Fig. 1
- ID
- ZDB-FIG-180703-1
- Publication
- Naini et al., 2018 - Surfen and oxalyl surfen decrease tau hyperphosphorylation and mitigate neuron deficits in vivo in a zebrafish model of tauopathy
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Surfen and oxalyl surfen are well tolerated by Tg[HuC::hTauP301L; DsRed] embryos. a Chemical structure of Surfen (1,3-bis(4-amino-2-methylquinolin-6-yl) urea), oxalyl surfen (N1,N2- bis(4-amino-2-methylquinolin-6-yl)oxalamide) and hemisurfen (1-(4-amino-2-methylquinolin-6- yl)urea). b Phenotypic analysis of 72 hpf wild-type (WT) and Tg[HuC::hTauP301L; DsRed] (hTauP301L) embryos incubated for 2 days in E3 medium containing 1% DMSO (hTauP301L?+?1% DMSO), 80 mM LiCl (hTauP301L?+?LiCl), 3 ?M surfen (hTauP301L?+?surfen), 2 ?M oxalyl surfen (hTauP301L?+?oxalyl surfen) or 3 ?M hemisurfen (hTauP301L?+?hemisurfen), showed that embryonic development is not impaired by the treatments. Magnification ×?40. c Survival rate of 72 hpf wild-type (WT) and Tg[HuC::hTauP301L; DsRed] (hTauP301L) embryos incubated for 2 days in E3 medium containing 1% DMSO (hTauP301L?+?1% DMSO), 80 mM LiCl (hTauP301L?+?LiCl), 3 ?M surfen (hTauP301L?+?surfen), 2 ?M oxalyl surfen (hTauP301L?+?oxalyl surfen), or 3 ?M hemisurfen (hTauP301L?+?hemisurfen), demonstrated that embryonic mortality was not significantly increased by treatments (n?=?250, P?>?0.05, Student?s t test) |