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Int. J. Mol. Sci. 2013, 14(7), 13109-13128; doi:10.3390/ijms140713109
Published: 25 June 2013
Abstract: Hormesis describes the drug action of low dose stimulation and high dose inhibition. The hormesis phenomenon has been observed in a wide range of biological systems. Although known in its descriptive context, the underlying mode-of-action of hormesis is largely unexplored. Recently, the hormesis concept has been receiving increasing attention in the field of aging research. It has been proposed that within a certain concentration window, reactive oxygen species (ROS) or reactive nitrogen species (RNS) could act as major mediators of anti-aging and neuroprotective processes. Such hormetic phenomena could have potential therapeutic applications, if properly employed. Here, we review the current theories of hormetic phenomena in regard to aging and neurodegeneration, with the focus on its underlying mechanism. Facilitated by a simple mathematical model, we show for the first time that ROS-mediated hormesis can be explained by the addition of different biomolecular reactions including oxidative damage, MAPK signaling and autophagy stimulation. Due to their divergent scales, the optimal hormetic window is sensitive to each kinetic parameter, which may vary between individuals. Therefore, therapeutic utilization of hormesis requires quantitative characterizations in order to access the optimal hormetic window for each individual. This calls for a personalized medicine approach for a longer human healthspan.
Since ancient times, people have proposed (and practiced) the idea that low doses of poison could be beneficial to health in the long run. The German philosopher Friedrich Nietzsche (1844–1900) made the famous statement that “What doesn’t kill us makes us stronger” (Was uns nicht umbringt macht uns stärker), probably to excuse his drinking habit. The old German Kanzler, Helmut Schmidt (born 1918), is well-known for his habitual cigarette consumption, however, even as a nonagenarian, he is admired both for his sharp thinking, and for his political engagement.
Indeed, studies have shown that dietary intake of moderate amounts of ethanol can double the lifespan of nematodes  and enhance memory in mice . In humans, it is well-known that high ethanol consumption is associated with heart disease, liver cirrhosis, neurological disorders and cancer . However, moderate drinkers have overall reduced mortality, especially of the kinds resulting from coronary heart disease and stroke [3,4]. In a similar vein, the apparent protective effect of cigarette smoking on Parkinson’s disease (PD) is one of the few consistent results in epidemiology [5,6], and could have a similar effect on Alzheimer’s dementia .
Such phenomena, distinguished by beneficial effects of apparently toxic agents at their low doses, have been known for centuries. Back in 1888, the German pharmacologist Hugo Schulz observed that small doses of multiple chemical disinfectants stimulate yeast growth [8,9]. However, the true origin of the word “hormesis” (derived from the ancient Greek term hormáein, which literally means “to excite”, or “to set in motion”) dates back to Chester Southam’s undergraduate thesis in 1941 as a better substitution for the word “toxicotrophism” (Figure 1). According to the original publication of Southam and Ehrlich in 1943, “The term hormesis (adj. hormetic) is proposed to designate such a stimulatory effect of sub-inhibitory concentrations of any toxic substance of any organism.” .
Essentially describing an overall biphasic shape of the dose response curve, hormesis seems to be quite commonplace: Bacteria tend to flourish in the presence of tiny amounts of antibiotics  and nematodes that have experienced a variety of environmental stresses including heat, hypoxia or elevated reactive oxygen species (ROS) exhibit extended lifespan . Insects treated with low doses of pesticides or ethanol generally live longer and produce more eggs . Short term ischemic treatment of human tissues increases their resistance to subsequent, long-term ischemia-reperfusion damages . Small doses of even the most harmful substances such as dioxin can stimulate beneficial responses that enhance the organism’s resistance against multiple stresses . With controversial, hormesis effects have also been observed with low dose radiation [15,16]. Recently, the term hormesis has been borrowed by the field of neurodegenerative diseases (ND) to describe possible protective effects of some neurotoxins. For example, amyloid-beta protein (Aβ) and the development of amyloid plaques have been considered as a hallmark in Alzheimer’s disease pathology . However, at physiological concentration, Aβ may actually have a protective effect on neurons . It enhances long term potentiation and memory, increases neurite outgrowth and produces presynaptic enhancement of neuronal plasticity .
Despite all these common examples, hormesis has been a topic of vigorous debate since its introduction [20,21]. Homeopathic practitioners worship the hormetic concept as the ultimate support for the therapeutic usage of highly poisonous drugs, whereas nonbelievers fiercely refuse this concept due to its principle reversal of toxicological dogma .
It is to be noticed here that, objectively, the term hormesis per se is merely a phenomenological description. In other words, hormesis is a symptom, not a diagnosis. Just like fever can have multiple medical diagnoses, the underlying mechanism of hormetic effects could be largely heterogeneous. Thus, a particular hormetic activity can only be fully described if there is an understanding of the biological processes underpinning that specific biphasic dose response . Edward Calabrese, an enduring advocate of the hormesis concept proposed the theory that low doses of toxins may trigger certain defensive responses that enable the organism to become more resistant to the same or similar stimuli . Indeed, an increasing number of hormetic effects have already been assigned to clear mechanisms: As a classical example, thermal stress induces the gene expression of heat-shock proteins [23,24]. The exposure to low dose pesticides can induce xenobiotic detoxification enzymes such as cytochrome P450 . Low-dose ultra violet (UV) radiation enhances the DNA base excision repair enzyme . In a sense, the development of acquired immunity through vaccination can also be termed hormesis, with its well-known pathogen T-cell interactions .
During the last decade, the word hormesis as the principle behavior of the stress-response has found a new lease on life in an old context : the biology of aging and age-related diseases . One reason for this is that hormetic effects typically occur over a relatively long time scale. Importantly, however, as mechanisms of aging have been revealed more and more clearly, people foresee potential, but immense, advantages of hormetic effects on aging [29,30]. Built on current understandings, this review aims to discuss the effects of hormesis in the context of aging and neurodegenerative diseases, with a special focus on the underlying hormetic mode-of-action involving reactive oxygen species. We will also envision how future studies will continue to refine our knowledge in this field, ultimately allowing us to profit from hormetic medical approaches.
2. ROS Hormesis in Aging and Neurodegenerative Diseases
Aging can be thought of as the multi-causal progressive failure of organism maintenance , with death as the final manifestation of the breakdown in homeostasis . Danham Harman’s free radical theory is one of the major hypotheses on aging mechanisms. It states that reactive oxygen species induce stochastic occurrence and accumulation of macromolecular damages, leading to a progressive decrease in the organism’s molecular fidelity . As the major biological building block, proteins are one of the prime targets for oxidative damage. The negatively charged superoxide anion (O2•−) targets iron-sulfur clusters in many proteins. Neutrally charged hydrogen peroxide (H2O2) reacts preferably with the cysteine thiols, leading to the generation of reversible and irreversible protein carbonyl derivatives. Oxidative damage also affects DNA and lipids, resulting in the accumulation of partially irreversible damages such as 8-oxo-7,8-dihydroguanine or peroxidized lipids [32,33].
A considerable portion of intracellular ROS results from the energy-producing metabolic activities of mitochondria. It is estimated that about 2% of oxygen consumption is converted to ROS during oxidative phosphorylation . Auto-oxidation of reduced respiratory components of the mitochondrial electron transport chain causes production of the superoxide anion and hydrogen peroxide. In the presence of iron, these can produce the highly reactive hydroxyl radical OH· via the Fenton reaction. OH· radicals can initiate chain reactions of lipid peroxidation while generating peroxyl- and alkoxyl radical intermediates . Moreover, mitochondrial superoxides may react with nitric oxide to produce peroxynitrite (ONOO−), a strong oxidant that can cause overwhelming oxidative injuries  (though reactive nitrogen species (RNS) are not the focus of this review).
Being both a major source, as well as the primary target of potentially harmful ROS, mitochondrial dysfunction is strongly associated with the onset of numerous age-related diseases , such as diabetes , cancer  and neurodegenerative conditions including Parkinson’s disease and Alzheimer’s disease [40,41]. Indeed, impairment of mitochondria has been assumed to be a main driving force of aging in itself [42,43].
2.1. ROS and Aging: Causal but Not Concomitant
Plenty of experimental findings have demonstrated increasing levels of ROS during organism aging . However, across aging models from yeast to mouse, enhanced ROS detoxification via endogenous or exogenous antioxidants failed to show consistent effects on lifespan . For instance, neither global reduction nor over-expression of manganese superoxide dismutase (SOD2), a major scavenger of superoxide molecules, alters lifespan, even though the enzyme activity was high enough to counteract the strong ROS effect of paraquat (N,N′-dimethyl-4,4′-bipyridinium dichloride) [45,46].
Moreover, numerous clinical interventions were unable to establish a positive association between antioxidant supplements and benefits to health: Most studies found a lack of correlation, and several studies even suggested severe adverse effects of antioxidant supplements on aging retardation [47,48]. Interestingly, this is consistently the case when antioxidants were applied simultaneously with lifespan-promoting measurements such as diet restriction or physical exercise [49–51]. For instance, it has been shown that long-term ascorbic acid supplements, an efficient free radical scavenger, diminished the exercise-induced adaptive responses in humans [52–54]. Combined, these facts raise the hypothesis that ROS may act as essential mediators promoting health and longevity in the frame of certain physiological adaptation processes [55,56].
2.2. Caloric Restriction Induced Lifespan Extension Is Mediated by ROS
As currently the most robust lifespan modulating measure; caloric restriction (CR); a 20%–40% reduction in caloric intake without malnutrition; has been consistently shown to increase lifespan in almost all model organisms investigated [28,57]. Rhesus monkeys under long-term CR demonstrated a prolonged time period of healthy living (or a prolonged “healthspan”); although the effect of CR on lifespan extension remains controversial . Profound beneficial effects of CR on health have also been frequently reported. For example; CR in humans clearly reduces the risk of type 2 diabetes and cardiovascular disease [59,60]. Long-term CR was reported to be highly effective in reducing the risk of atherosclerosis ; accompanied by significant improvement of vascular functions . Neuroprotective effects and promotion of adult neurogenesis were also observed in CR rodents .
For a period of time; the idea that CR exerts its beneficial effects by reducing the level of ROS; which is associated with a presumably decreased metabolic rate; was seen as a logical extension of Harman’s theory. However; accumulating evidence rejects this common expectation. It is now affirmed that CR increases the organism’s bodyweight-specific metabolic rate in all aging models investigated. This is observed through increased oxygen consumption; increased heat production; as well as increased total energy expenditure as a function of body mass [64–66]. It is probable that the initial energy deficit as a consequence of CR leads to an extensive aerobic metabolic shift in order to counteract it; this phenomenon was termed “mitohormesis” . Increased oxidative phosphorylation under CR has been observed in yeast; nematodes [68–70]; and in man . In addition; it has been demonstrated that CR also promotes mitochondrial biogenesis via a nitric oxide-mediated mechanism [72,73]. Importantly; such enhanced mitochondrial respiration is indeed correlated with an increased oxidative stress level ; as exemplified by an increased hydrogen peroxide concentration . Similarly, ROS up-regulation was also connected to the lifespan extension and health benefits associated with physical exercise in humans [35,76,77].
In 2007, it was reported that lifespan extension by CR in nematodes does require ROS . This was demonstrated by an elegant experiment employing two drugs that generate ROS: the respiratory inhibitor azide, which inhibits the respiratory complex IV and promotes H2O2 generation; and paraquat, which undergoes redox cycling to produce superoxides in vivo. At certain dosages, both of these ROS-inducers led to CR-like lifespan extension. Intriguingly, this effect was clearly abolished by the presence of antioxidants , and additional evidence was subsequently provided by other researchers as well [67,78]. These findings provided solid proof that an increased ROS formation, at least transiently, is essential for these promotions in longevity [33,69]. Bearing ROS’ damaging potential in mind, it becomes apparent that ROS can be justified as hormetic agents.
2.3. The Neuroprotective Potential of ROS Hormesis
Apart from the lifespan extending effect, it has been shown that ROS hormesis can also exert protective effects against neurodegenerative conditions . For example, Bonilla-Ramirez and co-workers treated the parkin knock-down Drosophila melanogaster with ROS-inducers such as paraquat and polyphenols (i.e., quercetin). Under these conditions, significantly higher lifespan as well as improved locomotor activity was observed in comparison to untreated controls .
Accumulating evidence of the possible neuroprotective potential of ROS hormesis comes from studies on a spectrum of substances called CR-mimetics, i.e., drugs or endogenous proteins that mimic some beneficial effect of CR. It was shown that low doses of resveratrol (4 μg/mouse/day) stimulated sensory neurons, and promoted hippocampal neurogenesis in the dentate gyrus and subventricular zone of adult mice . Within this hormetic window, cytokines such as BDNF (brain-derived neurotrophic factor) were released from the resveratrol-treated cells, resulting in both autocrine and paracrine neuroprotection. Interestingly, in a parallel study, high doses of resveratrol were shown to significantly inhibit proliferation and survival of mouse neuroprecursor cells both in vitro (>10 μM) and in vivo (25–250 μg/mouse/day) ; this is proposed to function via a ROS-mediated inhibition of BDNF secretion [83,84]. Together, these studies clearly demonstrated a biphasic hormetic curve of the neuroprotective effect of resveratrol, which is possibly mediated by ROS [85,86]. A similar mode-of-action could be assigned to curcumin, olive oil or green tea catechins [87,88]. Moreover, it has recently been shown that over-expression of neuroglobin, an oxygen binding and peroxynitrite-generating protein of the brain, can prevent or limit neuronal damage from beta-amyloid-induced neurotoxicity, stroke, and seizures in mice [89,90].
Apparently, the endogenously produced ROS stimulate certain adaptive responses that protect the organism from damages beyond ROS [46,56,57]. Hence, the logical next step is to depict the actual molecular mechanisms of these downstream adaptive responses.
3. ROS-Mediated Adaptive Responses
Almost six decades after the birth of Harman’s free radical theory, we now know that ROS and RNS are essential in many physiological processes [35,91]. In effect, although some of these species are indeed free radicals (paramagnetic molecular species with an unpaired electron), not all of them are equally reactive. Some of the species, such as superoxides, hydrogen peroxide or nitric oxide are stable enough to act as signaling molecules [35,92]. An increasing body of experimental findings favors the notion that ROS and RNS can act as triggers of dedicated adaptive cellular machinery that increase the organism’s stress resistance [67,93,94]. This includes antioxidant and heat shock responses, cell cycle regulation and apoptosis, DNA repair, fatty acid deacylation-reacylation, unfolded protein responses and autophagy stimulation  (Figure 2).
3.1. Antioxidant and Heat Shock Responses
Ample evidence suggests that an increased cellular ROS concentration induces cellular defense mechanisms involved in ROS detoxification, such as radical-scavenging enzymes and heat shock proteins [79,96,97]. In single eukaryotes like yeast, increased ROS levels lead to the activation of the redox-responsive transcription factors Msn2/4, which promote gene expression of the ROS-detoxification enzymes such as mitochondrial SOD, or heat shock proteins such as Hsp70 .
Multiple redox-sensitive heat shock factors exist in higher eukaryotes. For instance, heat shock factor 1 (HSF1) is normally maintained as a cytosolic monomer through its interaction with Hsp90, a constitutively expressed heat shock protein. When the cell is exposed to elevated levels of ROS, there is an accumulation of unfolded proteins that compete with HSF1 for Hsp90 binding. HSF1 released from the complex forms a homotrimer that can translocate into the nucleus and act as a transcription factor to promote target genes including Hsp27 and Hsp70 [99,100].
Apart from these heat shock factors, increased ROS concentration in mammals also results in the activation of additional transcription factors such as nuclear factor kappa B (NFκB) or cyclic AMP response element binding protein (CREB). These transcription factors trigger the expression of antioxidant enzymes, anti-apoptotic protein Bcl-2, and acute-phase proteins (haptoglobin, beta-fibrinogen) . In agreement with the hormesis concept, rodents exposed to CR exhibit elevated antioxidant defense capabilities [97,102–104], as well as enhanced heat shock protein production [97,103]. Furthermore, two different research groups proposed the hypoxia-inducible factor (HIF-1) as a convergence point of ROS hormesis and hypoxic signaling [105,106].
3.2. Cell Cycle Regulation and Selective Apoptosis
Multicellular organisms respond to ROS hormesis in a variety of ways that promote the organism’s survival as a whole. For example, cell growth and proliferation is orchestrated by protein kinase signaling pathways. Moderate concentration of ROS can stimulate cell proliferation by shifting the equilibrium between the phosphorylated and dephosphorylated forms of mitogen-activated kinases (MAPK) [107,108]. Specifically, the active site of the tyrosine phosphatase involved in the MAPK pathway contains a cysteine residue that is hypersensitive to ROS . Thus, this phosphatase is easily inactivated under elevated ROS. In turn, this causes a shift of balance towards the phosphorylated (active) receptor kinase molecules, resulting in an increased kinase activity. The net result is essentially the same as MAPK activation by growth factors [110,111].
On the other hand, when the dramatic ROS damage leads to extensive mitochondrial membrane permeabilization, the alternative strategy of the organism is to activate programmed cell death. For instance, increased production of hydrogen peroxide can cause the leakage of cytochrome c into the cytosol. Cytochrome c subsequently complexes with Apaf-1 (apoptosis protein-activating factor 1), dATP, and procaspase-9 to form an apoptosome. Facilitated by oxidative modification, caspase-9 in turn induces caspase-3 and caspase-7 activation [79,112–114]. This ultimately switches on the downstream apoptosis programs . Relatedly, recent studies have pointed out a possible conserved link between the lifespan-modulating effect of p53 (a tumor suppression protein) and its role in the regulation of hydrogen peroxide-mediated cell death .
3.3. Crosstalk of ROS Hormesis and the Unfolded Protein Response
Unfolded protein responses (UPR) represent another central mechanism of ROS hormesis in CR and aging . Metabolic stress-induced ROS-upregulation can trigger UPR—the endoplasmic reticulum-centered stress responses—in which several transcription regulating proteins are involved. This includes protein kinase RNA-like ER kinase (PERK), activating transcription factor 6 (ATF6) and inositol requiring endoplasmic reticulum RNAse alpha isoform (IRE1) .
PERK directly phosphorylates and activates the transcription factor NF-E2-related factor-2 (Nrf2). This contributes to cellular redox homeostasis by inducing the expression of various antioxidant genes and molecular chaperons in the ER [117,118]. ATF6 is cleaved by site-1 protease (S1P) and site-2 protease (S2P) in the Golgi apparatus to become activated. The cleaved N-terminal fragment of ATF6 acts as a transcription factor that migrates to the nucleus, where it induces expression of genes containing the ER stress response element. First described in yeast, IRE1 is susceptible to phosphorylation under elevated ROS. Phosphorylated IRE1 in turn cleaves the XBP1 (X-box binding protein 1) mRNA, resulting in the production of XBP1 proteins. XBP1 is a transcription factor that induces the expression of GRP78 (glucose-regulated protein 78), among other ER-stress proteins . Intrinsically, these three arms of the URP transduction are activated sequentially, with PERK being activated most rapidly, followed by ATF6 and lastly IRE1. Thus, time is allowed for the cell to resolve the stress and promote cell survival. However, if the ROS damages exceed a certain threshold, excessive activation of IRE1 ultimately allows the cell death programs to take over . Activation of the UPR through this process has been observed in post-mortem brain tissues of Parkinson’s disease and Alzheimer’s disease patients .
3.4. Autophagy Stimulation
Autophagy is a cellular catabolic process that is believed to act against aging, neurodegeneration and cancer [120,121]. The autophagy process involves a myriad of genes that orchestrate the selective engulfment of cytosol and cell organelles, autophagosome formation, and the trafficking and fusion of the autophagosome with the lysosome for final degradation. The autophagosome formation is initiated by Beclin 1 in mammals (Atg6 in yeast). Maturing of the autophagosome and its fusion with the lysosome requires LC3, one of the mammalian homologues of Atg8 in yeast . Specifically, one of the autophagy genes, Atg4, is a cystein protease hyper-sensitive to ROS. At this juncture, ROS and RNS can act as a molecular switch via the reactive thiol groups. Upon elevated ROS in the cell, Atg4 becomes predominantly oxidized. This in turn causes the accumulation of Atg8 phosphoethanolamine precursor that is required for the autophagosome formation . The stimulation of autophagy leads to increased turnover of proteins and defective mitochondria via lysosomal pathways . In addition, by sequestering cytochrome c, autophagy may also delay or prevent apoptosis, thus providing an opportunity for cellular recovery .
Autophagy up-regulation has been implemented in lifespan extensions induced by CR and under administration of CR-mimetics such as sirtuin activators , rapamycin , resveratrol [85,120] and spermidine [126,127]. Intrinsically, autophagy-based selective cellular partial degradation is essential for post-mitotic tissues like the brain. Matus and coworkers have proposed autophagy as a major protective mechanism underlying ROS hormesis to overcome neurodegeneration . This so-called “neurohormetic” effect of autophagy has been shown to suppress disease progression in animal models of Alzheimer’s disease, Parkinson’s disease, and stroke .
4. Possible Additive Nature of ROS Hormesis
Taken together, a large body of evidences supports the notion that several longevity-promoting interventions including CR and CR-mimetics (as well as physical exercise) may converge by causing an activation of mitochondrial oxygen consumption to promote increased formation of ROS. These ROS serve as a hormetic agent to activate a variety of downstream adaptive responses, which culminate in increased stress resistance, neuronal protection, and longevity [57,129].
Given the forthcoming consensus regarding the possible beneficial effects of ROS hormesis, and keeping in mind their obvious highly damaging potential, two open questions arise: First, what is the mechanistic foundation of the biphasic dose response dynamic? Second and more importantly, what are the major determinants of the hormetic window? These two questions led us to evaluate the quantitative data in the literature.
From a study of Bensaad and co-workers on the complex interplay of intracellular ROS and the p53-inducible proteins, it could be deduced that ROS-induced damage may be considered as linearly correlated with ROS concentration , whereas ROS-induced adaptive responses, such as DNA repair or autophagy stimulation, supposedly take a substrate-saturation kinetic. Based on these data, we set out to formulate a mathematical model attempting to describe the bifurcated effects of ROS. In our conceptual model, the correlation of human healthspan with ROS concentration was modeled by an additive effect of two elemental reactions: (i) ROS-induced damage; and (ii) ROS-induced adaptive responses. In the first elementary reaction, the ROS-induced damage was negatively, and linearly correlated with the ROS concentration. In the second reaction, the ROS-induced adaptive responses were set to be positively correlated with ROS, but bearing a saturation curve of ROS at about 200 μM (Figure 3a) . This dynamic property was modeled with Michaelis-Menten kinetics, which is frequently used as an approximation of the substance saturation phenomenon.
Combined, our model simulation gave a bi-phasic dose-response curve regarding ROS concentration vs. healthspan, which is typical for the hormesis phenomenon (Figure 3b). No significant effect was seen at ROS levels less than 20 μM. However, a beneficial or healthspan-extending effect of ROS was demonstrated with increasing ROS concentration, with an optimal ROS concentration (hormetic window) lying around 70 μM. ROS concentration higher than 120 μM was associated with a shortened healthspan. Thus, based on our model setting, ROS-induced hormesis in aging could be considered an integration of two opposite effects of ROS: ROS-induced damage, which is expressed as a linear descending curve in the ROS vs. damage diagram, and the ROS-stimulation of adaptive responses. This model presents a novel computational insight into the bi-phasic curve of ROS hormesis. Interestingly, in a study on human keratinocyte aging, 60 μM of hydrogen peroxide was shown to exert beneficial hormetic effects on telomere length maintenance . This is in keeping with our modeling prediction.
Notably, based on our mathematical model, the optimal hormetic dose of ROS for maximal healthspan is dependent on the individual kinetic parameters chosen for both ROS-induced damage and ROS-induced adaptive responses. Accordingly, maximizing the benefit of hormesis requires an optimized ROS concentration that enhances the stress response, while still staying far away from possible detrimental toxicity of ROS.
5. Potential Therapeutic Value of ROS Hormesis
Having these solid hormesis effects in hand, it is particularly inviting to think of its therapeutic potential. Oxidative stress and mitochondrial dysfunction have been implicated in multiple age-related pathologies . Regarding neurodegenerative diseases, imbalance of cellular homeostasis results in protein misfolding and accumulation of insoluble protein fibrils and aggregates (both inside and outside the cell) . With age, this further impedes the brain function accompanied by proteostasis breakdown. It is therefore tempting to consider interventions that employ transient ROS elevation to stimulate numerous endogenous cellular defense mechanisms.
Indeed, several experimental trials of ROS hormesis as a potential therapeutic strategy against ND and other age-related diseases have already been reported. For instance, low dose radiation, a process that generate ROS (albeit extracellular), has been shown to exert neuroprotective effects in mouse models of retinitis pigmentosa, a hereditary, progressive neurodegeneration that ultimately leads to blindness . Furthermore, in pancreatic beta-cells, sublethal exogenous H2O2 has been shown to induce secondary repair and defense mechanisms that counteract diabetes . In line with this, low doses of nicotine have been shown to stimulate mitochondrial autophagy in cultured human endothelial cells, possibly via a transient increase of ROS production [135,136]. Whether this could be associated with the beneficial effect on Parkinson’s disease prevention remains to be elucidated.
6. Conclusions and Perspectives
All living systems have the intrinsic ability to respond and adapt to external and internal sources of disturbance . Although the hazardous damaging effect of ROS is a settled issue, data summarized here support the theory that hormetic effects of ROS in aging and ND are obvious. In this regard, caloric restriction, CR-mimetics and physical exercise probably share several common mechanistic features that are mediated by increased ROS levels due to enhanced mitochondrial activity. This subsequently induces the organism’s adaptive responses and ultimately results in lifespan-extension and health promotion .
We welcome the renaissance of hormesis, but at the same time suggest that the word hormesis might currently be overblown, probably due to the great anticipation of the therapeutic potential of this phenomenon. It needs to be reiterated here that, all in all, hormetic effects tend to be small in size relative to the potentially fatal effects of these toxins. A better understanding of the biology underlying the bi-phasic dose response would be warranted to finally utilize these strategies for therapy promoting longer healthspan. Here, a critical key to the success of future medical intervention using the principle of hormesis is to get the right dose—the hormetic window , which will be anything but trivial [28,138]. This is because the parameters of each underlying sub-reaction are all dependent on individual reaction mechanisms. The dimension of the homeodynamic space of each patient is determined by their interacting genetic and epigenetic networks, which are part of the uniqueness of the individual [31,139]. Consequently, future investigations need to pay special attention to the inter-individual quantitative feature of the hormetic dose response when exploring therapy susceptibility . This necessitates the systematic collection of descriptive datasets on cohort study that facilitate sophisticated theoretical approaches . Albeit tedious, this would be an obligatory measure in ultimately utilizing the therapeutic potential of ROS hormesis against aging and age-related degenerative diseases.
In his later years, Friedrich Nietzsche seems to have given up being “stronger”, instead trying to avoid harshness and end his life at ease (he died at the age of 56). On the contrary, however, Mr. Helmut Schmidt still consumes a large number of cigarettes at every occasion. Perhaps his wisdom has led him to his personal optimal hormesis dose? Let’s keep our fingers crossed.
We cordially apologize to those scientists whose works relevant for the topic have not been cited due to limitation of space and our own ability. We thank Nicholas Jacobs and René Lang for their critical proofreading of this manuscript. This work was supported by the Berliner Chancengleichheitsprogramm.
Conflict of Interest
The authors declare no conflict of interest.
- Castro, P.V.; Khare, S.; Young, B.D.; Clarke, S.G. Caenorhabditis elegans battling starvation stress: Low levels of ethanol prolong lifespan in L1 larvae. PLoS One 2012, 7, e29984. [Google Scholar]
- Ritzmann, R.F.; Glasky, A.; Steinberg, A.; Melchior, C.L. The interaction of ethanol with the cognitive enhancers tacrine, physostigmine, and AIT-082. J. Gerontol 1994, 49, B51–B53. [Google Scholar]
- Briasoulis, A.; Agarwal, V.; Messerli, F.H. Alcohol consumption and the risk of hypertension in men and women: A systematic review and meta-analysis. J. Clin. Hypertens 2012, 14, 792–798. [Google Scholar]
- Marmot, M.G. Alcohol and coronary heart disease. Int. J. Epidemiol 2001, 30, 724–729. [Google Scholar]
- Maggio, R.; Riva, M.; Vaglini, F.; Fornai, F.; Racagni, G.; Corsini, G.U. Striatal increase of neurotrophic factors as a mechanism of nicotine protection in experimental parkinsonism. J. Neural Transm 1997, 104, 1113–1123. [Google Scholar]
- Quik, M. Smoking, nicotine and Parkinson’s disease. Trends Neurosci 2004, 27, 561–568. [Google Scholar]
- Baron, J.A. Beneficial effects of nicotine and cigarette smoking: The real, the possible and the spurious. Br. Med. Bull 1996, 52, 58–73. [Google Scholar]
- Calabrese, E.J. Historical blunders: How toxicology got the dose-response relationship half right. Cell. Mol. Biol 2005, 51, 643–654. [Google Scholar]
- Calabrese, E.J.; Baldwin, L.A. Defining hormesis. Hum. Exp. Toxicol 2002, 21, 91–97. [Google Scholar]
- Southam, C.M.; Ehrlich, J. Effects of Extract of western red cedar heartwood on certain wood-decaying fungi in culture. Phytopathology 1943, 33, 517–524. [Google Scholar]
- Kaiser, J. Hormesis. Sipping from a poisoned chalice. Science 2003, 302, 376–379. [Google Scholar]
- Cypser, J.R.; Tedesco, P.; Johnson, T.E. Hormesis and aging in Caenorhabditis elegans. Exp. Gerontol 2006, 41, 935–939. [Google Scholar]
- DeGracia, D.J.; Montie, H.L. Cerebral ischemia and the unfolded protein response. J. Neurochem 2004, 91. [Google Scholar] [CrossRef]
- Tuomisto, J.; Tuomisto, J.T. Is the fear of dioxin cancer more harmful than dioxin? Toxicol. Lett 2012, 210, 338–344. [Google Scholar]
- Feinendegen, L.E. Evidence for beneficial low level radiation effects and radiation hormesis. Br. J. Radiol 2005, 78, 3–7. [Google Scholar]
- Jaworowski, Z. Radiation hormesis—A remedy for fear. Hum. Exp. Toxicol 2010, 29, 263–270. [Google Scholar]
- Galimberti, D.; Scarpini, E. Alzheimer’s disease: From pathogenesis to disease-modifying approaches. CNS Neurol. Disord. Drug Targets 2011, 10, 163–174. [Google Scholar]
- Ittner, L.M.; Gotz, J. Amyloid-beta and tau—A toxic pas de deux in Alzheimer’s disease. Nat. Rev. Neurosci 2011, 12, 65–72. [Google Scholar]
- Morley, J.E.; Farr, S.A. Hormesis and amyloid-beta protein: Physiology or pathology? J. Alzheimers Dis 2012, 29, 487–492. [Google Scholar]
- Calabrese, E.J.; Baldwin, L.A. Toxicology rethinks its central belief. Nature 2003, 421, 691–692. [Google Scholar]
- Thayer, K.A.; Melnick, R.; Burns, K.; Davis, D.; Huff, J. Fundamental flaws of hormesis for public health decisions. Environ. Health Perspect 2005, 113, 1271–1276. [Google Scholar]
- Calabrese, E.J. Hormesis: A revolution in toxicology, risk assessment and medicine. EMBO Rep 2004, 5, S37–S40. [Google Scholar]
- Craig, E.A. The heat shock response. CRC Crit. Rev. Biochem 1985, 18, 239–280. [Google Scholar]
- Lindquist, S. The heat-shock response. Annu. Rev. Biochem 1986, 55, 1151–1191. [Google Scholar]
- Calabrese, E.J.; Baldwin, L.A.; Holland, C.D. Hormesis: A highly generalizable and reproducible phenomenon with important implications for risk assessment. Risk Anal 1999, 19, 261–281. [Google Scholar]
- Pollycove, M.; Feinendegen, L.E. Radiation-induced versus endogenous DNA damage: Possible effect of inducible protective responses in mitigating endogenous damage. Hum. Exp. Toxicol 2003, 22, 290–306, ; discussion 307, 315–317, 319–323.. [Google Scholar]
- Michalek, R.D.; Nelson, K.J.; Holbrook, B.C.; Yi, J.S.; Stridiron, D.; Danie, L.W.; Fetrow, J.S.; King, S.B.; Poole, L.B.; Grayson, J.M. The requirement of reversible cysteine sulfenic acid formation for T cell activation and function. J. Immunol 2007, 179, 6456–6467. [Google Scholar]
- Gems, D.; Partridge, L. Stress-response hormesis and aging: “That which does not kill us makes us stronger”. Cell Metab 2008, 7, 200–203. [Google Scholar]
- Hayflick, L. Biological aging is no longer an unsolved problem. Ann. N. Y. Acad. Sci. 2007, 1100. [Google Scholar] [CrossRef]
- Holliday, R. Aging is no longer an unsolved problem in biology. Ann. N. Y. Acad. Sci. 2006, 1067. [Google Scholar] [CrossRef]
- Rattan, S.I. Theories of biological aging: Genes, proteins, and free radicals. Free Radic. Res 2006, 40, 1230–1238. [Google Scholar]
- Bishop, N.A.; Guarente, L. Genetic links between diet and lifespan: Shared mechanisms from yeast to humans. Nat. Rev. Genet 2007, 8, 835–844. [Google Scholar]
- Pan, Y. Mitochondria, reactive oxygen species, and chronological aging: A message from yeast. Exp. Gerontol 2011, 46, 847–852. [Google Scholar]
- Joenje, H. Genetic toxicology of oxygen. Mutat. Res 1989, 219, 193–208. [Google Scholar]
- Afanas’ev, I. Reactive oxygen species signaling in cancer: Comparison with aging. Aging Dis 2011, 2, 219–230. [Google Scholar]
- Pacher, P.; Beckman, J.S.; Liaudet, L. Nitric oxide and peroxynitrite in health and disease. Physiol. Rev 2007, 87, 315–424. [Google Scholar]
- Lagouge, M.; Larsson, N.G. The role of mitochondrial DNA mutations and free radicals in disease and ageing. J. Intern. Med 2013, 273, 529–543. [Google Scholar]
- Wiederkehr, A.; Wollheim, C.B. Minireview: Implication of mitochondria in insulin secretion and action. Endocrinology 2006, 147, 2643–2649. [Google Scholar]
- Ristow, M. Oxidative metabolism in cancer growth. Curr. Opin. Clin. Nutr. Metab. Care 2006, 9, 339–345. [Google Scholar]
- Fukui, H.; Moraes, C.T. The mitochondrial impairment, oxidative stress and neurodegeneration connection: Reality or just an attractive hypothesis? Trends Neurosci 2008, 31, 251–256. [Google Scholar]
- Tatsuta, T.; Langer, T. Quality control of mitochondria: Protection against neurodegeneration and ageing. EMBO J 2008, 27, 306–314. [Google Scholar]
- Bratic, I.; Trifunovic, A. Mitochondrial energy metabolism and ageing. Biochim. Biophys. Acta 2010, 1797, 961–967. [Google Scholar]
- Galluzzi, L.; Kepp, O.; Trojel-Hansen, C.; Kroemer, G. Mitochondrial control of cellular life, stress, and death. Circ. Res 2012, 111, 1198–1207. [Google Scholar]
- Ugidos, A.; Nystrom, T.; Caballero, A. Perspectives on the mitochondrial etiology of replicative aging in yeast. Exp. Gerontol 2010, 45, 512–515. [Google Scholar]
- Van Remmen, H.; Ikeno, Y.; Hamilton, M.; Pahlavani, M.; Wolf, N.; Thorpe, S.R.; Alderson, N.L.; Baynes, J.W.; Epstein, C.J.; Huang, T.T.; et al. Life-long reduction in MnSOD activity results in increased DNA damage and higher incidence of cancer but does not accelerate aging. Physiol. Genomics 2003, 16, 29–37. [Google Scholar]
- Yang, W.; Hekimi, S. A mitochondrial superoxide signal triggers increased longevity in Caenorhabditis elegans. PLoS Biol 2010, 8, e1000556. [Google Scholar]
- Katsiki, N.; Manes, C. Is there a role for supplemented antioxidants in the prevention of atherosclerosis? Clin. Nutr 2009, 28, 3–9. [Google Scholar]
- Myung, S.K.; Kim, Y.; Ju, W.; Choi, H.J.; Bae, W.K. Effects of antioxidant supplements on cancer prevention: Meta-analysis of randomized controlled trials. Ann. Oncol 2010, 21, 166–179. [Google Scholar]
- Goto, S.; Radak, Z. Hormetic effects of reactive oxygen species by exercise: A view from animal studies for successful aging in human. Dose Response 2009, 8, 68–72. [Google Scholar]
- Liu, S.; Ajani, U.; Chae, C.; Hennekens, C.; Buring, J.E. Long-term beta-carotene supplementation and risk of type 2 diabetes mellitus: A randomized controlled trial. JAMA 1999, 282, 1073–1075. [Google Scholar]
- Song, Y.; Cook, N.R.; Albert, C.M.; van Denburgh, M.; Manson, J.E. Effects of vitamins C and E and beta-carotene on the risk of type 2 diabetes in women at high risk of cardiovascular disease: A randomized controlled trial. Am. J. Clin. Nutr 2009, 90, 429–437. [Google Scholar]
- Gomez-Cabrera, M.C.; Domenech, E.; Romagnoli, M.; Arduini, A.; Borras, C.; Pallardo, F.V.; Sastre, J.; Vina, J. Oral administration of vitamin C decreases muscle mitochondrial biogenesis and hampers training-induced adaptations in endurance performance. Am. J. Clin. Nutr. 2008, 87, 142–149. [Google Scholar]
- Khassaf, M.; McArdle, A.; Esanu, C.; Vasilaki, A.; McArdle, F.; Griffiths, R.D.; Brodie, D.A.; Jackson, M.J. Effect of vitamin C supplements on antioxidant defence and stress proteins in human lymphocytes and skeletal muscle. J. Physiol 2003, 549, 645–652. [Google Scholar]
- Ristow, M.; Zarse, K.; Oberbach, A.; Kloting, N.; Birringer, M.; Kiehntopf, M.; Stumvoll, M.; Kahn, C.R.; Bluher, M. Antioxidants prevent health-promoting effects of physical exercise in humans. Proc. Natl. Acad. Sci. USA 2009, 106, 8665–8670. [Google Scholar]
- Finley, L.W.; Haigis, M.C. The coordination of nuclear and mitochondrial communication during aging and calorie restriction. Ageing Res. Rev 2009, 8, 173–188. [Google Scholar]
- Woo, D.K.; Shadel, G.S. Mitochondrial stress signals revise an old aging theory. Cell 2011, 144, 11–12. [Google Scholar]
- Rattan, S.I. Hormesis in aging. Ageing Res. Rev 2008, 7, 63–78. [Google Scholar]
- Mattison, J.A.; Roth, G.S.; Beasley, T.M.; Tilmont, E.M.; Handy, A.M.; Herbert, R.L.; Lingo, D.L.; Allison, D.B.; Young, J.E.; Bryant, M.; et al. Impact of caloric restriction on health and survival in rhesus monkeys from the NIA study. Nature 2012, 489, 318–321. [Google Scholar]
- Castello, L.; Froio, T.; Cavallini, G.; Biasi, F.; Sapino, A.; Leonarduzzi, G.; Bergamini, E.; Poli, G.; Chiarpotto, E. Calorie restriction protects against age-related rat aorta sclerosis. FASEB J 2005, 19, 1863–1865. [Google Scholar]
- Colman, R.J.; Anderson, R.M.; Johnson, S.C.; Kastman, E.K.; Kosmatka, K.J.; Beasley, T.M.; Allison, D.B.; Cruzen, C.; Simmons, H.A.; Kemnitz, J.W.; et al. Caloric restriction delays disease onset and mortality in rhesus monkeys. Science 2009, 325, 201–204. [Google Scholar]
- Fontana, L.; Meyer, T.E.; Klein, S.; Holloszy, J.O. Long-term calorie restriction is highly effective in reducing the risk for atherosclerosis in humans. Proc. Natl. Acad. Sci. USA 2004, 101, 6659–6663. [Google Scholar]
- Meyer, T.E.; Kovacs, S.J.; Ehsani, A.A.; Klein, S.; Holloszy, J.O.; Fontana, L. Long-term caloric restriction ameliorates the decline in diastolic function in humans. J. Am. Coll. Cardiol 2006, 47, 398–402. [Google Scholar]
- Arumugam, T.V.; Gleichmann, M.; Tang, S.C.; Mattson, M.P. Hormesis/preconditioning mechanisms, the nervous system and aging. Ageing Res. Rev 2006, 5, 165–178. [Google Scholar]
- Barja, G. Mitochondrial oxygen consumption and reactive oxygen species production are independently modulated: Implications for aging studies. Rejuvenation Res 2007, 10, 215–224. [Google Scholar]
- Hulbert, A.J.; Clancy, D.J.; Mair, W.; Braeckman, B.P.; Gems, D.; Partridge, L. Metabolic rate is not reduced by dietary-restriction or by lowered insulin/IGF-1 signalling and is not correlated with individual lifespan in Drosophila melanogaster. Exp. Gerontol 2004, 39, 1137–1143. [Google Scholar]
- Selman, C.; Phillips, T.; Staib, J.L.; Duncan, J.S.; Leeuwenburgh, C.; Speakman, J.R. Energy expenditure of calorically restricted rats is higher than predicted from their altered body composition. Mech. Ageing Dev 2005, 126, 783–793. [Google Scholar]
- Ristow, M.; Zarse, K. How increased oxidative stress promotes longevity and metabolic health: The concept of mitochondrial hormesis (mitohormesis). Exp. Gerontol 2010, 45, 410–418. [Google Scholar]
- Lin, S.J.; Kaeberlein, M.; Andalis, A.A.; Sturtz, L.A.; Defossez, P.A.; Culotta, V.C.; Fink, G.R.; Guarente, L. Calorie restriction extends Saccharomyces cerevisiae lifespan by increasing respiration. Nature 2002, 418, 344–348. [Google Scholar]
- Schulz, T.J.; Zarse, K.; Voigt, A.; Urban, N.; Birringer, M.; Ristow, M. Glucose restriction extends Caenorhabditis elegans life span by inducing mitochondrial respiration and increasing oxidative stress. Cell Metab 2007, 6, 280–293. [Google Scholar]
- Sharma, P.K.; Agrawal, V.; Roy, N. Mitochondria-mediated hormetic response in life span extension of calorie-restricted Saccharomyces cerevisiae. Age 2011, 33, 143–154. [Google Scholar]
- Ames, B.N. Increasing longevity by tuning up metabolism. To maximize human health and lifespan, scientists must abandon outdated models of micronutrients. EMBO Rep 2005, 6, S20–S24. [Google Scholar]
- Nisoli, E.; Tonello, C.; Cardile, A.; Cozzi, V.; Bracale, R.; Tedesco, L.; Falcone, S.; Valerio, A.; Cantoni, O.; Clementi, E.; et al. Calorie restriction promotes mitochondrial biogenesis by inducing the expression of eNOS. Science 2005, 310, 314–317. [Google Scholar]
- Cerqueira, F.M.; Cunha, F.M.; Laurindo, F.R.; Kowaltowski, A.J. Calorie restriction increases cerebral mitochondrial respiratory capacity in a NO*-mediated mechanism: Impact on neuronal survival. Free Radic. Biol. Med 2012, 52, 1236–1241. [Google Scholar]
- Sies, H. Oxidative stress: Oxidants and antioxidants. Exp. Physiol 1997, 82, 291–295. [Google Scholar]
- Mesquita, A.; Weinberger, M.; Silva, A.; Sampaio-Marques, B.; Almeida, B.; Leao, C.; Costa, V.; Rodrigues, F.; Burhans, W.C.; Ludovico, P. Caloric restriction or catalase inactivation extends yeast chronological lifespan by inducing H2O2 and superoxide dismutase activity. Proc. Natl. Acad. Sci. USA 2010, 107, 15123–15128. [Google Scholar]
- Schulz, T.J.; Westermann, D.; Isken, F.; Voigt, A.; Laube, B.; Thierbach, R.; Kuhlow, D.; Zarse, K.; Schomburg, L.; Pfeiffer, A.F.H.; et al. Activation of mitochondrial energy metabolism protects against cardiac failure. Aging 2010, 2, 843–853. [Google Scholar]
- Warburton, D.E.; Nicol, C.W.; Bredin, S.S. Prescribing exercise as preventive therapy. CMAJ 2006, 174, 961–974. [Google Scholar]
- Hartwig, K.; Heidler, T.; Moch, J.; Daniel, H.; Wenzel, U. Feeding a ROS-generator to Caenorhabditis elegans leads to increased expression of small heat shock protein HSP-16.2 and hormesis. Genes Nutr 2009, 4, 59–67. [Google Scholar]
- Matus, S.; Castillo, K.; Hetz, C. Hormesis: Protecting neurons against cellular stress in Parkinson disease. Autophagy 2012, 8, 997–1001. [Google Scholar]
- Bonilla-Ramirez, L.; Jimenez-Del-Rio, M.; Velez-Pardo, C. Low doses of paraquat and polyphenols prolong life span and locomotor activity in knock-down parkin Drosophila melanogaster exposed to oxidative stress stimuli: Implication in autosomal recessive juvenile Parkinsonism. Gene 2013, 512, 355–363. [Google Scholar]
- Harada, N.; Zhao, J.; Kurihara, H.; Nakagata, N.; Okajima, K. Resveratrol improves cognitive function in mice by increasing production of insulin-like growth factor-I in the hippocampus. J. Nutr. Biochem 2011, 22, 1150–1159. [Google Scholar]
- Park, H.R.; Kong, K.H.; Yu, B.P.; Mattson, M.P.; Lee, J. Resveratrol inhibits the proliferation of neural progenitor cells and hippocampal neurogenesis. J. Biol. Chem 2012, 287, 42588–42600. [Google Scholar]
- Jones, R.G.; Plas, D.R.; Kubek, S.; Buzzai, M.; Mu, J.; Xu, Y.; Birnbaum, M.J.; Thompson, C.B. AMP-activated protein kinase induces a p53-dependent metabolic checkpoint. Mol. Cell 2005, 18, 283–293. [Google Scholar]
- Vingtdeux, V.; Giliberto, L.; Zhao, H.; Chandakkar, P.; Wu, Q.; Simon, J.E.; Janle, E.M.; Lobo, J.; Ferruzzi, M.G.; Davies, P.; et al. AMP-activated protein kinase signaling activation by resveratrol modulates amyloid-beta peptide metabolism. J. Biol. Chem 2010, 285, 9100–9113. [Google Scholar]
- Borriello, A.; Bencivenga, D.; Caldarelli, I.; Tramontano, A.; Borgia, A.; Pirozzi, V.A.; Oliva, A.; Ragione, F.D. Resveratrol and cancer treatment: Is hormesis a yet unsolved matter? Curr. Pharm. Des. 2013. in press. [Google Scholar]
- Kouda, K.; Iki, M. Beneficial effects of mild stress (hormetic effects): Dietary restriction and health. J. Physiol. Anthropol 2010, 29, 127–132. [Google Scholar]
- Speciale, A.; Chirafisi, J.; Saija, A.; Cimino, F. Nutritional antioxidants and adaptive cell responses: An update. Curr. Mol. Med 2011, 11, 770–789. [Google Scholar]
- Menendez, J.A.; Joven, J.; Aragones, G.; Barrajon-Catalan, E.; Beltran-Debon, R.; Borras-Linares, I.; Camps, J.; Corominas-Faja, B.; Cufi, S.; Fernandez-Arroyo, S.; et al. Xenohormetic and anti-aging activity of secoiridoid polyphenols present in extra virgin olive oil: A new family of gerosuppressant agents. Cell Cycle 2013, 12, 555–578. [Google Scholar]
- Lima, D.C.; Cossa, A.C.; Perosa, S.R.; de Oliveira, E.M.; da Silva, J.A., Jr; da Silva, F.M.J.; da Silva, I.R.; da Graca, N.-M.M.; Cavalheiro, E.A. Neuroglobin is up-regulated in the cerebellum of pups exposed to maternal epileptic seizures. Int. J. Dev. Neurosci. 2011, 29, 891–897. [Google Scholar]
- Yu, Z.; Liu, N.; Liu, J.; Yang, K.; Wang, X. Neuroglobin, a Novel Target for Endogenous Neuroprotection against Stroke and Neurodegenerative Disorders. Int. J. Mol. Sci 2012, 13, 6995–7014. [Google Scholar]
- Liochev, S.I. Reactive oxygen species and the free radical theory of aging. Free Radic. Biol. Med. 2013, 60. [Google Scholar] [CrossRef]
- Afanas’ev, I.B. On mechanism of superoxide signaling under physiological and pathophysiological conditions. Med. Hypotheses 2005, 64, 127–129. [Google Scholar]
- Feinendegen, L.E.; Bond, V.P.; Sondhaus, C.A.; Altman, K.I. Cellular signal adaptation with damage control at low doses versus the predominance of DNA damage at high doses. C. R. Acad. Sci. III 1999, 322, 245–251. [Google Scholar]
- Jones, S.A.; McArdle, F.; Jack, C.I.; Jackson, M.J. Effect of antioxidant supplementation on the adaptive response of human skin fibroblasts to UV-induced oxidative stress. Redox Rep 1999, 4, 291–299. [Google Scholar]
- Farooqui, A.A.; Horrocks, L.A.; Farooqui, T. Deacylation and reacylation of neural membrane glycerophospholipids. J. Mol. Neurosci 2000, 14, 123–135. [Google Scholar]
- Semsei, I.; Rao, G.; Richardson, A. Changes in the expression of superoxide dismutase and catalase as a function of age and dietary restriction. Biochem. Biophys. Res. Commun 1989, 164, 620–625. [Google Scholar]
- Youngman, L.D.; Park, J.Y.; Ames, B.N. Protein oxidation associated with aging is reduced by dietary restriction of protein or calories. Proc. Natl. Acad. Sci. USA 1992, 89, 9112–9116. [Google Scholar]
- Fontana, L.; Vinciguerra, M.; Longo, V.D. Growth factors, nutrient signaling, and cardiovascular aging. Circ Res 2012, 110, 1139–1150. [Google Scholar]
- Fulda, S.; Gorman, A.M.; Hori, O.; Samali, A. Cellular stress responses: Cell survival and cell death. Int. J. Cell Biol 2010. [Google Scholar] [CrossRef]
- Pirkkala, L.; Nykanen, P.; Sistonen, L. Roles of the heat shock transcription factors in regulation of the heat shock response and beyond. FASEB J 2001, 15, 1118–1131. [Google Scholar]
- Videla, L.A. Hormetic responses of thyroid hormone calorigenesis in the liver: Association with oxidative stress. IUBMB Life 2010, 62, 460–466. [Google Scholar]
- Ji, L.L.; Gomez-Cabrera, M.C.; Vina, J. Exercise and hormesis: Activation of cellular antioxidant signaling pathway. Ann. N. Y. Acad. Sci 2006, 1067, 425–435. [Google Scholar]
- Rao, G.; Xia, E.; Nadakavukaren, M.J.; Richardson, A. Effect of dietary restriction on the age-dependent changes in the expression of antioxidant enzymes in rat liver. J. Nutr 1990, 120, 602–609. [Google Scholar]
- Sreekumar, R.; Unnikrishnan, J.; Fu, A.; Nygren, J.; Short, K.R.; Schimke, J.; Barazzoni, R.; Nair, K.S. Impact of high-fat diet and antioxidant supplement on mitochondrial functions and gene transcripts in rat muscle. Am. J. Physiol. Endocrinol. Metab 2002, 282, E1055–E1061. [Google Scholar]
- Lee, S.J.; Hwang, A.B.; Kenyon, C. Inhibition of respiration extends C. elegans life span via reactive oxygen species that increase HIF-1 activity. Curr. Biol 2010, 20, 2131–2136. [Google Scholar]
- Xie, M.; Roy, R. Increased levels of hydrogen peroxide induce a HIF-1-dependent modification of lipid metabolism in AMPK compromised C. elegans dauer larvae. Cell Metab 2012, 16, 322–335. [Google Scholar]
- Suzuki, K.; Kodama, S.; Watanabe, M. Extremely low-dose ionizing radiation causes activation of mitogen-activated protein kinase pathway and enhances proliferation of normal human diploid cells. Cancer Res 2001, 61, 5396–5401. [Google Scholar]
- Tsutsui, T.; Tanaka, Y.; Matsudo, Y.; Hasegawa, K.; Fujino, T.; Kodama, S.; Barrett, J.C. Extended lifespan and immortalization of human fibroblasts induced by X-ray irradiation. Mol. Carcinog 1997, 18, 7–18. [Google Scholar]
- Van Montfort, R.L.; Congreve, M.; Tisi, D.; Carr, R.; Jhoti, H. Oxidation state of the active-site cysteine in protein tyrosine phosphatase 1B. Nature 2003, 423, 773–777. [Google Scholar]
- Juarez, J.C.; Manuia, M.; Burnett, M.E.; Betancourt, O.; Boivin, B.; Shaw, D.E.; Tonks, N.K.; Mazar, A.P.; Donate, F. Superoxide dismutase 1 (SOD1) is essential for H2O2-mediated oxidation and inactivation of phosphatases in growth factor signaling. Proc. Natl. Acad. Sci. USA 2008, 105, 7147–7152. [Google Scholar]
- Paulsen, C.E.; Truong, T.H.; Garcia, F.J.; Homann, A.; Gupta, V.; Leonard, S.E.; Carroll, K.S. Peroxide-dependent sulfenylation of the EGFR catalytic site enhances kinase activity. Nat. Chem. Biol 2012, 8, 57–64. [Google Scholar]
- Giorgio, M.; Migliaccio, E.; Orsini, F.; Paolucci, D.; Moroni, M.; Contursi, C.; Pelliccia, G.; Luzi, L.; Minucci, S.; Marcaccio, M.; et al. Electron transfer between cytochrome c and p66Shc generates reactive oxygen species that trigger mitochondrial apoptosis. Cell 2005, 122, 221–233. [Google Scholar]
- Orsini, F.; Migliaccio, E.; Moroni, M.; Contursi, C.; Raker, V.A.; Piccini, D.; Martin-Padura, I.; Pelliccia, G.; Trinei, M.; Bono, M.; et al. The life span determinant p66Shc localizes to mitochondria where it associates with mitochondrial heat shock protein 70 and regulates trans-membrane potential. J. Biol. Chem 2004, 279, 25689–25695. [Google Scholar]
- Zuo, Y.; Xiang, B.; Yang, J.; Sun, X.; Wang, Y.; Cang, H.; Yi, J. Oxidative modification of caspase-9 facilitates its activation via disulfide-mediated interaction with Apaf-1. Cell Res 2009, 19, 449–457. [Google Scholar]
- Tucci, P. Caloric restriction: Is mammalian life extension linked to p53? Aging 2012, 4, 525–534. [Google Scholar]
- Salminen, A.; Kaarniranta, K. ER stress and hormetic regulation of the aging process. Ageing Res. Rev 2010, 9, 211–217. [Google Scholar]
- Cullinan, S.B.; Diehl, J.A. PERK-dependent activation of Nrf2 contributes to redox homeostasis and cell survival following endoplasmic reticulum stress. J. Biol. Chem 2004, 279, 20108–20117. [Google Scholar]
- Cullinan, S.B.; Zhang, D.; Hannink, M.; Arvisais, E.; Kaufman, R.J.; Diehl, J.A. Nrf2 is a direct PERK substrate and effector of PERK-dependent cell survival. Mol. Cell. Biol 2003, 23, 7198–7209. [Google Scholar]
- Hoozemans, J.J.; van Haastert, E.S.; Nijholt, D.A.; Rozemuller, A.J.; Scheper, W. Activation of the unfolded protein response is an early event in Alzheimer’s and Parkinson’s disease. Neurodegener Dis 2012, 10, 212–215. [Google Scholar]
- Martins, I.; Galluzzi, L.; Kroemer, G. Hormesis, cell death and aging. Aging 2011, 3, 821–828. [Google Scholar]
- Szumiel, I. Radiation hormesis: Autophagy and other cellular mechanisms. Int. J. Radiat. Biol 2012, 88, 619–628. [Google Scholar]
- Eskelinen, E.L. New insights into the mechanisms of macroautophagy in mammalian cells. Int. Rev. Cell Mol. Biol 2008, 266, 207–247. [Google Scholar]
- Scherz-Shouval, R.; Shvets, E.; Fass, E.; Shorer, H.; Gil, L.; Elazar, Z. Reactive oxygen species are essential for autophagy and specifically regulate the activity of Atg4. EMBO J 2007, 26, 1749–1760. [Google Scholar]
- Salminen, A.; Kaarniranta, K.; Kauppinen, A. Crosstalk between Oxidative Stress and SIRT1: Impact on the Aging Process. Int. J. Mol. Sci 2013, 14, 3834–3859. [Google Scholar]
- Bjedov, I.; Toivonen, J.M.; Kerr, F.; Slack, C.; Jacobson, J.; Foley, A.; Partridge, L. Mechanisms of life span extension by rapamycin in the fruit fly Drosophila melanogaster. Cell Metab 2010, 11, 35–46. [Google Scholar]
- Eisenberg, T.; Knauer, H.; Schauer, A.; Buttner, S.; Ruckenstuhl, C.; Carmona-Gutierrez, D.; Ring, J.; Schroeder, S.; Magnes, C.; Antonacci, L.; et al. Induction of autophagy by spermidine promotes longevity. Nat. Cell Biol 2009, 11, 1305–1314. [Google Scholar]
- Morselli, E.; Marino, G.; Bennetzen, M.V.; Eisenberg, T.; Megalou, E.; Schroeder, S.; Cabrera, S.; Bénit, P.; Rustin, P.; Criollo, A.; et al. Spermidine and resveratrol induce autophagy by distinct pathways converging on the acetylproteome. J. Cell Biol 2011, 192, 615–629. [Google Scholar]
- Mattson, M.P.; Son, T.G.; Camandola, S. Viewpoint: Mechanisms of action and therapeutic potential of neurohormetic phytochemicals. Dose Response 2007, 5, 174–186. [Google Scholar]
- Ristow, M.; Schmeisser, S. Extending life span by increasing oxidative stress. Free Radic. Biol. Med 2011, 51, 327–326. [Google Scholar]
- Bensaad, K.; Cheung, E.C.; Vousden, K.H. Modulation of intracellular ROS levels by TIGAR controls autophagy. EMBO J 2009, 28, 3015–3026. [Google Scholar]
- Yokoo, S.; Furumoto, K.; Hiyama, E.; Miwa, N. Slow-down of age-dependent telomere shortening is executed in human skin keratinocytes by hormesis-like-effects of trace hydrogen peroxide or by anti-oxidative effects of pro-vitamin C in common concurrently with reduction of intracellular oxidative stress. J Cell. Biochem 2004, 93, 588–597. [Google Scholar]
- Alavez, S.; Vantipalli, M.C.; Zucker, D.J.; Klang, I.M.; Lithgow, G.J. Amyloid-binding compounds maintain protein homeostasis during ageing and extend lifespan. Nature 2011, 472, 226–229. [Google Scholar]
- Otani, A.; Kojima, H.; Guo, C.; Oishi, A.; Yoshimura, N. Low-dose-rate, low-dose irradiation delays neurodegeneration in a model of retinitis pigmentosa. Am. J. Pathol 2012, 180, 328–336. [Google Scholar]
- Li, N.; Stojanovski, S.; Maechler, P. Mitochondrial hormesis in pancreatic beta cells: Does uncoupling protein 2 play a role? Oxid. Med. Cell. Longev. 2012. [Google Scholar] [CrossRef]
- Duerrschmidt, N.; Hagen, A.; Gaertner, C.; Wermke, A.; Nowicki, M.; Spanel-Borowski, K.; Stepan, H.; Mohr, F.W.; Dhein, S. Nicotine effects on human endothelial intercellular communication via alpha4beta2 and alpha3beta2 nicotinic acetylcholine receptor subtypes. Naunyn Schmiedebergs Arch. Pharmacol 2012, 385, 621–632. [Google Scholar]
- Piri, M.; Nasehi, M.; Shahab, Z.; Zarrindast, M.R. The effects of nicotine on nitric oxide induced anxiogenic-like behaviors in the dorsal hippocampus. Neurosci. Lett 2012, 528, 93–98. [Google Scholar]
- Calabrese, E.J.; Mattson, M.P.; Calabrese, V. Dose response biology: The case of resveratrol. Hum. Exp. Toxicol 2010, 29, 1034–1037. [Google Scholar]
- Brink, T.C.; Demetrius, L.; Lehrach, H.; Adjaye, J. Age-related transcriptional changes in gene expression in different organs of mice support the metabolic stability theory of aging. Biogerontology 2009, 10, 549–564. [Google Scholar]
- Mao, L. Genetic Background Specific Hypoxia Resistance in Rat is Correlated with Balanced Activation of a Cross-Chromosomal Genetic Network Centering on Physiological Homeostasis. Front. Genet 2012. [Google Scholar] [CrossRef]
- Calabrese, V.; Cornelius, C.; Cuzzocrea, S.; Iavicoli, I.; Rizzarelli, E.; Calabrese, E.J. Hormesis, cellular stress response and vitagenes as critical determinants in aging and longevity. Mol. Aspects Med 2011, 32, 279–304. [Google Scholar]
- Calabrese, V.; Cornelius, C.; Dinkova-Kostova, A.T.; Calabrese, E.J.; Mattson, M.P. Cellular stress responses, the hormesis paradigm, and vitagenes: Novel targets for therapeutic intervention in neurodegenerative disorders. Antioxid. Redox Signal 2010, 13, 1763–1811. [Google Scholar]
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