tetramethylrhodamine and Myasthenia-Gravis

tetramethylrhodamine has been researched along with Myasthenia-Gravis* in 1 studies

Other Studies

1 other study(ies) available for tetramethylrhodamine and Myasthenia-Gravis

ArticleYear
Tetanic failure due to decreased endogenous adenosine A(2A) tonus operating neuronal Ca(v) 1 (L-type) influx in Myasthenia gravis.
    Journal of neurochemistry, 2011, Volume: 117, Issue:5

    In healthy motor endplates, tetanic depression is overcome by tonic adenosine A(2A) -receptor-mediated facilitation of transmitter release. The A(2A) receptor operates a coordinated shift from fast-desensitizing Ca(v) 2.1 (P/Q) calcium influx to long-lasting Ca(V) 1 (L) channels on motor nerve terminals. This study aimed at investigating whether A(2A) receptors-operated Ca(2+) influx via Ca(V) 1 (L)-type channels contribute to sustain acetylcholine release evoked by 50 Hz-bursts in toxin-induced Myasthenia gravis (TIMG) rats. In contrast to control animals, inhibition of [(3) H]acetylcholine (ACh) release by the Ca(V) 2.1 (P/Q) channel blocker, ω-Agatoxin IVA (100 nM), in TIMG rats had a higher magnitude than that observed with the Ca(V) 1 (L) channel blocker, nifedipine (1 μM). Adenosine deaminase (0.5 U/mL) and the A(2A) receptor antagonist, ZM 241385 (50 nM), decreased [(3) H]ACh release by a similar amount in control rats, but their effects were smaller in magnitude in myasthenic animals. The adenosine precursor, AMP (100 μM), increased (~40%) ACh release in both control and TIMG animals. Blockade of A(2A) , but not of A(1) , receptors prevented AMP-induced facilitation of transmitter release; nifedipine (1 μM) mimicked the effect of the A(2A) receptor antagonist. Video-microscopy studies designed to measure real-time transmitter exocytosis using the FM4-64 fluorescent dye fully supported radiochemical data. Thus, impairment of the adaptive shift from Ca(V) 2.1 (P/Q) to Ca(V) 1 (L) channels may contribute to tetanic failure in myasthenic rats. This parallels the reduction of adenosine A(2A) receptor tonus in TIMG animals, which might be restored by exogenous application of AMP.

    Topics: Acetylcholine; Adenosine; Adenosine Triphosphate; Animals; Bungarotoxins; Calcium Channel Blockers; Calcium Channels, L-Type; Calcium Channels, N-Type; Cholinesterase Inhibitors; Electric Stimulation; Exocytosis; Female; Fluorescent Dyes; Male; Membrane Potentials; Microscopy, Video; Motor Neurons; Muscle Contraction; Muscle, Smooth, Vascular; Myasthenia Gravis; Neurotransmitter Agents; Phrenic Nerve; Presynaptic Terminals; Rats; Receptor, Adenosine A2A; Rhodamines

2011