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. Author manuscript; available in PMC: 2013 Jan 17.
Published in final edited form as: Circulation. 2011 Dec 5;125(2):335–345. doi: 10.1161/CIRCULATIONAHA.111.045096

Table 1.

Death and neurological disability after transient fMCAO in S218L mutant mice.

Experiment 60 min fMCAO* 60 min fMCAO + MK-801# 30 min fMCAO
Gender, Genotype Male WT Male HET Male HOM Male WT Male HET Male WT Male HET Male HOM Female WT Female HET
N 9 23 8 9 10 9 5 4 6 8
Mortality 11% 35% 100% 0% 10% 0% 0% 75% 0% 0%
Functional outcome score 2 [2–3] 3 [2–5] 5 [5–5] 2 [1–2] 2 [1–2] 1 [1–2] 2 [1–2] 5 [4–5] 1 [0.3–1] 2 [1–2]

Functional outcome scores are shown as median [interquartile range]. 0 = best, 5 = worst, see Methods for the scoring system.

*

p<0.001 and p=0.008 for the effect of genotype on mortality and functional outcome score, respectively.

p=0.353 and p=0.757 for the effect of genotype on mortality and functional outcome score, respectively.

#

p=0.303 and p=0.315 for the effect of MK-801 on mortality and functional outcome score, respectively, in WT, and p=0.022 and p=0.009 for the effect of MK-801 on mortality and functional outcome score, respectively, in the S218L HET, compared to the untreated group.

p<0.001 and p=0.086 for the effect of genotype on mortality and functional outcome score in males, respectively, and p=0.02 for the effect of genotype on functional outcome score in females, after 30 min fMCAO. In the R192Q mutant strain, the mortality rate was 17%, 0% and 14% in WT, HET and HOM, respectively; neurological disability was not studied in this mutant strain.