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10.3390/brainsci10110807 http://scihub22266oqcxt.onion/10.3390/brainsci10110807 33142819!7693814!33142819     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Brain+Sci 2020 ; 10 (11): ä Nephropedia Template TP {{tp|p=33142819|t=2020. COVID-19 and Parkinson s Disease: Shared Inflammatory Pathways Under Oxidative Stress |pdf=|usr=}}{{33142819}} gab.com Text COVID-19 and Parkinson s Disease: Shared Inflammatory Pathways Under Oxidative Stress JO: Brain Sci http://www.kidney.de/pget.php?&tw=1&pmid=33142819 #FOAvip The current coronavirus pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has resulted in a serious global health crisis. It is a major concern for individuals living with chronic disorders such as Parkinson's disease (PD). Increasing evidence suggests an involvement of oxidative stress and contribution of NFkappaB in the development of both COVID-19 and PD. Although, it is early to identify if SARS-CoV-2 led infection enhances PD complications, it is likely that oxidative stress may exacerbate PD progression in COVID-19 affected individuals and/or vice versa. In the current study, we sought to investigate whether NFkappaB-associated inflammatory pathways following oxidative stress in SARS-CoV-2 and PD patients are correlated. Toward this goal, we have integrated bioinformatics analysis obtained from Basic Local Alignment Search Tool of Protein Database (BLASTP) search for similarities of SARS-CoV-2 proteins against human proteome, literature review, and laboratory data obtained in a human cell model of PD. A Parkinson's like state was created in 6-hydroxydopamine (6OHDA)-induced differentiated dopamine-containing neurons (dDCNs) obtained from an immortalized human neural progenitor cell line derived from the ventral mesencephalon region of the brain (ReNVM). The results indicated that SARS-CoV-2 infection and 6OHDA-induced toxicity triggered stimulation of caspases-2, -3 and -8 via the NFkappaB pathway resulting in the death of dDCNs. Furthermore, specific inhibitors for NFkappaB and studied caspases reduced the death of stressed dDCNs. The findings suggest that knowledge of the selective inhibition of caspases and NFkappaB activation may contribute to the development of potential therapeutic approaches for the treatment of COVID-19 and PD. Twit Text FOAVip COVID-19 and Parkinson s Disease: Shared Inflammatory Pathways Under Oxidative Stress ????Brain Sci http://www.kidney.de/pget.php?&tw=1&pmid=33142819 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=33142819 #FOAvip English Wikipedia <ref>{{Cite pmid|33142819}}</ref> COVID-19 and Parkinson s Disease: Shared Inflammatory Pathways Under Oxidative Stress #MMPMID33142819 Chaudhry ZL; Klenja D; Janjua N; Cami-Kobeci G; Ahmed BY Brain Sci 2020[Oct]; 10 (11): ä PMID33142819show ga The current coronavirus pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has resulted in a serious global health crisis. It is a major concern for individuals living with chronic disorders such as Parkinson's disease (PD). Increasing evidence suggests an involvement of oxidative stress and contribution of NFkappaB in the development of both COVID-19 and PD. Although, it is early to identify if SARS-CoV-2 led infection enhances PD complications, it is likely that oxidative stress may exacerbate PD progression in COVID-19 affected individuals and/or vice versa. In the current study, we sought to investigate whether NFkappaB-associated inflammatory pathways following oxidative stress in SARS-CoV-2 and PD patients are correlated. Toward this goal, we have integrated bioinformatics analysis obtained from Basic Local Alignment Search Tool of Protein Database (BLASTP) search for similarities of SARS-CoV-2 proteins against human proteome, literature review, and laboratory data obtained in a human cell model of PD. A Parkinson's like state was created in 6-hydroxydopamine (6OHDA)-induced differentiated dopamine-containing neurons (dDCNs) obtained from an immortalized human neural progenitor cell line derived from the ventral mesencephalon region of the brain (ReNVM). The results indicated that SARS-CoV-2 infection and 6OHDA-induced toxicity triggered stimulation of caspases-2, -3 and -8 via the NFkappaB pathway resulting in the death of dDCNs. Furthermore, specific inhibitors for NFkappaB and studied caspases reduced the death of stressed dDCNs. The findings suggest that knowledge of the selective inhibition of caspases and NFkappaB activation may contribute to the development of potential therapeutic approaches for the treatment of COVID-19 and PD. äCOVID-19 and Parkinson s Disease: Shared Inflammatory Pathways Under O(epmc).pdf DeepDyve Pubget Overpricing