Inability of rat alveolar macrophages to recycle L-citrulline to L-arginine despite induction of argininosuccinate synthetase mRNA and protein, and inhibition of nitric oxide synthesis by exogenous L-citrulline

Citation
R. Hammermann et al., Inability of rat alveolar macrophages to recycle L-citrulline to L-arginine despite induction of argininosuccinate synthetase mRNA and protein, and inhibition of nitric oxide synthesis by exogenous L-citrulline, N-S ARCH PH, 358(6), 1998, pp. 601-607
Citations number
36
Categorie Soggetti
Pharmacology & Toxicology
Journal title
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY
ISSN journal
00281298 → ACNP
Volume
358
Issue
6
Year of publication
1998
Pages
601 - 607
Database
ISI
SICI code
0028-1298(199812)358:6<601:IORAMT>2.0.ZU;2-#
Abstract
In the present study it was tested whether rat alveolar macrophages (AM Phi ) convert L-citrulline to L-arginine to maintain nitric oxide (NO) synthesi s under conditions of limited availability of L-arginine. Rat AM Phi (0.5 x 10(6) cells/well, cultured for 20 h in the absence or presence of 1 mu g/m l lipopolysaccharides, LPS), were incubated for 6 h in amino acid-free Kreb s solution and nitrite accumulation was determined as a measure of NO synth esis. After culture in the absence of LPS, nitrite in the incubation media was at the detection limit, independent of the addition of L-arginine or L- citrulline. AM Phi, cultured in the presence of LPS, produced about 4 nmol per 106 cells and 6 h nitrite, and L-arginine enhanced nitrite accumulation in a concentration-dependent manner, maximally about threefold (EC50: 55 m u M). In LPS-treated AM Phi L-citrulline (up to 10 mM) failed to enhance ni trite accumulation, but rather inhibited it by about 50% in the presence of 100 mu M L-arginine, i.e. when NO synthesis was enhanced. L-Arginine in th e culture medium was H-3-labelled and its metabolism analysed by HPLC. In m edium of AM Phi exposed to LPS [H-3]-L-arginine was reduced by about 60% af ter a 20-h culture period and this was almost balanced by an almost equal i ncrease in [H-3]-L-citrulline and [H-3]-L-ornithine, i.e. L-arginine was ma rkedly consumed. When [C-14]-L-citrulline was added to the culture medium o f AM Phi, no significant formation of [C-14]-L-arginine could be detected. On the other hand, argininosuccinate synthetase mRNA (by RT-PCR) and protei n (by Western blot) was marginally detectable in control AM Phi, but clearl y induced after exposure to LPS. Finally, L-citrulline was shown to inhibit L-arginine uptake in a concentration dependent manner, by about 50% at 10 mM. In conclusion, although the expression of argininosuccinate synthetase in r at AM Phi can be induced by LPS, AM Phi appear not to be able to recycle si gnificant amounts of L-citrulline to L-arginine to maintain sustained NO sy nthesis. On the contrary, at high concentrations L-citrulline can reduce NO synthesis, and this effect appears to be caused by inhibitory effects on L -arginine uptake.