Evidence-based strategies for the characterisation of human drug and chemical glucuronidation in vitro and UDP-glucuronosyltransferase reaction phenotyping

JO Miners, A Rowland, JJ Novak, K Lapham… - Pharmacology & …, 2021 - Elsevier
Enzymes of the UDP-glucuronosyltransferase (UGT) superfamily contribute to the
elimination of drugs from almost all therapeutic classes. Awareness of the importance of …

[HTML][HTML] Effects of telmisartan on metabolic syndrome components: a comprehensive review

M Imenshahidi, A Roohbakhsh… - Biomedicine & …, 2024 - Elsevier
Telmisartan is an antagonist of the angiotensin II receptor used in the management of
hypertension (alone or in combination with other antihypertensive agents. It belongs to the …

Physiologically based pharmacokinetic (PBPK) modeling to predict the pharmacokinetics of irbesartan in different CYP2C9 genotypes

CK Cho, P Kang, CG Jang, SY Lee, YJ Lee… - Archives of Pharmacal …, 2023 - Springer
Irbesartan, a potent and selective angiotensin II type-1 (AT1) receptor blocker (ARB), is one
of the representative medications for the treatment of hypertension. Cytochrome P450 (CYP) …

[HTML][HTML] Implementation of CYP2D6 copy-number imputation panel and frequency of key pharmacogenetic variants in Finnish individuals with a psychotic disorder

K Häkkinen, JI Kiiski, M Lähteenvuo, T Jukuri… - The …, 2022 - nature.com
We demonstrate that CYP2D6 copy-number variation (CNV) can be imputed using existing
imputation algorithms. Additionally, we report frequencies of key pharmacogenetic variants …

Methylophiopogonanone A is a naturally occurring broad‐spectrum inhibitor against human UDP‐glucuronosyltransferases: Inhibition behaviours and implication in …

QH Zhou, GH Zhu, YQ Song, YF Que… - Basic & Clinical …, 2021 - Wiley Online Library
Methylophiopogonanone A (MOA) is an abundant homoisoflavonoid in the Chinese herb
Ophiopogonis Radix. Recent investigations revealed that MOA inhibited several human …

Elucidating nonlinear pharmacokinetics of telmisartan: Integration of target‐mediated drug disposition and OATP1B3‐mediated hepatic uptake in a physiologically …

T Tsuchitani, A Tomaru, Y Aoki… - CPT …, 2024 - Wiley Online Library
Telmisartan, a selective inhibitor of angiotensin II receptor type 1 (AT1), demonstrates
nonlinear pharmacokinetics (PK) when orally administered in ascending doses to healthy …

[HTML][HTML] Exploring Variability in Rifampicin Plasma Exposure and Development of Anti-Tuberculosis Drug-Induced Liver Injury among Patients with Pulmonary …

A Kivrane, V Ulanova, S Grinberga, E Sevostjanovs… - Pharmaceutics, 2024 - mdpi.com
Genetic polymorphisms can exert a considerable impact on drug pharmacokinetics (PK) and
the development of adverse drug reactions (ADR). However, the effect of genetic …

Achieved dose and treatment discontinuation of candesartan in men and women with chronic heart failure: data from CHARM

H Qin, P Dewan, BT Santema, JM Ter Maaten… - ESC Heart …, 2024 - Wiley Online Library
Aims Angiotensin receptor blockers have been shown to reduce heart failure hospitalization
and cardiovascular mortality in men and women with heart failure with reduced ejection …

Pharmacogenomics of celiprolol–evidence for a role of P‐glycoprotein and organic anion transporting polypeptide 1A2 in celiprolol pharmacokinetics

P Hirvensalo, A Tornio, T Tapaninen… - Clinical and …, 2022 - Wiley Online Library
The aim of this study was to search for associations of genetic variants with celiprolol
pharmacokinetics in a large set of pharmacokinetic genes, and, more specifically, in a set of …

Studying Telmisartan Plasma Exposure, Kidney Distribution, Receptor Occupancy, and Response in Patients With Type 2 Diabetes Using [11C]Telmisartan

S van der Hoek, DJ Mulder… - Clinical …, 2022 - Wiley Online Library
The angiotensin receptor blocker telmisartan slows progression of kidney disease in
patients with type 2 diabetes (T2D), yet many patients remain at high risk for progressive …