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Recent News and Articles on the Keywords: long life + less insulin + insulin  Related to the article below (Last Update: 7/1/2008)

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Boston Globe
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all 30 news articles »
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Source: Google News

Insulin Resistance in Short Children with Intrauterine Growth Retardation 1 -
PL Hofman, WS Cutfield, EM Robinson, RN Bergman, … - Journal of Clinical Endocrinology & Metabolism, 1997 - Endocrine Soc
... dyslipidemia, and ischemic heart disease in late adult life. The long interval between
impaired S I and onset of ... defined term, with birth weight less than the ...

[PDF] … of the long-acting insulin analog insulin glargine (HOE901) in comparison with those of NPH insulin -
L Heinemann, R Linkeschova, K Rave, B Hompesch, M … - Diabetes Care, 2000 - profil-research.de
... subjects were connected to a Biostator (Life Science Instru ... ied whether this long
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-

Timing Requirements for Insulin/IGF-1 Signaling in C. elegans -
A Dillin, DK Crawford, C Kenyon - Science's STKE, 2002 - stke.sciencemag.org
... Therefore, the insulin/IGF-1 pathway appears to operate ... This seems less likely, because
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[CITATION] … , and improved quality of life in Type 1 diabetes mellitus with continuous subcutaneous insulin … -
R Linkeschova, M Raoul, U Bott, M Berger, M Spraul - Diabetic Medicine, 2002 - Blackwell Synergy
... followed for the initiation and long-term care ... the incidence of SH, with slightly
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Regulation of Hypoxic Death in C. elegans by the Insulin/IGF Receptor Homolog DAF-2 -
BA Scott, MS Avidan, CM Crowder - Science, 2002 - sciencemag.org
... in the homolog of the human insulin/IGF receptor ... 5). Two weakly Hyp alleles had
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Dietary Restriction in Long-Lived Dwarf Flies -
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daf-2, an Insulin Receptor-Like Gene That Regulates Longevity and Diapause in Caenorhabditis elegans -
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Polymorphic Variants of Insulin-Like Growth Factor I (IGF-I) Receptor and Phosphoinositide 3-Kinase … -
M Bonafe, M Barbieri, F Marchegiani, F Olivieri, E … - Journal of Clinical Endocrinology & Metabolism, 2003 - Endocrine Soc
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… bypass operation reduces the progression and mortality of non-insulin-dependent diabetes mellitus -
KG MacDonald, SD Long, MS Swanson, BM Brown, P … - Journal of Gastrointestinal Surgery, 1997 - Springer
... our on- going attempt to provide long-term follow ... median weight of the 1983
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Insulin Infusion and Intensive Injection Therapy in Type 1 Diabetes for Patients With Long-Standing … -
JH DeVries, FJ Snoek, PJ Kostense, N Masurel, RJ … - Diabetes Care, 2002 - Am Diabetes Assoc
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Source: Google Scholar

Key to a long life -- less insulin in the brain?

Last Updated: 2007-07-19 16:36:15 -0400 (Reuters Health)

WASHINGTON - Good, old-fashioned diet and exercise might keep you young by reducing the action of insulin in the brain, researchers reported on Thursday.

The investigators created mutant mice that over-ate, got fat and even had symptoms of diabetes, and yet lived 18 percent longer than normal lab mice. The secret: they lacked a certain key gene that affects insulin, the hormone that regulates glucose.

The genetic engineering mimicked the effects of eating less and exercising, the researchers report in the journal Science.

"This study provides a new explanation of why it's good to exercise and not eat too much," said Dr. Morris White, a Howard Hughes Medical Institute investigator at Children's Hospital in Boston who led the study.

The findings also raise questions about how desirable it is to use insulin to treat type 2 diabetes, said the researchers.

Doctors know that people who exercise regularly live longer on average. Researchers have also learned that putting animals on a strict diet makes them live longer, although this has not yet been shown to work in people.

So White's team sought to see if the two effects were linked. They looked at insulin, because both fasting and exercise make cells more insulin-sensitive, meaning they respond more efficiently to the effects of insulin.

They looked at the entire insulin pathway -- a series of actions in the cell that control the body's use of insulin.

White's team engineered mice that had no working copies of one of the genes involved in this pathway, called insulin receptor substrate 2 (Irs2).

BEST USE OF INSULIN

Mice with no copies of Irs2 had defective brains and diabetes. But mice with one working copy lived 18 percent longer than normal mice.

"What's more, the animals lived longer even though they had characteristics that should shorten their lives such as being overweight and having higher insulin levels in the blood," White said in a statement.

They were also more active than normal mice, and after eating, their brains had higher levels of a compound called superoxide dismutase, an antioxidant that protects cells from damage.

"Diet, exercise and lower weight keep your peripheral tissues sensitive to insulin," White said. That means the body needs to make less insulin.

"Since insulin turns on Irs2 in the brain, that means lower Irs2 activity, which we've linked to longer life span in the mouse," he said.

One obvious question is whether drugs can mimic the effects of having less Irs2, perhaps by interfering with its action. The researchers note that people who live to be 100 or more often have reduced insulin levels and their cells show better insulin sensitivity.

New diabetes drugs that increase insulin sensitivity may help, too, White said. But, he added: "The easiest way to keep insulin levels low in the brain is old-fashioned diet and exercise."

Copyright © 2007 Reuters Limited. All rights reserved. Republication or redistribution of Reuters content, including by framing or similar means, is expressly prohibited without the prior written consent of Reuters. Reuters shall not be liable for any errors or delays in the content, or for any actions taken in reliance thereon. Reuters and the Reuters sphere logo are registered trademarks and trademarks of the Reuters group of companies around the world.

 
 
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