Increased in vivo glucose recovery via nitric oxide release.


Autoria(s): Nichols, SP; Le, NN; Klitzman, B; Schoenfisch, MH
Data(s)

15/02/2011

Formato

1180 - 1184

Identificador

http://www.ncbi.nlm.nih.gov/pubmed/21235247

Anal Chem, 2011, 83 (4), pp. 1180 - 1184

http://hdl.handle.net/10161/10347

1520-6882

Relação

Anal Chem

10.1021/ac103070t

Tipo

Journal Article

Cobertura

United States

Resumo

The in vivo glucose recovery of subcutaneously implanted nitric oxide (NO)-releasing microdialysis probes was evaluated in a rat model using saturated NO solutions to steadily release NO. Such methodology resulted in a constant NO flux of 162 pmol cm(-2) s(-1) from the probe membrane over 8 h of perfusion daily. The in vivo effects of enhanced localized NO were evaluated by monitoring glucose recovery over a 14 day period, with histological analysis thereafter. A difference in glucose recovery was observed starting at 7 days for probes releasing NO relative to controls. Histological analysis at 14 days revealed lessened inflammatory cell density at the probe surface and decreased capsule thickness. Collectively, the results suggest that intermittent sustained NO release from implant surfaces may improve glucose diffusion for subcutaneously implanted sensors by mitigating the foreign body reaction.

Idioma(s)

ENG

Palavras-Chave #Animals #Cell Count #Glucose #Inflammation #Male #Microdialysis #Nitric Oxide #Rats