Pub Date : 2024-06-25DOI: 10.12116/j.issn.1004-5619.2023.330802
Jin-Ting Liu, Li-Ying Zhou, Jia-Hong Xiang, Zi-Yi Li, Wan-Ting Xie, Ke-Ming Yun, Yan Shi
Piperazines are a class of new psychoactive substances with hallucinogenic effects that affect the central nervous system by affecting the level of monoamine neurotransmitters. Abuse of piperazines will produce stimulating and hallucinogenic effects, accompanied by headache, dizziness, anxiety, insomnia, vomiting, chest pain, tachycardia, hypertension and other adverse reactions, and may even cause cardiovascular diseases and multiple organ failure and lead to death, seriously affecting human physical and mental health and public safety. The abuse of new psychoactive substance piperazines has attracted extensive attention from the international community. The study of its pharmacological toxicology and analytical methods has become a research hotspot in the field of forensic medicine. This paper reviews the in vivo processes, sample treatment and analytical methods of existing piperazines, in order to provide reference for forensic identification.
{"title":"Research Progress on Detection of New Psychoactive Substance Piperazines <i>in vivo</i>.","authors":"Jin-Ting Liu, Li-Ying Zhou, Jia-Hong Xiang, Zi-Yi Li, Wan-Ting Xie, Ke-Ming Yun, Yan Shi","doi":"10.12116/j.issn.1004-5619.2023.330802","DOIUrl":"https://doi.org/10.12116/j.issn.1004-5619.2023.330802","url":null,"abstract":"<p><p>Piperazines are a class of new psychoactive substances with hallucinogenic effects that affect the central nervous system by affecting the level of monoamine neurotransmitters. Abuse of piperazines will produce stimulating and hallucinogenic effects, accompanied by headache, dizziness, anxiety, insomnia, vomiting, chest pain, tachycardia, hypertension and other adverse reactions, and may even cause cardiovascular diseases and multiple organ failure and lead to death, seriously affecting human physical and mental health and public safety. The abuse of new psychoactive substance piperazines has attracted extensive attention from the international community. The study of its pharmacological toxicology and analytical methods has become a research hotspot in the field of forensic medicine. This paper reviews the <i>in vivo</i> processes, sample treatment and analytical methods of existing piperazines, in order to provide reference for forensic identification.</p>","PeriodicalId":12317,"journal":{"name":"法医学杂志","volume":"40 3","pages":"276-283"},"PeriodicalIF":0.0,"publicationDate":"2024-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142008566","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-06-25DOI: 10.12116/j.issn.1004-5619.2023.531002
Zhi-Wei Jiang, Ruo-Cheng Xia, Rui-Yang Tao, Cheng-Tao Li
Objectives: To establish a rapid, accurate, and sensitive multiplex PCR detection method for the simultaneous identification of the six common edible meats (beef, lamp, chicken, pork, goose, duck), and to evaluate its application value in meat adulteration identification.
Methods: Based on complete mitochondrial genomic sequences of six species in the GenBank database, DNA sequences (cattle:16S rRNA; sheep:COX-1; chickens:Cytb; pig:COX-1; goose:NADH2; duck:16S rRNA) with intra-species conservation and inter-species specificity were screened, and species-specific primers were designed to construct a multiplex PCR detection system that can simultaneously detect the meat of six common species. The species specificity, sensitivity and reproducibility of the system were studied, and the simulated mixture sample detection was performed.
Results: This study successfully constructed a multiplex PCR detection system that can detect the meats of six common species simultaneously. The system was not effective in DNA amplification of non-target species. When the DNA template sizes were 0.062 5-2 ng/μL, the amplified products of all six species could be detected. The duck component was still detected when the mixing ratio of duck and beef was as low as 0.5%.
Conclusions: This study constructs and establishes a multiplex PCR detection system with strong specificity, high sensitivity, and good reproducibility. It can accurately identify the components of animal origin in common edible meats and provide a simple and practical method for identifying adulteration of common edible meats and meat products in China.
目的建立一种快速、准确、灵敏的多重PCR检测方法,用于同时鉴定6种常见食用肉类(牛、灯、鸡、猪、鹅、鸭),并评价其在肉类掺假鉴定中的应用价值:方法:基于 GenBank 数据库中六种肉类的完整线粒体基因组序列,对其 DNA 序列(牛:16S rRNA;羊:COX-1;鸡:Cytb;猪:COX-1;鹅:NADH2;鸭:16S rRNA)的种内保守性和种间特异性,设计了种间特异性引物,构建了可同时检测 6 种常见肉类的多重 PCR 检测系统。研究了该系统的物种特异性、灵敏度和重现性,并进行了模拟混合样品检测:结果:本研究成功构建了一个可同时检测六种常见肉类的多重 PCR 检测系统。该系统对非目标物种的 DNA 扩增无效。当 DNA 模板大小为 0.062 5-2 ng/μL 时,可检测到所有六个物种的扩增产物。当鸭肉和牛肉的混合比例低至 0.5%时,仍能检测到鸭肉成分:本研究构建并建立了一种特异性强、灵敏度高、重现性好的多重 PCR 检测系统。结论:该研究构建并建立了特异性强、灵敏度高、重现性好的多重 PCR 检测系统,可准确鉴定常见食用肉类中的动物源性成分,为我国常见食用肉类及肉制品的掺假鉴别提供了一种简便实用的方法。
{"title":"Establishment and Validation of a Multiplex PCR Detection System for the Identification of Six Common Edible Meat Components.","authors":"Zhi-Wei Jiang, Ruo-Cheng Xia, Rui-Yang Tao, Cheng-Tao Li","doi":"10.12116/j.issn.1004-5619.2023.531002","DOIUrl":"https://doi.org/10.12116/j.issn.1004-5619.2023.531002","url":null,"abstract":"<p><strong>Objectives: </strong>To establish a rapid, accurate, and sensitive multiplex PCR detection method for the simultaneous identification of the six common edible meats (beef, lamp, chicken, pork, goose, duck), and to evaluate its application value in meat adulteration identification.</p><p><strong>Methods: </strong>Based on complete mitochondrial genomic sequences of six species in the GenBank database, DNA sequences (cattle:<i>16S rRNA</i>; sheep:<i>COX-1</i>; chickens:<i>Cytb</i>; pig:<i>COX-1</i>; goose:<i>NADH2</i>; duck:<i>16S rRNA</i>) with intra-species conservation and inter-species specificity were screened, and species-specific primers were designed to construct a multiplex PCR detection system that can simultaneously detect the meat of six common species. The species specificity, sensitivity and reproducibility of the system were studied, and the simulated mixture sample detection was performed.</p><p><strong>Results: </strong>This study successfully constructed a multiplex PCR detection system that can detect the meats of six common species simultaneously. The system was not effective in DNA amplification of non-target species. When the DNA template sizes were 0.062 5-2 ng/μL, the amplified products of all six species could be detected. The duck component was still detected when the mixing ratio of duck and beef was as low as 0.5%.</p><p><strong>Conclusions: </strong>This study constructs and establishes a multiplex PCR detection system with strong specificity, high sensitivity, and good reproducibility. It can accurately identify the components of animal origin in common edible meats and provide a simple and practical method for identifying adulteration of common edible meats and meat products in China.</p>","PeriodicalId":12317,"journal":{"name":"法医学杂志","volume":"40 3","pages":"254-260"},"PeriodicalIF":0.0,"publicationDate":"2024-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142008564","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objectives: To explore the effects of different test positions on quantitative muscle strength of wrist and finger flexor muscle groups and to establish a standardized muscle strength test protocol for each muscle group.
Methods: Forty healthy subjects (12 males and 28 females) were recruited. A portable digital quantitative muscle strength tester, Micro FET2TM, was used to measure the flexor muscle strength of each finger and the wrist joint at the 30° extension, 0° neutral, and 30° flexion, respectively. Palmar abduction strength of the thumb was measured at 30° and 60°, respectively. Ten subjects were randomly selected from the 40 subjects, and the quantitative muscle strength of each muscle group was tested again by the same operator after an interval of 10 to 15 days.
Results: Except for the fact that in males, there was no significant difference in flexor muscle strength of thumb and wrist joint between 30° of wrist extension and neutral 0° position, the muscle strength of the other fingers flexion and wrist palmar flexor showed the following characteristics:30° of wrist extension > neutral 0° position > 30° of flexion, and the PAST was 30°>60°; The flexor muscle strength of all the subjects was thumb > index finger > middle finger > ring finger > little finger; All muscle strength values of male were greater than those of female, and the difference was statistically significant (P<0.05); There was no significant difference between the left and right side muscle strength values of all subjects (P>0.05). The reliability of muscle strength values measured at different times in 10 subjects was good.
Conclusions: The quantitative muscle strength of each muscle group of the hand and wrist is affected by the test position, and a standardized and uniformed test position should be adopted in the actual identification. Micro FET2TM has good reliability for hand and wrist quantitative muscle strength testing. The 30° extension of the wrist can be used as the best standardized test position for the flexion muscle strength of each finger and wrist joint. The 30° position can be used as the best standardized test position for PAST.
{"title":"Effects of Different Test Positions on Quantitative Muscle Strength of Wrist and Finger Flexor Muscle Groups and Its Standardization.","authors":"Ze-Ren Yang, Dong Gao, Qing Xia, Dan Ran, Yan-Liang Sheng, Wen-Tao Xia","doi":"10.12116/j.issn.1004-5619.2023.230501","DOIUrl":"https://doi.org/10.12116/j.issn.1004-5619.2023.230501","url":null,"abstract":"<p><strong>Objectives: </strong>To explore the effects of different test positions on quantitative muscle strength of wrist and finger flexor muscle groups and to establish a standardized muscle strength test protocol for each muscle group.</p><p><strong>Methods: </strong>Forty healthy subjects (12 males and 28 females) were recruited. A portable digital quantitative muscle strength tester, Micro FET2<sup>TM</sup>, was used to measure the flexor muscle strength of each finger and the wrist joint at the 30° extension, 0° neutral, and 30° flexion, respectively. Palmar abduction strength of the thumb was measured at 30° and 60°, respectively. Ten subjects were randomly selected from the 40 subjects, and the quantitative muscle strength of each muscle group was tested again by the same operator after an interval of 10 to 15 days.</p><p><strong>Results: </strong>Except for the fact that in males, there was no significant difference in flexor muscle strength of thumb and wrist joint between 30° of wrist extension and neutral 0° position, the muscle strength of the other fingers flexion and wrist palmar flexor showed the following characteristics:30° of wrist extension > neutral 0° position > 30° of flexion, and the PAST was 30°>60°; The flexor muscle strength of all the subjects was thumb > index finger > middle finger > ring finger > little finger; All muscle strength values of male were greater than those of female, and the difference was statistically significant (<i>P</i><0.05); There was no significant difference between the left and right side muscle strength values of all subjects (<i>P</i>>0.05). The reliability of muscle strength values measured at different times in 10 subjects was good.</p><p><strong>Conclusions: </strong>The quantitative muscle strength of each muscle group of the hand and wrist is affected by the test position, and a standardized and uniformed test position should be adopted in the actual identification. Micro FET2<sup>TM</sup> has good reliability for hand and wrist quantitative muscle strength testing. The 30° extension of the wrist can be used as the best standardized test position for the flexion muscle strength of each finger and wrist joint. The 30° position can be used as the best standardized test position for PAST.</p>","PeriodicalId":12317,"journal":{"name":"法医学杂志","volume":"40 3","pages":"237-244"},"PeriodicalIF":0.0,"publicationDate":"2024-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142008563","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objectives: To screen biomarkers for forensic identification of acute myocardial infarction (AMI) by non-targeted metabolomic studies on changes of urine metabolites in rats with AMI.
Methods: The rat models of the sham surgery group, AMI group and hyperlipidemia + acute myocardial infarction (HAMI) group were established. Ultra-high performance liquid chromatography-mass spectrometry (UPLC-MS) was used to analyze the changes of urine metabolic spectrometry in AMI rats. Principal component analysis, partial least squares-discriminant analysis, and orthogonal partial least squares-discriminant analysis were used to screen differential metabolites. The MetaboAnalyst database was used to analyze the metabolic pathway enrichment and access the predictive ability of differential metabolites.
Results: A total of 40 and 61 differential metabolites associated with AMI and HAMI were screened, respectively. Among them, 22 metabolites were common in both rat models. These small metabolites were mainly concentrated in the niacin and nicotinamide metabolic pathways. Within the 95% confidence interval, the area under the curve (AUC) values of receiver operator characteristic curve for N8-acetylspermidine, 3-methylhistamine, and thymine were greater than 0.95.
Conclusions: N8-acetylspermidine, 3-methylhistamine, and thymine can be used as potential biomarkers for AMI diagnosis, and abnormal metabolism in niacin and nicotinamide may be the main causes of AMI. This study can provide reference for the mechanism and causes of AMI identification.
目的通过对急性心肌梗死大鼠尿液代谢物变化的非靶向代谢组学研究,筛选用于法医鉴定急性心肌梗死(AMI)的生物标志物:方法:建立假手术组、AMI 组和高脂血症+急性心肌梗死(HAMI)组大鼠模型。采用超高效液相色谱-质谱联用仪(UPLC-MS)分析 AMI 大鼠尿液代谢谱的变化。采用主成分分析、偏最小二乘判别分析和正交偏最小二乘判别分析筛选差异代谢物。MetaboAnalyst 数据库用于分析代谢途径富集情况,并获取差异代谢物的预测能力:结果:共筛选出 40 和 61 个分别与 AMI 和 HAMI 相关的差异代谢物。结果:分别筛选出了 40 和 61 个与 AMI 和 HAMI 相关的差异代谢物,其中 22 个代谢物在两种大鼠模型中都很常见。这些小代谢物主要集中在烟酸和烟酰胺代谢途径中。在 95% 的置信区间内,N8-乙酰精胺、3-甲基组胺和胸腺嘧啶的接收者运算特征曲线下面积(AUC)值均大于 0.95:N8-乙酰过氨酸、3-甲基组胺和胸腺嘧啶可作为诊断AMI的潜在生物标志物,烟酸和烟酰胺代谢异常可能是导致AMI的主要原因。本研究可为鉴别AMI的机制和原因提供参考。
{"title":"Urine Metabolites Changes in Acute Myocardial Infarction Rats via Metabolomic Analysis.","authors":"Nian-Nian Chen, Jiao-Fang Yu, Peng Wu, Li Luo, Ya-Qin Bai, Li-Kai Wang, Xiao-Qian Li, Zhan-Peng Li, Cai-Rong Gao, Xiang-Jie Guo","doi":"10.12116/j.issn.1004-5619.2023.431108","DOIUrl":"https://doi.org/10.12116/j.issn.1004-5619.2023.431108","url":null,"abstract":"<p><strong>Objectives: </strong>To screen biomarkers for forensic identification of acute myocardial infarction (AMI) by non-targeted metabolomic studies on changes of urine metabolites in rats with AMI.</p><p><strong>Methods: </strong>The rat models of the sham surgery group, AMI group and hyperlipidemia + acute myocardial infarction (HAMI) group were established. Ultra-high performance liquid chromatography-mass spectrometry (UPLC-MS) was used to analyze the changes of urine metabolic spectrometry in AMI rats. Principal component analysis, partial least squares-discriminant analysis, and orthogonal partial least squares-discriminant analysis were used to screen differential metabolites. The MetaboAnalyst database was used to analyze the metabolic pathway enrichment and access the predictive ability of differential metabolites.</p><p><strong>Results: </strong>A total of 40 and 61 differential metabolites associated with AMI and HAMI were screened, respectively. Among them, 22 metabolites were common in both rat models. These small metabolites were mainly concentrated in the niacin and nicotinamide metabolic pathways. Within the 95% confidence interval, the area under the curve (AUC) values of receiver operator characteristic curve for N8-acetylspermidine, 3-methylhistamine, and thymine were greater than 0.95.</p><p><strong>Conclusions: </strong>N8-acetylspermidine, 3-methylhistamine, and thymine can be used as potential biomarkers for AMI diagnosis, and abnormal metabolism in niacin and nicotinamide may be the main causes of AMI. This study can provide reference for the mechanism and causes of AMI identification.</p>","PeriodicalId":12317,"journal":{"name":"法医学杂志","volume":"40 3","pages":"227-236"},"PeriodicalIF":0.0,"publicationDate":"2024-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142008568","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objectives: To describe the current state of research and future research hotspots through a metrological analysis of the literature in the field of forensic anthropological remains identification research.
Methods: The data retrieved and extracted from the Web of Science Core Collection (WoSCC), the core database of the Web of Science information service platform (hereinafter referred to as "WoS"), was used to analyze the trends and topic changes in research on forensic identification of human remains from 1991 to 2022. Network visualisation of publication trends, countries (regions), institutions, authors and topics related to the identification of remains in forensic anthropology was analysed using python 3.9.2 and Gephi 0.10.
Results: A total of 873 papers written in English in the field of forensic anthropological remains identification research were obtained. The journal with the largest number of publications was Forensic Science International (164 articles). The country (region) with the largest number of published papers was China (90 articles). Katholieke Univ Leuven (Netherlands, 21 articles) was the institution with the largest number of publications. Topic analysis revealed that the focus of forensic anthropological remains identification research was sex estimation and age estimation, and the most commonly studied remains were teeth.
Conclusions: The volume of publications in the field of forensic anthropological remains identification research has a distinct phasing. However, the scope of both international and domestic collaborations remains limited. Traditionally, human remains identification has primarily relied on key areas such as the pelvis, skull, and teeth. Looking ahead, future research will likely focus on the more accurate and efficient identification of multiple skeletal remains through the use of machine learning and deep learning techniques.
{"title":"Bibliometric Analysis of Forensic Human Remains Identification Literature from 1991 to 2022.","authors":"Ji-Wei Ma, Ping Huang, Ji Zhang, Hai-Xing Yu, Yong-Jie Cao, Xiao-Tong Yang, Jian Xiong, Huai-Han Zhang, Yong Cang, Ge-Fei Shi, Li-Qin Chen","doi":"10.12116/j.issn.1004-5619.2023.430803","DOIUrl":"https://doi.org/10.12116/j.issn.1004-5619.2023.430803","url":null,"abstract":"<p><strong>Objectives: </strong>To describe the current state of research and future research hotspots through a metrological analysis of the literature in the field of forensic anthropological remains identification research.</p><p><strong>Methods: </strong>The data retrieved and extracted from the Web of Science Core Collection (WoSCC), the core database of the Web of Science information service platform (hereinafter referred to as \"WoS\"), was used to analyze the trends and topic changes in research on forensic identification of human remains from 1991 to 2022. Network visualisation of publication trends, countries (regions), institutions, authors and topics related to the identification of remains in forensic anthropology was analysed using python 3.9.2 and Gephi 0.10.</p><p><strong>Results: </strong>A total of 873 papers written in English in the field of forensic anthropological remains identification research were obtained. The journal with the largest number of publications was <i>Forensic Science International</i> (164 articles). The country (region) with the largest number of published papers was China (90 articles). Katholieke Univ Leuven (Netherlands, 21 articles) was the institution with the largest number of publications. Topic analysis revealed that the focus of forensic anthropological remains identification research was sex estimation and age estimation, and the most commonly studied remains were teeth.</p><p><strong>Conclusions: </strong>The volume of publications in the field of forensic anthropological remains identification research has a distinct phasing. However, the scope of both international and domestic collaborations remains limited. Traditionally, human remains identification has primarily relied on key areas such as the pelvis, skull, and teeth. Looking ahead, future research will likely focus on the more accurate and efficient identification of multiple skeletal remains through the use of machine learning and deep learning techniques.</p>","PeriodicalId":12317,"journal":{"name":"法医学杂志","volume":"40 3","pages":"245-253"},"PeriodicalIF":0.0,"publicationDate":"2024-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142008562","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}