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Published on: September 12, 2010
Control of light-sensitive current in salamander rods
1Physiological Laboratory, Cambridge.
Abstract:
1. The exponential decline of light-sensitive current seen after switch from Na+ to Li+ in the presence of Ca2+ probably depends on the activity of the phosphodiesterase (PDE) which hydrolyses cyclic GMP. 2. This probability is supported by experiments with suction electrodes which show that in toad and salamander rods the rate constant, b, of the exponential decline of current was increased at least 10-fold by moderate light intensities and decreased about 10-fold by 3-isobutyl-1-methylxanthine (IBMX), an inhibitor of PDE. 3. The rate constant b is about 3 times more sensitive to weak lights or to IBMX than the membrane current. This may be explained by a feed-back involving calcium ions which tends to hold current constant, perhaps by calcium inhibition of guanylate cyclase. 4. The time course of b, which probably represents the changes in PDE activity, was measured by switching from Na+ to Li+ at various times after a flash. The results suggest that a moderate flash (140 Rh) increased b about 7 times in 0.5 s and that b then declined with a time constant of 1.5-2 s. 5. Extrapolated values of the parameter b suggest that strong flashes (5000-10,000 Rh) increased b from 1 s-1 in the dark to perhaps 60 s-1 and that b continued to increase with flash strength for several log units after the current had reached saturation. 6. The observations in 4 and 5 fit well with the idea that b is related to PDE activity and that changes in the latter are sufficient to account for the rising phase of the flash response. 7. After a flash the light-sensitive current recovers much more rapidly than the time constant b-1, a discrepancy which is explained if a light flash causes a delayed increase in guanylate cyclase activity. 8. The apparent delayed increase in cyclase activation is consistent with an inhibitory effect of [Ca2+]i which is reduced when calcium is pumped out during the plateau of the response. 9. Experiments in which pulses of IBMX were applied at different times during a flash response support the idea that a flash causes a delayed increase in the rate of supply of cyclic GMP. Quantitative analysis of these and other tests with IBMX gave rate constants similar to those obtained by the Na+----Li+ method.
Insights
Light flashes increase phosphodiesterase (PDE) activity in retinal rods, influencing cyclic GMP levels and the light-sensitive current. This PDE activity is crucial for the flash response, with calcium ions playing a feedback role.
Area of Science:
- Phototransduction in retinal rods
- Cellular signaling pathways in vision
Background:
- The light-sensitive current in retinal rods is critical for vision.
- Cyclic guanosine monophosphate (cGMP) is a key second messenger in phototransduction.
- Phosphodiesterase (PDE) hydrolyzes cGMP, regulating its levels.
Purpose of the Study:
- To investigate the role of phosphodiesterase (PDE) activity in the decline of light-sensitive current.
- To elucidate the relationship between PDE activity, cyclic GMP hydrolysis, and the flash response in retinal rods.
- To explore the involvement of calcium ions and guanylate cyclase in phototransduction regulation.
Main Methods:
- Utilized the Na+/Li+ switch method in toad and salamander rods to measure the rate constant (b) of current decline.
- Employed suction electrodes to record light-sensitive currents.
- Administered 3-isobutyl-1-methylxanthine (IBMX), a PDE inhibitor, and varied light intensities.
- Applied light flashes of controlled strengths (e.g., 140 Rh, 5000-10,000 Rh).
Main Results:
- The rate constant (b) of current decline, indicative of PDE activity, increased significantly with light exposure and IBMX treatment.
- Moderate flashes (140 Rh) increased 'b' approximately 7-fold within 0.5 seconds, with subsequent decline.
- Strong flashes (5000-10,000 Rh) elevated 'b' substantially, suggesting PDE activity changes are sufficient to explain the flash response's rising phase.
- Light-sensitive current recovery was faster than the decline in 'b', suggesting a delayed increase in guanylate cyclase activity.
Conclusions:
- The activity of phosphodiesterase (PDE) is a primary determinant of the exponential decline in light-sensitive current following light stimulation.
- Changes in PDE activity, influenced by light and calcium ions, are sufficient to account for the rising phase of the visual flash response.
- A delayed activation of guanylate cyclase, possibly due to reduced calcium inhibition, explains the rapid current recovery post-flash.
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