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1.
Microbiol Resour Announc ; 13(2): e0101423, 2024 Feb 15.
Artículo en Inglés | MEDLINE | ID: mdl-38231185

RESUMEN

Actinobacteria produce about two-thirds of all naturally derived antibiotics currently in clinical use. Kitasatospora aureofaciens Tü117 is a species of Actinobacteria and produces α-lipomycin. We report the complete genome sequence of K. aureofaciens, composed of a single linear chromosome of 8,717,539 Mbp with a G + C content of 72.0%.

2.
J Clin Pharm Ther ; 44(6): 977-980, 2019 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-31468576

RESUMEN

WHAT IS KNOWN AND OBJECTIVE: Lenvatinib inhibits CYP2C8. (S)-Warfarin is metabolized to (S)-7-hydroxywarfarin by CYP2C9 and (S)-4'-hydroxywarfarin by CYP2C8. Here, we report drug interactions between warfarin and lenvatinib in a patient with CYP2C9*1/*3. CASE SUMMARY: The patient was administered warfarin. His international normalized ratio (INR) was 1.92 before lenvatinib administration. On day 8 after beginning 12 mg/day lenvatinib, plasma trough concentrations of lenvatinib and (S)-warfarin were 33.3 ng/mL and 0.67 µg/mL, respectively. On day 10, his INR increased to 3.48. WHAT IS NEW AND CONCLUSION: Lenvatinib-dependent (S)-warfarin inhibition could involve CYP2C9 and CYP2C8. After initiating warfarin plus lenvatinib, INR assays are necessary.


Asunto(s)
Citocromo P-450 CYP2C9/genética , Interacciones Farmacológicas/genética , Compuestos de Fenilurea/uso terapéutico , Quinolinas/uso terapéutico , Vitamina K Epóxido Reductasas/genética , Warfarina/uso terapéutico , Anciano , Citocromo P-450 CYP2C8/genética , Genotipo , Humanos , Masculino
3.
Xenobiotica ; 45(12): 1147-53, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26189776

RESUMEN

1. The purpose of the present study was to investigate the effect of tacrolimus concentration in blood 12 h after administration (C12h) on acute renal dysfunction in patients with lupus nephritis (LN) taking tacrolimus once daily. 2. Five of the 35 LN patients experienced tacrolimus-induced acute renal dysfunction. 3. The average annual C12h of tacrolimus was higher for patients with events of elevated serum creatinine level than for patients not experiencing these events [6.4 (5.6-8.8) versus 2.8 (2.2-4.6) ng/mL, respectively, p=0.001]. 4. The average annual tacrolimus C12h was higher for patients with CYP3A5*3/*3 (PM) than for patients with the CYP3A5*1 allele (EM) [4.6 (3.2-6.6) versus 2.5 (2.0-3.1) ng/mL, respectively, p=0.002]. 5. The area under the receiver operating characteristic was 0.887, which gave the best sensitivity (80.0%) and specificity (86.7%) at a tacrolimus C12h (average annual C12h or C12h at events) threshold of 5.2 ng/mL. 6. C12h measurements, CYP3A5 genotyping and dose adjustments of tacrolimus should be performed to prevent acute renal dysfunction in LN patients taking tacrolimus once daily.


Asunto(s)
Citocromo P-450 CYP3A/genética , Citocromo P-450 CYP3A/metabolismo , Inmunosupresores/efectos adversos , Enfermedades Renales/inducido químicamente , Nefritis Lúpica/complicaciones , Tacrolimus/efectos adversos , Adolescente , Adulto , Anciano , Área Bajo la Curva , Creatinina/sangre , Femenino , Genotipo , Humanos , Inmunosupresores/farmacocinética , Estimación de Kaplan-Meier , Enfermedades Renales/complicaciones , Masculino , Persona de Mediana Edad , Polimorfismo Genético , Tacrolimus/farmacocinética , Adulto Joven
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