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1 Institute of Neurobiology, Institutes of Brain Science, Fudan University, 220 Handan Road, Shanghai, 200433, China
2 Shanghai Institutes for Biological Sciences and Graduate School, Chinese Academy of Sciences, 320 Yueyang Road, Shanghai, 200031, China
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(Received 14 September 2005;
accepted after revision 18 October 2005;
first published online 20 October 2005)
Corresponding author X.-L. Yang: Institute of Neurobiology, Fudan University, 220 Handan Road, Shanghai, 200433, China. Email: xlyang{at}fudan.edu.cn
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Introduction |
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In the vertebrate retina, melatonin is produced by photoreceptors, and the synthesis and release of melatonin show a marked daily variation, being at higher levels at night and at lower levels during the daytime (Besharse & Iuvone, 1983; Tosini & Fukuhara, 2003). Melatonin concentration in the retina and its circadian changes have been determined in various species (Cahill, 1996; Alonso-Gomez et al. 2000; Tosini, 2000; Zawilska et al. 2003). Moreover, in situ hybridization and immunocytochemical studies have demonstrated the presence of melatonin receptors in the retina of various species (Reppert et al. 1995; Fujieda et al. 1999; Savaskan et al. 2002; Scher et al. 2002; Wiechmann, 2003; Wiechmann et al. 2004; Sallinen et al. 2005). Melatonin is implicated in many retinal functions, including retinomotor responses, rod disc shedding, and regulation of horizontal cell (HC) light responsiveness, dopamine release, etc. (see Vanecek, 1998 for review). It was recently shown in the fish retina that activation of melatonin receptors could regulate the activity of cone-driven HCs, an activity which is thought to be mediated by modulating dopamine release from interplexiform and amacrine cells (Ribelayga et al. 2004). Melatonin could also modulate receptors for other neurotransmitters expressed on retinal neurones. In cultured chick retinal neurones, melatonin receptors are coupled to adenylate cyclase, which is regulated by D1 dopamine receptors (Iuvone & Gan, 1995), reflecting a direct functional interaction of these two types of receptor. Modulation by melatonin of neurotransmitter–receptor systems in the retina, however, is not necessarily mediated by melatonin receptors. For instance, in isolated carp bipolar and amacrine-like cells, melatonin accelerates desensitization of GABAA receptor-mediated currents, which may be due to the allosteric action of melatonin bound to a site of the GABAA receptor (Li et al. 2001).
In the present work we show that the MT1 receptor is expressed on HCs in carp retina by using immunocytochemistry. We further present data showing, for the first time that melatonin potentiates glutamate-receptor-mediated currents recorded from isolated carp H1 cells via the activation of the MT1 receptor, which may be in part responsible for melatonin-caused reduction of the light responses of these cells. These results suggest that melatonin may probably play an important role in the circadian regulation by melatonin of light responsiveness of cone HCs via directly modifying the activity of glutamate receptors on these cells.
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Methods |
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Experiments were performed on the adult crucian carp (Carassius carassius) retina. The animal, maintained under 12 h : 12 h light:dark cycle for at least 1 week, was dark-adapted for 20 min prior to an experiment and then deeply anaesthetized with 0.01% tricaine methylsulphonate, before being decapitated and pithed. The eyeball was enucleated and hemisected under dim red light. Adequate care was taken to minimize pain and discomfort to animals in accordance with the National Institutes of Health guidelines for animal experimentation.
Immunocytochemistry and Western blot analysis
Procedures for immunocytochemical double-labelling analysis were basically similar to those used in a previous work, with minor modifications (Xu et al. 2003). In brief, isolated carp retinas were immersion-fixed in fresh 4% formaldehyde in phosphate buffer solution (PBS, pH 7.4) for 10 min at 4°C and then sequentially cryoprotected at 4°C in 10, 20 and 30% (w/v) sucrose in 0.1 M PBS for 2 h, 2 h, and overnight, respectively. They were embedded in OCT (Miles, Inc., Elkhart, IN, USA) and frozen by liquid nitrogen. Vertical sections were made at 14 µm thickness on a freezing microtome (Leica, Nussloch, Germany) and collected on gelatin chromium-coated slides. Indirect immunofluorescence labelling was performed for the preparations. The sections were blocked and permeabilized with 6% normal donkey serum, 1% normal bovine serum albumin and 0.2% Triton X-100 in PBS overnight at 4°C, followed by incubation with the primary antibodies goat polyclonal antibody against the MT1 receptor (sc-13186; Santa Cruz Biotechnology, CA, USA) and mouse monoclonal antibody against GAD67 (MAS5406; Chemicon, Temecula, CA, USA), at working dilutions of 1 : 500 and 1 : 1000, respectively. The secondary antibodies Texas-red-conjugated donkey anti-goat IgG and fluorescein isothiocyanate (FITC)-conjugated donkey anti-mouse IgG (Jackson ImmunoResearch Laboratories, West Grove, PA, USA), diluted to 1 : 200, were used to reveal the binding sites. The sections were incubated sequentially in the primary antibodies and secondary antibody at 4°C for 3 days and 2 h, respectively. Washed with PBS and coverslipped, fluorescently labelled sections were imaged with a Leica SP2 confocal laser scanning microscope (Leica, Mannheim, Germany) using a x63 oil-immersion objective lens. Single optical sections were made through the preparation at intervals of 1.0 µm.
Western blot analysis was conducted following the procedure previously described in detail (Zhao & Yang, 2001). The extract samples (2.0 mg ml–1, 20 µl) were loaded, subjected to 12% SDS-PAGE and electroblotted onto polyvinylidene fluoride (PVDF) membranes using the Mini-PROTEAN 3 Electrophoresis System and the Mini Trans-Blot Electrophoretic Transfer System (Bio-Rad, Hercules, CA, USA). The membranes were blocked with non-fat milk at room temperature for 2 h, and then incubated with the antibody against the MT1 receptor, at a working dilution of 1 : 1000, overnight at 4°C. The blots were washed, incubated with horseradish-peroxidase-conjugated donkey antigoat IgG (1 : 5000; Santa Cruz Biotechnology, USA) for 2 h at 4°C, and finally visualized with enhanced chemiluminescence (Amersham Biosciences, Arlington Height, IL, USA).
Whole-cell patch-clamp recording
HCs were acutely dissociated from retinas by enzymatic and mechanical treatments, as previously described (Lu et al. 1998). Chopped retina pieces were incubated in Hanks' solution with 60 U ml–1 papain (Caliochem-Novabiochem Corp., CA, USA) and 1 mg ml–1 cysteine for 30 min at 25°C. Hanks' solution contained (mM): NaCl 137, KCl 3, CaCl2 2, MgSO4 1, sodium pyruvate 1, NaH2PO4 1, NaHCO3 0.5, Hepes 20 and glucose 16, pH 7.4 adjusted with NaOH. After rinsing with fresh Hanks' solution, the papain-treated retina pieces were kept in normal Hanks' solution for up to 8 h at 4°C. Cells were freshly dissociated from the stored retina pieces by gentle trituration with fire-polished Pasteur pipettes, and the cell suspension was placed onto a plastic dish mounted on the stage of a phase-contrast microscope (IX70; Olympus Optical, Tokyo, Japan). Cells were bathed in Ringer solution containing (mM) NaCl 145, KCl 5, CaCl2 2, MgCl2 1, Hepes 10 and glucose 16, pH adjusted to 7.4 with NaOH. HCs were easily identified by their typical morphology and by the characteristic inwardly rectifying K+ current (Lasater, 1986; Lu et al. 1998). Whole-cell membrane currents of HCs, voltage-clamped at –60 mV, were recorded with pipettes of 5–7 M
resistance, when filled with a solution containing (mM) KCl 60, KF 50, CaCl2 1, MgCl2 1, EGTA 10, Hepes 10, ATP 4 and GTP 0.5, pH 7.3 adjusted with KOH, connected to an EPC9/2 patch-clamp amplifier (Heka, Germany). The liquid junction potential was compensated on-line. Fast capacitance and cell capacitance were cancelled by the circuit of the amplifier. Seventy per cent of the series resistance of the recording electrode was compensated. Analog signals were filtered at 2 kHz, sampled at 10 kHz, and stored on PC hard disk for further off-line analysis. Desensitization of the response to glutamate was fitted to a monoexponential equation: I(t) =Ax exp(–t/
) +C, where A is the peak current, t is time, is the time constant, and C is an offset. Dose–response relationships of glutamate-induced currents were fitted to the equation: I/Imax= 1/(1 + (EC50/[Glu])n), where I is the current response elicited by a given glutamate concentration [Glu], Imax is the response at a saturating concentration of glutamate, EC50 is the concentration of glutamate producing a half-maximal response, and n is the Hill coefficient. The normalized percentage potentiation of melatonin was calculated by the equation: (Imelatonin–Icontrol)/Icontrolx 100%. The data were all presented as means ±S.E.M. Student's paired t test was performed for statistical analysis.
All solutions were delivered using a stepper motor-based rapid solution changer RSC-100 (Bio-Logic Science Instruments, France), as described in detail previously (Lu et al. 1998). The recorded cells were lifted from the dish bottom, and completely bathed in the solution. The solution exchange could be completed in a few milliseconds (Lu et al. 1998).
Intracellular recording and photostimulation
Intracellular recordings were made from HCs in the isolated, superfused flat-mounted retina (Huang et al. 2004) during the daytime. The retina, superfused with oxygenated (95% O2, 5% CO2) Ringer solution, consisting of (mM) NaCl 116, KCl 2.4, CaCl2 1.2, MgCl2 1.2, NaHCO3 30, and glucose 10, buffered to pH 7.7, was illuminated diffusely from the photoreceptor side by a dual-beam photostimulator, which provided two coincident 8 mm-diameter spots around the electrode tip. Light intensities and wavelengths of the two beams were changed by calibrated neutral density and interference filters. All light intensities referred to in the text are in log units relative to the maximum intensity (logI= 0), which was 5.5 x 1013 quanta cm–2 s–1. Glass microelectrodes filled with 4 M potassium acetate and having a tip resistance of 70–150 M, in combination with an amplifier (MEZ 8300; Nihon Koden Corporation, Tokyo, Japan), were employed to record intracellular potentials. Cone- and rod-driven HCs were identified by reference to previously well-established criteria (cone HCs: Yang et al. 1982, 1983, 1994; Xu et al. 2001; rod HCs: Kaneko & Yamada, 1972; Yang et al. 1988, 1994).
Chemicals
All chemicals were obtained from Sigma Chemical Company (St Louis, MO, USA), unless otherwise specified, and most of them were freshly dissolved in Ringer solution. Melatonin, luzindole and K 185 were first dissolved in DMSO and then added to Ringer solution on the day of experiment. The final concentration of DMSO was less than 0.1% which had no effects on the glutamate-induced currents from isolated HCs, or on the membrane potential and light responses of these cells intracellularly recorded from the isolated, superfused retina.
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Results |
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The specificity of the MT1 receptor antibody was first tested using Western blot analysis. As shown in Fig. 1A, the antibody revealed a single immunoreactive band at approximately 37 kDa, which precisely corresponds to the predicted molecular mass of the receptor (Song et al. 1997). The specificity of the immunofluorescence labelling was then evaluated by omitting one or both of the two primary antibodies during the incubation. When one of the primary antibodies was omitted, only the immunoreactivity for the remaining antibody was revealed, and omission of the both eliminated any immunolabelling. It was further found that no cross-reactivity of species-specific secondary antibodies was observed when the retina preparation was stained by a mixture of the two secondary antibodies after incubation with one of the two primary antibodies. As shown in Fig. 1B, almost no immunoflorescence labelling could be found when the MT1 antibody was pre-absorbed with the immunizing antigen, indicating that the protein recognized by the rabbit anti-MT1 antiserum used in this work may most likely be the MT1 receptor. Figure 1C–F shows confocal laser scanning micrographs of the vertical sections of the carp retina double-labelled with the antibodies against the MT1 receptor and GAD67, a marker of GABAergic neurones. In the low-power micrograph (Fig. 1C), the MT1 immunoreactivity was diffusely distributed in the neural retina, with the labelling being rather strong in the outer plexiform layer (OPL) and the distal part of the inner nuclear layer (INL). The region of OPL and outer INL marked by the box is shown at higher magnification in Fig. 1D–F. From the merged image (Fig. 1F) of Fig. 1D, showing MT1 immunoreactivity, and Fig. 1E, showing GAD and MT1 immunoreactivity, it was clear that the somata of the HCs were strongly MT1 immunoreactive and the labelling delineated the cells, suggesting that the MT1 receptor may be predominantly expressed on the cell membrane. Processes of these HCs located in the OPL were also MT1 immunoreactive, though they could not be clearly distinguished.
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Carp retinal HCs exclusively express the AMPA-preferring glutamate receptor subtype (Lu et al. 1998). We first examined if and how melatonin modulates AMPA receptor-mediated currents of HCs. The experiments were mainly performed on H1 cells, which have a relatively small soma (10–20 µm in diameter) and limited process size. H1 cells, together with H2 and H3 cells, are known to be cone driven (Dowling, 1987). Some experiments were also done on H2 and H3 cells and no significant difference could be found in regard to melatonin modulation of glutamate-induced currents. Melatonin at concentrations ranging between 100 pM and 500 µM alone failed to induce any detectable current from H1 cells (data not shown). Figure 2A–D shows the effects of melatonin of increasing concentrations on the glutamate-induced current recorded from an H1 cell. The inward current response of the cell to 3 mM glutamate, a concentration that is little higher than the EC50 (1.08 mM) (Lu et al. 1998), recorded in normal Ringer solution, reached a peak in less than 2 ms, and then rapidly decayed to a much lower steady level (desensitization) with a time constant of 3.6 ms (Fig. 2A), which is typical of the AMPA receptor-mediated response (Lu et al. 1998). When the cell was incubated with 100 pM melatonin, both peak and steady-state currents of the response were gradually increased in size with time. The peak current was increased from the control level (381 pA) to a steady level of 448 pA in 2 min, whereas the steady-state current was increased from 39 to 45 pA (Fig. 2B). When the concentration of melatonin was increased to 10 nM, the peak and steady-state currents were further increased to 627 and 54 pA, respectively (Fig. 2C). Full recovery of the current response to the control level could be obtained after washout with Ringer solution for 3 min (Fig. 2D). This potentiation by melatonin of the glutamate current was seen in 58 out of 75 H1 cells tested. For the remaining 17 cells, glutamate current responses were almost unchanged by melatonin. It was noteworthy that the rise time and the desensitization course were hardly altered, while the peak amplitude was significantly potentiated. In Fig. 2E, the activation and desensitization courses of the responses shown in Fig. 2B and C were normalized and then superimposed on the control response at a much faster time scale. It was evident that these normalized responses precisely coincide with the control response. The 10–90% rise time of the control responses was 1.54 ± 0.16 ms, whereas that of the current responses obtained in the presence of 10 nM melatonin was 1.49 ± 0.20 ms (n= 12, P > 0.05). Meanwhile, the rate of desensitization of control responses (= 3.82 ± 0.47 ms) also remained unchanged in the presence of 10 nM melatonin (3.63 ± 0.41 ms, P > 0.05). The results obtained following the incubation of 100 pM melatonin were similar. To test if deactivation was affected by melatonin, the deactivation courses of the responses shown in Fig. 2B and C were normalized and compared at a much faster time scale by enlarging and superimposing them (Fig. 2F). It is clear that all these three traces coincide precisely.
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We also investigated the effects of melatonin on kainic acid (KA)-induced currents, which are sustained and do not show any desensitization (Lu et al. 1998). As shown in Fig. 2H, melatonin of 10 nM increased the current of the H1 cell from 704 to 989 pA. Similar results were obtained in four other H1 cells. The relative increase of the response amplitude was 26.8 ± 8.2% (P < 0.05, n= 5).
Melatonin increases both receptor efficacy and affinity for glutamate
We further determined the dose–response relationships of the glutamate-induced currents of H1 cells in the absence and presence of 10 nM melatonin to explore whether melatonin may change the affinity and efficacy of AMPA receptors of H1 cells for glutamate. For each of the cells tested, we recorded the responses to three concentrations of glutamate, first recorded in Ringer solution and then in the presence of melatonin. Relative potentiation was calculated for each of the doses. When the average dose–response relationship (Fig. 3, squares) based on the data pooled from between five and ten H1 cells obtained in the presence of 10 nM melatonin was compared to that determined in normal Ringer solution (circles), it was clear that the responses to glutamate of different concentrations, ranging from 0.1 mM to 10 mM (a saturating concentration that induced maximal current), were all potentiated to different extents. The Imax to 10 mM glutamate, was increased to 137.0% of the control level (P < 0.01), suggesting an increase in efficacy of glutamate. When the dose–response relationship obtained in the presence of 10 nM melatonin was further normalized by the amplitude of the maximal peak response to that obtained in normal Ringer solution, it was found that the curve obtained with 10 nM melatonin, as a whole, was shifted to the left along the abscissa, and the EC50 was reduced from 1.03 ± 0.04 mM (control) to 0.69 ± 0.02 mM, indicating an increased apparent affinity of glutamate receptors. It was noteworthy that the Hill coefficient was not significantly changed (1.52 ± 0.07 versus 1.49 ± 0.03, P > 0.05).
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We further examined how K 185, a specific antagonist of the MT2 receptor (Sugden et al. 1999; Faust et al. 2000) and luzindole, a competitive antagonist of both MT1 and MT2 receptors (Browning et al. 2000), may alter the effects of melatonin on the glutamate currents of H1 cells. Figure 4 shows the results of such an experiment obtained in an H1 cell. Similar to that shown in Fig. 2B, 10 nM melatonin significantly potentiated the peak current in response to 3 mM glutamate (Fig. 4B). When 10 nM melatonin was substituted by a mixture of 100 nM K 185 and 10 nM melatonin, the potentiated glutamate response was nearly unchanged (Fig. 4C). The cell was then washed out with normal Ringer solution for 3 min and the current recovered to the control level. With incubation of a mixture of 100 nM luzindole and 10 nM melatonin for another 2 min, however, the response was almost identical to the control response and no potentiation was observed at all (Fig. 4D), with a relative change of 99.1 ± 2.3% (P > 0.05, n= 6).
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It is well documented that melatonin receptors are coupled to G-protein and activation of these receptors may regulate several second messengers, among which cAMP and cGMP may be major ones (Vanecek, 1998). We therefore tested the effects of intracellular administrated cAMP and cGMP by adding these chemicals in the pipettes.
Figure 5A shows that internal infusion with 1 mM cAMP for 5 min did not change the peak amplitude of the response to 3 mM glutamate recorded in an H1 cell, but considerably potentiated the steady-state current, an effect that was quite different from the melatonin effect. In all seven cells tested, the steady-state current was increased by 71.3 ± 21.5% in the presence of 1 mM cAMP, while there was no significant change in peak amplitudes (102.4 ± 3.1% of control, P > 0.05). Internal infusion with 1 mM cGMP, however, clearly reduced the peak amplitude of the response. In the example shown in Fig. 5Ba, the peak amplitude of the response was 535 pA when sealing was just made (grey trace), but it gradually decreased in size and reached a steady level of 281 pA in 4 min (dark trace). Meanwhile, the steady-state current was also reduced in size from 51 to 28 pA. This effect of cGMP was reminiscent of the melatonin effect. It was of interest that the whole-current trace, when normalized, coincides with the control trace (see the inset). In five cells tested, internal infusion with 1 mM cGMP reduced the peak current amplitude to 48.4 ± 5.6% and the steady-state current to 54.3 ± 9.8% of the control levels (P < 0.001), respectively. Furthermore, when 10 nM melatonin was applied to the cGMP-filled cell, the glutamate current remained unchanged (100.5 ± 2.2%, n= 5, P > 0.05) (Fig. 5Bb). We also investigated the effects of methylene blue (MB), a guanosine cyclase inhibitor that decreases the intracellular concentration of cGMP, on the glutamate currents. As shown in Fig. 5Ca, melatonin of 10 nM potentiated the glutamate peak and steady-state currents of the H1 cell from 503 and 95 pA (control, grey trace) to 721 and 113 pA (MEL, dark trace), respectively. With incubation of 10 µM MB, the control glutamate peak and steady-state currents were also increased in size and reached a steady level of 802 and 122 pA (dark trace) in 5 min (Fig. 5Cb), but the desensitization kinetics was almost unchanged (= 3.5 ± 0.2 versus 3.5 ± 0.3 ms, n= 5, P > 0.05), as evidenced by the fact that the current response obtained in the presence of MB, when normalized, precisely coincides with the control response (see the inset), thus mimicking the effects of melatonin. In five cells tested, the peak and steady-state currents obtained with 10 µM MB were increased by 45.9 ± 6.1 and 38.3 ± 5.4%, respectively. ODQ, another guanosine cyclase inhibitor, had the effect similar to that of MB (n= 5, data not shown). It was further found that the glutamate currents of this cell remained unchanged when 10 nM melatonin was co-applied with 10 µM MB (Fig. 5Cc). The data obtained in all five cells tested indicated that peak current amplitudes obtained with a mixture of 10 µM MB and 10 nM melatonin were not significantly changed from those obtained with 10 µM MB alone (99.8 ± 1.9% of control, n= 5, P > 0.05). These results suggest that the potentiation by MB and melatonin of the glutamate current may be via the same pathway. We further examined if the effects of melatonin and MB may be additive when their concentrations were lower. Figure 5Da shows that melatonin of 1 nM potentiated the peak glutamate current of the H1 cell from 425 pA (control, grey trace) to 561 pA (MEL, dark trace). With incubation of 2 µM MB, the peak current was increased to 595 pA in 5 min (Fig. 5Db). When 1 nM melatonin was co-applied with 2 µM MB (Fig. 5Dc), the current was increased to 675 pA, a level significantly higher than that caused by either melatonin or MB. Similar results were obtained in four other H1 cell. Melatonin of 1 nM potentiated the glutamate currents by 30.1 ± 5.9%, whereas 2 µM MB potentiated those by 36.1 ± 5.8%. While both melatonin and MB were co-applied a larger (47.4 ± 9.2%) potentiation of glutamate currents was found.
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To explore physiological implication of the melatonin-induced potentiation of the glutamate response, we investigated effects of melatonin on light responses of cone HCs intracellularly recorded in the isolated, superfused retina.
After a preparation was set up in the perfusion chamber, light flashes of 500 nm (logI=–0.6) and 680 nm (logI=–0.6) were alternately presented at 1 Hz for about 5 min to release the cone system from the dark suppression (Xu et al. 2001). During the experiments, these two light flashes were alternately presented at intervals of 3 s, which is a routine experimental protocol in this laboratory that has been demonstrated to completely suppress the carp rod-driven light responses (Huang et al. 2004). Figure 6A illustrates the results obtained in a H1 cell. The light responses of this cell to test flashes of 500 nm (log I=–0.6) and 680 nm (log I=–0.6), predominantly activating short-wavelength sensitive cones, most probably green-sensitive (G) cones, and red-sensitive (R) cones, respectively (Yang et al. 1982, 1983, 1994), were of comparable amplitudes, but they exhibited different waveforms, suggesting that these responses were indeed driven by inputs from different types of cones. Application of 25 nM melatonin depolarized the H1 cell from –28 to –10 mV in 2 min. In association with the membrane depolarization, the light responses to both test flashes were reduced in amplitudes to the same extent (around 50% of the control responses). Co-application of 250 nM luzindole blocked the melatonin effects, and both membrane potential and light responses returned to the original levels obtained before the application of melatonin. Such results were consistently obtained in six other H1 cells. On average, the membrane potential of the cells was depolarized by 14.1 ± 2.1 mV, whereas the relative decrease of the amplitude was 46.7 ± 7.0% for green responses, and 47.1 ± 7.3% for red responses (n= 7).
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Modulation by melatonin of light responsiveness of cone HCs observed in the isolated retina might be a result of modified activity of D2-like dopamine receptors on photoreceptors due to melatonin-caused changes in dopamine release from interplexiform cells and amacrine cells, just like that reported recently (Ribelayga et al. 2004). The melatonin effects could also be a consequence of modulation of receptors for GABA and/or glycine expressed on these cells and/or on neurones presynaptic to these cells (see Kalloniatis & Tomisich, 1999; Yang, 2004 for review). The effects of melatonin on H1 cells were therefore studied in the presence of spiperone (a selective D2-like receptor antagonist), SCH 23390 (a selective and potent D1 receptor antagonist), picrotoxin (a non-selective Cl– channel blocker), and strychnine (a competitive antagonist of glycine receptors), and an example is shown in Fig. 6C. Co-application of 10 µM spiperone, 10 µM SCH 23390, 150 µM picrotoxin and 25 µM strychnine slightly (less than 5 mV) depolarized the cell, but hardly changed the light responses. Application of 25 nM melatonin, under these conditions, further depolarized the cell from –24 µM to –8 mV in 2 min. In association with the membrane depolarization, the light responses to both test flashes were reduced in amplitudes, like those observed in normal Ringer solution. Addition of 250 nM luzindole blocked these effects of melatonin, and both membrane potential and light responses returned to the original levels obtained before the application of melatonin. Such results were consistently obtained in five other H1 cells. On average, the membrane potential of the cells was depolarized by 11.2 ± 3.4 mV, whereas the relative decrease of the amplitude was 21.3 ± 8.4% for green responses and 21.6 ± 6.5% for red responses, respectively (n= 6).
As a comparison, rod HCs were intracellularly recorded and effects of melatonin on these cells were tested. Figure 6D shows that 25 nM melatonin slightly hyperpolarized the cell from a dark membrane potential of –26 to –30 mV and increased the amplitudes by about 20% for both green and red responses. These effects were quite different from those observed in the cone HCs. Again, the effects of melatonin could be reversed by adding 250 nM luzindole. Similar results were observed in eight other rod HCs. On average, the membrane potential of the cells was hyperpolarized by 2.8 ± 0.5 mV, whereas the relative increase of the amplitude was 26.5 ± 6.5% for green responses and 25.7 ± 6.2% for red responses (n= 9).
Effects of melatonin of high concentrations on glutamate currents and light responses of cone HCs
It was previously shown that melatonin of high concentration (500 µM) increased light responses of tiger salamander HCs (Wiechmann et al. 1988). We therefore tested effects of melatonin of high concentrations on both glutamate currents and light responses of H1 cells. When the concentration of melatonin was increased to 10 µM or higher, the effect of melatonin on glutamate current responses of H1 cells was quite different. A comparison of the responses to 3 mM glutamate obtained in normal Ringer solution (Fig. 7A) and in the presence of 100 µM melatonin (Fig. 7B) clearly shows that 100 µM melatonin did not potentiate, but reduced the peak amplitude of the response of an H1 cell (from 475 to 396 pA). Co-application with 250 µM luzindole did not reverse the effect of melatonin and instead further reduced the peak amplitude to 263 pA (Fig. 7C). The results obtained in seven other cells were quite similar. In the presence of 100 µM melatonin the glutamate current was reduced by 24.3 ± 4.4% (P < 0.05). Addition of 250 µM luzindole further reduced the current by 37.4 ± 4.7% (P < 0.05).
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Discussion |
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Although we were not sure from Fig. 1 if all subtypes of HCs (H1, H2, H3 and H4) (Dowling, 1987) were labelled by the anti-MT1 receptor antibody used, because the GAD-immunoreactive HCs could not be clearly identified, it was clear that somata and dendrites of GAD-labelled H1 cells, which are the most distally located of all HCs, were strongly MT1-immunoreactive and the labelling for MT1 was probably localized to the membrane of the H1 cells. This result is basically in agreement with the results obtained in other species by immunocytochemistry and in situ hybridization (Fujieda et al. 1999; Savaskan et al. 2002; Scher et al. 2002; Wiechmann, 2003; Sallinen et al. 2005).
Modulation by melatonin of glutamate currents of cone HCs
Our results showed that glutamate currents of cone HCs in carp retina were significantly potentiated by melatonin at rank orders of picomolar and nanomolar concentration in a dose-dependent manner. It should be emphasized that these concentrations of melatonin were most likely physiological ones (Faillace et al. 1996; Wan et al. 1999; Saenz et al. 2002; Wiechmann et al. 2003). The increase in maximal currents and the reduction of EC50 (Fig. 3) suggest that the potentiation may be due to an increase in both efficacy and apparent affinity of AMPA receptors for glutamate. The effect of melatonin on KA-induced currents was similar. The melatonin-caused potentiation could be blocked by luzindole, but not by K 185. Even though there is no specific antagonist of the MT1 receptor now available and luzindole works as a competitive antagonist of both MT1 and MT2 receptors (Browning et al. 2000), the different actions of luzindole and K 185 strongly suggest that the potentiation observed may be predominantly mediated by the MT1 receptor. While melatonin has been shown to modulate the GABA receptor on central neurones (Wan et al. 1999; Wu et al. 1999), the present work reports, for the first time, that melatonin could modulate AMPA receptor-mediated glutamatergic transmission by activating the MT1 receptor. It was of interest that melatonin did not change desensitization of the glutamate current, suggesting that melatonin might not interfere with physiological and biochemical processes which are responsible for receptor desensitization (Jones & Westbrook, 1996; Sun et al. 2002).
Melatonin of higher (micromolar) concentrations suppressed the glutamate currents, which could not be blocked by luzindole, suggesting that this effect of melatonin was unlikely mediated by the MT receptor. It is highly possible that this effect of melatonin may be due to an allosteric action caused by melatonin binding to a modulatory site on the AMPA receptor, which may not distinguish subtle difference between melatonin and luzindole. Action at an allosteric binding site on the intra- or extracellular surface of a receptor channel can cause changes in gating properties of the receptor (Changeux & Edelstein, 1998).
Possible mechanisms underlying the potentiation by melatonin of glutamate currents cAMP and cGMP are major intracellular second messengers that mediate melatonin regulation of cell functions (Vanecek, 1998). In a variety of cells melatonin does not alter basal cAMP levels but inhibits intracellular accumulation of cAMP (Reppert et al. 1994, 1995; Martensson & Andersson, 2000). In the carp cone HCs intracellular infusion of cAMP hardly changed the peak amplitude of the glutamate response, while it enhanced the steady-state current (Fig. 5A). This effect was quite different from that of melatonin on the glutamate response. Furthermore, since phosphorylation by cAMP-dependent protein kinase (PKA) of AMPA receptor was shown to enhance the activity of the receptor (Roche et al. 1996), the decrease of intracellular accumulation of cAMP by melatonin should have suppressed the glutamate response if the melatonin-caused potentiation observed in this work were mediated through cAMP. All these make it unlikely that cAMP may be a second messenger mediating the melatonin-induced potentiation.
Melatonin increases the intracellular concentration of cGMP in some cells (Vacas et al. 1981; Faillace et al. 1996), but decreases it in others (Vanecek & Vollrath, 1989; Petit et al. 1999; Saenz et al. 2002). Our results showed that, as observed in hybrid bass HCs (McMahon & Ponomareva, 1996), an increase in cGMP concentration by internal infusion reduced the amplitudes of both peak and steady-state glutamate currents (Fig. 5Ba) and the currents were not changed by the addition of 10 nM melatonin in the cGMP-filled cells (Fig. 5Bb). Moreover, a decrease of cGMP concentration in H1 cells by MB potentiated the amplitudes of both peak and steady-state currents, without affecting receptor desensitization, effects that were reminiscent of the melatonin effects on the currents (Fig. 5Cb), and the potentiation of the glutamate response by melatonin was no longer observed in the presence of MB (Fig. 5Cc). It was further found that the effects of melatonin and MB were additive when their concentrations were lower (Fig. 5D). All these results are suggestive of the involvement of cGMP in the melatonin-caused potentiation of the glutamate current. Of course, the possibility that melatonin and cGMP may affect AMPA receptor function through separate, but parallel pathways cannot be excluded.
Physiological roles of melatonin in the outer retina
Melatonin of 25 nM significantly depolarized the H1 cells and reduced light responses of these cells, intracellularly recorded in the isolated, superfused retina, which could be reversed by adding luzindole of 250 nM (Fig. 7A), suggesting that these effects of melatonin were mediated by the activation of the melatonin receptors. It seems unlikely that these effects of melatonin may be a consequence of its action on photoreceptors, since melatonin does not change the electroretinographic a wave in frog retina (Wiechmann et al. 2003) and no MT1 receptors are present on cones (Scher et al. 2002). While the possibility that these melatonin effects on cone HCs may be a consequence of melatonin-caused modulation of other receptors could not be fully ruled out, the fact that the melatonin effects persisted in the presence of spiperone, SCH 23390, picrotoxin and strychnine (Fig. 6C) suggests that the effects must be produced, at least in part, by a direct action of melatonin on the cone HCs. The reasons that melatonin caused the changes in membrane potential and light responses of cone HCs may be complicated. A possibility that activation of the MT1 receptor on H1 cells may lead to a stronger activation of the AMPA receptor on the cone HCs, probably through reducing the intracellular concentration of cGMP, thus making the membrane potential close to the reversal potential of the AMPA receptor (
0 mV) (Hirasawa et al. 2001). As a result of the reduced driving force, the light responses of these cells were reduced in size. With regard to the effects of melatonin on light responses of HCs, it is noted that 500 µM melatonin hyperpolarizes HCs and increases their light responses in the isolated, superfused tiger salamander retina (Wiechmann et al. 1988). We speculate that the effects of melatonin reported in that work may not be mediated by MT receptors and they could be attributed to the much higher concentration of melatonin (500 µM) used, 104 times higher than the concentration used in the present work, which could produce a possible allosteric action on the AMPA receptor of the HCs. In carp retina, melatonin of 250 µM also hyperpolarized the cone HCs (Fig. 7D), which was not reversed by luzindole.
In the teleost retina, circadian changes in the light responsiveness of L-type cone horizontal (H1) cells have been extensively studied (Wang & Mangel, 1996; Ribelayga et al. 2002, 2004). The light responses of H1 cells at night, compared with those recorded during the subjective day, are generally smaller in amplitude and slower. Moreover, application of melatonin during the subjective day makes the light responses of H1 cells smaller and slower, so that they resemble those typically observed during the subjective night, whereas superfusion of luzindole during the subjective night results in the night-like responses. Such modulation of the light responsiveness is thought be a result of melatonin modified activity of D2-like dopamine receptors on photoreceptors. In the present work, we also found that 25 nM melatonin reduced light responses of carp H1 cells, though no significant changes in response waveforms, similar to those reported in goldfish (Ribelayga et al. 2004), were observed, and these effects of melatonin were mediated by melatonin receptors, most likely the MT1 subtype, on the HCs. It should be indicated that rod signal was not detectable in light responses of H1 cells under our experimental conditions (see Results), even if rod signal could converge onto H1 cells through rod–cone coupling, as suggested by Wang & Mangel (1996). On the other hand, the experiments by Ribelayga et al. (2004) were conducted in fully dark adaptation; in other words, the experimental conditions used for this and the work of Ribelayga et al. work are not quite comparable. Our results therefore raise an alternative intriguing possibility that modulation by melatonin of cone HC light responsiveness may also involve modulation of AMPA receptor-mediated currents of these cells. This may be an additional mechanism underlying the effects of melatonin on cone-driven response of H1 cells that acts in concert with the mechanism proposed by Ribelayga et al. (2004).
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and •, respectively. For each cell, responses to three concentrations of glutamate were first recorded in Ringer solution and then in the presence of 10 nM melatonin. The response peaks obtained at different concentrations of glutamate were normalized to that of the response to 10 mM, a saturating concentration, of glutamate for each cell in the absence of melatonin. Curve fitting was performed for the averaged data, yielding EC50 values of 1.03 0.04 and 0.69 ± 0.02 mM in the absence and presence of 10 nM melatonin, respectively. The dashed curve is the normalized dose–response relationship in the presence of 10 nM melatonin, by that in normal Ringer solution, clearly demonstrating that the curve was shifted leftward by melatonin. Values in parentheses indicate the number of cells tested for each dose.
