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Canavanine-induced longevity in mice may require diets with greater than 15.7% protein
© Brown; licensee BioMed Central Ltd. 2005
- Received: 09 December 2004
- Accepted: 25 February 2005
- Published: 25 February 2005
Dietary administration of 1% canavanine had been shown to improve survival in female BALB/c mice consuming diets containing 23.4% protein (dry matter basis).
In order to determine if this effect also obtains at more moderate dietary protein concentrations, 30 female BALB/c mice were fed a basal diet with 14% protein (15.7% dry matter basis) and another 30 were fed the same diet plus 1% canavanine.
Neither mean (Control 873.2 d, Canavanine 870.0 d; SEM = 34.2 d; P = 0.949 from ANOVA) nor median (Control 902 d, Canavanine 884.5 d; P = 0.9058 from Mann-Whitney) lifespans differed between groups.
Although mean antinuclear antibody (ANA) titers did not differ between control and canavanine-treated mice at 833 days of age (19.84 vs 20.39 respectively; SEM = 2.64; P = 0.889 from ANOVA), one canavanine-treated mouse displayed an outlying ANA value of 50 (next lower value = 30) denoting possible early sign of incipient autoimmune disease in that individual.
There may be an interaction between dietary protein level and canavanine with respect to lifespan in mice.
- Basal Diet
- High Protein Diet
- Anti dsDNA Titer
- Sentinel Mouse
Canavanine has also been reported to induce a condition that mimics systemic lupus erythematosus (SLE) in primates [11, 12], to increase antibodies to nuclear components and promote SLE-like lesions in auto immune-susceptible (e.g., (NZB X NZW)F1) mice .
In our previous study , eighteen female BALB/c mice were fed a 23.4% protein diet containing 1.56% L-canavanine sulfate (equivalent to 1% L-canavanine base) and eighteen control mice received control diet (23.4% protein) from 84–477 days of age. More canavanine-fed mice (16 of 18) survived to age 477 days than those fed the basal diet (9 of 18) (X 2 with Yates correction = 24.8).
The death rate and median life span of control mice were consistent with previously reported survival studies of female BALB-C mice fed high protein diets . Necropsy and histopathology from both experimental animals and co-housed cages of contemporary sentinel mice performed by the University of California Comparative Pathology Laboratory (Davis, Ca.) did not detect any significant gross or histopathological lesions, parasites or pathogenic bacteria, viruses or mycoplasma. Serology results were negative as well. There was no evidence of infectious disease and no evidence of the lung tumors often found in older BALB-C mice . One sentinel, but no experimental animals, showed evidence of a lymphosarcoma.
Kristal and Yu  have suggested that aging "...results in deleterious changes in cellular, intercellular, tissue and organismic functions."
Apparently, canavanine postponed the type of physiological decline that results in earlier death due to the inability of these aging mice to maintain homeostasis in the face of undetectable disease or some other stress.
These were serendipitous findings during a project designed to explore the mechanism of diet-induced autoimmunity. Ironically, no positive ANAs or anti SSDNA or anti dsDNA titers were detected in these mice as a result of canavanine treatment.
Previous reports of life span extension by restricting the intake of energy , protein , tryptophan  and methionine  have been accompanied by severe reductions in growth and eventual body size relative to controls. The severe stunting usually associated with amino acid deficiency and extended life span was not observed in the BALBc mice .
Our earlier results did leave unanswered the question of whether canavanine was extending life or merely offsetting the life-shortening effects of a very high protein diet. Since the objectives of the original investigation were unrelated to lifespan determination and required the harvest of body tissues, full lifespan data were not available.
The purpose of the experiment reported here was to test the hypothesis that canavanine will reduce middle age mortality and extend the lifespan of female BALB/c mice consuming a diet containing moderate concentrations of protein (15.7% DMB).
Basal (Agway Prolab 1000)
Basal Diet + canavanine
Dry Master %
All others on DMBasis
Gross Energy kcal/g
Estimated Metabolizable Energy kcal/
At 833 days of age, blood samples were taken from the supraorbital sinus of the 37 surviving mice (19 controls and 18 canavanine-fed) and analyzed for antinuclear antibodies (ANA) by the methods of Naiki, et al .
Variations in lifespan and ANA values were evaluated by analyses of variance and median values were contrasted by the Mann Whitney procedure .
Although mean (20.39 vs 19.84) indices of ANA titers at 833 days of age were also similar for canavanine and control treatments, one canavanine-fed mouse displayed an unusually high titer (10X SEM above mean). (Figure 3).
Probable cause of death
Both Types of Tumor
Total With Any Tumor
The median longevity of control mice observed in this experiment (in which a 15.7% protein was fed) considerably exceeds that of the previous trial in which the basal diet contained 23.4% protein (902 d vs 449 d). Storer  fed BALB/c mice a diet of protein content between those two extremes (17%, but probably closer to 19% on a dry matter basis) and observed mean longevity for females of 575 d, a result falling between our two observations. That decreasing protein concentrations should extend rodent lifespan is not a unique finding, the phenomenon is well known. The apparent corrective effect of canavanine at high protein concentrations and lack of effect at more moderate concentrations does offer a new dimension to dietary modulation of longevity that bears further study.
A number of populations consume protein in amounts that far exceed known nutritional requirements (humans in some Western countries, alfalfa-fed horses in some Western States and pet dogs in most of the Northern Hemisphere). The impact of these protein intakes on human and domestic animal longevity and the possible corrective effects of non-protein amino acids on those effects should interest a variety of medical, veterinary and nutritional workers.
For the second time, we have failed to induce significant autoimmune disease signs with dietary canavanine in BALB/c mice. Since this can be done in autoimmune susceptible strains and hybrids and in the "normal" (DBA/2) strain of mice , genetic differences may play a role in an animal's response to this secondary plant compound.
These preliminary experiments were not contemporary comparisons, nor were they conducted with both sexes, with the same source of BALB/c mice, the same basal diets or at the same locations. Known autoimmune-susceptible lines were not challenged in those trials. Although the data from those trials did indicate a canavanine-protein concentration interaction, we propose a contemporary, comprehensive, integrated experiment including both autoimmune susceptible and more normal populations. The proposed work will be more conclusive and provide an opportunity to examine the generality of the canavanine longevity effect, suggest mechanisms for its occurrence and find out if positive effects on oxidation event-dependent aging might be offset by autoimmunity in susceptible individuals. Examination of such indices as tissue and urine nitrate/nitrite, 8-OH deoxyguanidine, canavanyl residues in specific and total proteins would all contribute to a better understanding of mechanisms of longevity modulation.
This and a previous study suggest that an interaction between dietary protein concentration and canavanine effects on longevity may exist in BALB/c mice. Contemporary trials that vary both protein and canavanine concentrations are needed to test this possibility more conclusively.
The author acknowledges M. Eric Gershwin for analyses of ANA in these mice and Thomas Kuntz for purification of the canavanine and preparation of experimental rations.
- Bell EA: Non-protein amino acids in leguminosae. Advances in legume systematics. 1978, Royal Botanical Gardens, Surrey, 2: 489-499.Google Scholar
- Hrabak A, Bajor T, Temesi A: Comparison of substrate and inhibitor specificity of arginase and nitric oxide (NO) synthase for arginine analogues and related compounds in murine and rat macrophages. Biochem Biophys Res Commun. 1994, 198 (1): 206-212. 10.1006/bbrc.1994.1029.View ArticleGoogle Scholar
- Krishna G: Inhibition of brain nitric oxide synthase expressed on CHO cells by canavanine. NIH Project number Z01HL04421-94. 1994, (CRISP Abstract)Google Scholar
- Umans JG, Samsel RW: L-Canavanine selectively augments contraction in aortas from endotoxemic rats. European Journal of Pharmacology. 1992, 210 (3): 343-346. 10.1016/0014-2999(92)90425-4.View ArticleGoogle Scholar
- Dokita S, Smith SD, Nishimoto T, Wheeler MA, Weiss RM: Involvement of nitric oxide and cyclic GMP in rabbit urethral relaxation. Eur J Pharmarol. 1994, 266 (3): 269-275. 10.1016/0922-4106(94)90136-8.View ArticleGoogle Scholar
- Thomas DA, Rosenthal GA: Toxicity and pharmacokinetics of the nonprotein amino acid L-canavanine in the rat. Toxicology and Applied Pharmacology. 1987, 91: 395-405. 10.1016/0041-008X(87)90061-5.View ArticleGoogle Scholar
- Thomas DA, Rosenthal GA: Metabolism of L-[guanidinooxy-14]canavanine in the rat. Toxicology and Applied Pharmacology. 1987, 91: 406-414. 10.1016/0041-008X(87)90062-7.View ArticleGoogle Scholar
- Crine P, Lemieux E: Incorporation of canavanine into rat pars intermedia proteins inhibits the maturation of pro-opiomelanocortin, the common precursor to adrenocorticotropin and beta-lipotropin. J Biol Chem. 1982, 257: 832-838.Google Scholar
- Rosenthal GA, Reighart JM, Hoffman JA: L-canavanine incorporation into vitellogenin and macromolecular conformation. J Biol Chem. 1989, 264 (23): 13693-13696.Google Scholar
- Brown DL: Reproductive toxicity and increased longevity in mice fed L-canavanine. J Anim Sci. 1994, 72 (Sup 1): 145-Google Scholar
- Malinow MR, Bardana EJ, Pirofsky B, Craig S, McLaughlin P: SLE-like syndrome in monkeys fed alfalfa sprouts: role of a non-protein amino acid. Science. 1982, 216: 415-417.View ArticleGoogle Scholar
- Montanaro A, Bardana EJ: Dietary amino acid-induced systemic lupus erythematosus. Rheumatic Disease Clinics of North America. 1991, 17: 323-333.Google Scholar
- Prete PE: Effects of L-canavanine on immune function in normal and autoimmune mice: disordered B-cell function by a dietary amino acid in the immunoregulation of autoimmune disease. Can J Physiol Pharmacol. 1985, 63: 843-854.View ArticleGoogle Scholar
- Brown DL, Naiki M, Gershwin ME: Does L- canavanine ingestion induce murine SLE? Paradoxical effects on survival of BALB/c mice. J Nutr Immun. 2000, 5 (3/4): 17-27.Google Scholar
- Roscoe B, Jackson Memorial Laboratory Staff: Biology of the Laboratory Mouse. 1966, New York, McGraw-Hill Book Company, 512-518.Google Scholar
- Kristal BS, Yu BP: Modulation of Aging Processes by Dietary Restriction. Edited by: Yu BP. 1994, Boca Raton, CRC Press Boca, 1-37.Google Scholar
- McCay CM: The effect of retarded growth upon the length of life span and upon the ultimate body size. J Nutr. 1935, 10: 63-79.Google Scholar
- Leto S, Kokkonen GC, Barrows CH: Dietary protein, life-span and biochemical variables in female mice. J Gerontol. 1976, 31: 144-148.View ArticleGoogle Scholar
- Ooka H, Segall PE, Timiras PS: Histology and survival in age-delayed low-tryptophan-fed rats. Mech Aging Dev. 1988, 43: 79-98. 10.1016/0047-6374(88)90099-1.View ArticleGoogle Scholar
- Orentreich N, Matias JR, DeFelice A, Zimmerman JA: Low methionine ingestion by rats extends life span. J Nutr. 1993, 123: 269-274.Google Scholar
- Rosenthal GA: Preparation and colorimetric analysis of L-canavanine. Anal Biochem. 1977, 77: 147-151. 10.1016/0003-2697(77)90299-8.View ArticleGoogle Scholar
- Naiki M, Yasuyuki I, Yuhsuke K, Osawa T: Effect of an autoreactive T cell clone from (NZB X NZW) F1 mice on the production of anti-DNA antibodies in vivo and in vitro. Immunology Letters. 1988, 18: 281-288. 10.1016/0165-2478(88)90175-7.View ArticleGoogle Scholar
- Snedecor GW, Cochran WG: Statistical methods. 1980, Ames, IA, Iowa State University Press, 7Google Scholar
- Storer JB: Longevity and gross pathology at death in 22 inbred mouse strains. J Gerontol. 1966, 21: 404-409.View ArticleGoogle Scholar
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