Regulation of the sensitivity of acetylcholine receptors to nicotine in rat habenula neurons

Academic Article

Abstract

  • 1. Time-dependent changes in nicotinic acetylcholine receptor (nAChR) function were studied in acutely isolated medial habenula neurons during whole-cell perfusion. 2. The peak amplitude of inward currents induced by 1 s pulses of nicotinic agonists, applied at 30 s intervals, gradually increased over the first several minutes of whole-cell recording. The ratio of response amplitudes at 1 and 15 min (t15/t1) was 1.9. Run-up of responses occurred independently of channel activation and was specific to nAChRs. 3. The channel blocker chlorisondamine (30 μM), co-applied with nicotine, was used to irreversibly block the majority (91%) of the nAChRs that opened in the first 2 min of recording. Run-up in the remaining 9% unblocked channels assessed at 15 min (t15/t2 = 3.4) was similar to that in control cells not exposed to nicotine and chlorisondamine simultaneously, implying that run-up is not due to the incorporation of new receptors. 4. A marked alteration in the sensitivity of nAChRs to extracellular Ca2+ was also observed during whole-cell perfusion. The ratio of current amplitudes obtained in 0.2 and 4.0 mM Ca2+ changed from 0.54 (t = 5 min) to 0.82 (t = 30 min). 5. Inward rectification of nicotine-induced responses was reduced during internal dialysis. Voltages for half-maximal conductance were -23.0 and -13.8 mV at 2 and 15 min, respectively. Inclusion of either free Mg2+ (∼2 mM) or spermine (100 μM) in the internal solution counteracted the change in rectification, but did not prevent run-up. 6. The period of run-up was followed by a use-dependent run-down phase. Little run-down in peak current amplitude was induced provided that agonist was applied infrequently (5 min intervals), whereas applications at 30 s intervals produced a loss of channel function after ∼15 min whole-cell perfusion. The time at which run-down began (∼5-30 min) was correlated with the initial rate of nAChR desensitization (∼200-4000 ms); slowly desensitizing nicotinic currents demonstrated delayed run-down. 7. We suggest that run-up of nAChR-mediated responses does not require receptor activation and may result from a change in channel open probability. We also hypothesize that channel run-down reflects accumulation of nAChRs in long-lived desensitized/inactivated states.
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    Author List

  • Hicks JH; Dani JA; Lester RAJ
  • Start Page

  • 579
  • End Page

  • 597
  • Volume

  • 529
  • Issue

  • 3