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. 2009 Apr 27;157(7):1157–1171. doi: 10.1111/j.1476-5381.2009.00196.x

Table 4.

Effect of NXY-059 on infarct volume by brain region subdivided by animal species and sex, and model of ischaemia

Group Experiments Animals Coefficient 95% CI P-value
Species
Total 18 442 −0.03 −0.04 to −0.02 <0.0001
Mice 1 9 −8.67 −19.69 to 2.36 0.12
Rats 15 401 −0.03 −0.04 to −0.02 <0.0001
Marmosets 2 32 −0.06 −0.10 to −0.01 0.01
Males 2 17 −0.02 −0.06 to 0.01 0.13
Females 2 15 −0.05 −0.09 to −0.005 0.03
Cortical 4 111 −0.08 −0.11 to −0.06 <0.0001
Rats 2 79 −0.13 −0.16 to −0.10 <0.0001
Marmosets 2 32 −0.04 −0.09 to 0.003 0.07
Males 2 17 −0.03 −0.10 to 0.03 0.32
Females 2 15 −0.04 −0.08 to 0.01 0.13
Subcortical 4 111 −0.10 −0.13 to −0.08 <0.0001
Rats 2 79 −0.13 −0.16 to −0.10 <0.0001
Marmosets 2 32 −0.07 −0.11 to −0.02 0.002
Males 2 17 −0.06 −0.13 to 0.01 0.11
Females 2 15 −0.07 −0.11 to −0.03 0.001
Model
Total
Transient 6 160 −0.05 −0.08 to −0.03 <0.0001
Permanent 11 258 −0.10 −0.13 to −0.08 <0.0001
Thrombotic 1 24 −0.06 −0.15 to 0.03 0.18

No data were available for cortical/subcortical volumes in mice. Analyses based on individual animal data only. Data are coefficients per 100 mg·kg−1 of total administered NXY-059 dose with standardization for model and adjustment for time to treatment; 95% confidence intervals (95% CI) and significance. Results in bold are statistically significant.

Permanent models only.

NXY-059, disodium 2,4-disulphophenyl-N-tert-butylnitrone.