| Literature DB >> 31100277 |
Palmer Taylor1, Shyong Yan-Jye2, Jeremiah Momper3, William Hou3, Gisela Andrea Camacho-Hernandez2, Zoran Radic'3, Yvonne Rosenberg4, Zrinka Kovarik5, Rakesh Sit6, K Barry Sharpless6.
Abstract
Since the development in the 1950's of 2-PAM (Pralidoxime), an antidote that reactivates organophosphate conjugated acetylcholinesterase in target tissues upon pesticide or nerve agent exposure, improvements in antidotal therapy have largely involved congeneric pyridinium aldoximes. Despite seminal advances in detailing the structures of the cholinesterases as the primary target site, progress with small molecule antidotes has yet to define a superior agent. Two major limitations are immediately apparent. The first is the impacted space within the active center gorge, particularly when the active center serine at its base is conjugated with an organophosphate. The reactivating nucleophile will have to negotiate the tortuous gorge terrain to access the phosphorus atom with its most nucleophilic form or ionization state, the oximate anion. A second limitation stems from the antidote crossing the blood-brain barrier sufficiently rapidly, since it is well documented that central acetylcholinesterase inhibition gives rise to cardiovascular and respiratory compromise. The associated hypoxia then leads to a sequelae of events, including poor perfusion of the brain and periphery, along with muscle fasciculation, tremors and eventually seizures. We consider both the barriers confronting and further achievements necessary to enhance efficacy of antidotes.Entities:
Keywords: Acetylcholinesterase; Nerve agent; Organophosphate; Oxime; RS194B antidote
Mesh:
Substances:
Year: 2019 PMID: 31100277 DOI: 10.1016/j.cbi.2019.05.015
Source DB: PubMed Journal: Chem Biol Interact ISSN: 0009-2797 Impact factor: 5.192