Article Figures & Data
Figures
- Fig. 1.
Effect of PGE2 on membrane properties of deep dorsal horn neurons. A, Depolarizing response produced by bath application of PGE2 (10 μm) recorded intracellularly in current-clamp mode in the presence of TTX (1 μm). Downward deflections are electrotonic voltage transients elicited by hyperpolarizing current pulses (amplitude, 0.15 nA; duration, 400 msec) to measure membrane input resistance (Rin). The PGE2-induced depolarization was associated with a decreasedRin. When the neuron was manually clamped (DC) to the resting membrane potential, the reduction inRin was unaffected. Therefore, the decreasedRin was not caused by activation of voltage-gated channels. B, Blind whole-cell patch-clamp recording of a PGE2 (5 μm)-induced inward current recorded in the presence of TTX (1 μm) from a neuron voltage clamped to −70 mV. This neuron was recorded from a slice with an attached dorsal root, permitting determination of the type of afferent input. Neurons with both A- and C-fiber inputs (bottom) responded to PGE2 with larger inward currents than neurons with purely A-fiber input. C, Both PGF2α (10 μm) and PGD2 (10 μm) were without effect in this PGE2 (10 μm)-responsive neuron.D, Intracellular recording from a deep dorsal horn neuron. Top, Bath-applied PGE2 (10 μm) elicited a membrane depolarization. At the resting membrane potential, dorsal root stimulation at A-fiber intensity (30 μA, 0.05 msec, 0.5 Hz) elicited subthreshold EPSPs. During the PGE2-induced depolarization, evoked EPSPs reached action potential threshold. Action potentials are indicated by dots. When the neuron was manually clamped (DC) to the resting membrane potential, action potentials disappeared. Bottom, EPSPs and action potentials are shown on an expanded time scale. Note that the amplitudes of EPSPs during DC are not significantly different from control, indicating that the generation of action potentials is not caused by the augmentation of transmitter release from presynaptic terminals. Three consecutive traces are superimposed in each stimulating condition.
- Fig. 2.
PGE2 acts postsynaptically. A, Whole-cell patch-clamp recording of a PGE2 (5 μm)-evoked inward current in a deep dorsal horn neuron with only A-fiber input. The PGE2-induced inward current was not blocked by perfusion with the Ca2+-free/high Mg2+ (5 mm) Krebs' solution. B, In contrast, dorsal root-evoked monosynaptic EPSCs were completely abolished by perfusion with the Ca2+-free/high Mg2+solution. Traces in A andB are from the same neuron. C, PGE2 did not affect the frequency of miniature EPSCs. The frequencies of miniature EPSCs before and during application of PGE2 were 46.2 and 44.3 Hz, respectively. This neuron responded to PGE2 with an inward current (see Fig. 1B).
- Fig. 3.
PGE2 has no effect on excitatory transmitter release in the SG (lamina II). A, The amplitude of Aδ-fiber (top traces) and C-fiber (bottom traces)-evoked monosynaptic EPSCs was not affected by PGE2 (10 μm). Five consecutive traces are superimposed for each condition. They were averaged, and the difference between baseline and peak current was measured. B, Summary of the PGE2 (10 μm) effects on the amplitude of dorsal root-evoked EPSCs. PGE2 did not significantly alter the amplitude of either Aδ- or C-fiber-evoked EPSCs in the SG (Aδ-fiber EPSC, p = 0.79, n = 9; C-fiber EPSC, p = 0.78, n = 8; pairedt test). The amplitudes of evoked EPSCs were measured 5–10 min after the start of PGE2 application. C, Miniature EPSCs recorded from a SG neuron in the presence of TTX (1 μm). The frequencies of mEPSCs were 22.6 and 22.2 Hz before and during application of PGE2, respectively. D, The effect of PGE2 (10 μm) on the frequency of mEPSCs. PGE2 did not significantly increase the frequency of mEPSCs in 14 of 15 SG neurons studied (p = 0.23, pairedt test). The frequency of mEPSCs was counted 5–10 min after the start of PGE2 application. All data were recorded at −70 mV.
- Fig. 4.
Effects of EP receptor agonists on membrane currents in deep dorsal horn neurons. A, An EP1 receptor agonist, 17-phenyl trinor prostaglandin E2 (10 μm), and an EP3 receptor agonist, sulprostone (10 μm), had no effect on membrane currents in neurons that responded to the nonselective EP receptor agonist, 19(R)-hydroxy prostaglandin E2 (10 μm). B, The selective EP2 receptor agonist, butaprost methyl ester (10 μm), induced an inward current similar to that produced by PGE2 (10 μm). C, Comparison of the effects of the different EP agonists. Points represent the mean ± SD of the percentage maximum response to PGE2 (10 μm).n = 3–6 in each group. EC50 values are 1.5 μm for PGE2, 2.3 μm for 19(R)-hydroxy prostaglandin E2, and 3.1 μm for butaprost methyl ester.
- Fig. 5.
Effects of membrane potential, flufenamic acid (FFA), andN-methyl-d-glucamine (NMDG) on PGE2-induced inward currents. A, This deep dorsal horn neuron was voltage clamped to different holding potentials, and PGE2 (10 μm, 60 sec)-induced inward currents were recorded. Note that responses become smaller as the membrane potential is depolarized. HP, Holding potential.B, Bath-applied PGE2 (5 μm) elicited an inward current in another neuron, as recorded by the whole-cell patch-clamp technique. FFA (50 μm) partially blocked the PGE2-induced inward current. Increasing the concentration of FFA to 100 μm almost completely blocked the PGE2-induced current, in a reversible fashion. C, Whole-cell patch-clamp recording reveals that application of FFA (100 μm) during the PGE2 (5 μm)-induced inward current reversed the effect of PGE2. D, Effect of decreasing extracellular Na+ on PGE2-induced inward currents. In normal Krebs' solution, bath-applied PGE2 (10 μm) induced an inward current. Changing the perfusion solution to a low Na+ solution, in which Na+ was replaced with NMDG+ (a membrane impermeable cation), reversed the PGE2-induced inward current nearly to control values. Returning to normal Krebs' solution restored the PGE2-induced inward current. The amplitudes of spontaneous EPSCs are truncated. Neurons were voltage clamped to −70 mV inB–D.
Tables
Superficial DH Deep DH Lamina II III, IV, V, VI Inward current 5/37 65/116 (patch clamp) 5 ± 2 pA 21 ± 16 pA Depolarization 1/16 18/23 (intracellular) 3 mV 8 ± 4 mV Total 6/53 83/139 (11%) (60%)
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