Blood glucose lowering property of water in oral insulin-fed diabetic rats

Context: In oral insulin delivery, blood glucose profiles of a subject can be a function of complicated transfer of water and insulin between gastrointestinal and blood compartments. Objective: This study examined the effects of orally administered water on blood glucose profiles of oral insulin-fed...

詳細記述

書誌詳細
出版年:Pharmaceutical Biology
第一著者: Wong T.W.; Sumiran N.; Mohd Mokhtar M.T.; Kadir A.
フォーマット: 論文
言語:English
出版事項: 2012
オンライン・アクセス:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84867423854&doi=10.3109%2f13880209.2012.679985&partnerID=40&md5=65e125869e4c07f50d5c6b09d22a1958
その他の書誌記述
要約:Context: In oral insulin delivery, blood glucose profiles of a subject can be a function of complicated transfer of water and insulin between gastrointestinal and blood compartments. Objective: This study examined the effects of orally administered water on blood glucose profiles of oral insulin-fed diabetic rats. The blood glucose, insulin and red blood cell concentration profiles of streptozotocin-induced diabetic rats were determined following administration of deionized water and insulin solution (14 IU/kg) with control receiving none. The aqueous solution samples were subjected to X-ray diffractometry (XRD), fourier transform infra-red spectroscopy (FTIR), viscometry and osmolality tests to elucidate the state of water-insulin interaction. Results and discussion: Deionized water reduced blood glucose concentration by more than 70% via dilution of systemic circulation. The addition of insulin into deionized water negated its blood glucose lowering property instead of no influence due to insulin had not shown marked oral bioavailability. The insulin interacted with water to form solution with higher viscosity and osmolality values. Conclusion: Insulin-water interaction could be one reason where water migration from the gastrointestinal lumen into systemic circulation is reduced and blood glucose lowering capacity of deionized water is negated. © 2012 Informa Healthcare USA, Inc.
ISSN:17445116
DOI:10.3109/13880209.2012.679985