Biomolecules & Therapeutics : eISSN 2005-4483 / pISSN 1976-9148

Cited by CrossRef (40)

  1. Tindaro Bongiovanni, Federico Genovesi, Monika Nemmer, Christopher Carling, Giampietro Alberti, Glyn Howatson. Nutritional interventions for reducing the signs and symptoms of exercise-induced muscle damage and accelerate recovery in athletes: current knowledge, practical application and future perspectives. Eur J Appl Physiol 2020
    https://doi.org/10.1007/s00421-020-04432-3
  2. İ. İpek Boşgelmez, Gülin Güvendik. Beneficial Effects of N-Acetyl-L-cysteine or Taurine Pre- or Post-treatments in the Heart, Spleen, Lung, and Testis of Hexavalent Chromium-Exposed Mice. Biol Trace Elem Res 2019;190:437
    https://doi.org/10.1007/s12011-018-1571-z
  3. Md. Jakaria, Shofiul Azam, Md. Ezazul Haque, Song-Hee Jo, Md. Sahab Uddin, In-Su Kim, Dong-Kug Choi. Taurine and its analogs in neurological disorders: Focus on therapeutic potential and molecular mechanisms. Redox Biology 2019;24:101223
    https://doi.org/10.1016/j.redox.2019.101223
  4. Riho Komatsuzawa, Teruo Miyazaki, Hajime Ohmori, Chitose Maruyama, Stephen W. Schaffer, Shigeru Murakami, Takashi Ito. Evaluation of taurine content on skeletal muscle of exercised rats using MALDI-TOF MS imaging analysis. JPFSM 2020;9:165
    https://doi.org/10.7600/jpfsm.9.165
  5. Zeynep Dicle Yıldız, Adile Merve Baki, Canan Başaran-Küçükgergin, Pervin Vural, Semra Doğru-Abbasoğlu, Müjdat Uysal. Protective effects of N-acetylcysteine and taurine on oxidative stress induced by chronic acetaldehyde administration in rat liver and brain tissues. 2019
    https://doi.org/10.25000/acem.579968
  6. Alessandra Agostini, Ding Yuchun, Bai Li, David A. Kendall, Marie-Christine Pardon. Sex-specific hippocampal metabolic signatures at the onset of systemic inflammation with lipopolysaccharide in the APPswe/PS1dE9 mouse model of Alzheimer’s disease. Brain, Behavior, and Immunity 2020;83:87
    https://doi.org/10.1016/j.bbi.2019.09.019
  7. Mujtaba Aamir Bhat, Khurshid Ahmad, Mohd Sajjad Ahmad Khan, Mudasir Ahmad Bhat, Ahmad Almatroudi, Safikur Rahman, Arif Tasleem Jan. Expedition into Taurine Biology: Structural Insights and Therapeutic Perspective of Taurine in Neurodegenerative Diseases. Biomolecules 2020;10:863
    https://doi.org/10.3390/biom10060863
  8. Fouzia Haider, Halina I. Falfushynska, Stefan Timm, Inna M. Sokolova. Effects of hypoxia and reoxygenation on intermediary metabolite homeostasis of marine bivalves Mytilus edulis and Crassostrea gigas. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology 2020;242:110657
    https://doi.org/10.1016/j.cbpa.2020.110657
  9. Vincent Chin-Hung Chen, Chun-Ching Chiu, Jun-Cheng Weng, Li-Jeng Chen, Jing Yi Siow, Tsai-Ching Hsu, Bor-Show Tzang. Taurine reduces hyperactive behavior in SHR rats through upregulating the proportion of CD4+CD25+Foxp3+ regulatory T cells. Journal of Functional Foods 2019;56:312
    https://doi.org/10.1016/j.jff.2019.03.032
  10. Mengjuan Liu, Jiaqi Wang, Hongping Tang, Li Fan, Liang Zhao, Hai-Bin Wang, Yan Zhou, Wen-Song Tan. Cell culture medium supplemented with taurine decreases basic charge variant levels of a monoclonal antibody. Biotechnol Lett 2018;40:1487
    https://doi.org/10.1007/s10529-018-2606-4
  11. Kyung Suk Cho, Manoj Kumar Neog, Joo Young Kim, Hyung-In Yang, Kyoung Soo Kim. Taurine 11. 2018.
    https://doi.org/10.1007/978-981-13-8023-5_3
  12. Jing Liu, Yongfei Ai, Xiaolin Niu, Fujun Shang, Zhili Li, Hui Liu, Wei Li, Wenshuai Ma, Ruirui Chen, Ting Wei, Xue Li, Xiaoli Li. Taurine protects against cardiac dysfunction induced by pressure overload through SIRT1–p53 activation. Chemico-Biological Interactions 2020;317:108972
    https://doi.org/10.1016/j.cbi.2020.108972
  13. M. Dan McKirnan, Yasuhiro Ichikawa, Zheng Zhang, Alice E. Zemljic-Harpf, Sili Fan, Dinesh Kumar Barupal, Hemal H. Patel, H. Kirk Hammond, David M. Roth. Metabolomic analysis of serum and myocardium in compensated heart failure after myocardial infarction. Life Sciences 2019;221:212
    https://doi.org/10.1016/j.lfs.2019.01.040
  14. Feng He, Ning Ma, Kaoru Midorikawa, Yusuke Hiraku, Shinji Oikawa, Yingxi Mo, Zhe Zhang, Kazuhiko Takeuchi, Mariko Murata. Taurine 11. 2019.
    https://doi.org/10.1007/978-981-13-8023-5_49
  15. Gerald S. Supinski, Lin Wang, Elizabeth A. Schroder, Leigh Ann P. Callahan. Taurine administration ablates sepsis induced diaphragm weakness. Respiratory Physiology & Neurobiology 2020;271:103289
    https://doi.org/10.1016/j.resp.2019.103289
  16. M. Li, C. M. Reynolds, C. Gray, R. Patel, D. M. Sloboda, M. H. Vickers. Long-term effects of a maternal high-fat: high-fructose diet on offspring growth and metabolism and impact of maternal taurine supplementation. J Dev Orig Health Dis 2020;11:419
    https://doi.org/10.1017/S2040174419000709
  17. Akash Kumar, Nabojit Das, Neeraj Kumar Satija, Kapil Mandrah, Somendu Kumar Roy, Raja Gopal Rayavarapu. A Novel Approach towards Synthesis and Characterization of Non-Cytotoxic Gold Nanoparticles Using Taurine as Capping Agent. Nanomaterials 2019;10:45
    https://doi.org/10.3390/nano10010045
  18. Ana Virel, Ilona Dudka, Rutger Laterveer, Sara af Bjerkén. 1H NMR profiling of the 6-OHDA parkinsonian rat brain reveals metabolic alterations and signs of recovery after N-acetylcysteine treatment. Molecular and Cellular Neuroscience 2019;98:131
    https://doi.org/10.1016/j.mcn.2019.06.003
  19. Guoyao Wu. Important roles of dietary taurine, creatine, carnosine, anserine and 4-hydroxyproline in human nutrition and health. Amino Acids 2020;52:329
    https://doi.org/10.1007/s00726-020-02823-6
  20. Mohammad Mehdi Ommati, Omid Farshad, Akram Jamshidzadeh, Reza Heidari. Taurine enhances skeletal muscle mitochondrial function in a rat model of resistance training. PharmaNutrition 2019;9:100161
    https://doi.org/10.1016/j.phanu.2019.100161
  21. Mengmeng Yu, Yang Wang, Zhe Wang, Yanxu Liu, Yang Yu, Xuejun Gao. Taurine Promotes Milk Synthesis via the GPR87-PI3K-SETD1A Signaling in BMECs. J. Agric. Food Chem. 2019;67:1927
    https://doi.org/10.1021/acs.jafc.8b06532
  22. Chunmei Jiang, Zhenzhu Li, Yihong Shi, Dan Guo, Bin Pang, Xianqing Chen, Dongyan Shao, Yanlin Liu, Junling Shi. Bacillus subtilis inhibits Aspergillus carbonarius by producing iturin A, which disturbs the transport, energy metabolism, and osmotic pressure of fungal cells as revealed by transcriptomics analysis. International Journal of Food Microbiology 2020;330:108783
    https://doi.org/10.1016/j.ijfoodmicro.2020.108783
  23. Cemal Orhan, Osman Kucuk, Nurhan Sahin, Mehmet Tuzcu, Kazim Sahin. Effects of taurine supplementation on productive performance, nutrient digestibility and gene expression of nutrient transporters in quails reared under heat stress. Journal of Thermal Biology 2020:102668
    https://doi.org/10.1016/j.jtherbio.2020.102668
  24. Ewelina Zaorska, Lenka Tomasova, Dominik Koszelewski, Ryszard Ostaszewski, Marcin Ufnal. Hydrogen Sulfide in Pharmacotherapy, Beyond the Hydrogen Sulfide-Donors. Biomolecules 2020;10:323
    https://doi.org/10.3390/biom10020323
  25. Kyoung Soo Kim, Hari Madhuri Doss, Hee-Jin Kim, Hyung-In Yang. Taurine Stimulates Thermoregulatory Genes in Brown Fat Tissue and Muscle without an Influence on Inguinal White Fat Tissue in a High-Fat Diet-Induced Obese Mouse Model. Foods 2020;9:688
    https://doi.org/10.3390/foods9060688
  26. Alessandra Stacchiotti, Gaia Favero, Antonio Lavazza, Maria Monsalve, Luigi Rodella, Rita Rezzani. Taurine Supplementation Alleviates Puromycin Aminonucleoside Damage by Modulating Endoplasmic Reticulum Stress and Mitochondrial-Related Apoptosis in Rat Kidney. Nutrients 2018;10:689
    https://doi.org/10.3390/nu10060689
  27. Milito, Brancaccio, D’Argenio, Castellano. Natural Sulfur-Containing Compounds: An Alternative Therapeutic Strategy against Liver Fibrosis. Cells 2019;8:1356
    https://doi.org/10.3390/cells8111356
  28. M. Prideaux, Y. Kitase, M. Kimble, T.M. O'Connell, L.F. Bonewald. Taurine, an osteocyte metabolite, protects against oxidative stress-induced cell death and decreases inhibitors of the Wnt/β-catenin signaling pathway. Bone 2020;137:115374
    https://doi.org/10.1016/j.bone.2020.115374
  29. Reza Heidari, Shima Behnamrad, Zahra Khodami, Mohammad Mehdi Ommati, Negar Azarpira, Afsaneh Vazin. The nephroprotective properties of taurine in colistin-treated mice is mediated through the regulation of mitochondrial function and mitigation of oxidative stress. Biomedicine & Pharmacotherapy 2019;109:103
    https://doi.org/10.1016/j.biopha.2018.10.093
  30. Adrian Post, M. Yusof Said, Antonio W. Gomes-Neto, Jennifer van der Krogt, Pim de Blaauw, Stefan P. Berger, Johanna M. Geleijnse, Karin Borgonjen, Else van den Berg, Harry van Goor, Gerald Rimbach, Ido P. Kema, Dimitrios Tsikas, M. Rebecca Heiner-Fokkema, Stephan J. L. Bakker. Urinary Taurine Excretion and Risk of Late Graft Failure in Renal Transplant Recipients. Nutrients 2019;11:2212
    https://doi.org/10.3390/nu11092212
  31. Zonglin Guo, Xiangzhen Ge, Ling Han, Lihua Yang, Qun-Li Yu. Ultrasound-assisted extraction and purification of taurine from bovine liver. Journal of Food Composition and Analysis 2020;90:103514
    https://doi.org/10.1016/j.jfca.2020.103514
  32. Petr D. Shabanov, Ludmila K. Khnychenko. Membranotropic activity of taurine derivatives. Medical academic journal 2020
    https://doi.org/10.17816/MAJ19074
  33. Chen Barazani, Haim Werner, Zvi Laron. Changes in plasma amino acids metabolites, caused by long-term IGF-I deficiency, are reversed by IGF-I treatment – A pilot study. Growth Hormone & IGF Research 2020;52:101312
    https://doi.org/10.1016/j.ghir.2020.02.001
  34. P.F. Surai, I.I. Kochish, M.T. Kidd. Taurine in poultry nutrition. Animal Feed Science and Technology 2020;260:114339
    https://doi.org/10.1016/j.anifeedsci.2019.114339
  35. Ilia A. Dereven’kov, Lubov V. Tsaba, Elizaveta A. Pokrovskaya, Sergei V. Makarov. Studies on the interaction of aquacobalamin with cysteinesulfinic and cysteic acids, hypotaurine and taurine. Journal of Coordination Chemistry 2018;71:3194
    https://doi.org/10.1080/00958972.2018.1515927
  36. Yuriy Balji, Martin Knicky, Galia Zamaratskaia. Perspectives and safety of horsemeat consumption. Int J Food Sci Technol 2020;55:942
    https://doi.org/10.1111/ijfs.14390
  37. Ghassan Bkaily, Ashley Jazzar, Alexandre Normand, Yanick Simon, Johny Al-Khoury, Danielle Jacques. Taurine and cardiac disease: state of the art and perspectives. Can. J. Physiol. Pharmacol. 2020;98:67
    https://doi.org/10.1139/cjpp-2019-0313
  38. Liwei Chen, Jingtao Zhang, Jean Pui Yi Teh, Bobby K. Cheon, Yifan Yang, Joergen Schlundt, Yulan Wang, Patricia L. Conway. Comparative Blood and Urine Metabolomics Analysis of Healthy Elderly and Young Male Singaporeans. J. Proteome Res. 2020
    https://doi.org/10.1021/acs.jproteome.0c00215
  39. Juan I Sbodio, Solomon H Snyder, Bindu D Paul. Regulators of the transsulfuration pathway. British Journal of Pharmacology 2019;176:583
    https://doi.org/10.1111/bph.14446
  40. Natalia I. Nesterova, Olesya V. Shcheblykina, Pavel D. Kolesnichenko, Arkady V. Nesterov, Dmitry V. Shcheblykin, Dmitry Yakovlev. Neuroprotective effects of taurine and 3-hydroxypyridine derivatives in the intracerebral hemorrhage model in rats. RRP 2019;5:87
    https://doi.org/10.3897/rrpharmacology.5.36988