posted on 2015-09-30, 00:00authored byXin Li, Rong-Rong Tao, Ling-Juan Hong, Juan Cheng, Quan Jiang, Ying-Mei Lu, Mei-Hua Liao, Wei-Feng Ye, Nan-Nan Lu, Feng Han, Yong-Zhou Hu, You-Hong Hu
Accumulating evidence suggests that
formation of peroxynitrite
(ONOO<sup>–</sup>) in the cerebral vasculature contributes
to the progression of ischemic damage, while the underlying molecular
mechanisms remain elusive. To fully understand ONOO<sup>–</sup> biology, efficient tools that can realize the real-time tracing
of endogenous ONOO<sup>–</sup> fluxes are indispensable. While
a few ONOO<sup>–</sup> fluorescent probes have been reported,
direct visualization of ONOO<sup>–</sup> fluxes in the cerebral
vasculature of live mice remains a challenge. Herein, we present a
fluorescent switch-on probe (<b>NP3</b>) for ONOO<sup>–</sup> imaging. <b>NP3</b> exhibits good specificity, fast response,
and high sensitivity toward ONOO<sup>–</sup> both in vitro
and in vivo. Moreover, <b>NP3</b> is two-photon excitable and
readily blood–brain barrier penetrable. These desired photophysical
and pharmacokinetic properties endow <b>NP3</b> with the capability
to monitor brain vascular ONOO<sup>–</sup> generation after
injury with excellent temporal and spatial resolution. As a proof
of concept, <b>NP3</b> has enabled the direct visualization
of neurovascular ONOO<sup>–</sup> formation in ischemia progression
in live mouse brain by use of two-photon laser scanning microscopy.
Due to these favorable properties, <b>NP3</b> holds great promise
for visualizing endogenous peroxynitrite fluxes in a variety of pathophysiological
progressions in vitro and in vivo.