Skip to main content

Advertisement

Log in

Beneficial effects of melatonin in a rat model of sporadic Alzheimer’s disease

  • Research Article
  • Published:
Biogerontology Aims and scope Submit manuscript

Abstract

Melatonin synthesis is disordered in patients with Alzheimer’s disease (AD). To determine the role of melatonin in the pathogenesis of AD, suitable animal models are needed. The OXYS rats are an experimental model of accelerated senescence that has also been proposed as a spontaneous rat model of AD-like pathology. In the present study, we demonstrate that disturbances in melatonin secretion occur in OXYS rats at 4 months of age. These disturbances occur simultaneously with manifestation of behavioral abnormalities against the background of neurodegeneration and alterations in hormonal status but before the signs of amyloid-β accumulation. We examined whether oral administration of melatonin could normalize the melatonin secretion and have beneficial effects on OXYS rats before progression to AD-like pathology. The results showed that melatonin treatment restored melatonin secretion in the pineal gland of OXYS rats as well as the serum levels of growth hormone and IGF-1, the level of BDNF in the hippocampus and the healthy state of hippocampal neurons. Additionally, melatonin treatment of OXYS rats prevented an increase in anxiety and the decline of locomotor activity, of exploratory activity, and of reference memory. Thus, melatonin may be involved in AD progression, whereas oral administration of melatonin could be a prophylactic strategy to prevent or slow down the progression of some features of AD pathology.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6

Similar content being viewed by others

References

  • Allen SJ, Watson JJ, Shoemark DK, Barua NU, Patel NK (2013) GDNF, NGF and BDNF as therapeutic options for neurodegeneration. Pharmacol Therapeut 138:155–175

    Article  CAS  Google Scholar 

  • Andersen P, Morris R, Amaral D, Bliss T, O’Kneefe J (2007) The Hippocampus Book. Oxford University Press, Inc., New York

    Google Scholar 

  • Bubenik GA, Konturek SJ (2011) Melatonin and aging: prospects for human treatment. J Physiol Pharmacol 62:13–19

    CAS  PubMed  Google Scholar 

  • Castellano JM, Deane R, Gottesdiener AJ, Verghese PhB, Stewart FR, West T, Paoletti AC, Kasper TR, DeMattos RB, Zlokovic BV, Holtzman DM (2012) Low-density lipoprotein receptor overexpression enhances the rate of brain-to-blood Aβ clearance in a mouse model of β-amyloidosis. Proc Natl Acad Sci USA 109:15502–15507

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Durany N, Michel T, Kurt J, Cruz-Sánchez FF, Cervás-Navarro J, Reiderer P (2000) Brain-derived neurotrophic factor and neurotrophin-3 levels in Alzheimer’s disease brains. Int J Dev Neurosci 18:807–813

    Article  CAS  Google Scholar 

  • Esposito E, Cuzzocrea S (2010) Antiinflammatory activity of melatonin in central nervous system. Curr Neuropharmacol 8:228–242

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Hardeland R (2012) Melatonin in aging and disease—multiple consequences of reduced secretion, options and limits of treatment. Aging Dis 3:194–225

    PubMed Central  PubMed  Google Scholar 

  • Jenwitheesuk A, Nopparat C, Mukda S, Wongchitrat P, Govitrapong P (2014) Melatonin regulates aging and neurodegeneration through energy metabolism, epigenetics, autophagy and circadian rhythm pathways. Int J Mol Sci 15:16848–16884

    Article  PubMed Central  PubMed  Google Scholar 

  • Kolosova NG, Stefanova NA, Muraleva NA, Skulachev VP (2012) The mitochondria-targeted antioxidant SkQ1 but not N-acetylcysteine reverses aging-related biomarkers in rats. Aging (Albany NY) 4:686–694

    CAS  Google Scholar 

  • Kozhevnikova OS, Korbolina EE, Stefanova NA, Muraleva NA, Orlov YL, Kolosova NG (2013) Association of AMD-like retinopathy development with an Alzheimer’s disease metabolic pathway in OXYS rats. Biogerontology 14:753–762

    Article  CAS  PubMed  Google Scholar 

  • Lin L, Huang QX, Yang SS, Chu J, Wang JZ, Tian Q (2013) Melatonin in Alzheimer’s disease. Int J Mol Sci 14:14575–14593

    Article  PubMed Central  PubMed  Google Scholar 

  • Moodly KK, Chan D (2014) The hippocampus in neurodegenerative disease. Front Neurol Neurosci 34:95–108

    Article  Google Scholar 

  • Nyberg F, Hallberg M (2013) Growth hormone and cognitive function. Nat Rev Endocrinol 9:357–365

    Article  CAS  PubMed  Google Scholar 

  • Paxinos G, Watson CH (2007) The rat brain in stereotaxic coordinates, 6th edn. Elsevier, Sydney

    Google Scholar 

  • Ramírez-Rodríguez G, Klempin F, Babu H, Benítez-King G, Kempermann G (2009) Melatonin modulates cell survival of new neurons in the hippocampus of adult mice. Neuropsychopharmacology 34:2180–2191

    Article  PubMed  Google Scholar 

  • Reichardt LF (2006) Neurotrophin-regulated signalling pathways. Philos Trans R Soc Lond B Biol Sci 361:1545–1564

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  • Sardi F, Fassina L, Venturini L, Inguscio M, Guerriero F, Rolfo E, Ricevuti G (2011) Alzheimer’s disease, autoimmunity and inflammation. The good, the bad and the ugly. Autoimmun Rev 11:149–153

    Article  CAS  PubMed  Google Scholar 

  • Shcheglova TV, Amstislavskaya TG, Kolosova NG (2002) Serotonin metabolism in the brain structures of prematurely ageing OXYS rats. Neurochemistry 19:269–273

    Google Scholar 

  • Snytnikova OA, Tsentalovich YP, Stefanova NA, Fursova AZh, Kaptein R, Sagdeev RZ, Kolosova NG (2012) The therapeutic effect of mitochondria-targeted antioxidant SkQ1 and Cistanche deserticola is associated with increased levels of tryptophan and kynurenine in the rat lenses. Dokl Biochem Biophys 447:300–303

    Article  CAS  PubMed  Google Scholar 

  • Stefanova NA, Fursova AZh, Kolosova NG (2010) Behavioral effects induced by mitochondria-targeted antioxidant SkQ1 in Wistar and senescence-accelerated OXYS rats. J Alzheimers Dis 21:479–491

    CAS  PubMed  Google Scholar 

  • Stefanova NA, Fursova AZh, Sarsenbaev KN, Kolosova NG (2011) Effects of Cistanche deserticola on behavior and signs of cataract and retinopathy in senescence-accelerated OXYS rats. J Ethnopharmacol 138:624–632

    Article  PubMed  Google Scholar 

  • Stefanova NA, Kozhevnikova OS, Vitovtov AO, Maksimova KYi, Logvinov SV, Rudnitskaya EA, Korbolina EE, Muraleva NA, Kolosova NG (2014a) Senescence-accelerated OXYS rats: a model of age-related cognitive decline with relevance to abnormalities in Alzheimer disease. Cell Cycle 13:1–12

    Article  Google Scholar 

  • Stefanova NA, Muraleva NA, Skulachev VP, Kolosova NG (2014b) Alzheimer’s disease-like pathology in senescence-accelerated OXYS rats can be partially retarded with mitochondria-targeted antioxidant SkQ1. J Alzheimers Dis 38:681–694

    CAS  PubMed  Google Scholar 

  • Wu YH, Swaab DF (2007) Disturbance and strategies for reactivation of the circadian rhythm system in aging and Alzheimer’s disease. Sleep Med 8:623–636

    Article  PubMed  Google Scholar 

  • Yanshole VV, Snytnikova OA, Kiryutin AS, Yanshole LV, Sagdeev RZ, Tsentalovich YP (2014) Metabolomics of the rat lens: a combined LC–MS and NMR study. Exp Eye Res 125:71–78

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

We thank Dr. Vadim V. Yanshole of the International Tomography Center SB RAS, for assistance with the liquid chromatography with mass spectrometry experiments. This work was supported by a grant from the Russian Foundation for Basic Research (project # 12-04-00091) and partially by grants from the government of the Russian Federation # 2012-220-03-435 and # 14.B25.31.0033. The mass spectrometric analysis involved financial support by the Russian Scientific Foundation (project # 14-14-00056).

Conflict of interest

The authors declare that they have no competing financial interests.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Natalia A. Stefanova.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Rudnitskaya, E.A., Maksimova, K.Y., Muraleva, N.A. et al. Beneficial effects of melatonin in a rat model of sporadic Alzheimer’s disease. Biogerontology 16, 303–316 (2015). https://doi.org/10.1007/s10522-014-9547-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10522-014-9547-7

Keywords

Navigation