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–) in the cerebral vasculature contributes
to the progression of ischemic damage, while the underlying molecular
mechanisms remain elusive. To fully understand ONOO– biology, efficient tools that can realize the real-time tracing
of endogenous ONOO– fluxes are indispensable. While
a few ONOO– fluorescent probes have been reported,
direct visualization of ONOO– fluxes in the cerebral
vasculature of live mice remains a challenge. Herein, we present a
fluorescent switch-on probe (NP3) for ONOO– imaging. NP3 exhibits good specificity, fast response,
and high sensitivity toward ONOO– both in vitro
and in vivo. Moreover, NP3 is two-photon excitable and
readily blood–brain barrier penetrable. These desired photophysical
and pharmacokinetic properties endow NP3 with the capability
to monitor brain vascular ONOO– generation after
injury with excellent temporal and spatial resolution. As a proof
of concept, NP3 has enabled the direct visualization
of neurovascular ONOO– formation in ischemia progression
in live mouse brain by use of two-photon laser scanning microscopy.
Due to these favorable properties, NP3 holds great promise
for visualizing endogenous peroxynitrite fluxes in a variety of pathophysiological
progressions in vitro and in vivo.