The water-soluble vitamin riboflavin (RF) is involved in key metabolic reactions and is essential for normal cellular functions and growth. Deficiency of RF occurs in humans during periods of physiological and pathological stress and leads to a variety of clinical abnormalities, including growth retardation and degenerative changes in the nervous system. The kidney is the main organ that eliminates RF from the body and therefore plays a key role in regulating body RF homeostasis. Depending on its plasma concentration, RF has been found to be transported bi-directionally in the renal tubule, i.e., reabsorbed and secreted. The reabsorption and secretion processes of RF represent movement of the vitamin across the highly polarized renal epithelial cells. These cells have two membrane domains-the brush border membrane (BBM) and basolateral membrane (BLM)- which are different in their composition, function and permeability. Little is known about the mechanisms involved in RF trans-epithelial transport processes (i.e., reabsorption and secretion) and of their individual trans-membrane transport events (influx and efflux) across the BBM and BLM. Also, nothing is known about the molecular nature of the transport systems involved. We will address these issues in this proposal. Membrane transport processes of many nutrients in different biological systems are regulated by their level in athe diet (i.e., in the body). The effect of RF deficiency and over-supplementation on RF renal reabsorption and secretion transport processes are not known and will be examined in this study. Thyroid hormone has profound effects on may aspects of RF metabolism and physiology, including the urinary excretion of the vitamin. The role of thyroid hormone in regulating RF renal transport processes is not known and will be investigated. Phenothiazine derivatives like chlorpromazine and antidepressant agents like imipramine and amitriptyline share structural similarities with RF and have been found to affect many aspects of normal RF metabolism nd physiology including its urinary excretion. The effects of these widely used therapeutic agents on RF renal transport processes are not known and will be examined. Transport studies will be performed using rabbit isolated perfused proximal tubules in vitro, purified BBM vesicles and BLM vesicles and primary cultures of renal proximal tubular epithelial cells. Expression cloning studies will be performed using Xenopus laevis oocytes. The results of these studies will provide valuable information regarding the cellular and molecular mechanisms of renal transport of an essential nutrient and of the factors that regulate and interfere with the transport processes involved. This should also significantly expand our knowledge in the general area of water-soluble vitamin nutrition and physiology.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK047203-03
Application #
2414855
Study Section
Nutrition Study Section (NTN)
Project Start
1995-05-01
Project End
1999-04-30
Budget Start
1997-05-01
Budget End
1998-04-30
Support Year
3
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of California Irvine
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
161202122
City
Irvine
State
CA
Country
United States
Zip Code
92697
Said, H M; Ortiz, A; Moyer, M P et al. (2000) Riboflavin uptake by human-derived colonic epithelial NCM460 cells. Am J Physiol Cell Physiol 278:C270-6
Yanagawa, N; Shih, R N; Jo, O D et al. (2000) Riboflavin transport by isolated perfused rabbit renal proximal tubules. Am J Physiol Cell Physiol 279:C1782-6
Said, H M (1999) Cellular uptake of biotin: mechanisms and regulation. J Nutr 129:490S-493S
Yanagawa, N; Pham, C; Shih, R N et al. (1999) Chloride dependency of renal brush-border membrane phosphate transport. Am J Physiol 277:F506-12
Kumar, C K; Nguyen, T T; Gonzales, F B et al. (1998) Comparison of intestinal folate carrier clone expressed in IEC-6 cells and in Xenopus oocytes. Am J Physiol 274:C289-94
Yanagawa, N; Jo, O D; Said, H M (1998) Riboflavin transport by rabbit renal basolateral membrane vesicles. Biochim Biophys Acta 1415:56-62
Said, H M; Ortiz, A; Ma, T Y et al. (1998) Riboflavin uptake by the human-derived liver cells Hep G2: mechanism and regulation. J Cell Physiol 176:588-94
Said, H M; Ortiz, A; McCloud, E et al. (1998) Biotin uptake by human colonic epithelial NCM460 cells: a carrier-mediated process shared with pantothenic acid. Am J Physiol 275:C1365-71
Kumar, C K; Yanagawa, N; Ortiz, A et al. (1998) Mechanism and regulation of riboflavin uptake by human renal proximal tubule epithelial cell line HK-2. Am J Physiol 274:F104-10
Kumar, C K; Moyer, M P; Dudeja, P K et al. (1997) A protein-tyrosine kinase-regulated, pH-dependent, carrier-mediated uptake system for folate in human normal colonic epithelial cell line NCM460. J Biol Chem 272:6226-31

Showing the most recent 10 out of 16 publications