Short- and long-term influences of hypoxia during early postnatal period of development on behavioral and hormonal responses in rats

Neuroscience Letters

Volumn 464, Issue 3, 2009, Pages 214-217

  Mikhailenko, Victor A ^a   Butkevich, Irina P ^a   Bagaeva, Tatyana R ^a   Makukhina, Galina V ^a   Otellin, Vladimir A ^a  

^a PAVLOV INSTITUTE OF PHYSIOLOGY   (Russian Federation)

Author keywords

Corticosterone; Depression; Hypoxia; Infant rats; Pain

Indexed keywords

CORTICOSTERONE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BEHAVIOR DISORDER; CONTROLLED STUDY; CORTICOSTERONE BLOOD LEVEL; DEPRESSION; FORCED SWIMMING TEST; HORMONE RESPONSE; HYPOXIA; IMMOBILIZATION; MALE; NEUROENDOCRINE SYSTEM; NONHUMAN; PAIN; PERINATAL PERIOD; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; RAT;

AGING; ANIMALS; ANIMALS, NEWBORN; ANOXIA; BEHAVIOR, ANIMAL; CORTICOSTERONE; DEPRESSION; PAIN; PAIN MEASUREMENT; RATS; RATS, WISTAR; STRESS, PSYCHOLOGICAL; TIME FACTORS;

EID: 70249088421     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neulet.2009.08.047     Document Type: Article

References (20)

1. Butkevich I.P., Barr G.A., and Vershinina E.A. Sex differences in formalin-induced pain in prenatally stressed infant rats. Eur. J. Pain 11 (2007) 888-894
2. Butkevich I.P., and Vershinina E.A. Maternal stress differently alters nociceptive behaviors in the formalin test in adult female and male rats. Brain Res. 961 (2003) 159-165
3. Detke M.J., Rickels M., and Lucki I. Active behaviors in the rat forced swimming test differentially produced by serotonergic and noradrenergic antidepressants. Psychopharmacology (Berl.) 121 (1995) 66-72
4. Filaretova L.P., Filaretov A.A., and Makara G.B. Corticosterone increase inhibits stress-induced gastric erosions in rats. Am. J. Physiol.: Gastrointest. Liver Physiol. 274 (1998) G1024-G1030
5. Grino M., Burgunder J.M., Eskay R.L., and Eiden L.E. Onset of glucocorticoid responsiveness of anterior pituitary corticotrophs during development is scheduled by corticotrophin-releasing factor. Endocrinology 124 (1989) 2686-2692
6. Jensen F.E. The role of glutamate receptor maturation in perinatal seizures and brain injury. Int. J. Dev. Neurosci. 20 (2002) 339-347
7. King T.E., and Barr G.A. Spinal cord ionotropic glutamate receptors function in formalin-induced nociception in preweaning rats. Psychopharmacology (Berl.) 192 (2007) 489-498
8. Lanoir J., Hilaire G., and Self I. Reduced density of functional 5-HT1A receptors in the brain, medulla and spinal cord of monoamine oxidase-a knockout mouse neonates. J. Comp. Neurol. 495 (2006) 607-623
9. Liu D., Diorio J., Tannenbaum B., Caldji C., Francis D., and Freedman A. Maternal care, hippocampal glucocorticoid receptors, and hypothalamic-pituitary-adrenal responses to stress. Science 277 (1997) 1659-1662
10. Mikhaǐlenko V.A., Butkevich I.P., Vershinina E.A., and Semenov P.O. Relationships between indices of persistent inflammatory pain response and the level of depression in prenatally stressed rats. Ross. Fiziol. Zh. Im. I. M. Sechenova 94 (2008) 1384-1392
11. Morley-Fletcher S., Darnaudery M., Koehl M., Casolini P., Van Reeth O., and Maccari S. Prenatal stress in rats predicts immobility behavior in the forced swim test. Effects of a chronic treatment with tianeptine. Brain Res. 989 (2003) 246-251
12. Northington F.J. Brief update on animal models of hypoxic-ischemic encephalopathy and neonatal stroke. ILAR J. 47 (2006) 32-38
13. Porsolt R.D., LePichon M., and Jalfre M. Depression: a new animal model sensitive to antidepressant treatments. Nature 266 (1977) 730-732
14. Raff H., Lee J.J., Widmaier E.P., Oaks M.K., and Engeland W.C. Basal and adrenocorticotropin-stimulated corticosterone in the neonatal rat exposed to hypoxia from birth: modulation by chemical sympathectomy. Endocrinology 145 (2004) 79-86
15. Rybnikova E., Vataeva L., Tyulkova E., Gluschenko T., Otellin V., Pelto-Huikko M., and Samoilov M. Mild hypoxia preconditioning prevents impairment of passive avoidance learning and suppression of brain NGFI-a expression induced by severe hypoxia. Behav. Brain Res. 160 (2005) 107-114
16. Vataeva L.A., Otellin V.A., Kassil' V.G., Kostkin V.B., Korzhevskiǐ D.E., Khozhaǐ L.I., and Gonchar V.S. Effect of hypoxia on early postnatal ontogenesis of rats: brain development and formation of behavior. Dokl. Acad. Nauk. 383 (1998) 409-411
17. Veenema A.H., Meijer O.C., de Kloet E.R., and Koolhaas J.M. Genetic selection for coping style predicts stressor susceptibility. J. Neuroendocrinol. 15 (2003) 256-267
18. Viggiano D. The hyperactive syndrome: metanalysis of genetic alterations, pharmacological treatments and brain lesions which increase locomotor activity. Behav. Brain Res. 194 (2008) 1-14
19. Walker C.D., Perin M., Vale W., and Rivier C. Ontogeny of the stress response in the rat: role of the pituitary and the hypothalamus. Endocrinology 118 (1986) 1445-1451
20. Yager J.Y., and Ashwal S. Animal models of perinatal hypoxic-ischemic brain damage. Pediatr. Neurol. 40 (2009) 156-167