@article{article_595655, title={The Dose-Duration-Effect Profile of Agmatine on Rat Primary Neuron Cell Culture}, journal={Erciyes Üniversitesi Veteriner Fakültesi Dergisi}, volume={16}, pages={86–91}, year={2019}, DOI={10.32707/ercivet.595655}, author={Binnetoğlu, Damla}, keywords={Agmatin,hücre ölümü,nöronal kültür,nöroproteksiyon}, abstract={<p class="MsoNormal" style="margin-bottom:.0001pt;text-align:justify;line-height:200%;"> <span style="font-family:Arial, sans-serif;font-size:13.3333px;">Agmatine is a newly found neurotransmitter and its role in important modulations of central nervous systems how the pharmacological importance of agmatine. The aim of this study was to investigate the possible toxic and proliferative effects of agmatine, which is known to have endogenous neuroprotective effect, on primary rat neuron culture. In this context, it has been tried to determine the possible toxic and protective effects of agmatine at 8 different exposure times at 5 different doses. Neuron cultures obtained from brain cortex in the neonatal rats are treated with agmatine at 15 min, 30 min, 1 h, 2 hours, 4 hours, 8 hours, 12 hours, 24 hours, doses of 10 </span> <sup style="font-size:10px;font-family:Arial, sans-serif;">-2 </sup> <span style="font-family:Arial, sans-serif;font-size:13.3333px;">, 10 </span> <sup style="font-size:10px;font-family:Arial, sans-serif;">-3 </sup> <span style="font-family:Arial, sans-serif;font-size:13.3333px;">, 10 </span> <sup style="font-size:10px;font-family:Arial, sans-serif;">-4 </sup> <span style="font-family:Arial, sans-serif;font-size:13.3333px;">, 10 </span> <sup style="font-size:10px;font-family:Arial, sans-serif;">-5 </sup> <span style="font-family:Arial, sans-serif;font-size:13.3333px;"> and 10 </span> <sup style="font-size:10px;font-family:Arial, sans-serif;">-6  </sup> <span style="font-family:Arial, sans-serif;font-size:13.3333px;">M. Then, the dose duration effect relationship was determined with MTT ( </span> <span style="font-family:Arial, sans-serif;font-size:13.3333px;">3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) </span> <span style="font-family:Arial, sans-serif;font-size:13.3333px;"> proliferation kit. According to the results of the viability assay, a statistically significant neuroprotective effect was observed in 10 </span> <sup style="font-size:10px;font-family:Arial, sans-serif;">-5  </sup> <span style="font-family:Arial, sans-serif;font-size:13.3333px;">and 10 </span> <sup style="font-size:10px;font-family:Arial, sans-serif;">-6  </sup> <span style="font-family:Arial, sans-serif;font-size:13.3333px;">M doses, especially in 1 hour and 24 hours exposure periods. In addition, proliferation was observed only at a concentration of 10 </span> <sup style="font-size:10px;font-family:Arial, sans-serif;">-4  </sup> <span style="font-family:Arial, sans-serif;font-size:13.3333px;">M for 24 hours. However, no statistically significant difference in toxic effect was observed. Consequently agmatine showed neuroprotective effect in the primary rat neuron culture, especially at the lowest dose and the longest exposure. </span> <br /> </p> <p class="MsoNormal" style="margin-top:6pt;margin-right:0cm;margin-bottom:6pt;margin-left:0cm;text-align:justify;line-height:200%;"> <span style="font-size:10pt;line-height:200%;font-family:Arial, ’sans-serif’;"> </span> </p> <p> </p>}, number={2}, publisher={Erciyes Üniversitesi}