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Role of nitric oxide in hypoxia-induced hyperventilation and hypothermia: participation of the locus coeruleus
Fabris, G; Anselmo-Franci, J. A; Branco, L. G. S.
  • Fabris, G; Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Fisiologia.
  • Anselmo-Franci, J. A; Universidade de São Paulo. Faculdade de Odontologia de Ribeirão Preto. Departamento de Morfologia, Estomatologia e Fisiologia.
  • Branco, L. G. S; Universidade de São Paulo. Faculdade de Odontologia de Ribeirão Preto. Departamento de Morfologia, Estomatologia e Fisiologia.
Braz. j. med. biol. res ; 32(11): 1389-98, Nov. 1999. ilus, graf
Article in English | LILACS | ID: lil-248433
RESUMO
Hypoxia elicits hyperventilation and hypothermia, but the mechanisms involved are not well understood. The nitric oxide (NO) pathway is involved in hypoxia-induced hypothermia and hyperventilation, and works as a neuromodulator in the central nervous system, including the locus coeruleus (LC), which is a noradrenergic nucleus in the pons. The LC plays a role in a number of stress-induced responses, but its participation in the control of breathing and thermoregulation is unclear. Thus, in the present study, we tested the hypothesis that LC plays a role in the hypoxia-induced hypothermia and hyperventilation, and that NO is involved in these responses. Electrolytic lesions were performed bilaterally within the LC in awake unrestrained adult male Wistar rats weighing 250-350 g. Body temperature and pulmonary ventilation (VE) were measured. The rats were divided into 3 groups control (N = 16), sham operated (N = 7) and LC lesioned (N = 19), and each group received a saline or an NG-nitro-L-arginine methyl ester (L-NAME, 250 µg/µl) intracerebroventricular (icv) injection. No significant difference was observed between control and sham-operated rats. Hypoxia (7 per cent inspired O2) caused hyperventilation and hypothermia in both control (from 541.62 + or - 35.02 to 1816.18 + or - 170.7 and 36.3 + or - 0.12 to 34.4 + or - 0.09, respectively) and LC-lesioned rats (LCLR) (from 694.65 + or - 63.17 to 2670.29 + or - 471.33 and 36 + or - 0.12 to 35.3 + or - 0.12, respectively), but the increase in VE was higher (P<0.05) and hypothermia was reduced (P<0.05) in LCLR. L-NAME caused no significant change in VE or in body temperature under normoxia, but abolished both the hypoxia-induced hyperventilation and hypothermia. Hypoxia-induced hyperventilation was reduced in LCLR treated with L-NAME. L-NAME also abolished the hypoxia-induced hypothermia in LCLR. The present data indicate that hypoxia-induced hyperventilation and hypothermia may be related to the LC, and that NO is involved in these responses.
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Full text: Available Index: LILACS (Americas) Main subject: Locus Coeruleus / Hypoxia, Brain / Hyperventilation / Hypothermia / Nitric Oxide Limits: Animals Language: English Journal: Braz. j. med. biol. res Journal subject: Biology / Medicine Year: 1999 Type: Article / Congress and conference

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Full text: Available Index: LILACS (Americas) Main subject: Locus Coeruleus / Hypoxia, Brain / Hyperventilation / Hypothermia / Nitric Oxide Limits: Animals Language: English Journal: Braz. j. med. biol. res Journal subject: Biology / Medicine Year: 1999 Type: Article / Congress and conference