Hormesis and Female Sex Hormones
The concept of hormesis reflects the pharmacological phenomenon of a substance producing diametrically different effects depending on the dose, thus negating the notion that dose-response curves are generally unidirectional . Although debated due to initially limited experimental evidence, the concept has been successively established as a relevant model for explaining the biological effects of certain substances . Another controversial subject during recent years is the menopausal hormone therapy debate. The effects of estrogens on stroke have been especially conflicting, since large epidemiological studies [3-5] and numerous animal studies [6-10] have found hormone therapy to be neuroprotective, while, on the contrary, the randomized controlled trial Women's Health Initiative (WHI)  reported increased stroke risk and some animal studies [12-15] have demonstrated increased ischemic lesions. Recent evidence indicates that estrogens' effects in rat stroke models may obey hormetic principles, so that physiological concentrations are protective while higher, prolonged concentrations are detrimental [16,17].
With the current widespread consumption of female sex hormones as contraceptive pills and menopausal hormone therapy, it is crucial to acknowledge the potentially hormetic effect patterns when designing animal studies, assessing study data and when planning clinical trials. This may be done by using a wide range of doses and by, at several relevant time-points, measuring the resulting in vivo serum concentrations of the hormone. Although all this may seem obvious, these measures to ensure study quality are unfortunately very commonly neglected. For illustrative purposes, we performed a literature review, covering the latest 100 articles describing administration of 17β-estradiol to rats or mice, retrieved when searching Medline (on the 25th of March 2011) with the terms “Estradiol and (rat or mouse)”. Of these 100 articles, published in 2010 and 2011, 86 described administration of only one 17β-estradiol dose, and only seven studies adopted more than two doses. It is interesting to note that in the study using the highest number of doses, a clear bidirectional dose-response relation was seen . Serum 17β-estradiol measurements were only performed in 27 of the studies, of which 25 only investigated one single time-point, which thus conveys little information about the serum concentrations before and after the exact moment the sample was taken (Table 1).
The aim of this review is to highlight the importance of taking hormesis into account in all studies investigating the biological effects of female sexual hormones. The fundamentals of hormesis are first described and discussed, and the definition adopted in this review is outlined (Section 2). Subsequently examples of female sex steroids demonstrating hormetic dose-response relations, including the abovementioned biphasic actions of estrogens in stroke, are presented (Section 3), followed by concluding remarks regarding the implications for menopausal hormone therapy research (Section 4).
2. The Concept of Hormesis
The first record of the term “hormesis” in scientific publications is found in the 1943 article by Southam and Ehrlich “Effects of extract of western red-cedar heartwood on certain wood-decaying fungi in culture”. The authors investigated the effects of a wide concentration range of an anti-fungal agent, finding that despite high concentration decreased the fungus growth, doses below the growth-inhibitory threshold actually stimulated it . Thus, this original adoption of the term described the phenomenon that merely depending on the dose, one substance could have diametrically different effects in a biological system. However, although Southam and Ehrlich were the first to use the term “hormesis” in scientific publications, the phenomenon had been acknowledged much earlier. Actually, already the ancient Greeks' proverb “meden agan” (nothing in excess), the Latin analogue “in medio stat virtus” (virtue stands in the middle), as well as Paracelsus well-known quote “Alle Dinge sind Gift und nichts ist ohne Gift, allein die Dosis macht es, dass ein Ding kein Gift ist” (all things are poison and nothing is without poison; only the dose makes a thing not a poison) reflects aspects of hormesis. The scientist most often attributed as the first to scientifically identify the hormetic phenomena, though without using the word “hormesis”, was Schultz, who in a series of studies as early as in the 1880's demonstrated e.g. that formic acid promoted fermentation in low doses while inhibiting it in higher doses .
Before and in parallel with the adoption of the term “hormesis” in the 1940's, numerous terms for similar phenomena were suggested, including “biphasic”, “bidirectional”, “non-monotonic”, “J-shaped”, “U-shaped” and “inverted U-shaped dose-response curves”, “β-curve”, “Arndt-Schultz' law” and “Huebbe's law”. The rich flora of terms has probably contributed to confusion and difficulty in properly investigating the phenomenon, thus the fundamental importance of clearly defining a term, such as “hormesis”, to precisely account for bidirectional dose-response relations of this sort cannot be overestimated.
As mentioned before, a lively debate concerning the definition and significance of hormesis has taken place in the scientific community in recent years [1,2,21,22]. One of the most influential scientists in the field is Calabrese, who has not only performed extensive literature analyses to assess the phenomenon's frequency and nature [23,24], but also in a series of reviews has revised the hormesis definition [2,25-28]. An important contribution by Calabrese in developing a scientifically sound definition of hormesis was the realization that the low-dose effect of hormesis should not necessarily be beneficial, since “beneficial” is an utterly complex and context-dependent expression .
A related question is if the mechanism(s) should be included in the definition of hormesis. In an attempt to more strictly define hormesis by attributing it to one common mechanism, it has been suggested that hormesis should be viewed as an adaptive action taken by the cell to minimize the damage from a toxic insult. This adaptation would in turn be direct or resulting from overcompensation by the toxic damage, in the latter case with a mandatory time delay [2,25,29]. However, it seems unnecessarily narrow to define one type of mechanisms for all types of hormetic dose-responses, as pointed out by Kendig et al. . Further, such a definition is unintuitive, probably unrelated to many of the instances in which the term has been used, and the classification of a dose-response relation becomes exceedingly complicated if an adaptive nature of the response needs to be proven in every single case. Adaptation to toxic insults can definitely be the one possible mechanism for certain hormetic responses, but the concept of hormesis should not be limited to this. Instead, Kendig et al. suggested that the definition of hormesis should solely be related to the bidirectional dose-response curve, and unrelated to its mechanism: “Hormesis is a dose-response relationship for a single endpoint that is characterized by reversal of response between low and high doses of chemicals, biological molecules, physical stressors, or any other initiators of a response” . In line with this definition, Conolly and Lutz illustratively demonstrated how different multi-mechanistic systems, including adaptations to damage, can render hormetic dose-response curves for certain endpoints. They thus highlighted that hormesis is most likely to occur in mechanistically complex systems, where a multitude of mechanisms with different potency and efficiency taken together can create a bidirectional pattern . The advantage of this definition is that it is intuitive, readily enables identification of hormesis and is far less speculative than the above mechanism-coupled definition.
It should be also emphasized that not all non-monotonic dose-response curves are included in the concept of hormesis, but that effects in both directions compared to the control group need to be demonstrated (Figure 1).
The debate concerning the nature of hormesis has largely been conducted within the realm of toxicological sciences, which has influenced the suggestions of how the term should be used. For example, the hormetic effect has most often been described as the sub-threshold stimulatory effect of a dose-toxicity curve, rather than e.g. the reversal of a drug's desired effect in doses above the therapeutic window . It is worth emphasizing that the hormetic stimulatory window of toxic substances and the therapeutic window of pharmaceuticals are conceptually similar , and merely reflects different aspects of the same phenomenon. The dominating influence of toxicologists in the debate has probably also contributed to the widespread idea that the low-dose effect in hormesis is generally an adaptive response, an assumption that evidently makes most sense in a toxicological perspective.
Another matter of debate, which also needs to be addressed when using the term “hormesis”, is its universality. The keenest proponents of hormesis have argued that hormesis is actually a more general phenomenon than the classical, well-established threshold theory, and should therefore be considered the default when assessing dose-response relations . Although it seems plausible that hormetic phenomena are more common than hitherto demonstrated, and although advocating the search for hormesis by using wide ranges of concentrations is much deserving, it seems as yet unwarranted to claim that hormesis is universal since the phenomenon probably relies on different mechanisms in different instances and therefore is highly context-dependent. Moreover, the claim for its superiority to the threshold model and its generalizability has probably fuelled much of the recent skepticism towards the concept of hormesis [1,22].
Thus when in the remaining article referring to hormesis, we adhere to the definition suggested by Kendig , and view hormesis as a dose-dependent bidirectional effector-endpoint relation, which is unrelated to the mechanism and should not, although seemingly common and underappreciated, be considered universal.
3. Female Sex Hormones and Hormesis
Progestagens and estrogens both exert their effects through multiple pathways, each of which may constitute highly complex signal systems. Progestagens mainly act via the two nuclear progesterone receptors A and B, which are both derived from the same gene , but often oppose each other's effects . There is also evidence of membrane-bound progesterone receptors [33,34], even though the pharmacological importance of these remains to be proven. In the case of estrogens, the classical pathway – the nuclear estrogen receptors α and β (ERα and ERβ)  – are complemented by effects mediated by membrane bound receptors, such as GPR30 , and also by direct effects including redox cycling . Further, at very high doses, 17β-estradiol is known to cause down-regulation of its own receptors  at the same time as stimulating other receptors of the nuclear receptor superfamily, thus activating a totally different set of genes in the toxicological compared to the physiological concentration range . It has furthermore been speculated that different subsets of membrane receptors, e.g. defined by their residence in membrane caveolae or lipid rafts, can result in non-monotonic dose-response relations . These multifaceted signal systems in turn affect a wide range of biological mechanisms, thus further adding to the intricacy of estrogens' and progestagens' effects. Given this complexity, far from the single-receptor situation which is the basis of the linear dose-response model, it is not unexpected that female sex hormones frequently produce hormetic phenomena. As aforementioned, complex signal pathways is what mechanistically allows hormesis to occur  (Figure 2).
There are numerous examples of estrogen and progestagen hormesis affecting a wide variety of endpoints, including cerebral ischemia [16,17], calcium content in bones , bone development , dopamine transporters and release [43,44], mammary gland differentiation [45,46], capillary endothelial cellular adhesion , plasminogen activator regulation , DNA synthesis in endothelial cells , insulin sensitivity , genital development [51-53], growth of cultured tumor cells [54-56], cardiac monophasic action potentials , levels of cytosolic magnesium ions , anxiety [59,60], sulfotransferase activity in cancer cells  and multiple inflammatory processes [62-67]. A few of these are presented below in detail to further highlight the hormetic potential of estrogens and progestagens.
3.1. Cerebral Ischemia
In 2005, Theodorsson et al. published a study originally designed to investigate if the earlier reported neuroprotective effects of estrogens could be explained by effects on the neuropeptide galanin . Numerous earlier animal stroke experiments had demonstrated neuroprotective effects of estrogens [7,68-70], however in this study 17β-estradiol unexpectedly turned out to be damaging . This raised the question of what methodological factor could be responsible for the diametrical discrepancy in results, and differences in estrogen administration regimes was in an early phase suspected to be the culprit. In the study by Theodorsson and Theodorsson a certain type of subcutaneously implanted slow-release pellets from the company Innovative Research of America (IRA) was used for administration of the hormone. Two subsequent trials investigated this method and the two other commonest methods for estrogen administration, and it was found that the IRA pellets in fact were exceptional in producing highly supraphysiological, long-lasting serum concentration peaks of 17β-estradiol, while the other methods rendered physiological levels or a pattern of short peaks [71,72]. Soon thereafter a meta-analysis of methods in estrogen-stroke rat experiments was published reporting that the high-dose IRA pellets were in fact the only methods capable of inducing increased damage, and that higher dosed pellets were most likely to be detrimental . The hypothesis was later also experimentally validated . Hence, it is very likely that at least part of the controversy of estrogens' effect in animal stroke models was caused by a hormetic phenomenon that remained unnoticed for a long time due to underestimation (including ours) of the importance of well-established administration regimens.
The mechanisms for estrogens' protective effects are probably multifactorial, including decreased apoptosis, decreased inflammation, beneficial vascular effects and growth factor modulation [37,73,74]. This has been given much attention because of the strong potential of the hormone as a neuroprotectant, contrasting the possibly detrimental effects of estrogens in stroke, for which few mechanistic suggestions have been investigated. However, in a recent review, it was hypothesized that hormetic effects of estrogens on inflammation could be the mechanism behind the hormone's paradoxical effects on stroke. This hypothesis was based on an assessment of several rat experimental studies showing increased [13,78,79] or decreased [80-82] cerebral inflammation in the light of earlier studies investigating the produced serum concentrations  and effects [16,17] of different estrogen administration regimes .
Differential effects of estrogens on stroke have, as mentioned earlier, not only been reported in animal models. An analogous controversy is obvious when assessing results from the larger studies in human populations [3-5,11,75]. Although the doses used in these different studies are somewhat too similar to each other to draw any conclusions about hormetic effects, it must be seen as possible that the U-shaped dose-response curves seen in animal models could also be relevant in human estrogen consumption in general, and HT in particular.
Concerning progesterone, it has likewise been suggested (however on relatively weak grounds) that low doses could be protective and higher doses could increase risk of cerebral ischemia due to the hormone's bidirectional, dose-dependent effects on cytosolic magnesium ions in cerebral vascular smooth muscle cells. Normal concentrations of cytosolic magnesium ions, which are sustained by low levels of female sex hormones, are beneficial for vascular function, while depletion of these ions, caused by high levels of progestagens, result in cerebral vasospasm. The vasospasm leads to decreased cerebral blood perfusion, which could be related to migraine headaches and perhaps also an increased risk of stroke .
Many of the known examples of hormesis need pharmacological manipulation of the active substance to appear. However, when it comes to estrogens' effects on inflammation, hormesis-like phenomena can actually be observed in vivo during pregnancy. Non-pregnant women are more Th1-tilted than men are, which has been assessed as an estrogenic effect, while the shift from Th1 to the antagonizing Th2 that appears during pregnancy has also largely been attributed to changes in female sexual steroids . Hence it seems that, even under physiological conditions, paradoxical suppression/potentiation of different parts of the immune system results from different concentrations of estrogens, which is compatible with the concept of hormesis, and thus it is easy to imagine that pharmacological hormone manipulations even more potently can exert such phenomena. Numerous studies have been dedicated to experimentally investigate estrogens' effects on inflammation, and the results reveal an almost unbelievable complexity, that however to a large part can be understood as consequences of the fairly logical overall effects of estrogens in pregnancy, aimed at avoiding abortion of the fetus .
Most experimental studies demonstrating hormetic phenomena of female sex hormones on inflammation suggest that low hormone concentrations are pro-inflammatory whereas high hormone concentrations are anti-inflammatory , such as the effects of estrogens on the pro-inflammatory cytokine IL-1 . Similar results have been reported when it comes to the effects on TNF [62,64,65], natural killer cells and adhesion molecules, all seeming to be inhibited by high estrogen and/or progestagen levels while being stimulated by low levels . Furthermore, inhibition of immune cell apoptosis has been demonstrated in lower levels than have the opposite . These observations seem to be well in line with the understanding of the anti-inflammatory role of the high estrogen concentrations during pregnancy. However, the complexity increases even more when the effects of estrogens on a broader range of cytokines is taken into consideration, since not only concentration, but also the type of effector cell, the cytokine milieu and other factors seem to be crucial . As abovementioned it was in a recent review hypothesized that high dose estrogen administration regimens could increase cerebral inflammation while low dose regimens exert the opposite effect, which is quite contrary to the pattern presented above. The discordant patterns concerning in which concentration-ranges estrogens are neuroprotective or neurotoxic could possibly result from organ differences or reflect discrepancies in the measured end-points.
In this section, the aspect of estrogen type also merits attention, even though it does not present a clear example of hormesis. Interestingly, CEE, which was used in WHI and then resulted in increased risk of stroke [11,75], has in several studies been reported to be pro-inflammatory in contrary to 17β-estradiol , which has been administered in virtually all animal studies reporting decreased risk of stroke . CEE regimes are generally considered more potent than 17β-estradiol regimes, even if the exact potency is difficult to compare.
Even though estrogens' actions on inflammation in different organ and cells are exceedingly complex and it is difficult to draw any firm conclusions, it is clear that estrogens are highly capable of exerting hormetic effects also in inflammation, and that this needs to be taken into account when studying relevant phenomena. Hormetic effects on inflammation are particularly interesting since they are not only relevant for, as aforementioned, stroke and obviously inflammatory disorders such as rheumatoid arthritis, but also for e.g. cardiovascular diseases, osteoporosis and cancer.
3.3. Cardiovascular Disease
Hormetic effects of female sex hormones on inflammation have, as aforementioned, far-reaching implications for cardiovascular diseases, since inflammation e.g. is a central process in the pathogenesis of atherosclerotic plaques  and in the development of myocardial infarction . However, there are also more specific examples of hormesis that can be relevant, such as the effects on the anticoagulant protein plasminogen activator. In a cell culture experiment using bovine aortic endothelial cells the effects of 17β-estradiol and progesterone on plasminogen activator was investigated. It was found that even though 17β-estradiol and progesterone concentrations corresponding to low physiological in vivo levels activated the protein, higher concentrations inhibited it, and thus it was concluded that in this respect, estrogens and progesterone in pharmacological doses can be thrombogenic .
Further, estrogens' effects on the DNA production in endothelial cells have been reported to obey hormetic principles. In a human umbilical smooth muscle cell line it was found that 17β-estradiol in physiological concentrations stimulated [3H]thymidine incorporation into DNA whereas pharmacological concentrations were inhibitory. These findings may have bearing on cardiovascular diseases because of the role of smooth muscle cells in atherosclerosis pathophysiology .
Insulin resistance is a prominent feature of the metabolic syndrome and thus intimately related to cardiovascular diseases. In a RCT of the effects on conjugated equine estrogens on insulin sensitivity in postmenopausal women it was shown that the standard dose of 0.625 mg/day increased while 1.25 mg/day decreased insulin sensitivity . This is a clear demonstration that the hormetic effects of female sex hormones can indeed prevail in clinical situations.
Another relevant example concerns arrhythmia, which is a central feature of several cardiac diseases. It has been reported that progesterone's modulation of action potentials in heart muscle also displays hormetic patterns, so that while low progesterone levels were found to shorten action potentials, high doses lengthened the same .
Progestagens have in several studies been reported to exert both anxiogenic and anxiolytic effects, in accordance with hormetic principles. Both animals and postmenopausal women treated with the progestagen allopregnanolone exhibit anxiogenic responses in the lower and anxiolytic responses in the higher dose-spectrum . These effects are supposedly mediated via allopregnanolone's effects the GABA(A) receptor . In a study of mouse behavior in a plus-maze, it was shown that low doses of pregnanolone sulfate increased anxiety, while high doses on the contrary were anxiolytic , which matches pregnanolone sulfate's bidirectional effects on the GABA(A) receptor .
Hormesis is a highly relevant concept for female sexual steroids' effects on many biological endpoints. This is particularly evident concerning estrogens, but there are also several examples of progestagen hormesis. The dominance of estrogens over progestagens concerning number of reported cases of hormesis probably reflects that the former hormone has been subjected to more intense research efforts, but can also be due to an actually stronger tendency of estrogens to produce hormetic dose-response relations.
Therefore experiments designed to elucidate the proper biological and therapeutic effects of female sex hormones should be performed with hormesis in mind. A wide range of doses should be adopted, and importantly, the biological relevance of these doses must be assessed by serum hormone measurements and subsequent comparison with the intended clinical/biological situation. Since HT is mainly given in a low dose range, it seems reasonable to primarily aim at simulating these levels, and it is of utmost importance that the measurements of hormone after hormone manipulation, e.g. in an animal, is performed in several time-points . The same caution of using several dose levels – though difficult – may also be of relevance in human studies where a single dose has hereto been the rule.
|Number of 17β-estradiol doses||Number of studies||Number of occasions of 17β-estradiol measurement||Number of studies|
- Kendig, E.L.; Le, H.H.; Belcher, S.M. Defining hormesis: Evaluation of a complex concentration response phenomenon. Int. J. Toxicol. 2010, 29, 235–246. [Google Scholar]
- Calabrese, E.J. Hormesis is central to toxicology, pharmacology and risk assessment. Hum. Exp. Toxicol. 2010, 29, 249–261. [Google Scholar]
- Paganini-Hill, A.; Ross, R.K.; Henderson, B.E. Postmenopausal oestrogen treatment and stroke: A prospective study. BMJ 1988, 297, 519–522. [Google Scholar]
- Falkeborn, M.; Persson, I.; Terent, A.; Adami, H.O.; Lithell, H.; Bergstrom, R. Hormone replacement therapy and the risk of stroke. Follow-up of a population-based cohort in Sweden. Arch. Intern. Med. 1993, 153, 1201–1209. [Google Scholar]
- Finucane, F.F.; Madans, J.H.; Bush, T.L.; Wolf, P.H.; Kleinman, J.C. Decreased risk of stroke among postmenopausal hormone users. Results from a national cohort. Arch. Intern. Med. 1993, 153, 73–79. [Google Scholar]
- Rau, S.W.; Dubal, D.B.; Bottner, M.; Gerhold, L.M.; Wise, P.M. Estradiol attenuates programmed cell death after stroke-like injury. J. Neurosci. 2003, 23, 11420–11426. [Google Scholar]
- Simpkins, J.W.; Rajakumar, G.; Zhang, Y.Q.; Simpkins, C.E.; Greenwald, D.; Yu, C.J.; Bodor, N.; Day, A.L. Estrogens may reduce mortality and ischemic damage caused by middle cerebral artery occlusion in the female rat. J. Neurosurg. 1997, 87, 724–730. [Google Scholar]
- Sandstrom, N.J.; Rowan, M.H. Acute pretreatment with estradiol protects against CA1 cell loss and spatial learning impairments resulting from transient global ischemia. Horm. Behav. 2007, 51, 335–345. [Google Scholar]
- Choi, Y.C.; Lee, J.H.; Hong, K.W.; Lee, K.S. 17 Beta-estradiol prevents focal cerebral ischemic damages via activation of Akt and CREB in association with reduced PTEN phosphorylation in rats. Fundam. Clin. Pharmacol. 2004, 18, 547–557. [Google Scholar]
- O'Donnell, M.E.; Lam, T.I.; Tran, L.Q.; Foroutan, S.; Anderson, S.E. Estradiol reduces activity of the blood-brain barrier Na-K-Cl cotransporter and decreases edema formation in permanent middle cerebral artery occlusion. J. Cereb. Blood Flow Metab. 2006, 26, 1234–1249. [Google Scholar]
- Rossouw, J.E.; Anderson, G.L.; Prentice, R.L.; LaCroix, A.Z.; Kooperberg, C.; Stefanick, M.L.; Jackson, R.D.; Beresford, S.A.; Howard, B.V.; Johnson, K.C.; et al. Risks and benefits of estrogen plus progestin in healthy postmenopausal women: Principal results from the women's health initiative randomized controlled trial. JAMA 2002, 288, 321–333. [Google Scholar]
- Theodorsson, A.; Theodorsson, E. Estradiol increases brain lesions in the cortex and lateral striatum after transient occlusion of the middle cerebral artery in rats: No effect of ischemia on galanin in the stroke area but decreased levels in the hippocampus. Peptides 2005, 26, 2257–2264. [Google Scholar]
- Yong, Y.; Xie, H.J.; Zhang, Y.F.; Yang, Q.D.; Liao, D.F.; Yang, H.L.; Yan, P.K.; Liu, Z.J. 17beta-estradiol potentiates ischemia-reperfusion injury in diabetic ovariectomized female rats. Brain Res. 2005, 1054, 192–199. [Google Scholar]
- Carswell, H.V.; Bingham, D.; Wallace, K.; Nilsen, M.; Graham, D.I.; Dominiczak, A.F.; Macrae, I.M. Differential effects of 17beta-estradiol upon stroke damage in stroke prone and normotensive rats. J. Cereb. Blood Flow Metab. 2004, 24, 298–304. [Google Scholar]
- Harukuni, I.; Hurn, P.D.; Crain, B.J. Deleterious effect of beta-estradiol in a rat model of transient forebrain ischemia. Brain Res. 2001, 900, 137–142. [Google Scholar]
- Strom, J.O.; Theodorsson, A.; Theodorsson, E. Dose-related neuroprotective versus neurodamaging effects of estrogens in rat cerebral ischemia: A systematic analysis. J. Cereb. Blood Flow Metab. 2009, 29, 1359–1372. [Google Scholar]
- Strom, J.O.; Theodorsson, E.; Holm, L.; Theodorsson, A. Different methods for administering 17beta-estradiol to ovariectomized rats result in opposite effects on ischemic brain damage. BMC Neurosci. 2010, 11, 39. [Google Scholar]
- Inagaki, T.; Gautreaux, C.; Luine, V. Acute estrogen treatment facilitates recognition memory consolidation and alters monoamine levels in memory-related brain areas. Horm. Behav. 2010, 58, 415–426. [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]
- Schulz, H.; Crump, T. NIH-98-134: Contemporary Medicine as Presented by its Practitioners Themselves, Leipzig, 1923:217-250. Nonlinearity Biol. Toxicol. Med. 2003, 1, 295–318. [Google Scholar]
- Jonas, W.B. A critique of “the scientific foundations of hormesis”. Crit. Rev. Toxicol. 2001, 31, 625–629. [Google Scholar]
- Mushak, P. Hormesis and its place in nonmonotonic dose-response relationships: Some scientific reality checks. Environ. Health Perspect. 2007, 115, 500–506. [Google Scholar]
- Calabrese, E.J.; Baldwin, L.A. The frequency of U-shaped dose responses in the toxicological literature. Toxicol. sci. 2001, 62, 330–338. [Google Scholar]
- Calabrese, E.J. Dose-response features of neuroprotective agents: An integrative summary. Crit. Rev. Toxicol. 2008, 38, 253–348. [Google Scholar]
- Calabrese, E.J.; Baldwin, L.A. Defining hormesis. Hum. Exp. Toxicol. 2002, 21, 91–97. [Google Scholar]
- Calabrese, E.J.; Baldwin, L.A. Hormesis: The dose-response revolution. Annu. Rev. Pharmacol. Toxicol. 2003, 43, 175–197. [Google Scholar]
- Calabrese, E.J. Hormesis-basic, generalizable, central to toxicology and a method to improve the risk-assessment process. Int. J. Occup. Environ. Health 2004, 10, 466–467. [Google Scholar]
- Calabrese, E.J.; Staudenmayer, J.W.; Stanek, E.J. Drug development and hormesis: Changing conceptual understanding of the dose response creates new challenges and opportunities for more effective drugs. Curr. Opin. Drug Discov. Devel. 2006, 9, 117–123. [Google Scholar]
- Stebbing, A.R.D. The kinetics of growth control on a colonial hydroid. J. Mar. Biol. Assoc. U.K. 1981, 61, 35–64. [Google Scholar]
- Conolly, R.B.; Lutz, W.K. Nonmonotonic dose-response relationships: Mechanistic basis, kinetic modeling, and implications for risk assessment. Toxicol. Sci. 2004, 77, 151–157. [Google Scholar]
- Giangrande, P.H.; McDonnell, D.P. The A and B isoforms of the human progesterone receptor: Two functionally different transcription factors encoded by a single gene. Recent Prog. Horm. Res. 1999, 54, 291–313, discussion 313-314. [Google Scholar]
- Vegeto, E.; Shahbaz, M.M.; Wen, D.X.; Goldman, M.E.; O'Malley, B.W.; McDonnell, D.P. Human progesterone receptor a form is a cell- and promoter-specific repressor of human progesterone receptor B function. Mol. Endocrinol. 1993, 7, 1244–1255. [Google Scholar]
- Blackmore, P.F. Extragenomic actions of progesterone in human sperm and progesterone metabolites in human platelets. Steroids 1999, 64, 149–156. [Google Scholar]
- Losel, R.; Dorn-Beineke, A.; Falkenstein, E.; Wehling, M.; Feuring, M. Porcine spermatozoa contain more than one membrane progesterone receptor. Int. J. Biochem. Cell Biol. 2004, 36, 1532–1541. [Google Scholar]
- Hanstein, B.; Djahansouzi, S.; Dall, P.; Beckmann, M.W.; Bender, H.G. Insights into the molecular biology of the estrogen receptor define novel therapeutic targets for breast cancer. Eur. J. Endocrinol. 2004, 150, 243–255. [Google Scholar]
- Funakoshi, T.; Yanai, A.; Shinoda, K.; Kawano, M.M.; Mizukami, Y. G protein-coupled receptor 30 is an estrogen receptor in the plasma membrane. Biochem. Biophys. Res. Commun. 2006, 346, 904–910. [Google Scholar]
- Simpkins, J.W.; Yi, K.D.; Yang, S.H. Role of protein phosphatases and mitochondria in the neuroprotective effects of estrogens. Front. Neuroendocrinol. 2009, 30, 93–105. [Google Scholar]
- Medlock, K.L.; Lyttle, C.R.; Kelepouris, N.; Newman, E.D.; Sheehan, D.M. Estradiol down-regulation of the rat uterine estrogen receptor. Proc. Soc. Exp. Biol. Med. 1991, 196, 293–300. [Google Scholar]
- Saal, F.S. Hormesis controversy. Environ. Sci. Technol. 2007, 41, 3. [Google Scholar]
- Watson, C.S.; Jeng, Y.J.; Kochukov, M.Y. Nongenomic signaling pathways of estrogen toxicity. Toxicol. Sci. 2010, 115, 1–11. [Google Scholar]
- Sato, K.; Nohtomi, K.; Shizume, K.; Demura, H.; Kanatani, H.; Kiyoki, M.; Ohashi, Y.; Ejiri, S.; Ozawa, H. 17 beta-estradiol increases calcium content in fetal mouse parietal bones cultured in serum-free medium only at physiological concentrations. Bone 1996, 19, 213–221. [Google Scholar]
- Calabrese, E.J. Estrogen and related compounds: Biphasic dose responses. Crit. Rev. Toxicol. 2001, 31, 503–515. [Google Scholar]
- Alyea, R.A.; Laurence, S.E.; Kim, S.H.; Katzenellenbogen, B.S.; Katzenellenbogen, J.A.; Watson, C.S. The roles of membrane estrogen receptor subtypes in modulating dopamine transporters in PC-12 cells. J. Neurochem. 2008, 106, 1525–1533. [Google Scholar]
- Cabrera, R.; Diaz, A.; Pinter, A.; Belmar, J. In vitro progesterone effects on 3H-dopamine release from rat corpus striatum slices obtained under different endocrine conditions. Life Sci. 1993, 53, 1767–1777. [Google Scholar]
- Vandenberg, L.N.; Wadia, P.R.; Schaeberle, C.M.; Rubin, B.S.; Sonnenschein, C.; Soto, A.M. The mammary gland response to estradiol: Monotonic at the cellular level, non-monotonic at the tissue-level of organization? J. Steroid Biochem. Mol. Biol. 2006, 101, 263–274. [Google Scholar]
- Kohlerova, E.; Skarda, J. Mouse bioassay to assess oestrogenic and anti-oestrogenic compounds: Hydroxytamoxifen, diethylstilbestrol and genistein. J. Vet. Med. A Physiol. Pathol. Clin. Med. 2004, 51, 209–217. [Google Scholar]
- Banerjee, S.K.; Campbell, D.R.; Weston, A.P.; Banerjee, D.K. Biphasic estrogen response on bovine adrenal medulla capillary endothelial cell adhesion, proliferation and tube formation. Mol. Cell Biochem. 1997, 177, 97–105. [Google Scholar]
- Sobel, M.I.; Winkel, C.A.; Macy, L.B.; Liao, P.; Bjornsson, T.D. The regulation of plasminogen activators and plasminogen activator inhibitor type 1 in endothelial cells by sex hormones. Am. J. Obstet. Gynecol. 1995, 173, 801–808. [Google Scholar]
- Somjen, D.; Kohen, F.; Jaffe, A.; Amir-Zaltsman, Y.; Knoll, E.; Stern, N. Effects of gonadal steroids and their antagonists on DNA synthesis in human vascular cells. Hypertension 1998, 32, 39–45. [Google Scholar]
- Lindheim, S.R.; Presser, S.C.; Ditkoff, E.C.; Vijod, M.A.; Stanczyk, F.Z.; Lobo, R.A. A possible bimodal effect of estrogen on insulin sensitivity in postmenopausal women and the attenuating effect of added progestin. Fertil. Steril. 1993, 60, 664–667. [Google Scholar]
- Putz, O.; Schwartz, C.B.; LeBlanc, G.A.; Cooper, R.L.; Prins, G.S. Neonatal low- and high-dose exposure to estradiol benzoate in the male rat: II. Effects on male puberty and the reproductive tract. Biol. Reprod. 2001, 65, 1506–1517. [Google Scholar]
- vom Saal, F.S.; Timms, B.G.; Montano, M.M.; Palanza, P.; Thayer, K.A.; Nagel, S.C.; Dhar, M.D.; Ganjam, V.K.; Parmigiani, S.; Welshons, W.V. Prostate enlargement in mice due to fetal exposure to low doses of estradiol or diethylstilbestrol and opposite effects at high doses. Proc. Natl. Acad. Sci. U.S.A. 1997, 94, 2056–2061. [Google Scholar]
- Putz, O.; Schwartz, C.B.; Kim, S.; LeBlanc, G.A.; Cooper, R.L.; Prins, G.S. Neonatal low- and high-dose exposure to estradiol benzoate in the male rat: I. Effects on the prostate gland. Biol. Reprod. 2001, 65, 1496–1505. [Google Scholar]
- Welshons, W.V.; Thayer, K.A.; Judy, B.M.; Taylor, J.A.; Curran, E.M.; vom Saal, F.S. Large effects from small exposures. I. Mechanisms for endocrine-disrupting chemicals with estrogenic activity. Environ. Health Perspect. 2003, 111, 994–1006. [Google Scholar]
- Amara, J.F.; Dannies, P.S. 17 beta-Estradiol has a biphasic effect on gh cell growth. Endocrinology 1983, 112, 1141–1143. [Google Scholar]
- Manni, A.; Badger, B.; Wright, C.; Ahmed, S.R.; Demers, L.M. Effects of progestins on growth of experimental breast cancer in culture: Interaction with estradiol and prolactin and involvement of the polyamine pathway. Cancer Res. 1987, 47, 3066–3071. [Google Scholar]
- Cheng, J.; Ma, X.; Zhang, J.; Su, D. Diverse modulating effects of estradiol and progesterone on the monophasic action potential duration in Langendorff-perfused female rabbit hearts. Fundam. Clin. Pharmacol. 2011. [Google Scholar] [CrossRef]
- Li, W.; Zheng, T.; Altura, B.M.; Altura, B.T. Sex steroid hormones exert biphasic effects on cytosolic magnesium ions in cerebral vascular smooth muscle cells: Possible relationships to migraine frequency in premenstrual syndromes and stroke incidence. Brain Res. Bull. 2001, 54, 83–89. [Google Scholar]
- Andreen, L.; Nyberg, S.; Turkmen, S.; van Wingen, G.; Fernandez, G.; Backstrom, T. Sex steroid induced negative mood may be explained by the paradoxical effect mediated by GABAA modulators. Psychoneuroendocrinology 2009, 34, 1121–1132. [Google Scholar]
- Melchior, C.L.; Ritzmann, R.F. Pregnenolone and pregnenolone sulfate, alone and with ethanol, in mice on the plus-maze. Pharmacol. Biochem. Behav. 1994, 48, 893–897. [Google Scholar]
- Chetrite, G.S.; Ebert, C.; Wright, F.; Philippe, A.C.; Pasqualini, J.R. Control of sulfatase and sulfotransferase activities by medrogestone in the hormone-dependent MCF-7 and T-47D human breast cancer cell lines. J. Steroid Biochem. Mol. Biol. 1999, 70, 39–45. [Google Scholar]
- Gilmore, W.; Weiner, L.P.; Correale, J. Effect of estradiol on cytokine secretion by proteolipid protein-specific T cell clones isolated from multiple sclerosis patients and normal control subjects. J. Immunol. 1997, 158, 446–451. [Google Scholar]
- Holladay, S.D.; Ehrich, M.; Gogal, R.M., Jr. Commentary on hormetic dose-response relationships in immunology: Occurrence, quantitative features of the dose response, mechanistic foundations, and clinical implications. Crit. Rev. Toxicol. 2005, 35, 299–302. [Google Scholar]
- Correale, J.; Arias, M.; Gilmore, W. Steroid hormone regulation of cytokine secretion by proteolipid protein-specific CD4+ T cell clones isolated from multiple sclerosis patients and normal control subjects. J. Immunol. 1998, 161, 3365–3374. [Google Scholar]
- Chao, T.C.; van Alten, P.J.; Greager, J.A.; Walter, R.J. Steroid sex hormones regulate the release of tumor necrosis factor by macrophages. Cell Immunol. 1995, 160, 43–49. [Google Scholar]
- Straub, R.H. The complex role of estrogens in inflammation. Endocr. Rev. 2007, 28, 521–574. [Google Scholar]
- Strom, J.O.; Theodorsson, A.; Theodorsson, E. Mechanisms of estrogens' dose-dependent neuroprotective and neurodamaging effects in experimental models of cerebral ischemia. Int. J. Mol. Sci. 2011, 12, 1533–1562. [Google Scholar]
- Toung, T.K.; Hurn, P.D.; Traystman, R.J.; Sieber, F.E. Estrogen decreases infarct size after temporary focal ischemia in a genetic model of type 1 diabetes mellitus. Stroke 2000, 31, 2701–2706. [Google Scholar]
- Yang, S.H.; Shi, J.; Day, A.L.; Simpkins, J.W. Estradiol exerts neuroprotective effects when administered after ischemic insult. Stroke 2000, 31, 745–749, discussion 749-750. [Google Scholar]
- Wise, P.M.; Dubal, D.B. Estradiol protects against ischemic brain injury in middle-aged rats. Biol. Reprod. 2000, 63, 982–985. [Google Scholar]
- Strom, J.O.; Theodorsson, E.; Theodorsson, A. Order of magnitude differences between methods for maintaining physiological 17beta-oestradiol concentrations in ovariectomized rats. Scand. J. Clin. Lab Invest. 2008, 68, 814–822. [Google Scholar]
- Theodorsson, A.; Hilke, S.; Rugarn, O.; Linghammar, D.; Theodorsson, E. Serum concentrations of 17beta-estradiol in ovariectomized rats during two times six weeks crossover treatment by daily injections in comparison with slow-release pellets. Scand. J. Clin. Lab Invest. 2005, 65, 699–705. [Google Scholar]
- Duckles, S.P.; Krause, D.N. Cerebrovascular effects of oestrogen: Multiplicity of action. Clin. Exp. Pharmacol. Physiol. 2007, 34, 801–808. [Google Scholar]
- Brown, C.M.; Suzuki, S.; Jelks, K.A.; Wise, P.M. Estradiol is a potent protective, restorative, and trophic factor after brain injury. Semin. Reprod. Med. 2009, 27, 240–249. [Google Scholar]
- Anderson, G.L.; Limacher, M.; Assaf, A.R.; Bassford, T.; Beresford, S.A.; Black, H.; Bonds, D.; Brunner, R.; Brzyski, R.; Caan, B.; et al. Effects of conjugated equine estrogen in postmenopausal women with hysterectomy: The Women's Health Initiative randomized controlled trial. JAMA 2004, 291, 1701–1712. [Google Scholar]
- Nicot, A. Gender and sex hormones in multiple sclerosis pathology and therapy. Front. Biosci. 2009, 14, 4477–4515. [Google Scholar]
- Polan, M.L.; Daniele, A.; Kuo, A. Gonadal steroids modulate human monocyte interleukin-1 (IL-1) activity. Fertil. Steril. 1988, 49, 964–968. [Google Scholar]
- Nordell, V.L.; Scarborough, M.M.; Buchanan, A.K.; Sohrabji, F. Differential effects of estrogen in the injured forebrain of young adult and reproductive senescent animals. Neurobiol. Aging 2003, 24, 733–743. [Google Scholar]
- Johnson, A.B.; Sohrabji, F. Estrogen's effects on central and circulating immune cells vary with reproductive age. Neurobiol. Aging 2005, 26, 1365–1374. [Google Scholar]
- Santizo, R.A.; Anderson, S.; Ye, S.; Koenig, H.M.; Pelligrino, D.A. Effects of estrogen on leukocyte adhesion after transient forebrain ischemia. Stroke 2000, 31, 2231–2235. [Google Scholar]
- Suzuki, S.; Brown, C.M.; Dela Cruz, C.D.; Yang, E.; Bridwell, D.A.; Wise, P.M. Timing of estrogen therapy after ovariectomy dictates the efficacy of its neuroprotective and antiinflammatory actions. Proc. Natl. Acad. Sci. USA 2007, 104, 6013–6018. [Google Scholar]
- Chiappetta, O.; Gliozzi, M.; Siviglia, E.; Amantea, D.; Morrone, L.A.; Berliocchi, L.; Bagetta, G.; Corasaniti, M.T. Evidence to implicate early modulation of interleukin-1beta expression in the neuroprotection afforded by 17beta-estradiol in male rats undergone transient middle cerebral artery occlusion. Int. Rev. Neurobiol. 2007, 82, 357–372. [Google Scholar]
- Libby, P.; Ridker, P.M.; Hansson, G.K. Inflammation in atherosclerosis: From pathophysiology to practice. J. Am. Coll. Cardiol. 2009, 54, 2129–2138. [Google Scholar]
- Jiang, B.; Liao, R. The paradoxical role of inflammation in cardiac repair and regeneration. J. Cardiovasc. Transl. Res. 2010, 3, 410–416. [Google Scholar]
- Puia, G.; Ducic, I.; Vicini, S.; Costa, E. Does neurosteroid modulatory efficacy depend on GABAA receptor subunit composition? Recept. Channels 1993, 1, 135–142. [Google Scholar]
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