Effects of ivermectin and midecamycin on ryanodine receptors and the Ca 2+ ‐ATPase in sarcoplasmic reticulum of rabbit and rat skeletal muscle
| Autor: | Jorgen Mould, Suzanne M. Curtis, Gerard P. Ahern, Suzy M. Pace, Angela F. Dulhunty, Pauline R. Junankar |
|---|---|
| Rok vydání: | 1999 |
| Předmět: |
Ruthenium red
Thapsigargin Physiology Lipid Bilayers Calcium-Transporting ATPases In Vitro Techniques Pharmacology Leucomycins Midecamycin Tacrolimus Binding Proteins chemistry.chemical_compound Caffeine parasitic diseases medicine Animals Immunophilins Muscle Skeletal Terminal cisternae Sirolimus Calcium metabolism Ivermectin Ryanodine receptor Endoplasmic reticulum Skeletal muscle Ryanodine Receptor Calcium Release Channel Original Articles musculoskeletal system Rats Sarcoplasmic Reticulum medicine.anatomical_structure Biochemistry chemistry Calcium Ca(2+) Mg(2+)-ATPase Macrolides Rabbits Muscle Contraction medicine.drug |
| Zdroj: | The Journal of Physiology. 514:313-326 |
| ISSN: | 1469-7793 0022-3751 |
| DOI: | 10.1111/j.1469-7793.1999.313ae.x |
| Popis: | 1. Ryanodine receptor (RyR) Ca2+ channels in the sarcoplasmic reticulum (SR) of skeletal muscle are regulated by the 12 kDa FK506- (or rapamycin-) binding protein (FKBP12). Rapamycin can also activate RyR channels with FKBP12 removed, suggesting that compounds with macrocyclic lactone ring structures can directly activate RyRs. Here we tested this hypothesis using two other macrocyclic lactone compounds, ivermectin and midecamycin. 2. Rabbit skeletal RyRs were examined in lipid bilayers. Ivermectin (cis, 0.66-40 microM) activated six of eight native, four of four control-incubated and eleven of eleven FKBP12-'stripped' RyR channels. Midecamycin (cis, 10-30 microM) activated three of four single native channels, six of eight control-incubated channels and six of seven FKBP12-stripped channels. Activity declined when either drug was washed out. 3. Neither ivermectin nor midecamycin removed FKBP12 from RyRs. Western blots of terminal cisternae (TC), incubated for 15 min at 37 C with 40 microM ivermectin or midecamycin, showed normal amounts of FKBP12. In contrast, no FKBP12 was detected after incubation with 40 microM rapamycin. 4. Ivermectin reduced Ca2+ uptake by the SR Ca2+-Mg2+-ATPase. Ca2+ uptake by TC fell to approximately 40% in the presence of ivermectin (10 microM), both with and without 10 microM Ruthenium Red. Ca2+ uptake by longitudinal SR also fell to approximately 40% with 10 microM ivermectin. Midecamycin (10 microM) reduced Ca2+ uptake by TC vesicles to approximately 76% without Ruthenium Red and to approximately 90 % with Ruthenium Red. 5. The rate of rise of extravesicular [Ca2+] increased approximately 2-fold when 10 microM ivermectin was added to TC vesicles that had been partially loaded with Ca2+ and then Ca2+ uptake blocked by 200 nM thapsigargin. Ivermectin also potentiated caffeine-induced Ca2+ release to approximately 140% of control. These increases in Ca2+ release were not seen with midecamycin. 6. Ivermectin, but not midecamycin, reversibly reduced Ca2+ loading in four of six skinned rat extensor digitorum longus (EDL) fibres to approximately 90%, and reversibly increased submaximal caffeine-induced contraction in five of eight fibres by approximately 110% of control. Neither ivermectin nor midecamycin altered twitch or tetanic tension in intact EDL muscle fibres within 20 min of drug addition. 7. The results confirm the hypothesis that compounds with a macrocyclic lactone ring structure can directly activate RyRs. Unexpectedly, ivermectin also reduced Ca2+ uptake into the SR. These effects of ivermectin on SR Ca2+ handling may explain some effects of the macrolide drugs on mammals. |
| Databáze: | OpenAIRE |
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