The present study was performed to investigate whether neomycin, an aminoglycoside, interacts with calcium channels in the frog rectus abdominis muscle. We thus examined the effects of methoxyverapamil (D600), a dihydropyridine-sensitive calcium channel antagonist, and neomycin on contractions induced by acetylcholine (ACh; 10-6, 3 × 10 -6, 5 × 10-6, 10-5 and 5 × 10 -5 M), electrical field stimulation (EFS; 5, 8, 10 Hz, 15 V, 1 ms) and potassium chloride (KCl; 40 mM) in isolated frog rectus abdominis muscle. D600 (10-6 - 3 × 10-4 M) exhibited a concentration dependent inhibitory action on contractions evoked by ACh, EFS and KCl. Neomycin (10-5-5 × 10-4 M) significantly inhibited the contractions elicited by ACh and EFS in a concentration de...
The effects of seven antibiotics (streptomycin, amikacin, polymyxin B, lincomycin, clindamycin, tetr...
In all four proboscis muscles of the whelk Buccinum undatum, the potassium-induced depolarization re...
4-Aminopyridine is widely used as a Kv channel blocker. However, its mechanism of action is still a ...
PubMedID: 10806525The present study was undertaken to investigate the postsynaptic effects of aminog...
The present study was undertaken to investigate the postsynaptic effects of aminoglycosides on contr...
The effects of verapamil in high concentration (0.5-5 mM) on electrical and mechanical responses, an...
Cumulation and interaction of neuromuscular blocking effects of neomycin and tubocurarine were deter...
AbstractIn this study we have investigated the actions of the aminoglycoside antibiotic neomycin on ...
Four groups of antibiotics (aminoglycosides, polymyxins, tetracyclines, and lincomycins) have neurom...
Neomycin is a potent inhibitor of skeletal muscle sarcoplasmic reticulum (SR) calcium release. To el...
ADAMS, H. RICHARD AND FRANK R. GOODMAN Differential inhibitory effect of neomvcin on contractile res...
Gentamicin in concentrations of 0.05-0.2 mmol litre"1 blocked neuromuscular transmission in the...
1. 1. Exposures for 30 min to Ca-free salines irreversibly inhibited responses of the odontophore pr...
The activity of single mechanosensitive channels was recorded from cell-attached patches on acutely ...
4-Aminopyridine is widely used as a Kv channel blocker. However, its mechanism of action is still a ...
The effects of seven antibiotics (streptomycin, amikacin, polymyxin B, lincomycin, clindamycin, tetr...
In all four proboscis muscles of the whelk Buccinum undatum, the potassium-induced depolarization re...
4-Aminopyridine is widely used as a Kv channel blocker. However, its mechanism of action is still a ...
PubMedID: 10806525The present study was undertaken to investigate the postsynaptic effects of aminog...
The present study was undertaken to investigate the postsynaptic effects of aminoglycosides on contr...
The effects of verapamil in high concentration (0.5-5 mM) on electrical and mechanical responses, an...
Cumulation and interaction of neuromuscular blocking effects of neomycin and tubocurarine were deter...
AbstractIn this study we have investigated the actions of the aminoglycoside antibiotic neomycin on ...
Four groups of antibiotics (aminoglycosides, polymyxins, tetracyclines, and lincomycins) have neurom...
Neomycin is a potent inhibitor of skeletal muscle sarcoplasmic reticulum (SR) calcium release. To el...
ADAMS, H. RICHARD AND FRANK R. GOODMAN Differential inhibitory effect of neomvcin on contractile res...
Gentamicin in concentrations of 0.05-0.2 mmol litre"1 blocked neuromuscular transmission in the...
1. 1. Exposures for 30 min to Ca-free salines irreversibly inhibited responses of the odontophore pr...
The activity of single mechanosensitive channels was recorded from cell-attached patches on acutely ...
4-Aminopyridine is widely used as a Kv channel blocker. However, its mechanism of action is still a ...
The effects of seven antibiotics (streptomycin, amikacin, polymyxin B, lincomycin, clindamycin, tetr...
In all four proboscis muscles of the whelk Buccinum undatum, the potassium-induced depolarization re...
4-Aminopyridine is widely used as a Kv channel blocker. However, its mechanism of action is still a ...