Source:http://linkedlifedata.com/resource/pubmed/id/17195423
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
2007-1-1
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pubmed:abstractText |
Exenatide (synthetic exendin-4) is the analog of glucagon-like peptide 1 (GLP-1), the major physiologic incretin. The latter is an intestinal hormone that enhances glucose-induced insulin secretion after meals. In addition, GLP-1 stimulates insulin synthesis, inhibits glucagon secretion, delays gastric emptying, and may promote satiety. These glucoregulatory actions help control plasma glucose in the postprandial period. However, in diabetes, the GLP-1 response to nutrient intake is impaired, leading to exacerbation of postprandial hyperglycemia. Exenatide was recently approved as adjunctive therapy in diabetic patients failing sulfonylureas and/or metformin. In clinical trials lasting 30 weeks, exenatide therapy was associated with moderate reduction in mean hemoglobin A1c (HbA1c) levels of approximately 0.8%, and an average weight loss of approximately 2 kg compared with baseline. Hypoglycemia was generally mild and occurred more commonly when exenatide was used in conjunction with sulfonylureas. The requirement of subcutaneous injections twice a day, and the frequent occurrence of nausea and vomiting, represent the main limitations of exenatide. Nevertheless, this agent may be a useful add-on therapy in obese diabetic patients with suboptimal control as a result of continuing weight gain and/or severe postprandial hyperglycemia. The introduction of GLP-1-based antidiabetic drugs is a novel and promising strategy to treat diabetes.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Adamantane,
http://linkedlifedata.com/resource/pubmed/chemical/Gastric Inhibitory Polypeptide,
http://linkedlifedata.com/resource/pubmed/chemical/Glucagon,
http://linkedlifedata.com/resource/pubmed/chemical/Hypoglycemic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Insulin,
http://linkedlifedata.com/resource/pubmed/chemical/Nitriles,
http://linkedlifedata.com/resource/pubmed/chemical/Peptides,
http://linkedlifedata.com/resource/pubmed/chemical/Pyrrolidines,
http://linkedlifedata.com/resource/pubmed/chemical/Venoms,
http://linkedlifedata.com/resource/pubmed/chemical/exenatide,
http://linkedlifedata.com/resource/pubmed/chemical/vildagliptin
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0038-4348
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
99
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1271-9
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:17195423-Adamantane,
pubmed-meshheading:17195423-Animals,
pubmed-meshheading:17195423-Diabetes Mellitus, Type 2,
pubmed-meshheading:17195423-Gastric Emptying,
pubmed-meshheading:17195423-Gastric Inhibitory Polypeptide,
pubmed-meshheading:17195423-Glucagon,
pubmed-meshheading:17195423-Humans,
pubmed-meshheading:17195423-Hypoglycemic Agents,
pubmed-meshheading:17195423-Insulin,
pubmed-meshheading:17195423-Nitriles,
pubmed-meshheading:17195423-Peptides,
pubmed-meshheading:17195423-Pyrrolidines,
pubmed-meshheading:17195423-Treatment Outcome,
pubmed-meshheading:17195423-Venoms
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pubmed:year |
2006
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pubmed:articleTitle |
Exenatide: a novel approach for treatment of type 2 diabetes.
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pubmed:affiliation |
Endocrinology Division, Olive View-UCLA Medical Center, 14445 Olive View Drive, Sylmar, CA 91342, USA. nmikhail@ladhs.org
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pubmed:publicationType |
Journal Article,
Review
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