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Canadian scientist mines drugs database for new diabetes treatment

Researchers develop cheap and efficient method to identify small molecules for diabetes treatment, finding NAADP plays a crucial role in insulin secretion. This discovery could lead to a new class of drugs to treat type 2 diabetes.

SourceBiotechnology and Biological Sciences Research Council·JournalNature Chemical Biology·DateFeb 23, 2009

Scientists mine drugs database for new diabetes treatment

Researchers at the University of Oxford have developed a cheap and efficient method to discover new drugs for type 2 diabetes. They identified a small molecule called Ned-19, which plays a crucial role in insulin secretion, representing a brand new target for diabetes drugs.

SourceBiotechnology and Biological Sciences Research Council·JournalNature Chemical Biology·DateFeb 22, 2009
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Insulin analogues: What's all the fuss?

A systematic review of insulin analogues found that they have minimal impact on managing type 1 and 2 diabetes, as well as gestational diabetes. However, rapid-acting insulin analogues may be cost-effective for adults with type 1 diabetes. Experts recommend educational programs to manage sugar levels over insulin analogues.

SourceCanadian Medical Association Journal·JournalCanadian Medical Association Journal·DateFeb 16, 2009

Can berberine enhance glucose-stimulated insulin secretion in rat islets?

A study published in the World Journal of Gastroenterology found that berberine increases insulin sensitivity in rat islets through the modulation of HNF4 alpha expression and glucokinase activity. Berberine enhances glucose-stimulated insulin secretion in a dose-dependent manner.

SourceWorld Journal of Gastroenterology·JournalWorld Journal of Gastroenterology·DateOct 31, 2008

New discovery a step towards better diabetes treatment

Researchers at Uppsala University develop new image analysis methods to study the release of insulin and cAMP in beta cells. The findings show that ATP causes an increase in cAMP concentration, which varies rhythmically and coincides with variations in calcium signals, resulting in pulsatile insulin secretion.

SourceUppsala University·JournalCell Metabolism·DateJul 1, 2008
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Fat cells send message that aids insulin secretion

Researchers at WashU Medicine found that fat cells release an enzyme called Nampt, which enhances glucose-stimulated insulin secretion from pancreatic beta cells. This discovery could lead to new methods for improving glucose metabolism in type 2 diabetic or insulin-resistant individuals.

SourceWashU Medicine·JournalCell Metabolism·DateNov 6, 2007

Insulin -- in need of some restraint?

Researchers at the Salk Institute found that knocking out the urocortin 3 gene protects mice against high-fat diet's harmful effects by reducing insulin production. This study suggests a new peptide plays a role in insulin secretion, offering potential therapeutic benefits for treating type 2 diabetes.

SourceSalk Institute·JournalProceedings of the National Academy of Sciences·DateMar 6, 2007

A non-invasive method for measuring beta cell mass during diabetes

Researchers have developed a non-invasive method to measure beta cell mass in individuals with diabetes using PET-based quantitation of VMAT2 receptors. This approach allows for the estimation of beta cell mass in rats with type 1 diabetes, providing insights into the pathogenesis of diabetes and potential therapeutic interventions.

SourceJCI Journals·JournalJournal of Clinical Investigation·DateMay 18, 2006
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MicroRNA study points to novel path for treating diabetes

A team of researchers has discovered that microRNA miR-375 regulates insulin secretion, opening up new avenues for understanding and treating diabetes. The study's findings define a biological function for a mammalian microRNA gene and highlight the importance of collaboration between computation and experiment in modern biology.

SourceNew York University·JournalNature·DateNov 10, 2004

Mouse model of type 2 diabetes

Researchers have developed a mouse model that replicates the clinical features of type 2 diabetes, enabling studies on pathogenesis and testing of new therapies. The strain of mice, generated by selectively mutating an insulin-like receptor in muscle cells, fully recapitulates the disease's progression.

SourceCold Spring Harbor Laboratory·JournalGenes & Development·DateJul 31, 2001

Fat cell defect may trigger insulin resistance in muscle and liver

Researchers at Beth Israel Deaconess Medical Center found that fat cells can trigger insulin resistance in muscle and liver, leading to type 2 diabetes. The study, published in Nature, reveals a potential new target for diabetes treatment and prevention by disrupting the communication between fat cells and other tissues.

SourceBeth Israel Deaconess Medical Center·JournalNature·DateFeb 7, 2001

University of Pittsburgh research may lead to new therapies for diabetes

Researchers at the University of Pittsburgh have developed transgenic mice that overexpress hepatocyte growth factor, leading to increased beta cell proliferation and insulin production. The study suggests that this approach may lead to new therapies for diabetes by enabling islet cells to proliferate and produce insulin more effectively.

SourceUniversity of Pittsburgh Medical Center·JournalJournal of Biological Chemistry·DateJan 14, 2000
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The CARDIA Study: Statement from Dr. Claude Lenfant, director, National Heart, Lung, and Blood Institute

The CARDIA Study found that high-fiber diets are associated with lower insulin levels, weight gain, and other cardiovascular disease risk factors in healthy, young black and white adults. The study of nearly 3,000 participants over 10 years revealed a significant inverse association between fiber consumption and CVD risk factors.

SourceNIH/National Heart, Lung and Blood Institute·DateOct 25, 1999

Stress, coping and biology intertwine for diabetes control

Researchers found that stress and coping measures can affect blood sugar control in people with diabetes. The study's biopsychosocial model suggests that psychological factors interact with biological factors to regulate blood sugar levels.

SourceCenter for Advancing Health·JournalJournal of Health and Social Behavior·DateJun 20, 1999

Adult-Onset Diabetes: An 'Imbalancing' Act

A new study reveals that adult-onset diabetics may be suffering from an 'imbalancing act' caused by a key enzyme called PFK, which regulates glucose metabolism. The researchers found that mice with abnormally high levels of the PFK-L sub-unit developed symptoms of Type II diabetes.

SourceAmerican Committee for the Weizmann Institute of Science·JournalDiabetes·DateOct 15, 1997
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New Oral Insulin Delivery System Shows Promise

Researchers at Purdue University have developed an oral delivery method for insulin that may eventually treat human diabetes. The method uses a gel-like material to protect insulin from stomach enzymes, allowing it to release the drug in a location where it can work.

SourcePurdue University·DateSep 4, 1997

Protein Reverses Vascular And Nerve Damage In Diabetic Rats

Researchers found that C-peptide protein repaired damaged blood vessels and nerves in diabetic rats, suggesting a new approach to preventing cardiovascular disease in both types of diabetes. The protein's unique mechanism of action may be key to understanding its effects on cell function.

SourceWashU Medicine·JournalScience·DateJul 24, 1997

MGH Researchers Find Link Between Leptin And Beta Cells Of Pancreas

Researchers found that leptin reduces insulin secretion in pancreatic beta cells by interacting with receptors and activating ion channels. The study suggests that treatment with leptin or sensitizing drugs may help prevent diabetes in obese individuals with fasting hyper-insulinemia.

SourceMassachusetts General Hospital·DateMay 27, 1997

Molecular Gates Show Promise For Drug Delivery

A graduate student at Purdue University has developed a gel-like material that expands and contracts in response to changes in acidity, mimicking the natural response of the body. The gel could be used as a 'molecular gate' to deliver insulin in real-time, responding to glucose levels.

SourcePurdue University·DateApr 16, 1997
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