|SkQ1 treatment and food restriction--two ways to retard an aging program of organisms.|
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|PMID: 22170754 Owner: NLM Status: MEDLINE|
|Effects of the mitochondria-targeted antioxidant SkQ1 and food restriction are compared. In both cases there is a remarkable increase in the median lifespan of organisms belonging to many different taxonomic ranks. Essentially, both SkQ1 treatment and restriction in food intake retard development of numerous adverse traits of senescence. This relationship could be predicted assuming that SkQ1 and food restriction inhibit the execution of an aging program. It is hypothesized that food restriction is perceived by organisms as a signal of starvation, which can be catastrophic for the population. Under these conditions, the organism switches off an aging program that is favorable for evolvability of the species but counterproductive for the individual. Unfortunately, food restriction is accompanied by some other effects, e.g., constant anxiety and attempts to scan as large a space as possible looking for food. Such side effects seem to be absent in the case of inhibition of the aging program by SkQ1.|
|Vladimir P Skulachev|
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|Type: Journal Article; Review|
|Title: Aging Volume: 3 ISSN: 1945-4589 ISO Abbreviation: Aging (Albany NY) Publication Date: 2011 Nov|
|Created Date: 2011-12-19 Completed Date: 2012-04-02 Revised Date: 2013-06-27|
Medline Journal Info:
|Nlm Unique ID: 101508617 Medline TA: Aging (Albany NY) Country: United States|
|Languages: eng Pagination: 1045-50 Citation Subset: IM|
|Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow 119991, Russia. email@example.com|
|APA/MLA Format Download EndNote Download BibTex|
Antioxidants / pharmacology*
Plastoquinone / analogs & derivatives*, pharmacology
|0/10-(6'-plastoquinonyl)decyltriphenylphosphonium; 0/Antioxidants; 4299-57-4/Plastoquinone|
Journal ID (nlm-ta): Aging (Albany NY)
Journal ID (publisher-id): ImpactJ
Publisher: Impact Journals LLC
Copyright: © 2011 Skulachev
Received Day: 8 Month: 12 Year: 2011
Accepted Day: 12 Month: 12 Year: 2011
collection publication date: Month: 11 Year: 2011
Electronic publication date: Day: 12 Month: 12 Year: 2011
Volume: 3 Issue: 11
First Page: 1045 Last Page: 1050
PubMed Id: 22170754
|SkQ1 treatment and food restriction — two ways to retard an aging program of organisms|
|Vladimir P. Skulachev|
|Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow 119991, Russia
|Correspondence: Correspondence to:Vladimir P. Skulachev, PhD;firstname.lastname@example.org
As geroprotectors, SkQ1 and food restriction are similar in two very important aspects. Both prolong lifespan in many species and retard development of numerous traits of aging [cf. 1-5 and 6, 7]. Furthermore, there is an indication that the food restriction effect includes at least one component characteristic of the mechanism of action of SkQ1, i.e. antioxidant activity at the mitochondrial level. Fernandes and coauthors  found that 40% caloric restriction resulted in a 10-fold increase in the lifespan of C57Bl/6 mice poisoned by the prooxidant paraquat, a cation with delocalized charge, which is targeted to mitochondria in its reduced form (I. I Severina et al., in preparation) 1.
The effect of food restriction on longevity was described in 1934, when McCay and coworkers  found that it extended the lifespan of rats (see also [11, 12]). The restriction was imposed at early stages of life and initially resulted in retardation of growth. When the food restriction was terminated, the animals rapidly increased in size to reach the average but lived longer by 70% (males) and 48% (females) than rats that were fed ad libitum over their whole life (cf. our data on a larger effect of SkQ1 on longevity in the mouse and mole-vole males than females ). A large decrease in death rates from pulmonary diseases and certain tumors was observed (again similar to SkQ1 [2, 3, 13]). It was also noted that food-restricted animals appeared active and young irrespective of their actual age (another similarity with SkQ1 [2, 3]).
Later, the positive effect of a certain food restriction on lifespan was demonstrated on a great variety of organisms — from yeast to rhesus monkeys and humans [6, 7, 14, 15]. With the appearance of Harman's hypothesis on the role of ROS in aging , this effect came to be explained in terms of a decreased volume of food being oxidized by oxygen and, as a consequence, a decreased production of ROS . That this assumption was invalid was evident already in early works on dietary restriction, when Will and McCay  reported that the heat production per kg body weight in the food-restricted rat cohort was higher rather than lower than in the control. Further research gave direct evidence against this commonly accepted viewpoint. First, it was found that for drosophila it is enough to starve for only the two first days of life to become long-lived to the same extent as if the flies were subjected to dietary restriction over their entire life  (similar relationships were revealed with SkQ1 ). Second, not only an excess of food, but also its smell attenuated the geroprotecting effect provided by food restriction on drosophila and C. elegans [20, 21]. These observations are unlikely to be specific for invertebrates. As far back as 1934, Robertson et al.  discovered in their experiments on mice that a two-day “fasting” every week is sufficient for their lifespan to be extended. Carr et al.  observed, again with mice, that reproductive ability lost by the end of the first year in the case of unrestricted feeding was preserved until at least the 21st month of life when the mice were limited in food ration over the first 11-15 months and then received food ad libitum (cf. SkQ1-induced fecundity increase of mice [2, 3] and mole-vole ). According to data of Stuchlikova et al. , rats, mice, and golden hamsters restricted in food ration by 50% over two years lived 20% longer than the controls. Dietary restriction during the first year of life prolonged the lifespan by 40-60%, and during the second year by only 30-40%.
Further research showed that the effect of dietary restriction involves both the carbohydrate and protein components of food. The effect of proteins restriction is associated with only one amino acid, viz. methionine [25-28]. Methionine is an essential amino acid that is not synthesized in mammals, so food is the only source of this compound. It was found that a diet in which proteins are replaced by a mixture of amino acids containing no methionine not only favors a longer life but decreases mitochondrial ROS generation and oxidative damage to mitochondrial DNA [27, 28]. Interestingly, dietary restriction has no effect on the oxidation of nuclear DNA .
In our opinion , food restriction is perceived by an organism as a worrying signal of food shortage. As known, starvation entails decline of many physiological functions, and in particular decreased fecundity . And this, in turn, jeopardizes the very existence of the population. To prevent, at least in part, such turn of events, it might be sufficient to cancel the aging program, thereby prolonging the reproductive period of the individual and thus increasing the total number of progeny. If this is the case, the impact of dietary restriction on lifespan is only indirectly related to ROS, rather being a regulatory effect. That is why such evidently signaling effects as a short-term fasting (or, vice versa, smell of food), rather than food shortage (or excess) over the entire life, exert a powerful effect on the life cycle parameters. It is remarkable that a temporary dietary restriction (fasting) is better than a constant restriction. The most probably, the signal of food shortage can be given for a fairly short time, whereas starving for a long time is harmful for an organism.
The signaling nature of the effect of dietary restriction provides a good rationale for the results of experiments with methionine. Apparently, the organism determines the amount of available food (and, first of all, essential amino acids required for protein synthesis) by monitoring the level of only one of the amino acids, specifically methionine.
Significantly, dietary restriction not only extends lifespan, but also prolongs youth, as already mentioned by McCay, the discoverer of this phenomenon . Quite illustrative in this respect is the recently reported results of studies by Weindruch and his group on primates . Twenty-year-long experiments on 76 macaques (started when the animals were from 7 to 14 years old) showed that a long-term 30% dietary restriction has the following effects: (1) a sharp decrease in age-related death rate (over 30 years, 20% against 50% in the control group fed ad libitum), (2) exclusion of diabetes from the causes of death, (3) halving the death rate from cancer (in macaques this is primarily intestine adenocarcinoma), (4) decrease in the death rate induced by cardiovascular diseases, (5) decrease in osteoporosis, (6) arrest of the development of such age-related traits as sarcopenia, decline in brain gray matter, alopecia, canities, etc. It is noteworthy that the majority of these effects are also characteristic of the action of SkQ1 [1-4]. By the age of 30 years, 80% of the surviving control macaques showed some traits of aging, whereas in the experimental group such traits were observed in only about 20% of the animals.
This experiment on monkeys is still far from completion, and, therefore, we can say nothing about the effect of dietary restriction on the maximal lifespan of primates. However, some data of this kind are available for rodents [12, 24]. Here it was found that the median lifespan in mice and hamsters increases much more markedly than the maximal lifespan (another similarity with the effect of SkQ1 [1-3]). The simplest mechanistic explanation of this phenomenon is arrest (or at least retardation) of an aging program. Therewith, other ontogenetic programs, first of all body growth, can also be retarded. These phenomena are observed with a rather severe and long-term fasting . However, a more moderate dietary restriction can prolong life without inhibiting growth .
This situation illustrates the very fact that moderate and severe starvations have opposite effects on physiological functions. Perhaps this explains contradictory data concerning the effect of food restriction on skeletal muscles and the immune system. On one hand, some authors state that it adversely affects both the muscle system and immunity2. On the other hand, Weindruch and coworkers  reported the lack of sarcopenia in food-restricted monkeys, and McCay and coworkers  observed resistance to pulmonary diseases in rats subjected to dietary restriction (cf. deceleration of age-dependent involution of the thymus and follicular spleen compartments in rats administered SkQ1 [3, 35])3.
The fact that dietary restriction adversely affects some vitally important parameters is not surprising. Animals usually do not tend to overeat even if they are not restricted in access to food. They normally eat as much as needed for healthy functioning. Therefore, long-term dietary restriction entails some disorders in vital functions. It is also clear that such disorders are more probable the longer is starvation. We already mentioned that long-term and continuous dietary restriction is not at all necessary for the geroprotecting effect. This explains the controversy in data on the effect of dietary restriction on lifespan as well as on state of the organism. In cases when dietary restriction was not too severe and not too long, positive effects were observed, whereas when gerontologists employed too severe restriction, unfavorable side effects occurred. Thus, it is commonly accepted that long-term dietary restriction decreases the frequency of estrous cycles (sometimes until they cease completely) , but in 1949 Carr and coworkers showed that temporary dietary restriction prolonged estrous cycles and favored their preservation until extreme old age . (The same effect was observed with SkQ1 [1, 3]). In principle, there is no need to starve over the whole life if starvation is a signal to switch off an aging program. However, there is a probability that too weak or delayed dietary restriction will only partially retard the program, and the geroprotecting effect will be weak.
Another circumstance should be taken into account when considering under-eating as a geroprotector for humans. Actually, if dietary restriction is a signal to warn about starvation, then the organism should respond not only by prolonging life to compensate for the decay of fecundity in lean years. Other responses are also quite possible, and some of them may prove not as attractive as extension of healthy life. For example, it was noted that a hungry mouse, once in a squirrel wheel, does not want to leave it and travels from 6 to 8 km overnight (with normal feeding this distance is always shorter than 1 km) . Obviously, this effect is not consistent with starvation-induced exhaustion and muscle weakness. More likely, we deal here with another response to the starvation signal: extreme anxiety and the attempt to scan as large a space as possible.
It should be mentioned in this context that SkQ1 does not influence the food intake by animals receiving it . Measurement of motivity of 15-20-month-old outbred mice and 129/sv mice showed that 5-250 nmol SkQ1/kg per day decreased rather than increased this parameter. In fact, the old control animals looked more agitated than the SkQ1-treated mice of the same age . An impression arises that SkQ is a “purer” way, when compared with starvation, to retard an aging program, not being accompanied by undesirable side effects.
Various strains of inbred mice may differ greatly in lifespan, which sometimes varies threefold [37, 38]. It seems possible that such a difference is sometimes due to mutations affecting execution of an aging program. In turn, food restriction, if it really inhibits an aging program, should be inefficient in strains already lacking such a program or mechanisms of food intake sensing. Recently, Sohal and coworkers compared C57Bl/6 mice (that respond to starvation with an increase in lifespan) and DBA/2 mice that do not show such an increase . Metabolic characteristics of DBA/2 mice were found to point to partial uncoupling of mitochondrial respiration and ADP phosphorylation, an effect strongly lowering mitochondrial ROS production in the resting state [39, 40]. Perhaps long-lived 129/sv mice, which are insensitive to SkQ1 with respect to lifespan and show regular estrous cycles for as long as 20 months even without SkQ1 , are similar to DBA/2 mice. Remarkably, 129/sv and DBA/2 mice show similar patterns of age-dependent changes of some gene transcripts, differing in this respect from BALB/c. However, C57Bl/6 mice, a line responding to food restriction, resemble DBA/2 if this criterion was applied . Quite recently, Hempenstall et al.  reported that food restriction-sensitive C57Bl/6 mice and insensitive DBA/2 mice oppositely responded to fasting when the blood glucose level was measured. In the first case, glucose level decreased, whereas in the latter case it increased. Blood glucose looks as a good candidate for a diet component to monitor food level of carbohydrates, just as blood methionine is such a component to monitor the level of proteins. If this is the case, it is hardly surprising that DBA/2 mice fail to recognize food restriction as a signal for a starvation period. It seems quite possible that mice of various lines differ in the threshold level of food restriction when diet limitation turns from a starvation signal to a harmful deficit of dietary components. This is never taken into account in caloric restriction studies. Apparently, commonly accepted 40% food restriction is close to such a threshold, thus resulting in great variation of responses of different strains of animals. The present situation in this field is exemplified by a recent publication of Liao at al.  who analyzed responses of 41 recombinant inbred strains of mice to 40% food restriction. For females, 8 lines responded to such restriction by an increase in lifespan, 10 by its decrease, and 21 showed no statistically reliable response. For males, these values were 2, 28, and 11. Unfortunately, each group was composed of only five animals living in one cage. For sure, food restriction worsened social climate in such small communities, resulting in increase in deviation of the lifespan data. In fact, in ad libitum groups this parameter varied from 407 to 1208 days for females and from 504 to 1152 days for males, whereas in food restricted groups it was 113 – 1225 days for females and 217-1215 days for males.
Another disadvantage of the abovementioned approach is that the most marked effect of food restriction is an increase in healthspan rather than lifespan. Large lifespan increase by switching off the aging program can be observed provided that ambient conditions are not artificially improved by, say, abolishing infection (a non-SPF vivarium or outdoor cages are better than an SPF vivarium). For further increase in lifespan, cancer must be somehow excluded. Both SkQ1 and food restriction are effective in retarding development of only a limited number of cancers, whereas others are resistant to these factors. Quite recently an example of a rodent cancelling its aging program and, moreover, solving the problem of cancer was described. We mean the naked mole-rat (Heterocephalus glaber). This animal of mouse size lives ten times longer than mice. The probability of its death does not increase with age , indicating that an aging program is not operating. The program seems to be switched off somewhere downstream of mitochondrial ROS since both the rate of ROS generation by resting mitochondria  and level of peroxidation of cellular biopolymers [44, 45] in the naked mole rats are higher than in mice. The latter finding is consistent with the observation that one of the major antioxidant enzymes, glutathione peroxidase, is 70-fold less active in naked mole-rats than in mice . The key for understanding this situation seems to be the observation that H2O2 fails to induce apoptosis in cultured arteria of naked mole rats . Age-related diseases are not known for naked mole-rats. And cancer has never been observed in naked mole-rats, necropsies failing to reveal tumors . This is apparently due to at least two additional lines of anticancer defense lacking in other rodents. Seluanov et al. reported  that naked mole-rat cells in culture express unusually high levels of the tumor suppressor p16INKYA, a protein responsible for contact inhibition of growth of cultured cells. Later Liang et al. showed  that oncogene expression in the naked mole-rat cells failed to produce cells competent in tumor expression when transferred to immunodeficient mice. The reason for such a failure is that these cells rapidly entered crisis, as evidenced by appearance of anaphase bridges, giant cells with enlarged nuclei, multinuclear cells, and cells with large number of chromosomes or abnormal chromatin. Crisis was also observed after >40 cell doublings of the naked mole-rat cells expressing an oncogene. Crisis in culture was prevented by additional infection of the cells with a retrovirus encoding telomere reverse transcriptase (hTERT). The authors suggested that such activity of hTERT is due to one of its extra-telomeric effects requiring an intracellular hTERT concentration higher than is normally present in naked mole-rat cells.
Apparently, the specific features of naked mole-rats preventing cancer are absent in other studied animals. Therefore, lifespan increase due to interruption of the aging program in these animals is not so strong as in naked mole-rats, since they die as a result of development of those types of cancer which are resistant to food restriction, SkQ1, or other geroprotectors that have been tested. The mole-vole (Ellobius talpinus) studied in our group  might represent an exception to this rule. As post mortem analysis showed, these rodents die almost exclusively due to infections or other non-cancer pathologies and live very much longer when treated with SkQ1. The effect of caloric restriction on mole voles is now being investigated.
The author of this manuscript has no conflict of interest to declare.
1Concerning decrease in mitochondrial ROS level by food restriction, see review by Gredilla and Barja 
2Fernandes and coworkers  noted that dietary restriction, especially at a young age, inhibits interleukin secretion by macrophages as a response to bacterial polysaccharides. In turn, this adversely affects resistance to sepsis and peritonitis [21, 31]. According to Gardner [32, 33], partial starvation abolishes resistance to influenza virus. For reviews, see Refs. [31, 34].
3As mentioned above, the effect of SkQ1 on longevity was especially strong in non-SPF vivaria. Apparently, a similar situation is inherent in the food restriction effect. Remarkably, the magnitude of the lifespan increase by food restriction was usually much stronger in experiments published in 1934-1975 (i.e. when SPF practice was unknown or not so widespread) than after 1975.
|ROS||reactive oxygen species|
|Anisimov VN,Egorov MV,Krasilshchikova MS,Manskikh VN,Lyamzaev KG,Manskikh VN,Moshkin MP,Novikov EA,Popovich IG,Rogovin KA,Shabalina IG,Shekarova ON,et al. Effect of mitochondria-targeted antioxidant SkQ1 on lifespan of rodentsAgingYear: 2011 (the 1st paper of this series)..|
|Anisimov VN,Bakeeva LE,Egormin PA,Filenko OF,Isakova EF,Manskikh VN,Mikhelson VM,Panteleeva AA,Pasyukova EG,Pilipenko DI,Piskunova TS,Popovich IG,et al. Mitochondria-targeted plastoquinone derivatives as tools to interrupt execution of the aging program. 5. SkQ1 prolongs lifespan and prevents development of traits of senescenceBiochemistry (Mosc)Year: 2008731329134219120018|
|Skulachev VP,Anisimov VN,Antonenko YN,Bakeeva LE,Chernyak BV,Erichev VP,Filenko OF,Kalinina NI,Kapelko VI,Kolosova NG,Kopnin BP,Korshunova GA,et al. An attempt to prevent senescence: a mitochondrial approachBiochim. Biophys. ActaYear: 2009178743746119159610|
|Skulachev MV,Antonenko YN,Anisimov VN,Chernyak BV,Cherepanov DA,Chistyakov VA,Egorov MV,Kolosova NG,Korshunova GA,Lyamzaev KG,Plotnikov EY,Roginsky VA,et al. Mitochondrial-targeted plastoquinone derivatives. Effect on senescence and acute age-related pathologiesCurr Drug TargetsYear: 20111280082621269268|
|Skulachev VP. How to Cancel the Aging Program of Organism?Russ. J. Gen. ChemYear: 20108015231541|
|Kompfort A. Year: 1979The Biology of SenescenceEdinburg-LondonChurchhill Livingstone|
|Austad SN. Year: 1997Why We Age?New YorkJohn Willey and Sons|
|Sun D,Muthukumar AR,Lawrence RA,Fernandes G. Effects of calorie restriction on polymicrobial peritonitis induced by cecum ligation and puncture in young C57BL/6 miceClin Diagn Lab ImmunolYear: 200181003101111527818|
|Gredilla R,Barja G. The role of oxidative stress in relation to caloric restriction and longevityEndocrinologyYear: 20051463713371715919745|
|McCay CM,Crowell MF. Prolonging the life spanSci. MonYear: 193439405414|
|McCay CM,Crowell MF,Maynard LA. The effect of retarded growth upon the length of life span and upon the ultimate body sizeJ NutrYear: 1935106379|
|McCay CM,Maynard LA,Barnes LL. Growth, aging, chronic diseases and lifespan in ratsArch BiochemYear: 19432469|
|Agapova LS,Chernyak BV,Domnina LV,Dugina VB,Efimenko AY,Fetisova EK,Ivanova OY,Kalinina NI,Khromova NV,Kopnin BP,Kopnin PB,Korotetskaya MV,et al. Mitochondria-targeted plastoquinone derivatives as tools to interrupt execution of the aging program. 3. Inhibitory effect of SkQ1 on tumor development from p53-deficient cellsBiochemistry (Mosc)Year: 2008731300131619120016|
|Colman RJ,Anderson RM,Johnson SC,Kastman EK,Kosmatka KJ,Beasley TM,Allison DB,Cruzen C,Simmons HA,Kemnitz JW,Weindruch R. Caloric restriction delays disease onset and mortality in rhesus monkeysScienceYear: 200932520120419590001|
|Holloszy JO,Fontana L. Caloric restriction in humansExp GerontolYear: 20074270971217482403|
|Harman D. Aging: a theory based on free radical and radiation chemistryJ GerontolYear: 19561129830013332224|
|Barja G. Rate of generation of oxidative stress-related damage and animal longevityFree Radic Biol MedYear: 2002331167117212398924|
|Will LC,McCay C.M.. Ageing, basal metabolism and retarded growthArch. Biochem.Year: 19432481|
|Mair W,Goymer P,Pletcher SD,Partridge L. Demography of dietary restriction and death in DrosophilaScienceYear: 20033011731173314500985|
|Libert S,Zwiener J,Chu X,Vanvoorhies W,Roman G,Pletcher SD. Regulation of Drosophila life span by olfaction and food-derived odorsScienceYear: 20073151133113717272684|
|Libert S,Pletcher SD. Modulation of longevity by environmental sensingCellYear: 20071311231123418160034|
|Robertson TB,Marston R,Walters JW. Influence of intermittent starvation and of intermittent starvation plus nucleic acid on growth and longevity in whyte miceAust J Exp Biol Med SciYear: 19341233|
|Carr CJ,King JT,Visscher B. Delay of senescence infertility by dietary restrictionProc Fedn Am Soc Exp. BiolYear: 1949822|
|Stuchlikova E,Juricova-Horakova M,Deyl Z. New aspects of the dietary effect of life prolongation in rodents. What is the role of obesity in aging?Exp GerontolYear: 1975101411441132453|
|Richie JP Jr.,Leutzinger Y,Parthasarathy S,Malloy V,Orentreich N,Zimmerman JA. Methionine restriction increases blood glutathione and longevity in F344 ratsFASEB JYear: 19948130213078001743|
|Miller RA,Buehner G,Chang Y,Harper JM,Sigler R,Smith-Wheelock M. Methionine-deficient diet extends mouse lifespan, slows immune and lens aging, alters glucose, T4, IGF-I and insulin levels, and increases hepatocyte MIF levels and stress resistanceAging CellYear: 2005411912515924568|
|Sanz A,Caro P,Ayala V,Portero-Otin M,Pamplona R,Barja G. Methionine restriction decreases mitochondrial oxygen radical generation and leak as well as oxidative damage to mitochondrial DNA and proteinsFASEB JYear: 2006201064107316770005|
|Caro P,Gomez J,Sanchez I,Garcia R,Lopez-Torres M,Naudi A,Portero-Otin M,Pamplona R,Barja G. Effect of 40% restriction of dietary amino acids (except methionine) on mitochondrial oxidative stress and biogenesis, AIF and SIRT1 in rat liverBiogerontologyYear: 20091057959219039676|
|Edman U,Garcia AM,Busuttil RA,Sorensen D,Lundell M,Kapahi P,Vijg J. Lifespan extension by dietary restriction is not linked to protection against somatic DNA damage in Drosophila melanogasterAging CellYear: 2009833133819627272|
|Berg BN,Simms HS. Nutrition and longevity in the rat. 3. Longevity and onset of disease with different levels of food intakeJ. NutrYear: 19607125526313855553|
|Hopkin K. Dietary drawbacksSci Aging Know EnvironYear: 2003814|
|Gardner EM. Caloric restriction decreases survival of aged mice in response to primary influenza infectionJ Gerontol A Biol Sci Med SciYear: 20056068869415983169|
|Ritz BW,Aktan I,Nogusa S,Gardner EM. Energy restriction impairs natural killer cell function and increases the severity of influenza infection in young adult male C57BL/6 miceJ NutrYear: 20081382269227518936230|
|Kristan DM. Calorie restriction and susceptibility to intact pathogensAge (Dordr)Year: 20083014715619424864|
|Obukhova LA,Skulachev VP,Kolosova NG. Mitochondria-targeted antioxidant SkQ1 inhibits age-dependent involution of the thymus in normal and senescence-prone ratsAgingYear: 2009138940120195490|
|Anisimov VN. AS “Mitotech” Report N 00011260. Year: 2010119|
|Forster MJ,Morris P,Sohal RS. Genotype and age influence the effect of caloric intake on mortality in miceFASEB JYear: 20031769069212586746|
|Liao CY,Rikke BA,Johnson TE,Diaz V,Nelson JF. Genetic variation in the murine lifespan response to dietary restriction: from life extension to life shorteningAging CellYear: 20109929519878144|
|Ferguson M,Rebrin I,Forster MJ,Sohal RS. Comparison of metabolic rate and oxidative stress between two different strains of mice with varying response to caloric restrictionExp GerontolYear: 20084375776318541398|
|Park SK,Kim K,Page GP,Allison DB,Weindruch R,Prolla TA. Gene expression profiling of aging in multiple mouse strains: identification of aging biomarkers and impact of dietary antioxidantsAging CellYear: 2009848449519555370|
|Hempenstall S,Picchio L,Mitchell SE,Speakman JR,Selman C. The impact of acute caloric restriction on the metabolic phenotype in male C57BL/6 and DBA/2 miceMech Ageing DevYear: 201013111111820064544|
|Buffenstein R. The naked mole-rat: a new long-living model for human aging researchJ Gerontol A Biol Sci Med SciYear: 2005601369137716339321|
|Lambert AJ,Boysen HM,Buckingham JA,Yang T,Podlutsky A,Austad SN,Kunz TH,Buffenstein R,Brand MD. Low rates of hydrogen peroxide production by isolated heart mitochondria associate with long maximum lifespan in vertebrate homeothermsAging CellYear: 2007660761817596208|
|Andziak B,Buffenstein R. Disparate patterns of age-related changes in lipid peroxidation in long-lived naked mole-rats and shorter-lived miceAging CellYear: 2006552553217129214|
|Andziak B,O'Connor TP,Qi W,DeWaal EM,Pierce A,Chaudhuri AR,Van Remmen H,Buffenstein R. High oxidative damage levels in the longest-living rodent, the naked mole-ratAging CellYear: 2006546347117054663|
|Andziak B,O'Connor TP,Buffenstein R. Antioxidants do not explain the disparate longevity between mice and the longest-living rodent, the naked mole-ratMech Ageing DevYear: 20051261206121216087218|
|Labinskyy N,Csiszar A,Orosz Z,Smith K,Rivera A,Buffenstein R,Ungvari Z. Comparison of endothelial function, O2−• and H2O2 production, and vascular oxidative stress resistance between the longest-living rodent, the naked mole rat, and miceAm J Physiol Heart Circ PhysiolYear: 2006291H2698270417090784|
|Seluanov A,Hine C,Azpurua J,Feigenson M,Bozzella M,Mao Z,Catania KC,Gorbunova V. Hypersensitivity to contact inhibition provides a clue to cancer resistance of naked mole-ratPNASYear: 2009106193521935719858485|
|Liang S,Mele J,Wu Y,Buffenstein R,Hornsby PJ. Resistance to experimental tumorigenesis in cells of a long-lived mammal, the naked mole-rat (Heterocephalus glaber)Aging CellYear: 2010962663520550519|
Keywords: Aging, mitochondria, food (caloric) restriction, SkQ1, mitochondria-targeted antioxidant.
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