| Literature DB >> 9930583 |
H Naito1, A Ohneda, R Kojima, T Sato, K Sasaki, Y Funayama, K Fukushima, C Shibata, S Matsuno, I Sasaki.
Abstract
Recent successful synthesis of human glicentin prompted us to establish an immunoassay method for determination of human glicentin in plasma. Human glicentin in plasma was measured using a newly developed sandwich ELISA. The mean fasting levels of human glicentin were 18.6+/-2.4 and 19.7+/-2.1 pM in normal subjects and diabetic patients, respectively. In diabetic patients with renal failure, plasma glicentin was elevated, exceeding 100 pM. In normal subjects, plasma glicentin increased to a peak level of about 130 pM at 60 min after an oral glucose load, and then decreased. In patients who underwent gastrectomy, plasma glicentin rapidly increased to a peak of about 300 pM at 30 min after oral glucose load. In a patient with short bowel syndrome plasma glicentin did not change following an oral glucose load. These results correspond with previous findings for gut glucagon-like immunoreactive materials (GLI) or enteroglucagon. We conclude that glicentin is secreted from the small intestine in response to intraluminal glucose stimulation in humans.Entities:
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Year: 1999 PMID: 9930583 DOI: 10.1016/s0167-0115(98)00144-x
Source DB: PubMed Journal: Regul Pept ISSN: 0167-0115