CHANGES IN PLASMA GLUTATHIONE CONCENTRATIONS, TURNOVER, AND DISPOSAL IN DEVELOPING RATS

We have previously shown that sinusoidal reduced glutathione (GSH) eff lux declines during development because of a declining maximum transpo rt rate [Am. J. Physiol. 261 (Gastrointest. Liver Physiol. 24): G648-G 656, 1991]. Because rat liver serves as the principal source of plasma GSH, we studied the response of plasma GSH to this declining inflow f rom liver. In immature (28- to 42-day) and mature (90- to 151-day) rat s we injected tracer boluses of [S-35]GSH intravenously and collected arterial samples over a 0.75- to 8-mi:n interval while plasma GSH pool remained at steady state!. Concentrations and radioactivities of GSH, oxidized glutathione (GSSG), cysteine (CYSH), cystine (CYSS), and cys teine-glutathione disulfides (CYSSG) and the radioactivities of protei ns were measured in plasma. Our results show the following changes in plasma concentrations (mu M): decreases in unbound (free) GSH (26.0 +/ - 2.1 to 12.4 +/- 0.98; P < 0.001), total unbound GSH equivalents GSH + 2GSSG (29.1 +/- 2.1 to 15.3 +/- 1.2; P < 0.001), total reducible (un bound + bound) GSH (39.3 +/- 2.2 to 28.9 +/- 2.6; P < 0.025!, and free CYSH (57.6 +/- 8.5 to 29.9 +/- 4.0; P < 0.05); no changes in GSSG (1. 57 +/- 0.27 vs. 1.47 +/- 0.41), CYSS (36.7 +/- 12 vs;. 43.4 +/- 17), a nd total unbound CYSH equivalents CYSH - 2CYSS (131 +/- 15 vs. 117 +/- 18); increases in total reducible (unbound + bound) CYSH (158 +/- 8.1 to 203 +/- 24; P < 0.05) and CYSSG (1.80 +/- 0.42 to 4.94 +/- 1.4 in IJ,M GSH equivalents; P < 0.05). A concurrent decline occurred in irre versible disposal rate (IDR) of plasma GSH from 38.5 +/- 4.9 to 16.4 /- 1.4 nmol.min(-1).ml(-1) (P < 0.001) as determined by compartmental analysis of tracer data. This 57% decrease in IDR parallels a decrease of 53% in the inflow of GSH estimated by perfused livers (17.0 to 8.0 nmol.min(-1).ml plasma(-1)). However, perfused liver estimates do not match >44-49% of plasma IDR. Thus perfused liver appears to underesti mate the true rate of sinusoidal GSH efflux taking place in vivo. Some earlier arteriovenous data and our present portal vein-to-hepatic vei n difference measurements appear to corroborate this view.