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Influence of glutathione on the bioactivity of subcutaneously or orally administered insulin to rats

Influence of glutathione on the bioactivity of subcutaneously or orally administered insulin to rats

Al-Kurdi, Zakieh I., Chowdhry, Babur Z., Leharne, Stephen A., Qinna, Nidal A., Al-Omari, Mahmoud M.H. and Badwan, Adnan A. (2015) Influence of glutathione on the bioactivity of subcutaneously or orally administered insulin to rats. Protein and Peptide Letters, 22 (6). pp. 489-496. ISSN 0929-8665 (Print), 1875-5305 (Online) (doi:10.2174/0929866522666150421112645)

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Abstract

The effect of reduced (GSH) and oxidized (GSSG) glutathione on the bioactivity of insulin was studied. A polyelectrolyte complex (PEC) of insulin with low molecular weight chitosan (13 kDa) was prepared and characterized. The PEC was then solubilized, in the presence and absence of GSH and GSSG, in a reverse micelle consisting of oleic acid and two surfactants (PEG-8 caprylic/capric glycerides and polyglycerol-6-dioleate). The in vitro and in vivo performances of the reverse micelle formulations (RMFs) were evaluated in rats. At pH 6.5 the association efficiency of the PEC was 76.2%. In vitro insulin release from the RMs was negligible at pH 1.2 and was markedly increased at pH 6.8. The hypoglycemic activity of insulin in the PEC was reduced when administered via the subcutaneous route, regardless of the GSH content. On the other hand, the presence of GSSG significantly enhanced hypoglycemia. When the RMF was administered via the oral route, the presence of GSH had no effect on the hypoglycemic activity of insulin compared with the GSH free system. However, the presence of GSSG in the oral preparation increased the hypoglycemic activity of insulin; probably by inhibiting insulin degradation, thereby prolonging its effect. Thus, incorporation of GSSG in the RMF reduces blood glucose levels in rats and protects insulin from degradation.

Item Type: Article
Uncontrolled Keywords: bioactivity, glutathione, low molecular weight chitosan, nanoparticles, oral insulin
Subjects: Q Science > QD Chemistry
Faculty / Department / Research Group: Faculty of Engineering & Science
Last Modified: 14 Oct 2016 09:34
Selected for GREAT 2016: None
Selected for GREAT 2017: None
Selected for GREAT 2018: None
URI: http://gala.gre.ac.uk/id/eprint/13776

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