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3 protocols using ac1903

1

Chemical Screening for Cell Viability

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Dimethylsulfoxide (DMSO), Minimum Essential Medium Eagle (EMEM, M0643), sodium bicarbonate (NaHCO3), noble agar (A5431), resazurin sodium salt (199303), Vincristine (V0400000), Lomustine (L5918), YM-58483 (Y4895), Synta66 (SML1949), GSK1016790A (G0798), HC-067047 (SML0143), AC1903 (SML2244), ML218 (SML0385), Mibefradil dihydrochloride hydrate (M5441), NNC55-0396 hydrate (N0287), Yoda1 (SML1558), Verapamil hydrochloride (V4629) and Nifedipine (N7634) were purchased from Sigma-Aldrich (Ryde, NSW, Australia). IA65 was a kind gift from Professor William Denny and Dr. Ralph Stevenson, and was synthesised as previously described [28 (link)]. CellTiter-Fluorâ„¢ Cell Viability (G6081) was obtained from Promega (Madison, WA, USA).
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2

Gadolinium-based Contrast Agent Characterization

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GDD and Gd-DTPA were purchased from Selleck. Magnevist and Gadavist were purchased from Bayer Healthcare Pharmaceutical (Whippany, NJ, USA). GdCl3, histamine, AC1903, and other salts used in the experimental solutions were purchased from Sigma-Aldrich (St. Louis, MO, USA).
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3

TRPC5 Inhibition Ameliorates Proteinuria

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DOX-dependent proteinuria was induced as described above. TRPC5 inhibitors, 0.3 mg/kg (low dose) and 1 mg/kg (high dose) of ML204 or 0.75 mg/kg (low dose) and 1.5 mg/kg (high dose) of AC1903 were dissolved in dimethylsulfoxide (DMSO) and injected into mice 48 and 76 hrs after DOX-chow addition to establish the effect of TRPC5 inhibition on ACR. ML204 and AC1903 were obtained from Sigma-Aldrich. Control mice received only the vehicle.
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