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. 2002 Nov 13;24(1):47–53. doi: 10.1016/0165-5728(89)90097-0

β-Endorphin alters a viral induced central nervous system disease in normal mice but not in nude mice

Sharon C Doll 1, Terry C Johnson 1,
PMCID: PMC7119888  PMID: 2553770

Abstract

A single intracerebroventricular injection of 100 ng of β-endorphin altered the course of the central nervous system (CNS) infection of a temperature-sensitive mutant of vesicular stomatitis virus (VSV), tsG31-KS5. When mice were administered β-endorphin and then 24 h later infected intracerebrally with tsG31-Ks5 VSV, 70% of the animals died within 8 days of infection. In comparison, less than 10% of the animals had died after 21 days when infected with tsG31-KS5 VSV alone. When mice were injected with β-endorphin and tsG31-KS5 VSV simultaneously, or with β-endorphin 21 days after infection, the more aggressive clinical disease was not observed. Superficially, the more lethal disease induced by β-endorphin appeared to be a result of a mild hypothermia caused by the neuropeptide. β-Endorphin, however, did not influence the disease in nude (nu/nu) mice even though their core temperatures were reduced to an extent similar to that of BALB/c (+/+) mice, implicating the involvement of T lymphocytes in the alteration of the course of infection in normal mice.

Keywords: Endorphin-β, Central nervous system disease, Neuropeptide, Vesicular stomatitis virus, temperature-sensitive, Athymic nude mouse

References

  1. Angeletti R.H., Hickey W.F. A neuroendocrine marker in tissues of the immune system. Science. 1985;230:89–90. doi: 10.1126/science.3898368. [DOI] [PubMed] [Google Scholar]
  2. Dal Canto M.C., Rabinowitz S.G., Johnson T.C., Hughes J.V. Ultrastructural-immunohistochemical evidence for a maturation defect of temperature-sensitive G31 vesicular stomatitis virus in murine spinal cord neurons. Infect. Immun. 1979;24:276–281. doi: 10.1128/iai.24.1.276-281.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Doll S.C., Johnson T.C. Neuropeptide-induced hypothermia and the course of central nervous system disease mediated by temperature-sensitive mutants of vesicular stomatitis virus. J. Virol. 1985;55:583–587. doi: 10.1128/jvi.55.3.583-587.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Doll S.C., Johnson T.C. Reconstitution with T-lymphocytes protects nude mice from a central nervous system disorder induced by a temperature-sensitive vesicular stomatitis virus. J. Gen. Virol. 1988;68:1969–1977. doi: 10.1099/0022-1317-69-8-1969. [DOI] [PubMed] [Google Scholar]
  5. Doll S.C., Johnson T.C. Proceedings of the New York Academy of Sciences Second International Congress of Neuroimmunology. 1989. A study of persistent viral infections using nude mice and a temperature-sensitive mutant of vesicular stomatitis virus. (in press) [DOI] [PubMed] [Google Scholar]
  6. Elizan T.S., Maker H., Yahr M.D. Neurotransmitter synthesizing enzymes in experimental viral encephalitis. J. Neural Transm. 1983;57:139–147. doi: 10.1007/BF01245114. [DOI] [PubMed] [Google Scholar]
  7. Esterling B., Rabin B.S. Stress-induced alteration of T-lymphocyte subsets and humoral immunity in mice. Behav. Neurosci. 1987;101:115–119. doi: 10.1037//0735-7044.101.1.115. [DOI] [PubMed] [Google Scholar]
  8. Fishman P.S., Gass J.S., Swoveland P.T., Lave E., Highkin M.D., Weiss S.R. Infection of the basal ganglia by a murine coronavirus. Science. 1985;229:877–879. doi: 10.1126/science.2992088. [DOI] [PubMed] [Google Scholar]
  9. Gilman S.C., Schwartz J.M., Milner R.J., Bloom F.E., Feldman J.D. Vol. 79. 1982. β-Endorphin enhances lymphocyte proliferative responses; pp. 4226–4230. (Proc. Natl. Acad. Sci. U.S.A.). [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Hall N.R., McGillis J.P., Spangelo B.L., Healy D.L., Goldstein A.L. Immunomodulatory peptides and the central nervous system. Springer Semin. Immunopathol. 1985;8:153–164. doi: 10.1007/BF00197253. [DOI] [PubMed] [Google Scholar]
  11. Hoffman-Goetz L., Keir R., Thorne R., Houston M.E., Young C. Chronic exercise stress in mice depresses splenic T lymphocyte mitogenesis in vitro. Clin. Exp. Immunol. 1986;66:551–557. [PMC free article] [PubMed] [Google Scholar]
  12. Horta-Barbosa L., Fuccillo D.A., Sever J.L., Zeman W. Subacute sclerosing panencephalitis: isolation of measles virus from a brain biopsy. Nature. 1969;221:974–976. doi: 10.1038/221974a0. [DOI] [PubMed] [Google Scholar]
  13. Hughes J.V., Doll S.C., Johnson T.C. Hypothermia-inducing peptide promotes recovery of vesicular stomatitis virus from persistent animal infections. Virol. 1985;53:781–785. doi: 10.1128/jvi.53.3.781-785.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Johnson R.T. Relapsing and remitting viral diseases of the nervous system. Trends Neurosci. 1984;7:207–209. [Google Scholar]
  15. Johnson T.C. Slow virus diseases. In: Youmans G., Paterson P., Sommers H., editors. The Biologic and Clinical Basis of Infectious Diseases. 3rd edn. W.B. Saunders; Philadelphia, PA: 1986. pp. 45–64. [Google Scholar]
  16. Kindred B. Deficient and sufficient immune systems in the nude mice. In: Gershwin M.E., Merchant B., editors. Immunologic Defects in Laboratory Animals. Plenum Press; New York: 1981. pp. 215–265. [Google Scholar]
  17. Millan M.J. Multiple opioid systems and pain. Pain. 1986;27:303–347. doi: 10.1016/0304-3959(86)90158-2. [DOI] [PubMed] [Google Scholar]
  18. Pringle C.R. The induction and genetic characterization of conditional lethal mutants of vesicular stomatitis virus induced by 5-fluorouracil, 5-azacytidine, and ethyl methane sulfonate. J. Virol. 1970;5:559–567. doi: 10.1128/jvi.5.5.559-567.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Puppo F., Corsini G., Mangini P., Bottaro L., Barreca T. Influence of β-endorphin on phytohemagglutinin-induced lymphocyte proliferation and on the expression of mononuclear cell surface antigens in vitro. Immunopharmacology. 1985;10:119–125. doi: 10.1016/0162-3109(85)90037-2. [DOI] [PubMed] [Google Scholar]
  20. Rabinowitz S.G., Dal Canto M.C., Johnson T.C. Comparison of central nervous system disease produced by wild-type and temperature-sensitive mutants of vesicular stomatitis virus. Infect. Immun. 1976;13:1242–1249. doi: 10.1128/iai.13.4.1242-1249.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Reichman M.F., Pringle C.R., Follet E.A.C. Defective particles in BHK cells infected with temperature-sensitive mutants of vesicular stomatitis virus. J. Virol. 1971;8:154–158. doi: 10.1128/jvi.8.2.154-160.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Roos R.P., Richards O.C., Green J., Ehrenfeld E. Characterization of a cell culture persistently infected with the DA strain of Theiler's murine encephalomyelitis virus. J. Virol. 1982;43:1118–1122. doi: 10.1128/jvi.43.3.1118-1122.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Shavit Y., Lewis J.W., Terman G.W., Gale R.P., Liebeskind J.C. Opioid peptides mediate the suppressive effect of stress on natural killer cell cytotoxicity. Science. 1984;223:188–190. doi: 10.1126/science.6691146. [DOI] [PubMed] [Google Scholar]
  24. Simpson R.W., McGinty L., Simon C.A., Smith C.A., Godzesik C.W., Boyd R.J. Association of parvoviruses with rheumatoid arthritis of humans. Science. 1984;223:1425–1428. doi: 10.1126/science.6701529. [DOI] [PubMed] [Google Scholar]
  25. Taylor J.W., Kaiser E.T. The structural characterization of β-endorphin and related peptide hormones and neurotransmitters. Pharmacol. Rev. 1986;38:291–319. [PubMed] [Google Scholar]
  26. Tseng L., Higgins M.J., Hong J., Hudson P.M., Fujimoto J.M. Release of immunoreactive Met-enkephalin from the spinal cord by intraventricular β-endorphin but not morphine in anesthetized rats. Brain Res. 1985;343:60–69. doi: 10.1016/0006-8993(85)91158-8. [DOI] [PubMed] [Google Scholar]
  27. Tyler K.L., Bronson R.T., Byers D.B., Fields B. Molecular basis of viral neurotropism: experimental reovirus infection. Neurology. 1985;35:88–92. doi: 10.1212/wnl.35.1.88. [DOI] [PubMed] [Google Scholar]
  28. Van Epps D.E., Saland L. β-Endorphin and met-enkephalin stimulate human peripheral blood mononuclear cell chemotaxis. J. Immunol. 1984;132:3046–3053. [PubMed] [Google Scholar]

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