Neuroscience Letters 590 (2015) 132–133
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Corrigendum
Corrigendum to “Preconditioning effect of (S)-3,5-dihydroxyphenylglycine on ischemic injury in middle cerebral artery occluded Sprague–Dawley rats” [Neurosci. Lett. 588 (2015) 137–141] Nik Nasihah Nik Ramli a , Nursyazwani Omar a , Andrean Husin b,c , Zalina Ismail d , Rosfaiizah Siran d,e,∗ a
Institute of Medical Molecular Biotechnology, Universiti Teknologi MARA, 47000 Selangor, Malaysia Faculty of Dentistry, Universiti Teknologi MARA, 40450 Shah Alam, Selangor, Malaysia c Brain and Neuroscience Communities of Research, Universiti Teknologi MARA, 40450 Shah Alam, Selangor, Malaysia d Brain Research and Information Network, Centre for Neurocognitive Sciences, Universiti Sains Malaysia, 16150 Kelantan, Malaysia e Faculty of Medicine, Universiti Teknologi MARA, 47000 Selangor, Malaysia b
The authors regret a number of minor errors in the published version of this article. The affiliations for Rosfaiizah Siran were incorrect and the correct affiliations appear above. In Section 2.4.1, the number of hours in the first sentence was incorrect and should have been: “All the rats were subjected to modified neurological severity scores (mNSS) behavioral test after 24 h of MCAO”. In Figs. 1 and 3b, the x-axis was mislabelled “saline” and should have been “control”. The corrected figures appear below:
Fig. 1 Modified neurological severity scores in ischemic (control) and pretreated with (S)-3,5-DHPG (1, 10 and 100 M) rats. Each value represents means ± S.E.M. **P < 0.01 compared to control.
DOI of original article: http://dx.doi.org/10.1016/j.neulet.2014.12.062. ∗ Corresponding author at: Faculty of Medicine, Universiti Teknologi MARA, 47000 Sungai Buluh Campus, Selangor, Malaysia. Tel.: +60 361267172; fax: +60 361265224. E-mail address:
[email protected] (R. Siran). http://dx.doi.org/10.1016/j.neulet.2015.01.061 0304-3940/© 2015 Elsevier Ireland Ltd. All rights reserved.
N.N.N. Ramli et al. / Neuroscience Letters 590 (2015) 132–133
Fig. 3 (b) One and 10 M (S)-3,5-DHPG pretreated ischemic rats showed significant decrease (**P < 0.01) against the control rats. The authors would like to apologise for any inconvenience caused.
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