The NAD+ precursors, nicotinic acid and nicotinamide protect cells against apoptosis induced by a multiple stress inducer, deoxycholate

被引:95
作者
Crowley, CL
Payne, CM [1 ]
Bernstein, H
Bernstein, C
Roe, D
机构
[1] Univ Arizona, Coll Med, Dept Microbiol & Immunol, Tucson, AZ 85724 USA
[2] Univ Arizona, Arizona Canc Ctr, Div Biometry, Tucson, AZ 85724 USA
关键词
nicotinic acid; nicotinamide; NAD; NF-kappa B; GRP78; PARP;
D O I
10.1038/sj.cdd.4400658
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
The bile salt, sodium deoxycholate (NaDOC), is a natural detergent that promotes digestion of fats. At high physiologic levels, NaDOC activates many stress-response pathways and induces apoptosis in various cell types. NaDOC induces DNA damage and activates poly(ADP-ribose) polymerase (PARP), an enzyme that utilizes NAD(+) as a substrate to repair DNA. NaDOC also induces oxidative stress, endoplasmic reticulum (ER) stress and contributes to protein malfolding. The NAD(+) precursors, nicotinic acid (NA) and nicotinamide (NAM) were found to protect cells against NaDOC-induced apoptosis. NA and NAM also decreased constitutive levels of both activated NF-kappa B and GRP78, two proteins that respond to oxidative stress. However, the mechanism by which NA and NAM protects cells against apoptosis does not involve a reduction in constitutive levels of oxidative stress. NA or NAM treatment increased the protein levels of glyceraldehyde-3-phosphate dehydrogense (GAPDH), a multi-functional enzyme, in the nucleus and cytoplasm, respectively. NAM did not activate the promoter/response elements of 13 stress response genes nor reduce intracellular non-protein thiols, suggesting that if is non-toxic to cells, NAM thus has promise as a dietary supplement to help prevent disorders involving excessive apoptosis.
引用
收藏
页码:314 / 326
页数:13
相关论文
共 119 条
[41]  
HILL MJ, 1986, DIETARY FIBER BASIC, P497
[42]  
HOCKENBERY D, 1995, AM J PATHOL, V146, P16
[43]   Inhibition of NADPH supply by 6-aminonicotinamide: effect on glutathione, nitric oxide and superoxide in J774 cells [J].
Hothersall, JS ;
Gordge, M ;
Noronha-Dutra, AA .
FEBS LETTERS, 1998, 434 (1-2) :97-100
[44]   Oxidative stress increases glyceraldehyde-3-phosphate dehydrogenase mRNA levels in isolated rabbit aorta [J].
Ito, Y ;
Pagano, PJ ;
Tornheim, K ;
Brecher, P ;
Cohen, RA .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1996, 270 (01) :H81-H87
[45]  
JACKSON TM, 1995, J NUTR, V125, P1455
[46]   Age-related neurodegeneration and oxidative stress - Putative nutritional intervention [J].
Joseph, JA ;
Denisova, N ;
Fisher, D ;
Shukitt-Hale, B ;
Bickford, P ;
Prior, R ;
Cao, GH .
NEUROLOGIC CLINICS, 1998, 16 (03) :747-+
[47]  
KALTSCHMIDT C, 1995, BIOL CHEM H-S, V376, P9
[48]   BILE-SALT ACID INDUCTION OF DNA DAMAGE IN BACTERIAL AND MAMMALIAN-CELLS - IMPLICATIONS FOR COLON CANCER [J].
KANDELL, RL ;
BERNSTEIN, C .
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL, 1991, 16 (3-4) :227-238
[49]   Free radical-induced megamitochondria formation and apoptosis [J].
Karbowski, M ;
Kurono, C ;
Wozniak, M ;
Ostrowski, M ;
Teranishi, M ;
Nishizawa, Y ;
Usukura, J ;
Soji, T ;
Wakabayashi, T .
FREE RADICAL BIOLOGY AND MEDICINE, 1999, 26 (3-4) :396-409
[50]   APOPTOSIS - BASIC BIOLOGICAL PHENOMENON WITH WIDE-RANGING IMPLICATIONS IN TISSUE KINETICS [J].
KERR, JFR ;
WYLLIE, AH ;
CURRIE, AR .
BRITISH JOURNAL OF CANCER, 1972, 26 (04) :239-+