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Diabetes occurs when there is a dis-balance between the demand and production of the hormone insulin.
When food is taken, it is broken down into smaller components. Sugars and carbohydrates are thus broken down into glucose for the body to utilize them as an energy source. The liver is also able to manufacture glucose.
In normal persons the hormone insulin, which is made by the beta cells of the pancreas, regulates how much glucose is in the blood. When there is excess of glucose in blood, insulin stimulates cells to absorb enough glucose from the blood for the energy that they need.
Insulin also stimulates the liver to absorb and store any excess glucose that is in the blood. Insulin release is triggered after a meal when there is a rise in blood glucose. When blood glucose levels fall, during exercise for example, insulin levels fall too.
High insulin will promote glucose uptake, glycolysis (break down of glucose), and glycogenesis (formation of storage form of glucose called glycogen), as well as uptake and synthesis of amino acids, proteins, and fat.
Low insulin will promote gluconeogenesis (breakdown of various substrates to release glucose), glycogenolysis (breakdown of glycogen to release gluose), lipolysis (breakdown of lipids to release glucose), and proteolysis (breakdown of proteins to release glucose). Insulin acts via insulin receptors.
|
Liver |
Adipose or fat Tissue |
Muscle |
High insulin |
Glycolysis |
Triglyceride synthesis |
Amino acid uptake |
Low insulin |
Gluconeogenesis |
Lipolysis |
Proteolysis |
Hormones that raise blood sugar include glucagon, epinephrine and norepinephrine, cortisol, Growth hormone etc. These hormones are released due to stress. Thus during phases of stress like an infection, surgery or pregnancy diabetes control worsens and blood sugar rises.
In this condition the immune system attacks and destroys the insulin producing beta cells of the pancreas. There is beta cell deficiency leading to complete insulin deficiency. Thus is it termed an autoimmune disease where there are anti insulin or anti-islet cell antibodies present in blood. These cause lymphocytic infiltration and destruction of the pancreas islets. The destruction may take time but the onset of the disease is rapid and may occur over a few days to weeks.
There may be other autoimmune conditions associated with type 1 diabetes including vitiligo and hypothyroidism. Type 1 diabetes always requires insulin therapy, and will not respond to insulin-stimulating oral drugs.
This condition is caused by a relative deficiency of insulin and not an absolute deficiency. This means that the body is unable to produce adequate insulin to meet the needs. There is Beta cell deficiency coupled with peripheral insulin resistance.
Peripheral insulin resistance means that although blood levels of insulin are high there is no hypoglycaemia or low blood sugar. This may be due to changes in the insulin receptors that bring about the actions of the insulin.
Obesity is the main cause of insulin resistance. In most cases over time the patients need to take insulin when oral drugs fail to stimulate adequate insulin release.
|
Type 1 Diabetes |
Type 2 Diabetes |
Etiology |
Autoimmune |
Peripheral insulin resistance |
Formerly known as |
IDDM |
NIDDM or “adult onset” diabetes |
Age of onset |
Younger |
Older |
Obesity |
Rare |
Common |
Family History |
Rare |
Common |
HLA association/Genetic association |
Yes |
No |
Ketosis |
Yes |
No |
Insulin resistance |
No |
Yes |
Presence of body’s own insulin |
No |
Yes |
Respond to Oral Agents |
No |
Yes |
Gestational diabetes is caused when there are excessive counter-insulin hormones of pregnancy. This leads to a state of insulin resistance and high blood sugar in the mother. There may be defective insulin receptors.
Pathophysiology behind symptoms and complications of diabetes