AI Article Synopsis

  • The study aimed to assess the long-term effects of endothelin-1 on retinal health in mice using various imaging techniques.
  • Mice were injected with different doses of ET-1, and their retinal response and cell survival were monitored over several weeks using tests like electroretinograms and optical coherence tomography.
  • Findings revealed that high doses of ET-1 caused immediate constriction of retinal blood vessels and a measurable loss of retinal cells over time, indicating that ET-1 has both transient and long-lasting impacts on retinal structure and function.

Article Abstract

Purpose: To study the long-term effects of endothelin-1 (ET-1)-induced retinal pathologies in mouse, using clinically relevant tools.

Methods: Adult C57BL/6 mice (7-9 weeks old) were intravitreally injected with PBS (n = 10) or 0.25 (n = 8), 0.5 (n = 8), or 1 nmol ET-1 (n = 9) and examined using electroretinogram, optical coherence tomography (OCT), and Doppler OCT at baseline and postinjection days 10, 28, and 56. Retinal ganglion cell (RGC) survival in retinal whole mount was quantified at days 28 and 56.

Results: ET-1 induced immediate retinal arterial constriction. The significantly reduced total blood flow and positive scotopic threshold response in the 0.5- and 1-nmol ET-1 groups at day 10 were recovered at day 28. A-wave magnitude was also significantly reduced at days 10 and 28. While a comparable and significant reduction in retinal nerve fiber layer thickness was detected in all ET-1 groups at day 56, the 1-nmol group was the earliest to develop such change at day 28. All ET-1 groups showed a transient inner retinal layer thinning at days 10 and 28 and a plateaued outer layer thickness at days 10 to 56. The 1-nmol group showed a significant RGC loss over all retinal locations examined at day 28 as compared with PBS control. As for the lower-dosage groups, significant RGC density loss at central and midperipheral retina was detected at day 56 when compared with day 28.

Conclusions: ET-1 injection in mice resulted in a transient vascular constriction and reduction in retinal functions, as well as a gradual loss of retinal nerve fiber layer and RGC in a dose-dependent manner.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10424801PMC
http://dx.doi.org/10.1167/iovs.64.11.15DOI Listing

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