Heterogeneity of the infant stage of rat development: Inflammatory pain response, depression-related behavior, and effects of prenatal stress

Brain Research

Volumn 1286, Issue , 2009, Pages 53-59

  Butkevich, Irina P ^a   Mikhailenko, Victor A ^a   Vershinina, Elena A ^a   Semionov, Pavel O ^a   Otellin, Vladimir A ^a   Aloisi, Anna Maria ^b  

^a PAVLOV INSTITUTE OF PHYSIOLOGY   (Russian Federation)

^b UNIVERSITY OF SIENA   (Italy)

Author keywords

Body weight; Forced swim test; Formalin induced pain; Infant rats; Prenatal stress

Indexed keywords

FORMALDEHYDE;

ANIMAL BEHAVIOR; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BODY WEIGHT; BRAIN DEVELOPMENT; CONTROLLED STUDY; DEPRESSION; EMOTIONALITY; IMMOBILIZATION; MALE; MATURATION; NONHUMAN; ONTOGENY; PAIN; PERINATAL PERIOD; PRENATAL STRESS; PRIORITY JOURNAL; RAT;

ANIMALS; ANIMALS, NEWBORN; BODY WEIGHT; DEPRESSION; FEMALE; INFLAMMATION; MALE; PAIN; PREGNANCY; PRENATAL EXPOSURE DELAYED EFFECTS; RATS; RATS, WISTAR; STRESS, PSYCHOLOGICAL;

RATTUS;

EID: 68049093925     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.brainres.2009.06.055     Document Type: Article

References (52)

1. Alberts J.R. Infancy. In: Whishaw I.Q., and Kolb B. (Eds). The Behavior of the Laboratory Rat (2005), University Press, Oxford 266-277
2. Anand, K.J.S., 2006. Pain Clinical Updates IASP. XIV, 1-4.
3. Andrews M.H., and Matthews S.G. Programming of the hypothalamo-pituitary-adrenal axis: serotonergic involvement. Stress 7 (2004) 15-27
4. Baccei, M., Fitzgerald, M., 2006. Development of pain pathways and mechanisms. In: Wall and Melzack's Textbook of Pain. S.B. McMahon, M. Koltzenburg, eds. 5th ed. Elsevier, Amsterdam; Churchill Livingstone, London, pp. 143-158.
5. Barr G.A. Maturation of the biphasic behavioral and heart rate response in the formalin test. Pharmacol. Biochem. Behav. 60 (1998) 329-335
6. Bell J., Zhang X., and Whitaker-Azmitia P.M. 5-HT3 receptor-active drugs alter development of spinal serotonergic innervation: lack of effect of other serotonergic agents. Brain Res. 571 (1992) 293-297
7. Biones-Aranda A., Lopez-Rubalcava C., and Picazo O. Influence of forced swimming-induced stress on the anxiolytic-like effect of 5-HT(1A) agents in mice. Psychopharmacology (Berl.) 162 (2002) 147-155
8. Butkevich I.P., Barr G.A., and Otellin V.A. Effect of prenatal stress on behavioral and neural indices of formalin-induced pain in infant rats. Abstracts, 35st Annual Meeting of Soc. for Neurosci. N 512.4. Washington, DC: Society of Neuroscience (2005)
9. Butkevich I.P., Mikhailenko V.A., Vershinina E.A., Khozhai L.I., Grigorev I.P., and Otellin V.A. Reduced serotonin synthesis during early embryogeny changes effect of subsequent prenatal stress on persistent pain in the formalin test in adult male and female rats. Brain Res. 1042 (2005) 144-159
10. Butkevich I.P., Barr G.A., Mikhailenko V.A., and Otelllin V.A. Increased formalin-induced pain and expression of fos neurons in the lumbar spinal cord of prenatally stressed infant rats. Neurosci. Lett. 403 (2006) 222-226
11. Butkevich I.P., Mikhailenko V.A., Khozhai L.I., and Otellin V.A. Pain sensitivity during ontogeny and long-term effects of prenatal noxious events. In: Hodgson D.M., and Coe C.L. (Eds). Perinatal Programming. Early Life Determinants of Adult Health and Disease (2006), Taylor and Francis, London and New York 211-222
12. 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
13. Butkevich I.P., Mikhailenko V.A., Vershinina E.A., and Otellin V.A. Prenatal imbalance between serotonergic and hypothalamo-pituitary-adrenocortical systems and body weight during different periods of rat ontogeny. Dokl. Biol. Sci. 422 (2008) 1-4
14. Butkevich I., Mikhailenko V., Semionov P., Bagaeva T., Otellin V., and Aloisi A.M. Effects of maternal corticosterone and stress on behavioral and hormonal indices of formalin pain in male and female offspring of different ages. Horm. Behav. 55 (2009) 149-157
15. Capone F., and Aloisi A.M. Refinement of pain evaluation techniques. The formalin test. Ann. 1st Super Sanità 40 (2004) 223-229
16. Dubuisson D., and Dennis S.G. The formalin test: a quantitative study of the analgesic effects of morphine, meperidine and brain stimulation in rats and cats. Pain 4 (1977) 161-174
17. Fitzgerald M. Developmental biology of inflammatory pain. Br. J. Anaesthesia 75 (1995) 177-185
18. Fitzgerald M. The development of nociceptive circuits. Nat. Rev., Neurosci. 6 (2005) 507-520
19. Fitzgerald M. Infant pain traces. Pain 125 (2006) 204-205
20. Fitzgerald M., and Beggs S. The neurobiology of pain: developmental aspects. Neuroscience 7 (2001) 246-257
21. Fitzgerald M., and Koltzenburg M. The functional development of descending inhibitory pathways in the dorsolateral funiculus of the newborn rat cord. Brain Res. 389 (1986) 261-270
22. 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 corticotropin-releasing factor. Endocrinology 124 (1989) 2686-2692
23. Grunau R.V., Whitfield M.F., Petrie J.H., and Fryer E.L. Early pain experience, child and family factors, as precursors of somatization: a prospective study of extremely premature and full-term children. Pain 56 (1994) 353-359
24. Guy E.R., and Abbott F.V. The behavioral response to formalin in preweanling rats. Pain 51 (1992) 81-90
25. Hayashi A., Nagaoka M., Yamada K., Ichitani Y., Miake Y., and Okado N. Maternal stress induces synaptic loss and developmental disabilities of offspring. Int. J. Dev. Neurosci. 16 (1998) 209-216
26. Hill M.N., Brotto L.A., Lee T.T., and Gorzalka B.B. Corticosterone attenuates the antidepressant-like effects elicited by melatonin in the forced swim test in both male and female rats. Prog. Neuropsychopharmacol. Biol. Psychiatry. 27 (2003) 905-911
27. Huizink A.C., Mulder E.J., and Buitelaar J.K. Prenatal stress and risk for psychopathology: specific effects or induction of general susceptibility?. Psychol. Bull. 130 (2004) 115-142
28. Jacobs B.L., and Azmitia E.C. Structure and function of the brain serotonin system. Physiol. Rev. 72 (1992) 165-229
29. Karandrea D., Kittas C., and Kitraki E. Forced swimming differentially affects male and female brain corticosteroid receptors. Neuroendocrinology 75 (2002) 217-226
30. 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
31. King T.E., Cheng J., Wang S., and Barr G.A. Maturation of NK1 receptor involvement in the nociceptive response to formalin. Synapse 36 (2000) 254-266
32. 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. Compar. Neurol. 495 (2006) 607-623
33. Larsson B.A. Pain and pain relief during the neonatal period. Early pain experiences can result in negative late-effects. Lakartidningen 98 (2001) 1656-1662
34. Leibowitz S.F., and Alexander J.T. Hypothalamic serotonin in control of eating behavior, meal size, and body weight. Biol. Psychiatry 44 (1998) 851-864
35. Maccari S., and Morley-Fletcher S. Effects of prenatal restraint stress on the hypothalamus-pituitary-adrenal axis and related behavioral and neurobiological alterations. Psychoendocrinology Suppl. 1 (2007) S10-S15
36. McCleane G. Antidepressants as analgesics. CNS Drugs 22 (2008) 139-156
37. Mico J.A., Berrocoso E., Ortega-Alvaro A., Gibert-Rahola J., and Rojas-Corrales M.O. The role of 5-HT1A receptors in research strategy for extensive pain treatment. Curr. Top. Med. Chem. 6 (2006) 1997-2003
38. 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
39. Porsolt R.D., LePichon M., and Jalfre M. Depression: a new animal model sensitive to antidepressant treatments. Nature 266 (1977) 730-732
40. Praag H.M. Can stress cause depression?. World J. Biol. Psychiatry 6 Suppl. 2 (2005) 5-22
41. Pryce C.R. Postnatal ontogeny of expression of the corticosteroid receptor genes in mammalian brains: inter-species and intra-species differences. Brain Res. Rev. 57 (2008) 596-605
42. Rokyta R. Fetal pain. Neuroendocrinol. Lett. 29 (2008) 807-814
43. Seckl J.R. Prenatal glucocorticoids and long-term programming. Eur. J. Endocrinol. 151 Suppl. 3 (2004) 49-62
44. Seckl J.R. Glucocorticoids, developmental "programming" and the risk of affective dysfunction. Prog. Brain Res. 167 (2008) 17-34
45. Slotkin T.A., Barnes G.A., McCook E.C., and Seidler F.J. Programming of brainstem serotonin transporter development by prenatal glucocorticoids. Dev. Brain Res. 93 (1996) 155-161
46. Van den Hove D.L.A., Lauder J.M., Scheepens A., Prickaerts J., Blanco C.E., and Steinbusch H.W.M. Prenatal stress in the rat alters 5-HT1A receptor binding in the ventral hippocampus. Brain Res. 1090 (2006) 29-34
47. 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
48. Weinstock M. The potential influence of maternal stress hormones on development and mental health of the offspring. Brain Behav. Immun. 19 (2005) 296-308
49. Weinstock M. The role of prenatal stress in the programming of behavior. In: Hodgson D.M., and Coe C.L. (Eds). Perinatal Programming: Early Life Determinants of Adult Health and Disease (2006), Taylor and Francis, London, New York 241-252
50. Weinstock M. The long-term behavioural consequences of prenatal stress. Neurosci. Biobehav. Rev. 32 (2008) 1073-1086
51. Yi D.K., and Barr G.A. Formalin-induced c-fos expression in the spinal cord of fetal rats. Pain 73 (1997) 347-354
52. Zimmermann M. Ethical guidelines for investigations of experimental pain in conscious animals. Pain 16 (1983) 109-110