Laboratory Animal Research最新文献

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Single injection of very mild dose botulinum toxin in the vastus lateralis improves testicular spermatogenesis and sperm motility in ageing experimental mice 股外侧肌单次注射极轻剂量肉毒杆菌毒素可改善衰老实验小鼠睾丸精子发生和精子活力
IF 2.9
Laboratory Animal Research Pub Date : 2022-03-04 DOI: 10.1186/s42826-022-00117-4
R. K. Radhakrishnan, Sowbarnika Ravichandran, Aishwarya Sukesh, B. Kadalmani, M. Kandasamy
{"title":"Single injection of very mild dose botulinum toxin in the vastus lateralis improves testicular spermatogenesis and sperm motility in ageing experimental mice","authors":"R. K. Radhakrishnan, Sowbarnika Ravichandran, Aishwarya Sukesh, B. Kadalmani, M. Kandasamy","doi":"10.1186/s42826-022-00117-4","DOIUrl":"https://doi.org/10.1186/s42826-022-00117-4","url":null,"abstract":"","PeriodicalId":17993,"journal":{"name":"Laboratory Animal Research","volume":"38 1","pages":""},"PeriodicalIF":2.9,"publicationDate":"2022-03-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"65797510","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}
引用次数: 2
Comparison of cisplatin-induced anti-tumor response in CT26 syngeneic tumors of three BALB/c substrains. 顺铂诱导的三种BALB/c亚株CT26同基因肿瘤的抗肿瘤反应比较
IF 2.9
Laboratory Animal Research Pub Date : 2021-12-08 DOI: 10.1186/s42826-021-00110-3
Jeong Eun Gong, You Jung Jin, Ji Eun Kim, Yun Ju Choi, Su Jin Lee, Kil Soo Kim, Young Suk Jung, Joon Yong Cho, Yong Lim, Hyun Gu Kang, Dae Youn Hwang
{"title":"Comparison of cisplatin-induced anti-tumor response in CT26 syngeneic tumors of three BALB/c substrains.","authors":"Jeong Eun Gong,&nbsp;You Jung Jin,&nbsp;Ji Eun Kim,&nbsp;Yun Ju Choi,&nbsp;Su Jin Lee,&nbsp;Kil Soo Kim,&nbsp;Young Suk Jung,&nbsp;Joon Yong Cho,&nbsp;Yong Lim,&nbsp;Hyun Gu Kang,&nbsp;Dae Youn Hwang","doi":"10.1186/s42826-021-00110-3","DOIUrl":"https://doi.org/10.1186/s42826-021-00110-3","url":null,"abstract":"<p><strong>Background: </strong>To determine whether the background of BALB/c substrains affects the response to anti-tumor drugs, we measured for alterations in tumor growth, histopathological structure of the tumor, and expressions of tumor-related proteins in three BALB/c substrains derived from different sources (BALB/cKorl, BALB/cA and BALB/cB), after exposure to varying concentrations of cisplatin (0.1, 1 and 5 mg/kg).</p><p><strong>Results: </strong>Cisplatin treatment induced similar responses for body and organ weights, serum analyzing factors, and blood analyzing factors in all BALB/c substrains with CT26 syngeneic tumor. Few differences were detected in the volume and histopathological structure of the CT26 tumor. Growth inhibition of CT26 tumors after exposure to cisplatin was greater in the BALB/cB substrain than BALB/cKorl and BALB/cA substrains, and a similar pattern was observed in the histopathological structure of tumors. However, the expression levels of other tumor-related factors, including Ki67, p27, p53, Bcl-2-associated X protein (Bax), B-cell lymphoma 2 (Bcl-2), caspase-3 (Cas-3), matrix metallopeptidase 2 (MMP2) and vascular endothelial growth factor (VEGF) proteins, were constantly maintained in the tumors of all three substrains after cisplatin treatment. A similar decrease pattern was observed for the expressions of inflammatory cytokines, including interleukin (IL)-1β, IL-6 and IL-10, in the CT26 tumors of the three BALB/c substrains.</p><p><strong>Conclusions: </strong>Taken together, results of the present study indicate that the genetic background of the three BALB/c substrains has no major effect on the therapeutic responsiveness of cisplatin, except growth and histopathology of the CT26 syngeneic tumor.</p>","PeriodicalId":17993,"journal":{"name":"Laboratory Animal Research","volume":"37 1","pages":"33"},"PeriodicalIF":2.9,"publicationDate":"2021-12-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8653566/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39578156","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Sensitivity to tumor development by TALEN-mediated Trp53 mutant genes in the susceptible FVB/N mice and the resistance C57BL/6 mice. 易感FVB/N小鼠和耐药C57BL/6小鼠中talen介导的Trp53突变基因对肿瘤发展的敏感性
IF 2.9
Laboratory Animal Research Pub Date : 2021-11-29 DOI: 10.1186/s42826-021-00107-y
Woo Bin Yun, Ji Eun Kim, Mi Lim Lee, Jun Young Choi, Jin Ju Park, Bo Ram Song, Byeong Cheol Kang, Ki Taek Nam, Han-Woong Lee, Dae Youn Hwang
{"title":"Sensitivity to tumor development by TALEN-mediated Trp53 mutant genes in the susceptible FVB/N mice and the resistance C57BL/6 mice.","authors":"Woo Bin Yun,&nbsp;Ji Eun Kim,&nbsp;Mi Lim Lee,&nbsp;Jun Young Choi,&nbsp;Jin Ju Park,&nbsp;Bo Ram Song,&nbsp;Byeong Cheol Kang,&nbsp;Ki Taek Nam,&nbsp;Han-Woong Lee,&nbsp;Dae Youn Hwang","doi":"10.1186/s42826-021-00107-y","DOIUrl":"https://doi.org/10.1186/s42826-021-00107-y","url":null,"abstract":"<p><strong>Background: </strong>This study was undertaken to compare the sensitivities of mice strains during tumor induction by transcription activator-like effector nucleases (TALEN)-mediated Trp53 mutant gene. Alterations of their tumorigenic phenotypes including survival rate, tumor formation and tumor spectrum, were assessed in FVB/N-Trp53<sup>em2Hwl</sup>/Korl and C57BL/6-Trp53<sup>em1Hwl</sup>/Korl knockout (KO) mice over 16 weeks.</p><p><strong>Results: </strong>Most of the physiological phenotypes factors were observed to be higher in FVB/N-Trp53<sup>em2Hwl</sup>/Korl KO mice than C57BL/6-Trp53<sup>em1Hwl</sup>/Korl KO mice, although there were significant differences in the body weight, immune organ weight, number of red blood cells, mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), mean corpuscular hemoglobin concentration (MCHC), platelet count (PLT), total bilirubin (Bil-T) and glucose (Glu) levels in the KO mice relative to the wild type (WT) mice. Furthermore, numerous solid tumors were also observed in various regions of the surface skin of FVB/N-Trp53<sup>em2Hwl</sup>/Korl KO mice, but were not detected in C57BL/6-Trp53<sup>em1Hwl</sup>/Korl KO mice. The most frequently observed tumor in both the Trp53 KO mice was malignant lymphoma, while soft tissue teratomas and hemangiosarcomas were only detected in the FVB/N-Trp53<sup>em2Hwl</sup>/Korl KO mice.</p><p><strong>Conclusions: </strong>Our results indicate that the spectrum and incidence of tumors induced by the TALEN-mediated Trp53 mutant gene is greater in FVB/N-Trp53<sup>em2Hwl</sup>/Korl KO mice than C57BL/6-Trp53<sup>em1Hwl</sup>/Korl KO mice over 16 weeks.</p>","PeriodicalId":17993,"journal":{"name":"Laboratory Animal Research","volume":"37 1","pages":"32"},"PeriodicalIF":2.9,"publicationDate":"2021-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8628475/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39785840","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Inflammatory response in the mid colon of ICR mice treated with polystyrene microplastics for two weeks. 用聚苯乙烯微塑料治疗两周后ICR小鼠中结肠的炎症反应。
IF 2.9
Laboratory Animal Research Pub Date : 2021-11-22 DOI: 10.1186/s42826-021-00109-w
Yun Ju Choi, Ji Eun Kim, Su Jin Lee, Jeong Eun Gong, You Jeong Jin, Sungbaek Seo, Jae Ho Lee, Dae Youn Hwang
{"title":"Inflammatory response in the mid colon of ICR mice treated with polystyrene microplastics for two weeks.","authors":"Yun Ju Choi,&nbsp;Ji Eun Kim,&nbsp;Su Jin Lee,&nbsp;Jeong Eun Gong,&nbsp;You Jeong Jin,&nbsp;Sungbaek Seo,&nbsp;Jae Ho Lee,&nbsp;Dae Youn Hwang","doi":"10.1186/s42826-021-00109-w","DOIUrl":"https://doi.org/10.1186/s42826-021-00109-w","url":null,"abstract":"<p><strong>Background: </strong>The oral administration of polystyrene-microplastics (PS-MPs) causes chronic constipation of ICR mice, but there are no reports on their effects on the inflammatory response in the colon. To determine if the oral administration of MPs causes inflammation in the colon, the changes in the apoptosis-associated speck like protein containing a caspase recruitment domain (ASC)-inflammasome pathway, nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) signaling pathway, and inflammatory cytokine expression were evaluated in the mid colon of ICR mice treated with 0.5 μm size PS-MPs for two weeks.</p><p><strong>Results: </strong>The thicknesses of the mucosa, muscle, flat luminal surface, and crypt layer were decreased significantly (p < 0.01) in the mid colon of the MPs treated group compared to the Vehicle treated group. On the other hand, a remarkable increase in the expression levels of NOD-like receptor pyrin domain-containing protein (NLRP) 3, ASC, and Cleaved Caspase (Cas)-1 protein was observed in the MPs treated group. In addition, similar increasing pattern in the levels of p-NF-κB and phospho-inhibitory subunit of NF-κB (p-IkB) α protein was detected. Four inflammatory cytokines, including NF-κB, interleukin (IL)-6, tumor necrosis factor (TNF)-α, and IL-1β, showed an increased expression level after the MPs treatment.</p><p><strong>Conclusions: </strong>Therefore, the present study suggests that PS-MPs can be a novel cause of an inflammatory response in the mid colon of ICR mice.</p>","PeriodicalId":17993,"journal":{"name":"Laboratory Animal Research","volume":"37 1","pages":"31"},"PeriodicalIF":2.9,"publicationDate":"2021-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607556/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39915801","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 11
Ventilator-induced lung-injury in mouse models: Is there a trap? 小鼠模型中呼吸机引起的肺损伤:有陷阱吗?
IF 2.9
Laboratory Animal Research Pub Date : 2021-10-29 DOI: 10.1186/s42826-021-00108-x
Jon Petur Joelsson, Saevar Ingthorsson, Jennifer Kricker, Thorarinn Gudjonsson, Sigurbergur Karason
{"title":"Ventilator-induced lung-injury in mouse models: Is there a trap?","authors":"Jon Petur Joelsson,&nbsp;Saevar Ingthorsson,&nbsp;Jennifer Kricker,&nbsp;Thorarinn Gudjonsson,&nbsp;Sigurbergur Karason","doi":"10.1186/s42826-021-00108-x","DOIUrl":"https://doi.org/10.1186/s42826-021-00108-x","url":null,"abstract":"<p><p>Ventilator-induced lung injury (VILI) is a serious acute injury to the lung tissue that can develop during mechanical ventilation of patients. Due to the mechanical strain of ventilation, damage can occur in the bronchiolar and alveolar epithelium resulting in a cascade of events that may be fatal to the patients. Patients requiring mechanical ventilation are often critically ill, which limits the possibility of obtaining patient samples, making VILI research challenging. In vitro models are very important for VILI research, but the complexity of the cellular interactions in multi-organ animals, necessitates in vivo studies where the mouse model is a common choice. However, the settings and duration of ventilation used to create VILI in mice vary greatly, causing uncertainty in interpretation and comparison of results. This review examines approaches to induce VILI in mouse models for the last 10 years, to our best knowledge, summarizing methods and key parameters presented across the studies. The results imply that a more standardized approach is warranted.</p>","PeriodicalId":17993,"journal":{"name":"Laboratory Animal Research","volume":"37 1","pages":"30"},"PeriodicalIF":2.9,"publicationDate":"2021-10-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8554750/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39575087","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 9
Surgical removal of a telemetry system in a cynomolgus monkey (Macaca fascicularis): a 12-month observation study. 手术切除食蟹猴(Macaca fascularis)的遥测系统:为期12个月的观察研究。
IF 2.9
Laboratory Animal Research Pub Date : 2021-10-16 DOI: 10.1186/s42826-021-00106-z
Doo-Wan Cho, Hyoung-Yun Han, Mi-Jin Yang, Dong Ho Woo, Su-Cheol Han, Young-Su Yang
{"title":"Surgical removal of a telemetry system in a cynomolgus monkey (Macaca fascicularis): a 12-month observation study.","authors":"Doo-Wan Cho,&nbsp;Hyoung-Yun Han,&nbsp;Mi-Jin Yang,&nbsp;Dong Ho Woo,&nbsp;Su-Cheol Han,&nbsp;Young-Su Yang","doi":"10.1186/s42826-021-00106-z","DOIUrl":"https://doi.org/10.1186/s42826-021-00106-z","url":null,"abstract":"<p><strong>Background: </strong>Telemetry is a wireless implanted device that measures biological signals in conscious animals and usually requires surgery for its removal when the study is finished. After removing the device, the animals are either used for other studies or euthanatized.</p><p><strong>Case presentation: </strong>Herein, we report the case of a living cynomolgus monkey (Macaca fascicularis) that was used for the entire experimental period, instead of euthanasia, after surgical removal of an implanted telemetry system. Radiography was used to determine the status of the implanted telemetry, following which, a repair surgery was performed for removing the system; clinical signs were used to preserve the life of the cynomolgus monkey. Postoperative clinical signs, food consumption, hematology, and serum biochemistry were examined during the 12-month observational period. No abnormal readings or conditions were observed in the subject after implant removal.</p><p><strong>Conclusions: </strong>This study may be a useful case report for living cynomolgus monkeys in telemetry implantations used throughout the study period. We suggest minimizing the suffering and improving the welfare of these animals.</p>","PeriodicalId":17993,"journal":{"name":"Laboratory Animal Research","volume":"37 1","pages":"29"},"PeriodicalIF":2.9,"publicationDate":"2021-10-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8520245/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39526201","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Reduced receptor for advanced glycation end products is associated with α-SMA expression in patients with idiopathic pulmonary fibrosis and mice. 特发性肺纤维化患者和小鼠中晚期糖基化终产物受体减少与α-SMA表达相关。
IF 2.9
Laboratory Animal Research Pub Date : 2021-10-02 DOI: 10.1186/s42826-021-00105-0
Hyosin Baek, Soojin Jang, Jaehyun Park, Jimin Jang, Jooyeon Lee, Seok-Ho Hong, Woo Jin Kim, Sung-Min Park, Se-Ran Yang
{"title":"Reduced receptor for advanced glycation end products is associated with α-SMA expression in patients with idiopathic pulmonary fibrosis and mice.","authors":"Hyosin Baek,&nbsp;Soojin Jang,&nbsp;Jaehyun Park,&nbsp;Jimin Jang,&nbsp;Jooyeon Lee,&nbsp;Seok-Ho Hong,&nbsp;Woo Jin Kim,&nbsp;Sung-Min Park,&nbsp;Se-Ran Yang","doi":"10.1186/s42826-021-00105-0","DOIUrl":"https://doi.org/10.1186/s42826-021-00105-0","url":null,"abstract":"<p><strong>Background: </strong>Idiopathic pulmonary fibrosis (IPF) is a chronic and progressive interstitial lung disease. Despite alveolar epithelial cells is crucial role in lung, its contribution and the associated biomarker remain unknown in the pathogenesis of IPF. Recently, environmental factors including stone dust, silica and cigarette smoking were found as risk factors involved in IPF. Receptor for advanced glycation end products (RAGE) is a member of the immunoglobulin super family of cell surface receptors. It has been shown that interaction between RAGE and its ligands on immune cells mediates cellular migration and regulation of pro-inflammation. RAGE is highly expressed in the lung, in particular, alveolar epithelial cells. Therefore, we determined whether RAGE expression is associated with fibrosis-associated genes in patients with IPF and mice.</p><p><strong>Results: </strong>When bleomycin (BLM) was intratracheally administered to C57BL/6 mice for 1, 2 weeks, macrophage and neutrophils were significantly increased. The fibrotic nodule formed and accumulation of collagen was determined after BLM injection in H&E- and Masson's trichrome staining. Levels of elastin, Col1a1 and fibronectin were increased in quantitative real-time PCR and protein levels of α-SMA was increased in western blot analysis. In the lung tissues of 1 mg/kg BLM-induced mice, RAGE expression was gradually decreased in 1- and 2 weeks in immunohistochemistry and western blot analysis, and 3 mg/kg of BLM-induced mice exhibited decreased RAGE levels while α-SMA expression was increased. We next determined RAGE expression in the lungs of IPF patients using immunohistochemistry. As a result, RAGE expression was decreased, while α-SMA expression was increased compared with non-IPF subjects.</p><p><strong>Conclusions: </strong>Our findings suggest that reduced RAGE was associated with increased fibrotic genes in BLM-induced mice and patients with IPF. Therefore, RAGE could be applied with a biomarker for prognosis and diagnosis in the pathogenesis of IPF.</p>","PeriodicalId":17993,"journal":{"name":"Laboratory Animal Research","volume":"37 1","pages":"28"},"PeriodicalIF":2.9,"publicationDate":"2021-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8487524/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39480168","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Zebrafish toxicological screening could aid Leishmaniosis drug discovery. 斑马鱼毒理学筛选有助于利什曼病药物的发现。
IF 2.9
Laboratory Animal Research Pub Date : 2021-09-16 DOI: 10.1186/s42826-021-00104-1
Hirla Costa Silva Fukushima, Ricardo Lacava Bailone, Tatiana Corrêa, Helena Janke, Luís Kluwe De Aguiar, Princia Grejo Setti, Ricardo Carneiro Borra
{"title":"Zebrafish toxicological screening could aid Leishmaniosis drug discovery.","authors":"Hirla Costa Silva Fukushima,&nbsp;Ricardo Lacava Bailone,&nbsp;Tatiana Corrêa,&nbsp;Helena Janke,&nbsp;Luís Kluwe De Aguiar,&nbsp;Princia Grejo Setti,&nbsp;Ricardo Carneiro Borra","doi":"10.1186/s42826-021-00104-1","DOIUrl":"https://doi.org/10.1186/s42826-021-00104-1","url":null,"abstract":"<p><strong>Background: </strong>Recently a screen from a library of 1.8 million compounds identified in vitro a potent activity of the 2-aminobenzimidazoles series against Leishmania infantum, the etiological agent responsible by over 20.000 deaths each year. Several analogs were synthesized and in vitro tested through an optimization program, leading to a promising 2-aminobenzimidazoles derived compound (2amnbzl-d) that was progressed to in vivo mice studies. However, the not expected toxic effects prevented its progression to more advanced preclinical and clinical phases of drug development. Due to limitations of cell models in detecting whole organism complex interactions, 90% of the compounds submitted to pre-clinical tests are reproved. The use of Zebrafish embryo models could improve this rate, saving mammals, time and costs in the development of new drugs. To test this hypothesis, we compared 2amnbzl-d with two compounds with already established safety profile: carbamazepine and benznidazole, using an embryo Zebrafish platform based on acute toxicity, hepatotoxicity, neurotoxicity and cardiotoxicity assays (Pltf-AcHpNrCd).</p><p><strong>Results: </strong>Tests were performed blindly, and the results demonstrated the presence of lethal and teratogenic effects (CL50%: 14.8 µM; EC50%: 8.6 µM), hepatotoxic in concentrations above 7.5 µM and neurotoxic in embryos exposed to 15 µM of 2amnbzl-d. Nevertheless, benznidazole exposition showed no toxicity and only the 100 µM of carbamazepine induced a bradycardia.</p><p><strong>Conclusions: </strong>Results using Pltf-AcHpNrCd with zebrafish reproduced that found in the toxicological tests with mammals to a portion of the costs and time of experimentation.</p>","PeriodicalId":17993,"journal":{"name":"Laboratory Animal Research","volume":"37 1","pages":"27"},"PeriodicalIF":2.9,"publicationDate":"2021-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8444568/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39423349","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Transgenic fluorescent zebrafish lines that have revolutionized biomedical research. 转基因荧光斑马鱼已经彻底改变了生物医学研究。
IF 2.9
Laboratory Animal Research Pub Date : 2021-09-08 DOI: 10.1186/s42826-021-00103-2
Chong Pyo Choe, Seok-Yong Choi, Yun Kee, Min Jung Kim, Seok-Hyung Kim, Yoonsung Lee, Hae-Chul Park, Hyunju Ro
{"title":"Transgenic fluorescent zebrafish lines that have revolutionized biomedical research.","authors":"Chong Pyo Choe,&nbsp;Seok-Yong Choi,&nbsp;Yun Kee,&nbsp;Min Jung Kim,&nbsp;Seok-Hyung Kim,&nbsp;Yoonsung Lee,&nbsp;Hae-Chul Park,&nbsp;Hyunju Ro","doi":"10.1186/s42826-021-00103-2","DOIUrl":"https://doi.org/10.1186/s42826-021-00103-2","url":null,"abstract":"<p><p>Since its debut in the biomedical research fields in 1981, zebrafish have been used as a vertebrate model organism in more than 40,000 biomedical research studies. Especially useful are zebrafish lines expressing fluorescent proteins in a molecule, intracellular organelle, cell or tissue specific manner because they allow the visualization and tracking of molecules, intracellular organelles, cells or tissues of interest in real time and in vivo. In this review, we summarize representative transgenic fluorescent zebrafish lines that have revolutionized biomedical research on signal transduction, the craniofacial skeletal system, the hematopoietic system, the nervous system, the urogenital system, the digestive system and intracellular organelles.</p>","PeriodicalId":17993,"journal":{"name":"Laboratory Animal Research","volume":"37 1","pages":"26"},"PeriodicalIF":2.9,"publicationDate":"2021-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8424172/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39396262","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 26
A comparative review on heart ion channels, action potentials and electrocardiogram in rodents and human: extrapolation of experimental insights to clinic. 鼠与人心脏离子通道、动作电位及心电图的比较研究:实验与临床的推论。
IF 2.9
Laboratory Animal Research Pub Date : 2021-09-08 DOI: 10.1186/s42826-021-00102-3
Siyavash Joukar
{"title":"A comparative review on heart ion channels, action potentials and electrocardiogram in rodents and human: extrapolation of experimental insights to clinic.","authors":"Siyavash Joukar","doi":"10.1186/s42826-021-00102-3","DOIUrl":"https://doi.org/10.1186/s42826-021-00102-3","url":null,"abstract":"<p><p>Electrocardiogram (ECG) is a non-invasive valuable diagnostic tool that is used in clinics for investigation and monitoring of heart electrical rhythm/conduction, ischemia/injury of heart, electrolyte disturbances and agents/drugs induced cardiac toxicity. Nowadays using animal models to study heart diseases such as electrical and mechanical disturbance is common. In addition, given to ethical consideration and availability, the use of small rodents has been a top priority for cardiovascular researchers. However, extrapolation of experimental findings from the lab to the clinic needs sufficient basic knowledge of similarities and differences between heart action potential and ECG of rodents and humans in normal and disease conditions. This review compares types of human action potentials, the dominant ion currents during action potential phases, alteration in ion channels activities in channelopathies-induced arrhythmias and the ECG appearance of mouse, rat, guinea pig, rabbit and human. Also, it briefly discusses the responsiveness and alterations in ECG following some interventions such as cardiac injury and arrhythmia induction. Overall, it provides a roadmap for researchers in selecting the best animal model/species whose studies results can be translated into clinical practice. In addition, this study will also be useful to biologists, physiologists, pharmacologists, veterinarians and physicians working in the fields of comparative physiology, pharmacology, toxicology and diseases.</p>","PeriodicalId":17993,"journal":{"name":"Laboratory Animal Research","volume":"37 1","pages":"25"},"PeriodicalIF":2.9,"publicationDate":"2021-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8424989/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39398243","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 30
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