Insulin signal transduction pathway
Insulin Signal Transduction Pathway
The insulin signal transduction pathway is a critical cellular mechanism that regulates glucose homeostasis and metabolism in the body. This pathway is activated by the hormone insulin, which is secreted by the beta cells of the pancreas in response to elevated blood glucose levels. The pathway involves a series of molecular interactions that lead to the uptake of glucose by cells, particularly in muscle and adipose tissue.
Overview
Insulin is a peptide hormone that plays a vital role in regulating carbohydrate and fat metabolism. When insulin binds to its receptor on the cell surface, it triggers a cascade of events that facilitate the uptake of glucose and its conversion into energy or storage as glycogen.
Insulin Receptor
The insulin receptor is a transmembrane receptor that belongs to the tyrosine kinase family. It is composed of two alpha and two beta subunits. Upon insulin binding, the receptor undergoes autophosphorylation, activating its intrinsic kinase activity.
Signal Transduction
The activated insulin receptor phosphorylates insulin receptor substrates (IRS), which serve as docking proteins for downstream signaling molecules. This leads to the activation of the phosphoinositide 3-kinase (PI3K) pathway and the mitogen-activated protein kinase (MAPK) pathway.
PI3K Pathway
The PI3K pathway is crucial for the metabolic actions of insulin. PI3K phosphorylates phosphatidylinositol (4,5)-bisphosphate (PIP2) to generate phosphatidylinositol (3,4,5)-trisphosphate (PIP3). PIP3 recruits protein kinase B (PKB/Akt) to the membrane, where it is activated. Akt plays a key role in promoting glucose uptake by translocating GLUT4 vesicles to the cell surface.
MAPK Pathway
The MAPK pathway is involved in the mitogenic effects of insulin. It is activated through the Ras protein, leading to a cascade that involves Raf, MEK, and ERK kinases. This pathway regulates cell growth and differentiation.
Biological Effects
The primary effect of insulin signaling is the reduction of blood glucose levels. Insulin promotes the uptake of glucose into cells, enhances glycogen synthesis, and inhibits gluconeogenesis in the liver. It also stimulates lipogenesis and inhibits lipolysis, contributing to fat storage.
Pathophysiology
Dysregulation of the insulin signal transduction pathway is associated with insulin resistance, a hallmark of type 2 diabetes mellitus. In insulin resistance, cells fail to respond adequately to insulin, leading to elevated blood glucose levels and compensatory hyperinsulinemia.
Related Pages
Transform your life with W8MD's budget GLP-1 injections from $125.
W8MD offers a medical weight loss program to lose weight in Philadelphia. Our physician-supervised medical weight loss provides:
- Most insurances accepted or discounted self-pay rates. We will obtain insurance prior authorizations if needed.
- Generic GLP1 weight loss injections from $125 for the starting dose.
- Also offer prescription weight loss medications including Phentermine, Qsymia, Diethylpropion, Contrave etc.
NYC weight loss doctor appointments
Start your NYC weight loss journey today at our NYC medical weight loss and Philadelphia medical weight loss clinics.
- Call 718-946-5500 to lose weight in NYC or for medical weight loss in Philadelphia 215-676-2334.
- Tags:NYC medical weight loss, Philadelphia lose weight Zepbound NYC, Budget GLP1 weight loss injections, Wegovy Philadelphia, Wegovy NYC, Philadelphia medical weight loss, Brookly weight loss and Wegovy NYC
|
WikiMD's Wellness Encyclopedia |
| Let Food Be Thy Medicine Medicine Thy Food - Hippocrates |
Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.
Translate this page: - East Asian
中文,
日本,
한국어,
South Asian
हिन्दी,
தமிழ்,
తెలుగు,
Urdu,
ಕನ್ನಡ,
Southeast Asian
Indonesian,
Vietnamese,
Thai,
မြန်မာဘာသာ,
বাংলা
European
español,
Deutsch,
français,
Greek,
português do Brasil,
polski,
română,
русский,
Nederlands,
norsk,
svenska,
suomi,
Italian
Middle Eastern & African
عربى,
Turkish,
Persian,
Hebrew,
Afrikaans,
isiZulu,
Kiswahili,
Other
Bulgarian,
Hungarian,
Czech,
Swedish,
മലയാളം,
मराठी,
ਪੰਜਾਬੀ,
ગુજરાતી,
Portuguese,
Ukrainian
Contributors: Prab R. Tumpati, MD