Abstract:
:In rat brain microvessels, tetrahydroaminoacridine (THA) caused a significant inhibition of both acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) activities, in a dose-dependent manner. THA resulted to be a more potent inhibitor of BuChE than AChE. Lineweaver-Burk plots showed that Km (app) and V were altered by THA, indicating mixed competitive/non-competitive inhibition. The results of the present study also established that the three molecular forms of BuChE (G1, G2 and G4), recently described to be present in brain microvessels, are inhibited after THA treatment.
journal_name
Life Scijournal_title
Life sciencesauthors
Catalán RE,Martínez AM,Aragonés MD,Miguel BG,Hernández F,Cruz Edoi
10.1016/0024-3205(93)90553-fsubject
Has Abstractpub_date
1993-01-01 00:00:00pages
1165-72issue
14eissn
0024-3205issn
1879-0631pii
0024-3205(93)90553-Fjournal_volume
53pub_type
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