Neuroprotective FK506 does not alter in vivo nitric oxide production during ischemia and early reperfusion in rats

Thomas J. Toung, Anish Bhardwaj, Valina L. Dawson, Ted M. Dawson, Richard J. Traystman, Patricia D. Hurn

Research output: Contribution to journalArticle

51 Citations (Scopus)

Abstract

Background and Purpose - Previous studies have demonstrated that the immunosuppressant FK506 provides neuroprotection in experimental brain injury and suggest that this action may be mediated by suppression of neuronal nitric oxide synthase activation that occurs after ischemic depolarization. We sought to determine whether FK506 reduces histological injury after middle cerebral artery occlusion (MCAO) in the rat and whether the neuroprotective effect is mediated via suppression of in vivo nitric oxide (NO) production during ischemia or early reperfusion. Methods - Under controlled conditions of normoxia, normocarbia, and normothermia, halothane-anesthetized male Wistar rats were subjected to 2 hours of MCAO by the intraluminal occlusion technique in a blinded, randomized experimental trial. Ipsilateral parietal cortical laser-Doppler flowmetry was monitored throughout ischemia. Animals were randomly assigned to 4 pretreatment groups: intravenous FK506 0.3 mg/kg or 1.0 mg/kg, vehicle (cremaphor), or an equivalent volume of saline administered 30 minutes before MCAO. Infarction volume was assessed by a triphenyltetrazolium chloride staining at 22 hours of reperfusion. In separate experiments, microdialysis probes were placed bilaterally into the striatum. Rats were perfused with artificial cerebrospinal fluid containing 3 μmol/L [14C]-L-arginine for 3 hours and then subjected to 2 hours of right MCAO. Intravenous 0.3 mg/kg FK506 or cremaphor was given 30 minutes before right MCAO. Right-left differences between [14C]-L-citrulline in the effluent were assumed to reflect differences in NO production. Results - All values are mean±SE. FK506 at 0.3 mg/kg reduced infarction volume in cortex: 40±12 mm3 compared with saline (109±15 mm3) and cremaphor vehicle (148±23) (P<0.05). Striatal infarction was also reduced by low-dose FK506: 16±4 mm3 versus 36±4 mm3 and 34±4 mm3 in saline and vehicle groups, respectively (P<0.05). High-dose treatment reduced infarction volume in cortex (61±14 mm3, P<0.05 from saline and vehicle groups) and in striatum (22±5 mm3, P<0.05 from saline and vehicle groups). [14C]-L-citrulline recovery via microdialysis was markedly enhanced in ischemic compared with nonischemic striatum. However; ischemia-evoked [14C]-L-citrulline recovery was not different in FK506-treated rats compared with vehicle-treated animals. Conclusions - These data demonstrate that FK506 provides robust neuroprotection against transient focal cerebral ischemia in the rat. The mechanism of protection in vivo is not through attenuation of ischemia- evoked NO production during MCAO and early reperfusion.

Original languageEnglish (US)
Pages (from-to)1279-1285
Number of pages7
JournalStroke
Volume30
Issue number6
StatePublished - Jun 1999
Externally publishedYes

Fingerprint

Tacrolimus
Reperfusion
Middle Cerebral Artery Infarction
Nitric Oxide
Ischemia
Citrulline
Infarction
Microdialysis
Corpus Striatum
Nitric Oxide Synthase Type I
Laser-Doppler Flowmetry
Transient Ischemic Attack
Neuroprotective Agents
Halothane
Immunosuppressive Agents
Brain Injuries
Cerebrospinal Fluid
Arginine
Wistar Rats
Staining and Labeling

Keywords

  • Immunosuppressive agents
  • Microdialysis
  • Nitric oxide
  • Rats
  • Stroke

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine
  • Neuroscience(all)

Cite this

Toung, T. J., Bhardwaj, A., Dawson, V. L., Dawson, T. M., Traystman, R. J., & Hurn, P. D. (1999). Neuroprotective FK506 does not alter in vivo nitric oxide production during ischemia and early reperfusion in rats. Stroke, 30(6), 1279-1285.

Neuroprotective FK506 does not alter in vivo nitric oxide production during ischemia and early reperfusion in rats. / Toung, Thomas J.; Bhardwaj, Anish; Dawson, Valina L.; Dawson, Ted M.; Traystman, Richard J.; Hurn, Patricia D.

In: Stroke, Vol. 30, No. 6, 06.1999, p. 1279-1285.

Research output: Contribution to journalArticle

Toung, TJ, Bhardwaj, A, Dawson, VL, Dawson, TM, Traystman, RJ & Hurn, PD 1999, 'Neuroprotective FK506 does not alter in vivo nitric oxide production during ischemia and early reperfusion in rats', Stroke, vol. 30, no. 6, pp. 1279-1285.
Toung, Thomas J. ; Bhardwaj, Anish ; Dawson, Valina L. ; Dawson, Ted M. ; Traystman, Richard J. ; Hurn, Patricia D. / Neuroprotective FK506 does not alter in vivo nitric oxide production during ischemia and early reperfusion in rats. In: Stroke. 1999 ; Vol. 30, No. 6. pp. 1279-1285.
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AU - Toung, Thomas J.

AU - Bhardwaj, Anish

AU - Dawson, Valina L.

AU - Dawson, Ted M.

AU - Traystman, Richard J.

AU - Hurn, Patricia D.

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N2 - Background and Purpose - Previous studies have demonstrated that the immunosuppressant FK506 provides neuroprotection in experimental brain injury and suggest that this action may be mediated by suppression of neuronal nitric oxide synthase activation that occurs after ischemic depolarization. We sought to determine whether FK506 reduces histological injury after middle cerebral artery occlusion (MCAO) in the rat and whether the neuroprotective effect is mediated via suppression of in vivo nitric oxide (NO) production during ischemia or early reperfusion. Methods - Under controlled conditions of normoxia, normocarbia, and normothermia, halothane-anesthetized male Wistar rats were subjected to 2 hours of MCAO by the intraluminal occlusion technique in a blinded, randomized experimental trial. Ipsilateral parietal cortical laser-Doppler flowmetry was monitored throughout ischemia. Animals were randomly assigned to 4 pretreatment groups: intravenous FK506 0.3 mg/kg or 1.0 mg/kg, vehicle (cremaphor), or an equivalent volume of saline administered 30 minutes before MCAO. Infarction volume was assessed by a triphenyltetrazolium chloride staining at 22 hours of reperfusion. In separate experiments, microdialysis probes were placed bilaterally into the striatum. Rats were perfused with artificial cerebrospinal fluid containing 3 μmol/L [14C]-L-arginine for 3 hours and then subjected to 2 hours of right MCAO. Intravenous 0.3 mg/kg FK506 or cremaphor was given 30 minutes before right MCAO. Right-left differences between [14C]-L-citrulline in the effluent were assumed to reflect differences in NO production. Results - All values are mean±SE. FK506 at 0.3 mg/kg reduced infarction volume in cortex: 40±12 mm3 compared with saline (109±15 mm3) and cremaphor vehicle (148±23) (P<0.05). Striatal infarction was also reduced by low-dose FK506: 16±4 mm3 versus 36±4 mm3 and 34±4 mm3 in saline and vehicle groups, respectively (P<0.05). High-dose treatment reduced infarction volume in cortex (61±14 mm3, P<0.05 from saline and vehicle groups) and in striatum (22±5 mm3, P<0.05 from saline and vehicle groups). [14C]-L-citrulline recovery via microdialysis was markedly enhanced in ischemic compared with nonischemic striatum. However; ischemia-evoked [14C]-L-citrulline recovery was not different in FK506-treated rats compared with vehicle-treated animals. Conclusions - These data demonstrate that FK506 provides robust neuroprotection against transient focal cerebral ischemia in the rat. The mechanism of protection in vivo is not through attenuation of ischemia- evoked NO production during MCAO and early reperfusion.

AB - Background and Purpose - Previous studies have demonstrated that the immunosuppressant FK506 provides neuroprotection in experimental brain injury and suggest that this action may be mediated by suppression of neuronal nitric oxide synthase activation that occurs after ischemic depolarization. We sought to determine whether FK506 reduces histological injury after middle cerebral artery occlusion (MCAO) in the rat and whether the neuroprotective effect is mediated via suppression of in vivo nitric oxide (NO) production during ischemia or early reperfusion. Methods - Under controlled conditions of normoxia, normocarbia, and normothermia, halothane-anesthetized male Wistar rats were subjected to 2 hours of MCAO by the intraluminal occlusion technique in a blinded, randomized experimental trial. Ipsilateral parietal cortical laser-Doppler flowmetry was monitored throughout ischemia. Animals were randomly assigned to 4 pretreatment groups: intravenous FK506 0.3 mg/kg or 1.0 mg/kg, vehicle (cremaphor), or an equivalent volume of saline administered 30 minutes before MCAO. Infarction volume was assessed by a triphenyltetrazolium chloride staining at 22 hours of reperfusion. In separate experiments, microdialysis probes were placed bilaterally into the striatum. Rats were perfused with artificial cerebrospinal fluid containing 3 μmol/L [14C]-L-arginine for 3 hours and then subjected to 2 hours of right MCAO. Intravenous 0.3 mg/kg FK506 or cremaphor was given 30 minutes before right MCAO. Right-left differences between [14C]-L-citrulline in the effluent were assumed to reflect differences in NO production. Results - All values are mean±SE. FK506 at 0.3 mg/kg reduced infarction volume in cortex: 40±12 mm3 compared with saline (109±15 mm3) and cremaphor vehicle (148±23) (P<0.05). Striatal infarction was also reduced by low-dose FK506: 16±4 mm3 versus 36±4 mm3 and 34±4 mm3 in saline and vehicle groups, respectively (P<0.05). High-dose treatment reduced infarction volume in cortex (61±14 mm3, P<0.05 from saline and vehicle groups) and in striatum (22±5 mm3, P<0.05 from saline and vehicle groups). [14C]-L-citrulline recovery via microdialysis was markedly enhanced in ischemic compared with nonischemic striatum. However; ischemia-evoked [14C]-L-citrulline recovery was not different in FK506-treated rats compared with vehicle-treated animals. Conclusions - These data demonstrate that FK506 provides robust neuroprotection against transient focal cerebral ischemia in the rat. The mechanism of protection in vivo is not through attenuation of ischemia- evoked NO production during MCAO and early reperfusion.

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