WBR0875: Difference between revisions
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White MF, Kahn CR. The insulin signaling system. J Biol Chem. 1994;269(1):1-4. | White MF, Kahn CR. The insulin signaling system. J Biol Chem. 1994;269(1):1-4. | ||
|AnswerA=RAS/MAP kinase pathway | |AnswerA=RAS/MAP kinase pathway | ||
|AnswerAExp=The RAS/MAPK pathway is responsible for the effects of insulin on cell growth and DNA synthesis. It is not associated | |AnswerAExp=The RAS/MAPK pathway is responsible for the effects of insulin on cell growth and DNA synthesis. It is not associated glycogen synthesis. | ||
|AnswerB=APC/Beta-catenin pathway | |AnswerB=APC/Beta-catenin pathway | ||
|AnswerBExp=The APC/Beta-catenin pathway in essential in Wnt signaling and gene regulation. It is not involved in glucose absorption or glycogen synthesis. | |AnswerBExp=The APC/Beta-catenin pathway in essential in Wnt signaling and gene regulation. It is not involved in glucose absorption or glycogen synthesis. |
Revision as of 01:56, 24 November 2013
Author | [[PageAuthor::Rim Halaby, M.D. [1]]] |
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Exam Type | ExamType::USMLE Step 1 |
Main Category | MainCategory::Biochemistry |
Sub Category | SubCategory::Endocrine |
Prompt | [[Prompt::A researcher is studying the effects of insulin on human muscle cells. After successfully culturing a line of skeletal muscle cells, he applies doses of insulin in small increments and then monitors the effective changes by analyzing samples of cell lysate and samples of the culture broth. He notices that as insulin doses increase the intracellular concentration of glycogen increases while the extracellular concentration of glucose steadily decreases. Which of the following intracellular pathways in responsible for the regulation of both occurrences?]] |
Answer A | AnswerA::RAS/MAP kinase pathway |
Answer A Explanation | AnswerAExp::The RAS/MAPK pathway is responsible for the effects of insulin on cell growth and DNA synthesis. It is not associated glycogen synthesis. |
Answer B | AnswerB::APC/Beta-catenin pathway |
Answer B Explanation | AnswerBExp::The APC/Beta-catenin pathway in essential in Wnt signaling and gene regulation. It is not involved in glucose absorption or glycogen synthesis. |
Answer C | AnswerC::Adenylate cyclase/PKA pathway |
Answer C Explanation | AnswerCExp::The adenylate cyclase/PKA pathway is not associated with insulin signaling. |
Answer D | AnswerD::Fas/FADD pathway |
Answer D Explanation | AnswerDExp::The Fas/FADD pathway is involved in apoptosis signaling. It is not associated with insulin signaling. |
Answer E | AnswerE::PI3k pathway |
Answer E Explanation | AnswerEExp::The PI3k pathway is the second messenger pathway involved in increasing glucose uptake and glycogen synthesis after insulin signaling. |
Right Answer | RightAnswer::E |
Explanation | [[Explanation::Insulin is a peptide hormone, produced by beta cells of the pancreas, and is central to regulating carbohydrate and fat metabolism in the body. Insulin causes cells in the liver, skeletal muscles, and fat tissue to absorb glucose from the blood and produce glycogen (liver and muscle) and triglycerides (adipocytes). Insulin binding to its receptor causes downstream activation of 2 processes: The RAS/MAPK pathway and the PI3k pathway. Both glucose absorption and glycogen synthesis are due to the effects of PI3k pathway activation. PI3K leads to PIP3 formation that activates protein kinase B. PKB phosphorylates glycogen synthase kinase and inactivates it leading to increased activity of glycogen synthase. PKB also facilitates GLUT-4 expression leading to increased glucose uptake. The RAS/MAPK pathway is responsible for the effects of insulin on cell growth and DNA synthesis.
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Approved | Approved::No |
Keyword | WBRKeyword::PI3K pathway, WBRKeyword::insulin, WBRKeyword::glycogen, WBRKeyword::glucose |
Linked Question | Linked:: |
Order in Linked Questions | LinkedOrder:: |