Protection from glutathione depletion by a glyconutritional mixture of saccharides

Citation
D. Busbee et al., Protection from glutathione depletion by a glyconutritional mixture of saccharides, AGE, 22(4), 1999, pp. 159-165
Citations number
32
Categorie Soggetti
Medical Research General Topics
Journal title
AGE
ISSN journal
01619152 → ACNP
Volume
22
Issue
4
Year of publication
1999
Pages
159 - 165
Database
ISI
SICI code
0161-9152(199910)22:4<159:PFGDBA>2.0.ZU;2-#
Abstract
A complex glyconutritional (GN) mixture of mono- ,di- and polysaccharides w as investigated to assess its capacity to protect two different types of ro dent cells, rat hepatocytes and mouse splenocytes, from depletion of glutat hione by a sulfhydryl-reactive mycotoxin, patulin, or by coxsackievirus B3 (CVB3) infection, respectively. Rat hepatocytes were treated with the GN mi xture in vitro or received carrier medium only prior to treatment with patu lin. When treated with the GN mixture prior to patulin exposure hepatocytes demonstrated protection against depletion of intracellular reduced glutath ione(GSH). Cells treated with the GN for up to 15 hours prior to patulin ex posure showed no increase in protection of GSH above that demonstrated by e el Is treated for 3 hours. Mice were infected with CVB3 and one treatment g roup was injected intraperitoneally with the GN once a week. Animals were s plenectomized each month over a ten month treatment for analysis of spleen monocytic cells. Splenocytes from mice treated with the GN mixture did not show the virally-associated depletion of intracellular GSH or damage to pan creatic acini observed in CVB3 inoculated but non-ON-treated mice. Animals from which spleen cells were taken for analysis showed no decrease in anti- CVB3 antibodies and no decrease in viral titers to accompany or explain the normal levels of intracellular GSH. These data strongly suggest that a com plex mixture of exogenous saccharides exerts a protective effect on liver c ells in vitro in that the cells are protected from chemically initiated dep letion of intracellular GSH, and on spleen cells in vivo in that the cells are protected against a CVB3-initiated decrease in intracellular GSH and in crease in pancreatic acini damage.