Uses
AR-R 17779 Hydrochloride is a selective α7 nicotinic receptor agonist.
Biological Activity
ar-r 17779 is a selective agonist of α7 nicotinic acetylcholine receptor (α7-nachr) [1] with an ec50 of 21 μm to rat α7-nachrs expressed in xenopus oocytes [2].nicotine enhances cognitive functions, e.g. learning, attention, retention and memory in both humans and animals, via activation of brain nicotinic acetylcholine receptors (nachrs). these receptors are homo- or heteropentameric ligand-gated ion channels. the most common nicotinic receptors found in the brain are the α4β2-nachr and the α7-nachr [3].the expression of cd38, cd138, and bcl-6, was sensitive to regulation via nachrs. daudi cells exposed to ar-r 17779 ± methyllycaconitine (mla) resulted in only moderate changes in the gene expression of cd38, cd138 and bcl-6, but ar-r 17779 alone significantly (p< 0.05) increased protein levels of cd38 and cd138. that means the effect of ar-r 17779 was abolished by mla [4].cholesterol is necessary for the homeostasis of acetylcholine receptor (achr) levels for ion translocation and at the plasmalemma [5]. in apoe-deficient mice, ar-r 17779 significantly reduced atherosclerotic plaque area in the thoracic aorta, and lowered heart rate, blood pressure, serum triglyceride level and serum total cholesterol level compared with which in ang ii + hfd mice. treatment with ar-r 17779 in mice did not result in any sickness behavior or apparent abnormalities. at the end of the experiment, the serum concentration of ar-r 17779 was 1.18 ± 0.17 μm. in apoe-deficient mice, treatment with ar-r 17779 resulted in significantly reduced aortic diameter comparable to control mice (0.81 ± 0.11 mm, p< 0.0001 vs. ang ii + hfd) [1].
Biochem/physiol Actions
AR-R17779 is a nicotinic acetylcholine receptor alpha7 full agonist that targets α7 nAChR with high affinity (Ki = 92 nM/rat α7 against 5 nM α-BTX vs.16 μM/rat α4β2 against 3 nM (-)-nicotine) and selectivity (EC50 = 6.2/10/12.7 μM using human/rat/monkey α7 nAChR-Xenopus oocyte by whole cell voltage clamp, no antagonistic activity against acetylcholine using human α4β2-, α3β4-, α3β2-, α3β2α5-expressing oocytes or antagonistic activity against 5-HT using rat 5HT3a-exxpressing oocytes). AR-R17779 exhibits cognition-improving efficacy in rats (1-20 mg/kg s.c) and mice (1-20 mg/kg i.p.) in vivo and is widely employed for studying other α7 nAChR-dependent physiological functions.
in vivo
AR-R17779 (1-5 mg/kg; i.p. twice a day for 7 d) ameliorates arthritis, reduces synovial inflammation, delays onset of disease and protects against joint destruction[3].
AR-R17779 (1-10 mg/kg; s.c. for 3 weeks) improves learning in two radial-arm maze tasks and reverses working memory impairment caused by fimbria-fornix sections in rats[2].
| Animal Model: | Male DBA/1 mice (8-10 weeks) were subjected to unilateral cervical vagotomy or sham surgery, after which arthritis was induced with type II collagen[3] |
| Dosage: | 1, 2.5, 5 mg/kg |
| Administration: | I.p. twice daily from day 20 until day 26 |
| Result: | Ameliorated arthritis and delayed onset of disease.
Reduced erosive disease, cartilage degradation and synovial inflammation.
Reduced TNFα levels in plasma and synovial tissue.
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References
[1]. toru hashimoto, toshihiro ichiki, ayawatanabe, et al. stimulation of α7 nicotinic acetylcholine receptor by ar-r17779 suppresses atherosclerosis and aortic aneurysm formation in apolipoprotein e-deficient mice. vascular pharmacology, 2014, 61:49-55.
[2]. rudy schreiber, marion dalmus and jean de vry. effects of α4/β2- and α7-nicotine acetylcholine receptor agonists on prepulse inhibition of the acoustic startle response in rats and mice. psychopharmacology, 2002, 159:248-257.
[3]. marja van kampen, karin selbach, renate schneider, et al. ar-r 17779 improves social recognition in rats by activation of nicotinic α7 receptors. psychopharmacology, 2004, 172:375-383.
[4]. juan arredondo, denys omelchenko, alexander i chernyavsky, et al. functional role of the nicotinic arm of the acetylcholine regulatory axis in human b-cell lines. journal of experimental pharmacology, 2009, 1:1-7.
[5]. virginia borroni and francisco j. barrantes. cholesterol modulates the rate and mechanism of acetylcholine receptor internalization. j. biol. chem., 2011, 286(19):17122-32.
