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1878年至2023年药理学教科书中记载的毛果芸香碱和毒扁豆碱临床相关性的下降:给未来(药理学)教科书作者的九条关键信息

The decline in the clinical relevance of pilocarpine and physostigmine monitored in pharmacology textbooks from 1878 to 2023: nine take-home messages for future (pharmacology) textbook authors.

作者信息

Ludwig Laureen, Seifert Roland

机构信息

Institute of Pharmacology, Hannover Medical School, Carl-Neuberg-Straße 1, Hannover, 30625, Germany.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2025 May;398(5):5171-5193. doi: 10.1007/s00210-024-03558-x. Epub 2024 Nov 12.

DOI:10.1007/s00210-024-03558-x
PMID:39531042
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11985697/
Abstract

In a recent study, using hydrogen cyanide as paradigm, we have shown that pharmacological knowledge evolves non-linearly ( https://pubmed.ncbi.nlm.nih.gov/38900251/ ). The aim of this study was to investigate the changes in the presentation of the drugs pilocarpine and physostigmine in textbooks from 1878 to 2023. The categories of structure, molecular mechanism of action, pharmacokinetics, effects, indications, adverse drug reactions, interactions, and contraindications were evaluated. The pharmacological knowledge on the molecular mechanism, chemical structure, and pharmacokinetics of pilocarpine and physostigmine changed the most during the period of 150 years. Until 1944, textbooks did not mention a molecular mechanism of action of pilocarpine and from 1951 onwards they described the activation of muscarinic acetylcholine receptors as the molecular basis of pilocarpine's effect. Until 1944, most textbooks on physostigmine also did not mention the molecular mechanism of action. From 1951 onwards, the reversible inhibition of acetylcholinesterase is mentioned as the mechanism of action of physostigmine. In contrast, in the categories effects, indications, adverse drug reactions, interactions, and contraindications, the detected changes in the pharmacological knowledge presented were comparatively smaller. Older pharmacology textbooks were better than newer ones at discussing changes in knowledge and scientific errors. We noted substantial differences in the presentation of pilocarpine and physostigmine among German and US pharmacology textbooks. We show a decline of the clinical relevance of both drugs and their presentation in pharmacological textbooks with physostigmine being virtually irrelevant. But modern textbooks still discuss physostigmine substantially, fitting to studies on the obsolete drug reserpine ( https://pubmed.ncbi.nlm.nih.gov/38103060/ ). Thus, textbooks often far lag clinical practice. Google Scholar conveys the incorrect impression that physostigmine is clinically more relevant than it is. An exponential decline in prescription numbers is a robust indicator of clinical obsolescence. From our study, we extract nine easily implementable take-home messages for future (pharmacology) textbook authors to ensure that this traditional teaching format will prevail against the competition of allegedly more "modern" teaching media.

摘要

在最近一项以氰化氢为范例的研究中,我们已经表明药理学知识呈非线性发展(https://pubmed.ncbi.nlm.nih.gov/38900251/)。本研究的目的是调查1878年至2023年教科书里毛果芸香碱和毒扁豆碱这两种药物呈现内容的变化。对结构、作用分子机制、药代动力学、效应、适应证、药物不良反应、相互作用和禁忌证等类别进行了评估。在150年期间,关于毛果芸香碱和毒扁豆碱的分子机制、化学结构和药代动力学的药理学知识变化最大。直到1944年,教科书都未提及毛果芸香碱的作用分子机制,从1951年起,它们将毒蕈碱型乙酰胆碱受体的激活描述为毛果芸香碱效应的分子基础。直到1944年,大多数关于毒扁豆碱的教科书也未提及作用分子机制。从1951年起,毒扁豆碱的作用机制被提及为乙酰胆碱酯酶的可逆抑制。相比之下,在效应、适应证、药物不良反应、相互作用和禁忌证等类别中,所呈现的药理学知识的检测变化相对较小。旧版药理学教科书在讨论知识变化和科学错误方面比新版更好。我们注意到德国和美国药理学教科书在毛果芸香碱和毒扁豆碱的呈现上存在很大差异。我们发现这两种药物的临床相关性及其在药理学教科书中的呈现均有所下降,毒扁豆碱实际上已无相关性。但现代教科书仍大量讨论毒扁豆碱,这与对过时药物利血平的研究情况相符(https://pubmed.ncbi.nlm.nih.gov/38103060/)。因此,教科书往往远远落后于临床实践。谷歌学术给人一种错误印象,即毒扁豆碱在临床上比实际情况更具相关性。处方数量呈指数下降是临床过时的有力指标。从我们的研究中,我们为未来(药理学)教科书作者提炼出九条易于实施的关键信息,以确保这种传统教学形式能够在据称更“现代”的教学媒体的竞争中胜出。

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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2772/11985697/f542192ae3c3/210_2024_3558_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2772/11985697/573d6973a283/210_2024_3558_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2772/11985697/6d27eb5a6154/210_2024_3558_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2772/11985697/52d04b6082fb/210_2024_3558_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2772/11985697/98eb6b8a7cfa/210_2024_3558_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2772/11985697/b6fd928e9811/210_2024_3558_Fig13_HTML.jpg
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