Arginine supplementation is well tolerated but does not enhance mitogen-induced lymphocyte proliferation in elderly nursing home residents with pressure ulcers

被引:33
作者
Langkamp-Henken, B
Herrlinger-Garcia, KA
Stechmiller, JK
Nickerson-Troy, JA
Lewis, B
Moffatt, L
机构
[1] Univ Florida, Coll Agr & Life Sci, Gainesville, FL 32611 USA
[2] Univ Florida, Coll Nursing, Gainesville, FL 32611 USA
关键词
D O I
10.1177/0148607100024005280
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Immune function declines with age, increasing risk for infection and delaying wound healing. Arginine enhances immune function and healing of standardized wounds in healthy elderly persons. The purpose of this study was to determine what level of arginine supplementation was orally and metabolically tolerated and effective in enhancing immune function in elderly persons with pressure ulcers. Methods: Residents with one or more pressure ulcers were recruited from two local nursing homes. Subjects were randomized to receive 0 g (n = 10; age, 82 +/- 3 years), 8.5 g (n = 11; 81 +/- 3 years), or 17 g (n = 11; 87 +/- 2 years) of supplemental arginine each day for 4 weeks. Oral tolerance, ie, absence of nausea, vomiting, abdominal distention, or diarrhea, was assessed daily. Metabolic tolerance was assessed weekly by evaluating serum electrolytes. Lymphocyte proliferation to phytohemagglutinin and interleukin 2 production were measured at baseline and after 4 weeks of supplementation as indicators of immune function. Results: Supplemental arginine significantly increased plasma arginine levels and was orally and metabolically tolerated with no complaints of abdominal distress or no clinically relevant changes in electrolyte levels among groups. Lymphocyte proliferation and interleukin 2 production were significantly different between nursing homes. When data from nursing homes were considered individually, arginine supplementation did not enhance the proliferative response. In subjects from nursing home 2 only, there was a 38% and 75% decrease (p < .05) in lymphocyte proliferation with 8.5 and 17 g of supplemental arginine, respectively. Interleukin 2 produc- tion was no different among supplementation groups. Conclusions: Pharmacologic doses of arginine were well tolerated but did not enhance lymphocyte proliferation or interleukin 2 production in nursing home residents with pressure ulcers. Clinical Relevancy: Enteral formulas supplemented with pharmacologic levels of arginine are frequently administered to elderly persons. This study demonstrates that; the very old can tolerate these nitrogen loads if baseline renal function is normal and fluid intake is Encouraged. Further research needs to be completed investigating the effect of arginine supplementation on immune function in this population before recommending arginine use.
引用
收藏
页码:280 / 287
页数:8
相关论文
共 30 条
[1]   METABOLIC AND IMMUNE EFFECTS OF ARGININE IN POST-INJURY HYPERALIMENTATION [J].
BARBUL, A ;
SISTO, DA ;
WASSERKRUG, HL ;
YOSHIMURA, NN ;
EFRON, G .
JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE, 1981, 21 (11) :970-974
[2]  
BARBUL A, 1981, SURGERY, V90, P244
[3]  
BARBUL A, 1990, SURGERY, V108, P331
[4]   INTRAVENOUS HYPERALIMENTATION WITH HIGH ARGININE LEVELS IMPROVES WOUND-HEALING AND IMMUNE FUNCTION [J].
BARBUL, A ;
FISHEL, RS ;
SHIMAZU, S ;
WASSERKRUG, HL ;
YOSHIMURA, NN ;
TAO, RC ;
EFRON, G .
JOURNAL OF SURGICAL RESEARCH, 1985, 38 (04) :328-334
[5]   WOUND-HEALING AND THYMOTROPIC EFFECTS OF ARGININE - A PITUITARY MECHANISM OF ACTION [J].
BARBUL, A ;
RETTURA, G ;
LEVENSON, SM ;
SEIFTER, E .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1983, 37 (05) :786-794
[6]   L-arginine-induced vasodilation in healthy humans:: Pharmacokinetic-pharmacodynamic relationship [J].
Bode-Böger, SM ;
Böger, RH ;
Galland, A ;
Tsikas, D ;
Frölich, JC .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1998, 46 (05) :489-497
[7]  
CERRA FB, 1991, NUTRITION, V7, P193
[8]  
Chorinchath BB, 1996, J IMMUNOL, V156, P1525
[9]   Arginine-supplemented diet decreases expression of inflammatory cytokines and improves survival in burned rats [J].
Cui, XL ;
Iwasa, M ;
Iwasa, Y ;
Ogoshi, S .
JOURNAL OF PARENTERAL AND ENTERAL NUTRITION, 2000, 24 (02) :89-96
[10]   IMMUNE AND METABOLIC EFFECTS OF ARGININE IN THE SURGICAL PATIENT [J].
DALY, JM ;
REYNOLDS, J ;
THOM, A ;
KINSLEY, L ;
DIETRICKGALLAGHER, M ;
SHOU, J ;
RUGGIERI, B .
ANNALS OF SURGERY, 1988, 208 (04) :512-523