Aminoglycoside antibiotics induce pH-sensitive activation of the calcium-sensing receptor
| Autor: | Donald T. Ward, Malcolm N. Jones, Darren Holden, Daniela Riccardi, Stuart J McLarnon, Austin C. Elliott |
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| Rok vydání: | 2002 |
| Předmět: |
Agonist
medicine.medical_specialty medicine.drug_class Intracellular pH education Biophysics Receptors Cell Surface Transfection Biochemistry Internal medicine medicine Extracellular Humans Receptor Molecular Biology Cells Cultured reproductive and urinary physiology Chemistry Aminoglycoside HEK 293 cells Cell Biology Neomycin Hydrogen-Ion Concentration female genital diseases and pregnancy complications Anti-Bacterial Agents body regions Low Density Lipoprotein Receptor-Related Protein-2 Endocrinology Tobramycin Calcium-sensing receptor Receptors Calcium-Sensing human activities medicine.drug |
| Zdroj: | Biochemical and Biophysical Research Communications. 297:71-77 |
| ISSN: | 0006-291X |
| Popis: | The aminoglycoside antibiotic (AGA) neomycin is a known agonist of the extracellular calcium-sensing receptor (CaR). To test whether other AGA drugs stimulate the CaR, we studied the relative effects of four AGAs on intracellular Ca(2+) concentration ([Ca(2+)](i)) using CaR-transfected human embryonic kidney (HEK)-293 cells. Gentamicin, tobramycin, and neomycin evoked dose-dependent increases in [Ca(2+)](i) with EC(50) values of 258, 177, and 43 microM, respectively, in CaR-transfected, but not in non-transfected cells. Kanamycin was ineffective at doses1mM. Thus, AGAs stimulate the CaR with a rank order of potency that correlates positively with the number of their attached amino groups. The CaR is expressed on the apical surface of renal proximal tubule cells, which is also the site of AGA endocytosis and nephrotoxicity. In the current study, reducing extracellular pH from 7.4 to 6.9, to mimic the luminal pH of the proximal tubule, enhanced the sensitivity of the CaR to tobramycin, suggesting that the AGAs may be more potent CaR agonists in the proximal tubule than elsewhere. This pH effect was not observed when stimulating CaR with the non-ionizable agonist, Gd(3+), suggesting that the enhanced AGA effect is due to increased ionization of the drug. Thus, we show that a number of AGA drugs are capable of CaR activation and that their potency most likely relates to the number of their amino side chains and to their pH-dependent charge characteristics. The contribution of CaR activation to the pharmacological/toxicological effects of these AGAs remains to be determined. |
| Databáze: | OpenAIRE |
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