T. Noda, R. Kato, Yasuyuki Ozato, Y. Kawai, M. Yamamoto, Yuya Kagawa, Misa Azuma, Kojiro Yamamoto, Mika Kusanagi, Kiyoaki Uryu, Hiromasa Harada, Y. Ijiri, T. Hayashi, Kazuhiko Tanaka
{"title":"血浆对乙酰氨基酚葡萄糖醛酸/对乙酰氨基酚浓度比降低提示对乙酰氨基酚诱导的肝损伤的发生","authors":"T. Noda, R. Kato, Yasuyuki Ozato, Y. Kawai, M. Yamamoto, Yuya Kagawa, Misa Azuma, Kojiro Yamamoto, Mika Kusanagi, Kiyoaki Uryu, Hiromasa Harada, Y. Ijiri, T. Hayashi, Kazuhiko Tanaka","doi":"10.1002/bdd.2316","DOIUrl":null,"url":null,"abstract":"Acetaminophen (APAP)‐induced liver injury (AILI) is the most common cause of acute liver failure. Although the mechanisms that trigger AILI are well known, it is less understood how to halt AILI progression and facilitate liver recovery. Therefore, it is necessary to understand the pathophysiology of APAP hepatotoxicity in patients and to examine predictive/preventive markers. In a clinical study, we had a case in which aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels increased in a patient with a low ratio of APAP glucuronide concentration (AP‐G)/APAP plasma concentration. Then a reverse translational study was conducted for clarifying this clinical question. The relationship between plasma AP‐G/APAP concentration ratio and the levels of AST and ALT was examined by in vivo and in vitro experiments. In in vivo experiments, 10‐week‐old rats showed lower UGT activity, lower AP‐G/APAP concentration ratios, and higher AST and ALT levels than 5‐week‐old rats. This suggests an inverse correlation between the AP‐G/APAP concentration ratio and the AST, ALT levels in APAP‐treated rats. Furthermore, as a result of the in vitro experiment, it was confirmed that the cell viability decreased when the AP‐G/APAP concentration ratio in the culture medium decreased. Since the decrease in the plasma AP‐G/APAP concentration ratio appears earlier than the increase of AST and ALT levels, the ratio might be a presymptomatic marker of AILI. When APAP is used for a long time, it is recommended to perform therapeutic drug monitoring of the AP‐G/APAP concentration ratio, which is a predictive/preventive marker of AILI.","PeriodicalId":8865,"journal":{"name":"Biopharmaceutics & Drug Disposition","volume":"43 1","pages":"108 - 116"},"PeriodicalIF":1.7000,"publicationDate":"2022-05-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Decreased plasma acetaminophen glucuronide/acetaminophen concentration ratio warns the onset of acetaminophen‐induced liver injury\",\"authors\":\"T. Noda, R. Kato, Yasuyuki Ozato, Y. Kawai, M. Yamamoto, Yuya Kagawa, Misa Azuma, Kojiro Yamamoto, Mika Kusanagi, Kiyoaki Uryu, Hiromasa Harada, Y. Ijiri, T. Hayashi, Kazuhiko Tanaka\",\"doi\":\"10.1002/bdd.2316\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Acetaminophen (APAP)‐induced liver injury (AILI) is the most common cause of acute liver failure. Although the mechanisms that trigger AILI are well known, it is less understood how to halt AILI progression and facilitate liver recovery. Therefore, it is necessary to understand the pathophysiology of APAP hepatotoxicity in patients and to examine predictive/preventive markers. In a clinical study, we had a case in which aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels increased in a patient with a low ratio of APAP glucuronide concentration (AP‐G)/APAP plasma concentration. Then a reverse translational study was conducted for clarifying this clinical question. The relationship between plasma AP‐G/APAP concentration ratio and the levels of AST and ALT was examined by in vivo and in vitro experiments. In in vivo experiments, 10‐week‐old rats showed lower UGT activity, lower AP‐G/APAP concentration ratios, and higher AST and ALT levels than 5‐week‐old rats. This suggests an inverse correlation between the AP‐G/APAP concentration ratio and the AST, ALT levels in APAP‐treated rats. Furthermore, as a result of the in vitro experiment, it was confirmed that the cell viability decreased when the AP‐G/APAP concentration ratio in the culture medium decreased. Since the decrease in the plasma AP‐G/APAP concentration ratio appears earlier than the increase of AST and ALT levels, the ratio might be a presymptomatic marker of AILI. 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Decreased plasma acetaminophen glucuronide/acetaminophen concentration ratio warns the onset of acetaminophen‐induced liver injury
Acetaminophen (APAP)‐induced liver injury (AILI) is the most common cause of acute liver failure. Although the mechanisms that trigger AILI are well known, it is less understood how to halt AILI progression and facilitate liver recovery. Therefore, it is necessary to understand the pathophysiology of APAP hepatotoxicity in patients and to examine predictive/preventive markers. In a clinical study, we had a case in which aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels increased in a patient with a low ratio of APAP glucuronide concentration (AP‐G)/APAP plasma concentration. Then a reverse translational study was conducted for clarifying this clinical question. The relationship between plasma AP‐G/APAP concentration ratio and the levels of AST and ALT was examined by in vivo and in vitro experiments. In in vivo experiments, 10‐week‐old rats showed lower UGT activity, lower AP‐G/APAP concentration ratios, and higher AST and ALT levels than 5‐week‐old rats. This suggests an inverse correlation between the AP‐G/APAP concentration ratio and the AST, ALT levels in APAP‐treated rats. Furthermore, as a result of the in vitro experiment, it was confirmed that the cell viability decreased when the AP‐G/APAP concentration ratio in the culture medium decreased. Since the decrease in the plasma AP‐G/APAP concentration ratio appears earlier than the increase of AST and ALT levels, the ratio might be a presymptomatic marker of AILI. When APAP is used for a long time, it is recommended to perform therapeutic drug monitoring of the AP‐G/APAP concentration ratio, which is a predictive/preventive marker of AILI.
期刊介绍:
Biopharmaceutics & Drug Dispositionpublishes original review articles, short communications, and reports in biopharmaceutics, drug disposition, pharmacokinetics and pharmacodynamics, especially those that have a direct relation to the drug discovery/development and the therapeutic use of drugs. These includes:
- animal and human pharmacological studies that focus on therapeutic response. pharmacodynamics, and toxicity related to plasma and tissue concentrations of drugs and their metabolites,
- in vitro and in vivo drug absorption, distribution, metabolism, transport, and excretion studies that facilitate investigations related to the use of drugs in man
- studies on membrane transport and enzymes, including their regulation and the impact of pharmacogenomics on drug absorption and disposition,
- simulation and modeling in drug discovery and development
- theoretical treatises
- includes themed issues and reviews
and exclude manuscripts on
- bioavailability studies reporting only on simple PK parameters such as Cmax, tmax and t1/2 without mechanistic interpretation
- analytical methods