Metronomic capecitabine inhibits liver transplant rejection in rats by triggering recipients' T cell ferroptosis.

BACKGROUND: Capecitabine (CAP) is a classic antimetabolic drug and has shown potential antirejection effects after liver transplantation (LT) in clinical studies. Our previous study showed that metronomic CAP can cause the programmed death of T cells by inducing oxidative stress in healthy mice. Ferroptosis, a newly defined non-apoptotic cell death that occurs in response to iron overload and lethal levels of lipid peroxidation, is an important mechanism by which CAP induces cell death. Therefore, ferroptosis may also play an important role in CAP-induced T cell death and play an immunosuppressive role in acute rejection after trans-plantation. AIM: To investigate the functions and underlying mechanisms of antirejection effects of metronomic CAP. METHODS: A rat LT model of acute rejection was established, and the effect of metronomic CAP on splenic hematopoietic function and acute graft rejection was evaluated 7 d after LT. In vitro, primary CD3+ T cells were sorted from rat spleens and human peripheral blood, and co-cultured with or without 5-fluorouracil (5-FU) (active agent of CAP). The levels of ferroptosis-related proteins, ferrous ion concentration, and oxidative stress-related indicators were observed. The changes in mito-chondrial structure were observed using electron microscopy. RESULTS: With no significant myelotoxicity, metronomic CAP alleviated graft injury (Banff score 9 vs 7.333, P < 0.001), prolonged the survival time of the recipient rats (11.5 d vs 16 d, P < 0.01), and reduced the infiltration rate of CD3+ T cells in peripheral blood (6.859 vs 3.735, P < 0.001), liver graft (7.459 vs 3.432, P < 0.001), and spleen (26.92 vs 12.9, P < 0.001), thereby inhibiting acute rejection after LT. In vitro, 5-FU, an end product of CAP metabolism, induced the degradation of the ferritin heavy chain by upregulating nuclear receptor coactivator 4, which caused the accumulation of ferrous ions. It also inhibited nuclear erythroid 2 p45-related factor 2, heme oxygenase-1, and glutathione peroxidase 4, eventually leading to oxidative damage and ferroptosis of T cells. CONCLUSION: Metronomic CAP can suppress acute allograft rejection in rats by triggering CD3+ T cell ferroptosis, which makes it an effective immunosuppressive agent after LT.

Flocculation-ultrasonic assisted extraction and solid phase clean-up for determination of polycyclic aromatic hydrocarbons in water rich in colloidal particulate with high performance liquid chromatography and ultraviolet-fluorescence detection.

In the present work, a simple method of sample preparation for the determination of polycyclic aromatic hydrocarbons (PAHs) in water rich in colloidal particulate was developed. The technique was mainly based on the effect of the flocculation of aluminum sulfate and the adsorption of the flocculation aid florisil. The method contained three steps: flocculation, ultrasonic extraction, and solid-phase extraction cleanup. Major parameters of the procedure were optimized with high performance liquid chromatography (HPLC) separation and ultraviolet-fluorescence detection. When 250 mL model sample containing 16 EPA PAHs was processed, the developed method provided detection limits in the range of 0.02-5 ng/L. Both spiked and non-spiked polluted river water samples rich in suspended particles and organic matters were analyzed. Recoveries and relative standard deviations for the 16 PAHs were in ranges of 86-94% and 3-13% (n=5), respectively.

Flow-injection analysis for the determination of total inorganic carbon and total organic carbon in water using the H2O2-luminol-uranine chemiluminescent reaction.

In the presence of carbonate and uranine, the chemiluminescent intensity from the reaction of luminol with hydrogen peroxide was dramatically enhanced in a basic medium. Based on this fact and coupled with the technique of flow-injection analysis, a highly sensitive method was developed for the determination of carbonate with a wide linear range. The method provided the determination of carbonate with a wide linear range of 1.0 x 10(-10)-5.0 x 10(-6) mol L(-1) and a low detection limit (S/N = 3) of carbonate of 1.2 x 10(-11) mol L(-1). The average relative standard deviation for 1.0 x 10(-9)-9.0 x 10(-7) mol L(-1) of carbonate was 3.7% (n = 11). Combined with the wet oxidation of potassium persulfate, the method was applied to the simultaneous determination of total inorganic carbon (TIC) and total organic carbon (TOC) in water. The linear ranges for TIC and TOC were 1.2 x 10(-6)-6.0 x 10(-2) mg L(-1) and 0.08-30 mg L(-1) carbon, respectively. Recoveries of 97.4-106.4% for TIC and 96.0-98.5% for TOC were obtained by adding 5 or 50 mg L(-1) of carbon to the water samples. The relative standard deviations (RSDs) were 2.6-4.8% for TIC and 4.6-6.6% for TOC (n = 5). The mechanism of the chemiluminescent reaction was also explored and a reasonable explanation about chemical energy transfer from luminol to uranine was proposed.

Post-column detection of benzenediols and 1,2,4-benzenetriol based on acidic potassium permanganate chemiluminescence.

Based on the sensitizing effect of formic acid on the chemiluminescence (CL) reaction of polyhydroxylbenzenes with acidified potassium permanganate and the combination technique of high-performance liquid chromatography (HPLC), a sensitive, selective and simple post-column CL detection method for simultaneously determining catechol, resorcinol, hydroquinone and 1,2,4-benzenetriol is described. The optimal conditions for the CL detection and HPLC separation were carried out. The linear ranges were: 6.0 x 10(-3)-1.5 mg/L for hydroquinone, 8.0 x 10(-3)-1.5 mg/L for 1,2,4-benzenetriol, 1.0 x 10(-2)-2.0 mg/L for resorcinol and 1.0 x 10(-2)-2.5 mg/L for catechol, respectively. The detection limits are: 3.2 x 10(-3) mg/L for hydroquinone, 3.9 x 10(-3) mg/L for 1,2,4-benzenetriol, 4.7 x 10(-3) mg/L for resorcinol and 5.2 x 10(-3) mg/L for catechol, respectively. Combining with solid phase extraction, the proposed method has been successfully applied to the determination of the polyhydroxylbenzenes in river water. The recoveries for three benzentriols were 92.1-95.4% and 82.0% for 1,2,4-benzenetriol, respectively.