysis and gluconeogenesis. Thus, understanding and managing carbohydrate metabolism disorders is crucial not only for maintaining nutritional health but also for managing stress responses and chronic conditions like diabetes.
From Chapter 28:
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