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Neurochemical research2001; 26(3); 231-234; doi: 10.1023/a:1010964500370

High intensity light increases olfactory bulb melatonin in Venezuelan equine encephalitis virus infection.

Abstract: In mice infected with the Venezuelan equine encephalomyelitis (VEE) virus and exposed to high intensity light (2500 lux) with a 12 h light: 12 h dark photoperiod, a significant increase in the levels of melatonin in the olfactory bulb was observed. The significance of these findings deserves further studies to understand the mechanisms involved in this effect since the olfactory bulbs have been proposed as first portal for VEE virus entry into the CNS. The increase in melatonin content could represent one of the mechanisms of defense against the viral attack.
Publication Date: 2001-08-10 PubMed ID: 11495546DOI: 10.1023/a:1010964500370Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research aims to explore the effect of high-intensity light on mice infected with Venezuelan equine encephalomyelitis virus wherein an increase of melatonin levels in their olfactory bulb was observed.

Study Background

  • The research conducted is an exploration of the Venezuelan equine encephalomyelitis (VEE) virus in mice.
  • The VEE virus is a mosquito-borne viral pathogen that can cause severe inflammation of the brain and spinal cord in horses and humans.
  • The study focuses on the impact of high-intensity light (measuring 2500 lux) on infected mice, particularly concerning the levels of melatonin in the olfactory bulb.

Methodology

  • Infected mice were subjected to an environment with high-intensity light set in a photoperiod of 12 hours light to 12 hours dark.
  • Observations were made regarding any changes or effects presented in the melatonin levels of the infected mice’s olfactory bulb.

Findings

  • The experimental condition resulted in a significant increase in the levels of melatonin found in the olfactory bulb of the infected mice.
  • The olfactory bulb is proposed to be the first entry point of the VEE virus into the central nervous system (CNS). The increase in melatonin content could potentially indicate a defensive mechanism against the viral attack.

Significance and Future Implications

  • The findings of the study, despite being significant, require further investigation to fully comprehend the mechanisms responsible for this effect.
  • If the increase in melatonin content is confirmed to be a defensive mechanism, this could open doors for potential treatments or preventions for VEE virus infection in the future.

Cite This Article

APA
Medina-Leendertz S, Valero N, Chacín-Bonilla L, Añez F, Giraldoth D, Arias J, Espina G, Díaz S, Bonilla E. (2001). High intensity light increases olfactory bulb melatonin in Venezuelan equine encephalitis virus infection. Neurochem Res, 26(3), 231-234. https://doi.org/10.1023/a:1010964500370

Publication

ISSN: 0364-3190
NlmUniqueID: 7613461
Country: United States
Language: English
Volume: 26
Issue: 3
Pages: 231-234

Researcher Affiliations

Medina-Leendertz, S
  • Department of Neurobiology, INBIOMED-FUNDACITE-ZULIA, Maracaibo, Venezuela. smedina@hotmail.com
Valero, N
    Chacín-Bonilla, L
      Añez, F
        Giraldoth, D
          Arias, J
            Espina, G
              Díaz, S
                Bonilla, E

                  MeSH Terms

                  • Animals
                  • Circadian Rhythm
                  • Dose-Response Relationship, Radiation
                  • Encephalomyelitis, Venezuelan Equine / metabolism
                  • Encephalomyelitis, Venezuelan Equine / physiopathology
                  • Light
                  • Male
                  • Melatonin / metabolism
                  • Mice
                  • Olfactory Bulb / metabolism
                  • Olfactory Bulb / physiopathology
                  • Olfactory Bulb / radiation effects

                  References

                  This article includes 20 references
                  1. Tamarkin L, Baird CJ, Almeida OF. Melatonin: a coordinating signal for mammalian reproduction?. Science 1985 Feb 15;227(4688):714-20.
                    pubmed: 3881822doi: 10.1126/science.3881822google scholar: lookup
                  2. Bonilla E, Valero-Fuenmayor N, Pons H, Chacín-Bonilla L. Melatonin protects mice infected with Venezuelan equine encephalomyelitis virus.. Cell Mol Life Sci 1997 May;53(5):430-4.
                    pubmed: 9176561doi: 10.1007/s000180050051google scholar: lookup
                  3. Conti A, Conconi S, Hertens E, Skwarlo-Sonta K, Markowska M, Maestroni JM. Evidence for melatonin synthesis in mouse and human bone marrow cells.. J Pineal Res 2000 May;28(4):193-202.
                  4. Medina S, Valero-Fuenmayor N, Chacín-Bonilla L, Añez F, Giraldoth D, Arias J, Espina G, Achong AY, Bonilla E. Exposure to 2500 lux increases serum melatonin in Venezuelan equine encephalomyelitis.. Neurochem Res 1999 Jun;24(6):775-8.
                    pubmed: 10447461doi: 10.1023/a:1020735730869google scholar: lookup
                  5. Danes L, Rychterová V, Kliment V, Hrusková J. Penetration of Venezuelan equine encephalomyelitis virus into the brain of guinea pigs and rabbits after intranasal infection.. Acta Virol 1973 Mar;17(2):138-46.
                    pubmed: 4144277
                  6. Reiter RJ. Normal patterns of melatonin levels in the pineal gland and body fluids of humans and experimental animals.. J Neural Transm Suppl 1986;21:35-54.
                    pubmed: 3018145
                  7. Maestroni GJ, Cosentino M, Marino F, Togni M, Conti A, Lecchini S, Frigo G. Neural and endogenous catecholamines in the bone marrow. Circadian association of norepinephrine with hematopoiesis?. Exp Hematol 1998 Nov;26(12):1172-7.
                    pubmed: 9808057
                  8. Goldman BD, Darrow JM. The pineal gland and mammalian photoperiodism.. Neuroendocrinology 1983 Nov;37(5):386-96.
                    pubmed: 6316190doi: 10.1159/000123579google scholar: lookup
                  9. Pedersen CE Jr, Eddy GA. Separation, isolation, and immunological studies of the structural proteins of Venezuelan equine encephalomyelitis virus.. J Virol 1974 Oct;14(4):740-4.
                    pubmed: 4214289doi: 10.1128/JVI.14.4.740-744.1974google scholar: lookup
                  10. Ryzhikov AB, Ryabchikova EI, Sergeev AN, Tkacheva NV. Spread of Venezuelan equine encephalitis virus in mice olfactory tract.. Arch Virol 1995;140(12):2243-54.
                    pubmed: 8572944doi: 10.1007/BF01323243google scholar: lookup
                  11. Johnson RT, Mims CA. Pathogenesis of viral infections of the nervous system.. N Engl J Med 1968 Jan 4;278(1):23-30 contd.
                    pubmed: 4295224doi: 10.1056/NEJM196801042780106google scholar: lookup
                  12. Rollag MD, Niswender GD. Radioimmunoassay of serum concentrations of melatonin in sheep exposed to different lighting regimens.. Endocrinology 1976 Feb;98(2):482-9.
                    pubmed: 1248456doi: 10.1210/endo-98-2-482google scholar: lookup
                  13. Park SJ, Tokura H. Bright light exposure during the daytime affects circadian rhythms of urinary melatonin and salivary immunoglobulin A.. Chronobiol Int 1999 May;16(3):359-71.
                    pubmed: 10373104doi: 10.3109/07420529909116864google scholar: lookup
                  14. Azuma H, Yamatodani A, Yagi A, Nishimura T, Wada H. Influence of intensity of illumination during the light period on diurnal variations of pineal indoles in rats and mice.. Neurosci Lett 1990 Oct 30;119(1):15-8.
                    pubmed: 2097578doi: 10.1016/0304-3940(90)90744-tgoogle scholar: lookup
                  15. Vogel P, Abplanalp D, Kell W, Ibrahim MS, Downs MB, Pratt WD, Davis KJ. Venezuelan equine encephalitis in BALB/c mice: kinetic analysis of central nervous system infection following aerosol or subcutaneous inoculation.. Arch Pathol Lab Med 1996 Feb;120(2):164-72.
                    pubmed: 8712896
                  16. Lewy AJ, Sack RL, Miller LS, Hoban TM. Antidepressant and circadian phase-shifting effects of light.. Science 1987 Jan 16;235(4786):352-4.
                    pubmed: 3798117doi: 10.1126/science.3798117google scholar: lookup
                  17. Reiter RJ. Action spectra, dose-response relationships, and temporal aspects of light's effects on the pineal gland.. Ann N Y Acad Sci 1985;453:215-30.
                  18. Pévet P. The role of the pineal gland in the photoperiodic control of reproduction in different hamster species.. Reprod Nutr Dev (1980) 1988;28(2B):443-58.
                    pubmed: 3045927doi: 10.1051/rnd:19880310google scholar: lookup
                  19. Charles PC, Walters E, Margolis F, Johnston RE. Mechanism of neuroinvasion of Venezuelan equine encephalitis virus in the mouse.. Virology 1995 Apr 20;208(2):662-71.
                    pubmed: 7747437doi: 10.1006/viro.1995.1197google scholar: lookup
                  20. Reiter RJ. Pineal melatonin: cell biology of its synthesis and of its physiological interactions.. Endocr Rev 1991 May;12(2):151-80.
                    pubmed: 1649044doi: 10.1210/edrv-12-2-151google scholar: lookup

                  Citations

                  This article has been cited 2 times.
                  1. Cross KM, Landis DM, Sehgal L, Payne JD. Melatonin for the Early Treatment of COVID-19: A Narrative Review of Current Evidence and Possible Efficacy. Endocr Pract 2021 Aug;27(8):850-855.
                    doi: 10.1016/j.eprac.2021.06.001pubmed: 34119679google scholar: lookup
                  2. Bonilla E, Valero N, Chacín-Bonilla L, Medina-Leendertz S. Melatonin and viral infections. J Pineal Res 2004 Mar;36(2):73-9.