The amount of thiolic antioxidant ingestion needed to improve several immune functions is higher in aged than in adult mice

被引:37
作者
De La Fuente, M
Miquel, J
Catalán, MP
Víctor, VM
Guayerbas, N
机构
[1] Univ Complutense, Fac Biol, Dept Anim Physiol, E-28040 Madrid, Spain
[2] Univ Alicante, Dept Biotechnol, E-03080 Alicante, Spain
关键词
ageing; ROS; thiolic antioxidants; macrophage; lymphocyte; diet;
D O I
10.1080/10715760290006439
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
With aging there is an increase of oxidative stress due to an imbalance between the oxidant production and the antioxidant levels in favor of the former. Since immune cell functions are specially linked to reactive oxygen species (ROS) generation, the oxidant/antioxidant balance is essential for these cells. Although low levels of antioxidants cause a decrease in immune function, very high levels of antioxidant compounds could show prooxidant effects. In the present work, we have studied the effect of diet supplementation, for 4 weeks, with two different doses of two thiolic antioxidants, namely thioproline (TP) and N-acetylcysteine (NAC), at 0.1% (w/w) and 0.3% (w/w, of each antioxidant) on the main immune system cells, i.e.: macrophages, lymphocytes and natural killer (NK) cells of adult (33+/-1 week old) and aged (73+/-1 week old) female Swiss mice. Two groups of animals, adult and aged mice, fed standard diet were used as controls. The results show that the ingestion of 0.1% doses of thiols, improves, in the adult mice, several immune functions such as the chemotaxis, capacity of both macrophages and lymphocytes, the phagocytosis of macrophages, the lymphoproliferative response to the mitogen Con A and the NK activity. Moreover, no change was observed in adherence capacity of immune cells, and superoxide production was decreased. By contrast, in aged mice the ingestion of these amounts of antioxidants did not change the immune functions studied with the exception of NK activity, which was stimulated. The ingestion of 0.3% of antioxidants by adult mice only increased some immune functions such as adherence and superoxide production, which are markers of oxidative stress. Other functions such as chemotaxis or lymphoproliferative response decreased. However, the ingestion of these very high amounts of thiols by aged animals increased the phagocytosis, the NK activity and specially the lymphoproliferative response to the mitogen, a function that is very depressed with aging.
引用
收藏
页码:119 / 126
页数:8
相关论文
共 38 条
[1]  
BAGASRA O, 1988, IMMUNOLOGY, V65, P405
[2]   Changes in several functions of murine peritoneal macrophages by N-acetylcysteine and thioproline ingestion.: Comparative effect between two strains of mice [J].
Blanco, B ;
Ferrández, RD ;
Correa, R ;
Del Rio, M ;
Guaza, C ;
Hernanz, A ;
De la Fuente, M .
BIOFACTORS, 1999, 10 (2-3) :179-185
[3]   Oxidative changes associated with β-carotene and α-tocopherol enrichment of human low-density lipoproteins [J].
Bowen, HT ;
Omaye, ST .
JOURNAL OF THE AMERICAN COLLEGE OF NUTRITION, 1998, 17 (02) :171-179
[4]   Graying of the immune system - Can nutrient supplements improve immunity in the elderly? [J].
Chandra, RK .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1997, 277 (17) :1398-1399
[5]   Lignans from Kadsura angustifolia [J].
Chen, YG ;
Qin, GW ;
Xie, YY ;
Cheng, KF ;
Lin, ZW ;
Sun, HD ;
Kang, YH ;
Han, BH .
JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH, 1998, 1 (02) :125-131
[6]  
COQUETTE A, 1986, ARCH INT PHYSL BIOCH, V94, P529
[7]   Improvement of murine immune functions in vitro by thioproline [J].
Correa, R ;
Del Río, M ;
De la Fuente, M .
IMMUNOPHARMACOLOGY, 1999, 44 (03) :281-291
[8]   Effect of a diet supplemented with thioproline on murine macrophage function in a model of premature ageing [J].
Correa, R ;
Blanco, B ;
Del Río, M ;
Victor, V ;
Guayerbas, N ;
Medina, S ;
De la Fuente, M .
BIOFACTORS, 1999, 10 (2-3) :195-200
[9]   Anti-oxidants as modulators of immune function [J].
De la Fuente, M ;
Victor, VM .
IMMUNOLOGY AND CELL BIOLOGY, 2000, 78 (01) :49-54
[10]  
De la Fuente M, 2000, BRIT J NUTR, V84, P25