Multivariate statistical batch processing (BP) analysis of H-1 NMR urine spectra was employed to establish time-dependent metabolic variations in animals treated with the model hepatotoxin, alpha-naphthylisothiocyanate (ANIT). ANIT (100 mg kg(-1)) was administered orally to rats (n = 5) and urine samples were collected from dosed and matching control rats at time-points up to 168 h post-dose. Urine samples were measured via H-1 NMR spectroscopy and partial least squares (PLS) based batch processing analysis was used to interpret the spectral data, treating each rat as an individual batch comprising a series of timed urine samples. A model defining the mean urine profile over the 7 day study period was established, together with model confidence limits (+/-3 standard deviation), for the control group. Samples obtained from ANIT treated animals were evaluated using the control model. Time-dependent deviations from the control model were evident in all ANIT treated animals consisting of glycosuria, bile aciduria, an initial decrease in taurine levels followed by taurinuria and a reduction of tricarboxylic acid cycle intermediate excretion. BP provided an efficient means of visualising the biochemical response to ANIT in terms of both inter-animal variation and net variation in metabolite excretion profiles. BP also allowed multivariate statistical limits for normality to be established and provided a template for defining the sequence of time-dependent metabolic consequences of toxicity in NMR based metabonomic studies.
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Univ London Imperial Coll Sci Technol & Med, Fac Med, Div Biomed Sci, Biol Chem Sect, London SW7 2AZ, EnglandUniv London Imperial Coll Sci Technol & Med, Fac Med, Div Biomed Sci, Biol Chem Sect, London SW7 2AZ, England
Nicholson, JK
Connelly, J
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Univ London Imperial Coll Sci Technol & Med, Fac Med, Div Biomed Sci, Biol Chem Sect, London SW7 2AZ, EnglandUniv London Imperial Coll Sci Technol & Med, Fac Med, Div Biomed Sci, Biol Chem Sect, London SW7 2AZ, England
Connelly, J
Lindon, JC
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Univ London Imperial Coll Sci Technol & Med, Fac Med, Div Biomed Sci, Biol Chem Sect, London SW7 2AZ, EnglandUniv London Imperial Coll Sci Technol & Med, Fac Med, Div Biomed Sci, Biol Chem Sect, London SW7 2AZ, England
Lindon, JC
Holmes, E
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Univ London Imperial Coll Sci Technol & Med, Fac Med, Div Biomed Sci, Biol Chem Sect, London SW7 2AZ, EnglandUniv London Imperial Coll Sci Technol & Med, Fac Med, Div Biomed Sci, Biol Chem Sect, London SW7 2AZ, England
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Univ London Imperial Coll Sci Technol & Med, Fac Med, Div Biomed Sci, Biol Chem Sect, London SW7 2AZ, EnglandUniv London Imperial Coll Sci Technol & Med, Fac Med, Div Biomed Sci, Biol Chem Sect, London SW7 2AZ, England
Nicholson, JK
Connelly, J
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机构:
Univ London Imperial Coll Sci Technol & Med, Fac Med, Div Biomed Sci, Biol Chem Sect, London SW7 2AZ, EnglandUniv London Imperial Coll Sci Technol & Med, Fac Med, Div Biomed Sci, Biol Chem Sect, London SW7 2AZ, England
Connelly, J
Lindon, JC
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Univ London Imperial Coll Sci Technol & Med, Fac Med, Div Biomed Sci, Biol Chem Sect, London SW7 2AZ, EnglandUniv London Imperial Coll Sci Technol & Med, Fac Med, Div Biomed Sci, Biol Chem Sect, London SW7 2AZ, England
Lindon, JC
Holmes, E
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h-index: 0
机构:
Univ London Imperial Coll Sci Technol & Med, Fac Med, Div Biomed Sci, Biol Chem Sect, London SW7 2AZ, EnglandUniv London Imperial Coll Sci Technol & Med, Fac Med, Div Biomed Sci, Biol Chem Sect, London SW7 2AZ, England