ArticleThe Journal of physiology2007
Proton modulation of ion channels in isolated horizontal cells of the goldfish retina.
Article in The Journal of physiology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 20 citations in OpenAlex.
- Spontaneous action potentials in retinal horizontal cells of goldfish (Journal of neurophysiology · 2019Article
- Voltage- and calcium-gated ion channels of neurons in the vertebrate retina.Progress in retinal and eye research · 2019Review
- Advancing the pH hypothesis of negative feedback to photoreceptors: sources of protons and a role for bicarbonate in feedback.The Journal of physiology · 2017Article
- Calcium dynamics and regulation in horizontal cells of the vertebrate retina: lessons from teleosts.Journal of neurophysiology · 2017Review
- Lateral interactions in the outer retina.Progress in retinal and eye research · 2012Review
- Guinea pig horizontal cells express GABA, the GABA-synthesizing enzyme GAD 65, and the GABA vesicular transporter.The Journal of comparative neurology · 2010Article
- A genetically encoded ratiometric sensor to measure extracellular pH in microdomains bounded by basolateral membranes of epithelial cells.Pflugers Archiv : European journal of physiology · 2008Article
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Transient changes in extracellular pH (pH(o)) occur in the retina and may have profound effects on neurotransmission and visual processing due to the pH sensitivity of ion channels. The present study characterized the effects of acidification on the activity of membrane ion channels in isolated horizontal cells (HCs) of the goldfish retina using whole-cell patch-clamp recording. Currents recorded from HCs were characterized by prominent inward rectification at potentials negative to -80 mV, a negative slope conductance between -70 and -40 mV, a sustained inward current, and outward rectification positive to 40 mV. Inward currents were identified as those of inward rectifier K(+) (Kir) channels and Ca(2+) channels by their sensitivity to 10 mM Cs(+) or 20 microm Cd(2+), respectively. Both of these currents were reduced when pH(o) decreased from 7.8 to 6.8. Glutamate (1 mM)-activated currents were also identified, as were hemichannel currents that were enhanced by removal of extracellular Ca(2+) and application of 1 mM quinidine. Both glutamate-activated and hemichannel currents were suppressed by a similar reduction of pH(o). When all of these H(+)-inhibited currents were blocked, a small, sustained inward current at -60 mV increased following a decrease in pH(o) from 7.8 to 6.8. In addition, slope conductance between -70 and -20 mV increased during this acidification. Suppression of this H(+)-activated current by removal of extracellular Na(+), and an extrapolated E(rev) near E(Na), indicated that this current was carried predominantly by Na(+) ions.
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