1 copolamine completely blocked the effects of arecoline.

2  and sensitize worms to the toxic effects of arecoline.

3 ol and approximately 30-230 times lower than arecoline.

4 zamine alkaloids is described, starting from arecoline.

5 ubthreshold) could potentiate the effects of arecoline, a cholinergic agonist, or L-glutamate, a glut

6                                Specifically, arecoline, a major betel nut alkaloid, reduced miR329, m

7 le repolarization--when worms are exposed to arecoline, a muscarinic agonist.

8 l agonist iperoxo (IXO), the partial agonist arecoline (ARC), and the inverse agonist 3-quinuclidinyl

9             While 11 compounds (aldosterone, arecoline, bortezomib, dasatinib, decitabine, dexamethas

10                      Moreover, we identified arecoline hydrobromide (AH) as a covalent ACAT1 inhibito

11 of this class were synthesized starting from arecoline hydrobromide and obtained in optically pure fo

12 ll members of this series were prepared from arecoline hydrobromide in optically pure form and were e

13 d the dose of bicuculline, in the septum, or arecoline in the hippocampus that was needed to improve

14  than before PAR training, blocked the usual arecoline-induced enhancement of response latencies.

15  into the septum, but it reduced the dose of arecoline needed to improve retention in the hippocampus

16 t of increasing the doses of bicuculline and arecoline needed to improve retention.

17 ected into the septum, increased the dose of arecoline needed to improve retention.

18                           The dose of either arecoline or L-glutamate needed to improve retention was

19 omimetic drugs, either a muscarinic agonist (arecoline, pilocarpine or oxotremorine), an acetylcholin

20 ing muscarinic cholinergic receptor agonist, arecoline, resulted in an even more impressive suppressi

21 scopolamine was given to young rats prior to arecoline, the dose-effect curve for enhanced latency ti

22                       We found that 4NQO and arecoline upregulated miR-211 expression in OSCC cells.