Diet and individuality in detoxification

References

• Kim H., Yoon Y. J., Shon J. H., Cha I. J., Shin J. G., Liu K. H. Inhibitory effects of fruit juices on CYP3A activity. Drug Metab Dispos 2006; 34: 521–523
   PubMed Web of Science ®Google Scholar
• Arbuthnot J. An essay concerning the nature of ailments, 3rd ed. J. Tonson pub, London 1735; 64
   Google Scholar
• Johnson S. Dictionary of the English Language Vol 1, 1st ed. W. Strahan Ltd, London 1755
   Google Scholar
• Tressl R., Holzer M., Apetz M. Formation of flavour components in asparagus. J Agric Food Chem 1977; 25: 455–463
   Google Scholar
• Waring R. H., Mitchell S. C., Fenwick G. R. The chemical nature of the urinary odour produced by man after asparagus ingestion. Xenobiotica 1987; 17: 1363–1371
   PubMed Web of Science ®Google Scholar
• Mitchell S. C., Waring R. H., Land D., Thorpe W. V. Odorous urine following asparagus ingestion in man. Experientia 1987; 43: 382–383
   PubMedGoogle Scholar
• Turner F., Smith G., Sachse C., Lightfoot T., Garner R. C., Wolf C. R., Forman D., Bishop D. T., Barrett J. H. Vegetable, fruit and meat consumption and potential risk modifying genes in relation to colorectal cancer. Int J Cancer 2004; 112: 259–264
   PubMed Web of Science ®Google Scholar
• MCMJ Stroombergen. Toxicological aspects of glutathione and glutathione‐S‐transferase. 1997, PhD Thesis, University of Birmingham
   Google Scholar
• Awasthi Y. C., Sharma R., Singhal S. S. Human glutathione‐S‐transferases. Int J Biochem 1994; 26: 295–308
   PubMedGoogle Scholar
• Moon Y. J., Wang X., Morris M. E. Dietary flavonoids: Effects on xenobiotic and carcinogen metabolism. Toxicol In Vitro 2006; 20: 187–210
   PubMed Web of Science ®Google Scholar
• Mandlekar S., Hong J. L., Kong A. N. Modulation of metabolic enzymes by dietary phytochemicals: a review of mechanisms underlying beneficial versus unfavorable effects. Curr Drug Metab 2006; 7: 661–675
   PubMed Web of Science ®Google Scholar
• Habig W. H., Jakoby W. B. Assays for differentiation of glutathione‐S‐transferases. Meth Enzymol 1981; 77: 398–405
   PubMedGoogle Scholar
• Alam Z., Coombes N., Waring R. H., Williams A. C., Steventon G. B. Platelet sulphotransferase activity, plasma sulphate levels and sulphation capacity in patients with migraine and tension headache. Cephalalgia 1997; 17: 761–764
   PubMed Web of Science ®Google Scholar
• Marazzitti D., Bonuccelli U., Nuti A., Toni C., Pedri S., Palego L., Pavese N., Lucetti C., Muratorio A., Cassano G. B. Platelet 3H‐imipramine binding and sulphotransferase activity in primary headache. Cephalalgia 1994; 14: 210–214
   PubMedGoogle Scholar
• Millichip J. G., Yee M. M. The diet factor in pediatric and adolescent migraine. Pediatr Neurol 2003; 28: 9–15
   PubMedGoogle Scholar
• Ghazali R. A., Waring R. H. The effects of flavonoids on human phenolsulphotransferases; potential in drug metabolism and chemoprevention. Life Sci 1999; 65: 1625–1632
   PubMed Web of Science ®Google Scholar
• Harris R. M., Waring R. H. Dietary modulation of human phenolsulphotransferase activity. Xenobiotica 1996; 12: 1241–1247
   Google Scholar
• Grant E. C. Food allergies and migraine. Lancet 1979; 1: 966–969
   PubMed Web of Science ®Google Scholar
• Harris R. M., Wood D. M., Blagg S., Owen K., Hughes P. J., Waring R. H., Kirk C. J. Phytoestrogens are potent inhibitors of oestrogen sulphation: Implications for breast cancer risk and treatment. J Clin Endocrinol Metab 2004; 89: 1779–1787
   PubMed Web of Science ®Google Scholar
• Waring R. H., Ayers S., Gesche A. J., Glatt H‐R., Meinl W., Jarratt P., Kirk C. J., Pettitt T., Rea D., Harris R. M. Phyto‐ and xeno‐estrogens: The contribution of diet and the environment to endocrine disruption. J Steroid Biochem Mol Biol. (in press)
   Google Scholar
• Dawson P. A., Markovich D. Pathogenetics of the human SLC26 transporters. Curr Med Chem 2005; 12: 385–396
   PubMed Web of Science ®Google Scholar
• Davies E., Tsang C‐W., Ghazali A. R., Harris R. M., Waring R. H. Effects of culture with TNF‐alpha, TGF‐beta and insulin on sulphotransferase (SULT 1A1 and 1A3) activity in human colon and neuronal cell lines. Toxicol In Vitro 2004; 18: 749–754
   PubMedGoogle Scholar
• Dawson P. A., Markovich D. Pathogenetics of the human SLC26 transporters. Curr Med Chem 2005; 12: 385–396
   PubMed Web of Science ®Google Scholar
• Parsons R. B., Waring R. H., Williams A. C., Ramsden D. B. Cysteine dioxygenase: Regional localisation of protein and mRNA in rat brain. J Neurosci Res 2001; 65: 78–84
   PubMedGoogle Scholar
• Klovrza L. V. Sulphur metabolism in clinical disease., 2006 PhD Thesis, University of Birmingham
   Google Scholar
• Wilkinson L. J., Waring R. H. Cysteine dioxygenase; modulation of expression in human cell lines by cytokines with control of sulphate formation. Toxicol In Vitro 2002; 16: 481–483
   PubMed Web of Science ®Google Scholar
• Bradley H., Gough A., Sokhi R. S., Hassell A., Waring R. H., Emery P. Sulphate metabolism is abnormal in patients with rheumatoid arthritis: Confirmation by in vivo biochemical findings. J Rheumatol 1994; 21: 1192–1196
   PubMed Web of Science ®Google Scholar
• Caramaschi P., Biasi D., Colombatti M., Pieropan S., Martinelli N., Carletto A., Volpe A., Pacor L. M., Bambara L. M. Anti‐TNF alpha therapy in rheumatoid arthritis and autoimmunity. Rheumatol Int 2006; 26: 209–214
   PubMed Web of Science ®Google Scholar
• Nakamura K., Honda K., Mizutani T., Akiho H., Harada N. Novel strategies for the treatment of inflammatory bowel disease: Selective inhibition of cytokines and adhesion molecules. World J Gastroenterol 2006; 12: 4628–4635
   PubMed Web of Science ®Google Scholar
• Holgate S. T. Cytokine and anti‐cytokine therapy for the treatment of asthma and allergic disease. Cytokine 2004; 28: 152–157
   PubMed Web of Science ®Google Scholar
• Bradford M. M. A rapid and sensitive method for the quantification of microgram quantities of protein utilising the principle of protein‐dye binding. Anal Biochem 1976; 72: 248–254
   PubMed Web of Science ®Google Scholar
• Johnston J. B., Murray K., Cain R. B. Microbial metabolism of aryl sulphonates: A re‐assessment of colorimetric methods for the determination of sulphite and their use in measuring desulphonation of aryl and alkylbenzene sulphonates. Antonie van Leeuwenhoek 1975; 41: 493–511
   PubMedGoogle Scholar
• Jackson S. G., McCandless E. L. Simple rapid turbidometric determination of inorganic sulfate and/or protein. Anal Biochem 1978; 90: 802–805
   PubMed Web of Science ®Google Scholar
• Bradley H., Waring R. H., Emery P., Arthur V. Metabolism of low dose paracetamol in patients with rheumatoid arthritis. Xenobiotica 1991; 21: 689–693
   PubMed Web of Science ®Google Scholar
• Waring R. H., Harris R. M. Sulphation and gut function in autistic spectrum disorders: The potential role of nutrition. The Nutrition Practitioner 2005; 6: 1–10
   Google Scholar
• Ramsden D. B., Parsons R. B., Ho S. L., Xie T., Waring R. H., Williams A. C. Further studies in xenbiotic metabolism and Parkinson's disease. Adv Neurol 2001; 86: 105–113
   PubMedGoogle Scholar