Among the many animal models of retinitis pigmentosa (RP), the most extensively characterized animal is the rd1 mouse. Recent studies showed that the neurophysiological properties of rd1 retinas differ significantly from those of normal retina; the presence of an oscillatory rhythmic activity (~10 Hz) both in retinal ganglion cell (RGC) spikes and field potentials (slow wave component, SWC). However, lesser studies have been done regarding electrical characteristics of rd10 retina, carrying the mutation of same rod-PDE gene and showing a later onset degeneration of photoreceptors. Therefore, in this study, we compared the oscillatory rhythm in RGC spike and SWC between rd1 and rd10 mice in different postnatal ages to understand neural code used by two diseased retinas to communicate with the brain. Extracellular action potentials are recorded by 8 × 8 MEA from the RGC in the in vitro whole mount retina. 4 and 8 weeks in rd1 mice and 4, 10, 15, and 20 weeks in rd10 mice were used (n=3 for each postnatal age). From the raw waveform of retinal recording, RGC Spikes and SWC were isolated by using 200 Hz high-pass filter and 20 Hz low-pass filter, respectively. Fourier transform was performed for detection of oscillatory rhythm in RGC spikes and SWC. In rd1 mice, there is no statistical difference between the frequency of SWC and spike in 4 weeks [p>0.05; spike 9.3 ± 0.9 Hz (n=40), SWC 9.3 ± 1.5 Hz (n=25)] and 8 weeks [p>0.05; spike 10.0 ± 1.3 Hz (n=87), SWC 10.9 ± 1.7 Hz (n=25)]. While in rd10 mice there is no statistical differences among the SWC through 4 ~ 20 weeks, significant differences were observed between the frequency of RGC spike and SWC and also among RGC spikes [4 weeks (p<0.001): spike 5.5 ± 1.3 Hz (n=59), SWC 10.8 ± 3.1 Hz (n=14); 10 weeks (p<0.001): spike 6.8 ± 3.8 Hz (n=79), SWC 10.3 ± 2.6 Hz (n=25); 15 weeks (p<0.05): spike 3.9 ± 0.7 Hz (n=33), SWC 9.9 ± 1.2 Hz (n=25); 20 weeks (p<0.05): spike 4.4 ± 1.2 Hz (n=53), SWC 9.8 ± 1.2 Hz (n=25)].
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http://dx.doi.org/10.1109/IEMBS.2011.6090255 | DOI Listing |
Invest Ophthalmol Vis Sci
January 2025
Southwest Hospital/Southwest Eye Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
Purpose: Previous studies have reported divergent sexual responses to aging; however, specific variations in gene expression between aging males and females and their potential association with age-related retinal diseases remain unclear. This study collected data from public databases and developed a comprehensive comparison of retina between aging females and males.
Methods: Single-cell RNA (scRNA) and bulk RNA sequencing data of the aging retina from females and males in public databases were utilized for integrated analysis to investigate sex-biased expression in retina.
Nat Commun
January 2025
Center for Synaptic Neuroscience, Istituto Italiano di Tecnologia, Genova, Italy.
The lack of effective therapies for visual restoration in Retinitis pigmentosa and macular degeneration has led to the development of new strategies, such as optogenetics and retinal prostheses. However, visual restoration is poor due to the massive light-evoked activation of retinal neurons, regardless of the segregation of visual information in ON and OFF channels, which is essential for contrast sensitivity and spatial resolution. Here, we show that Ziapin2, a membrane photoswitch that modulates neuronal capacitance and excitability in a light-dependent manner, is capable of reinstating, in mouse and rat genetic models of photoreceptor degeneration, brisk and sluggish ON, OFF, and ON-OFF responses in retinal ganglion cells evoked by full-field stimuli, with reactivation of their excitatory and inhibitory conductances.
View Article and Find Full Text PDFCurr Biol
January 2025
Synaptic Physiology Section, National Institute of Neurological Disorder and Stroke, National Institutes of Health, Bethesda, MD 20814, USA. Electronic address:
The neurovascular unit (NVU), comprising vascular, glial, and neural elements, supports the energetic demands of neural computation, but this aspect of the retina's trilaminar vessel network is poorly understood. Only the innermost vessel layer-the superficial vascular plexus (SVP)-is associated with astrocytes, like brain capillaries, whereas radial Müller glia interact with vessels in the other layers. Using serial electron microscopic reconstructions from mouse and primate retina, we find that Müller processes cover capillaries in a tessellating pattern, mirroring the wrapping of brain capillaries by tiled astrocytic endfeet.
View Article and Find Full Text PDFPharmaceuticals (Basel)
November 2024
Department of Integrative Pathophysiology and Therapies, Andalusian Molecular Biology and Regenerative Medicine Centre (CABIMER), Junta de Andalucía, CSIC, Universidad de Sevilla, Universidad Pablo de Olavide, Avda. Américo Vespucio 24, 41092 Seville, Seville, Spain.
Background: Retinitis pigmentosa (RP), the leading cause of inherited blindness in adults, is marked by the progressive degeneration of rod photoreceptors in the retina. While gene therapy has shown promise in treating RP in patients with specific mutations, no effective therapies currently exist for the majority of patients with diverse genetic backgrounds. Additionally, no intervention can yet prevent or delay photoreceptor loss across the broader RP patient population.
View Article and Find Full Text PDFbioRxiv
December 2024
Department of Ophthalmology & Visual Sciences and Department of Biochemistry & Molecular Medicine, West Virginia University, Morgantown, WV 26506, United States.
Rod photoreceptor neurons in the retina detect scotopic light through the visual pigment rhodopsin (Rho) in their outer segments (OS). Efficient Rho trafficking to the OS through the inner rod compartments is critical for long-term rod health. Given the importance of protein trafficking to the OS, less is known about the trafficking of rod synaptic proteins.
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