Skip to main content
Log in

Adrenalectomy increases local cerebral blood flow in the rat hippocampus

  • Published:
Pflügers Archiv Aims and scope Submit manuscript

Abstract

The present study examined the effect of glucocorticoid manipulations on local cerebral blood flow in the hippocampus. We measured local cerebral blood flow in the hippocampus at 1-h intervals over a 1-day period in freely moving rats, by means of the H2 clearance method, before and after sham adrenalectomy, adrenalectomy or adrenalectomy with corticosterone replacement. We also measured local cerebral blood flow in the prefrontal cortex before and after adrenalectomy. Four weeks after the adrenalectomy, hippocampal blood flow at each time of day was an average of 47% greater than before the operation, showing diurnal variation as before. After the sham adrenalectomy or adrenalectomy with corticosterone replacement, hippocampal blood flow did not change significantly with respect to either its level or its diurnal variation. Local cerebral blood flow in the prefrontal cortex increased by only 19% after adrenalectomy. The present study demonstrates that adrenalectomy causes a remarkable increase in hippocampal blood flow, probably due to a lack of corticosterone.

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.

Similar content being viewed by others

References

  1. Albe-Fessard D, Stutinsky F, Libouban S (1966) Atlas stereotaxique du diencéphale de rat blanc. Centre National de la Recherche Scientifique, Paris

    Google Scholar 

  2. Bryan RM, King J (1988) Glucocorticoids modulate the effect of plasma epinephrine on regional glucose utilization. Soc Neurosci Abstr 14:997

    Google Scholar 

  3. Cheifetz P, Gaffud N, Dingman JF (1968) Effects of bilateral adrenalectomy and continuous light on the circadian rhythm of corticotropin in female rats. Endocrinology 82:1117–1124

    Google Scholar 

  4. Eckenstein F, Baughman RW (1984) Two types of cholinergic innervation in cortex, one co-localized with vasoactive intestinal polypeptide. Nature 309:153–155

    Google Scholar 

  5. Endo Y, Jin-nai J, Endo M, Fujita K, Kimura F (1990) Diurnal variation of cerebral blood flow in rat hippocampus. Stroke 21:1464–1469

    Google Scholar 

  6. Foreman DL, Sanders M, Bloor CM (1976) Total and regional cerebral blood flow during moderate and severe exercise in miniature swine. J Appl Physiol 40:191–195

    Google Scholar 

  7. Gilad GM, Mahon BD, Finkelstein Y, Koffler B, Gilad VH (1985) Stress-induced activation of the hippocampal cholinergic system and the pituitary-adrenocortical axis. Brain Res 347:404–408

    Google Scholar 

  8. Heistad DD, Marcus ML, Said SI, Gross PM (1980) Effect of acetylcholine and vasoactive intestinal peptide on cerebral blood flow. Am J Physiol 239: H73-H80

    Google Scholar 

  9. Heistad DD, Busija DW, Marcus ML (1981) Neural effects on cerebral vessels: alteration of pressure-flow relationship. Fed Proc 40:2317–2321

    Google Scholar 

  10. Hiroshige T (1974) Circadian rhythm of corticotropin-releasing activity in the rat hypothalamus: an attempt at physiological validation. In: Kawakami M (ed) Biological rhythm in neuroendocrine activity. Igaku Shoin Tokyo, pp 267–280

    Google Scholar 

  11. Hiroshige T, Sakakura M (1971) Circadian rhythm of corticotropin-releasing activity in the hypothalamus of normal and adrenalectomized rats. Neuroendocrinology 7:25–36

    Google Scholar 

  12. Joës M, de Kloet ER (1991) Effect of corticosteroid hormone on electrical activity in rat hippocampus. J Steroid Biochem Mol Biol 40:83–86

    Google Scholar 

  13. Kadekaro M, Ito M, Gross PM (1988) Local cerebral glucose utilization is increased in acutely adrenalectomized rats. Neuroendocrinology 47:329–334

    Google Scholar 

  14. Kety SS, Schmidt CF (1945) The determination of cerebral blood flow in man by the use of nitrous oxide in low concentrations. Am J Physiol 143:53–66

    Google Scholar 

  15. Khadouri C, Marsy S, Barlet-Bas C, Doucet A (1987) Effect of adrenalectomy on NEM-sensitive ATPase along rat nephron and on urinary acidification. Am J Physiol 253:F495-F499

    Google Scholar 

  16. Landfield PW, Waymire JC, Lynch G (1978) Hippocampal aging and adrenocorticoids: quantitative correlations. Science 202:1098–1102

    Google Scholar 

  17. Landfield PW, Baskin E, Pitler T (1981) Brain aging correlates: retardation by hormonal-pharmacological treatments. Science 214:581–584

    Google Scholar 

  18. Landgraf R, Mitro A, Hess J (1978) Regional net uptake of 14C-glucose by rat brain under the influence of corticosterone. Endocrinol Exp 12:119–129

    Google Scholar 

  19. Martin AJ, Friston KJ, Colebatch JG, Frackowiak RSJ (1991) Decrease in regional cerebral blood flow with normal aging. J Cereb Blood Flow Metab 11:684–689

    Google Scholar 

  20. McEwen BS, Gould E (1990) Adrenal steroid influences on the survival of hipocampal neurons. Biochem Pharmacol 40: 2393–2402

    Google Scholar 

  21. McEwen BS, de Kloet ER, Rostene W (1986) Adrenal steroid receptors and actions in the nervous system. Physiol Rev 66: 1121–1188

    Google Scholar 

  22. Meyer JS, Micco DJ, Stephenson BS, Krey LC, McEwen BS (1979) Subcutaneous implantation method for chronic glucocorticoid replacement therapy. Physiol Behav 22:867–870

    Google Scholar 

  23. Munck A, Guyre PM, Holbrook NJ (1984) Physiological functions of glucocorticoids in stress and their relation to pharmacological actions. Endocr Rev 5:25–44

    Google Scholar 

  24. Pfaff DW, Silva MT, Weiss JM (1971) Telemetered recording of hormone effects on hippocampal neurons. Science 172:394–395

    Google Scholar 

  25. Reichle ME (1987) Circulatory and metabolic correlates of brain function in normal humans. In: Mountcastle DB, Plum F & Geiger SR (eds) Handbook of physiology: the nervous system. Higher functions of the brain, section 1, vol. 5, part 2. American Physiological Society, Bethesda, pp 643–674

    Google Scholar 

  26. Reul JMHM, de Kloet ER (1985) Two receptor system for corticosterone in rat brain: microdistribution and differential occupation. Endocrinology 117: 2505–2511

    Google Scholar 

  27. Sapolsky RM (1985) A mechanism for glucocorticoid toxicity in the hippocampus: increased neuronal vulnerability to metabolic insults. J Neurosci 5:1228–1232

    Google Scholar 

  28. Sato A, Sato Y (1992) Regulation of regional cerebral blood flow by cholinergic fibers originating in the basal forebrain. Neurosci Res 14:242–274

    Google Scholar 

  29. Scremin OU, Rovere AA, Raynald AC, Giardini A (1973) Cholinergic control of blood flow in the cerebral cortex of the rat. Stroke 4:232–239

    Google Scholar 

  30. Sloviter RS, Valiquette G, Abrams GM, Ronk EC, Sollas AL, Paul LA, Neubort S (1989) Selective loss of hippocampal granule cells in the mature rat brain after adrenalectomy. Science 243:535–538

    Google Scholar 

  31. Takebe K, Sakakura M, Mashimo K (1972) Continuance of diurnal rhythmicity of CRF activity in hypophysectomized rats. Endocrinology 90:1515–1520

    Google Scholar 

  32. Van Den Berg DTWM, de Kloet ER, Van Dijken HH, De Jong W (1990) Differential central effects of mineralocorticoid and glucocorticoid agonists and antagonists on blood pressure. Endocrinology 126:118–124

    Google Scholar 

  33. Vidal C, Jordan W, Zieglgänsberger W (1986) Corticosterone reduces the excitability of hippocampal pyramidal cells in vitro. Brain Res 383:54–59

    Google Scholar 

  34. Wallis CJ, Gregory TJ, Printz MP (1982) Relationship between regional brain angiotensinogen and local blood flow and volume in the adrenalectomized rat: application of approach to quantification of brain corticosterone receptors. J Neurochem 39:111–116

    Google Scholar 

  35. Will PC, Barnett ME (1983) A sugar and electrolyte drinking solution for long-term maintenance of adrenalectomized rats. Lab Anim Sci 33:172–174

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Endo, Y., Nishimura, J.I. & Kimura, F. Adrenalectomy increases local cerebral blood flow in the rat hippocampus. Pflügers Arch. 426, 183–188 (1994). https://doi.org/10.1007/BF00374770

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00374770

Key words

Navigation