Role of signaling pathways in the regulation of folate transport in ethanol-fed rats

被引:23
作者
Hamid, Abid [1 ]
Kaur, Jyotdeep [1 ]
机构
[1] Postgrad Inst Med Educ & Res, Dept Biochem, Chandigarh 160012, India
关键词
Crypt villus axis; Reduced folate carrier; Alcoholism; Signaling; Protein kinase; BRUSH-BORDER MEMBRANE; WATER-SOLUBLE VITAMINS; INTESTINAL-ABSORPTION; CHRONIC-ALCOHOLISM; EPITHELIAL-CELLS; PROTEIN-KINASE; COLON-CANCER; CARRIER; EXPRESSION; DEFICIENCY;
D O I
10.1016/j.jnutbio.2008.03.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Folate is an essential cofactor for normal cellular proliferation and tissue regeneration. Alcohol-associated folate deficiency is common, primarily due to intestinal malabsorption, the mechanism of which needs attention, The aim of the present study was to evaluate the regulatory events of folate transport in experimental alcohol ingestion. For this, male Wistar rats were fed I g/kg body weight/day ethanol (20% solution) orally for 3 months and folate transport was Studied in isolated intestinal epithelial cells across the crypt villus axis. The role of different signaling pathways in folate transport regulation was evaluated independently to that of reduced folate carrier (RFC) expression. The results showed that differentiated cells of villus possess high folate uptake activity as compared to mid villus and crypt base cells. During chronic ethanol ingestion, decrease in transport was observed all along the crypt villus axis but was more pronounced at proliferating crypt base stein cells. Studying the effect of modulators of signaling pathways revealed the folate transport system to be under the regulation of cAMP-dependent protein kinase A (PKA), the activity of which was observed to decrease upon alcohol ingestion. In addition, protein kinase C might have a role in folate transport regulation during alcoholic conditions. The deregulation ill the folate transport system was associated with a decrease ill RFC expression, which may result in lower transport efficiency observed at absorptive surface ill alcohol-fed rats. The study highlights the role that perturbed regulatory pathways and RFC expression play in the decreased folate transport at brush border surface during alcohol ingestion. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:291 / 297
页数:7
相关论文
共 27 条
[1]   Kinetic characteristics of folate binding to rat renal brush border membrane in chronic alcoholism [J].
Hamid, A ;
Kaur, J .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2005, 280 (1-2) :219-225
[2]   Down-regulation of reduced folate carrier may result in folate malabsorption across intestinal brush border membrane during experimental alcoholism [J].
Hamid, Abid ;
Wani, Nissar Ahmad ;
Rana, Satyavati ;
Vaiphei, Kim ;
Mahmood, Akhtar ;
Kaur, Jyotdeep .
FEBS JOURNAL, 2007, 274 (24) :6317-6328
[3]   Evaluation of the kinetic properties of the folate transport system in intestinal absorptive epithelium during experimental ethanol ingestion [J].
Hamid, Abid ;
Kaur, Jyotdeep ;
Mahmood, Akhtar .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2007, 304 (1-2) :265-271
[4]   Chronic alcoholism alters the transport characteristics of folate in rat renal brush border membrane [J].
Hamid, Abid ;
Kaur, Jyotdeep .
ALCOHOL, 2006, 38 (01) :59-66
[5]  
Homann N, 2000, INT J CANCER, V86, P169, DOI 10.1002/(SICI)1097-0215(20000415)86:2<169::AID-IJC4>3.0.CO
[6]  
2-3
[7]  
KAUR J, 1992, NUTRITION, V8, P338
[8]  
KAUR J, 1994, INDIAN J MED RES, V100, P289
[9]   MODIFIED PROCEDURE FOR RAPID PREPARATION OF EFFICIENTLY TRANSPORTING VESICLES FROM SMALL INTESTINAL BRUSH-BORDER MEMBRANES - THEIR USE IN INVESTIGATING SOME PROPERTIES OF D-GLUCOSE AND CHOLINE TRANSPORT-SYSTEMS [J].
KESSLER, M ;
ACUTO, O ;
STORELLI, C ;
MURER, H ;
MULLER, M ;
SEMENZA, G .
BIOCHIMICA ET BIOPHYSICA ACTA, 1978, 506 (01) :136-154
[10]   A protein-tyrosine kinase-regulated, pH-dependent, carrier-mediated uptake system for folate in human normal colonic epithelial cell line NCM460 [J].
Kumar, CK ;
Moyer, MP ;
Dudeja, PK ;
Said, HM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (10) :6226-6231