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Does adenosine A1 receptor stimulation causes QRS prolongation by blocking beta adrenergic receptors in amitriptyline poisoning?

Authors :
Akgun Arıcı, M. Aylin
Kalkan, Sule
Demir, Omer
Hocaoglu Aksay, Nil
Gidener, Sedef
Tuncok, Yesim
Source :
Toxicology Letters. Apr2009, Vol. 186 Issue 2, p130-138. 9p.
Publication Year :
2009

Abstract

Abstract: Aims: To investigate the role of beta receptor blockade via adenosine A1 receptor stimulation on amitriptyline-induced QRS prolongation. Methods: Isolated rat hearts were randomized into three groups (n =8 for each group). After pretreatment with 5% dextrose (control) or DPCPX (8-cyclopentyl-1,3-dipropylxanthine), or propranolol+DPCPX, amitriptyline infusion was given to all groups. Intact beta adrenergic receptor response was verified with a bolus dose of isoproteranol (3×10−5 M). Results: Amitriptyline (5.5×10−5 M) infusion following pretreatment with 5% dextrose or 10−4 M DPCPX prolonged QRS by 40–110% and 30–75%, respectively. After the beta receptor blockade with 10−2 M propranolol bolus, amitriptyline infusion following pretreatment with DPCPX prolonged QRS by 40–130%. Amitriptyline infusion following pretreatment with DPCPX (10−4 M) shortened the QRS at 40, 50 and 60 min significantly when compared to propranolol+DPCPX group (168.8±4.9%, p <0.05; 170.8±6.9%, p <0.01; 174.0±6.9%, p <0.01, respectively). Amitriptyline infusion following pretreatment with 5% dextrose prolonged QRS duration significantly at 50th minutes (209.5±6.1%, p <0.05) compared to DPCPX pretreatment group. Conclusion: DPCPX pretreatment shortened amitriptyline-induced QRS prolongation. Beta adrenergic receptor blockade enhanced QRS prolongation shortened by DPCPX pretreatment. Adenosine A1 receptor stimulation related to beta adrenergic receptor blockade may play a role in amitriptyline-induced QRS prolongation in isolated rat hearts. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
03784274
Volume :
186
Issue :
2
Database :
Academic Search Index
Journal :
Toxicology Letters
Publication Type :
Academic Journal
Accession number :
36898921
Full Text :
https://doi.org/10.1016/j.toxlet.2009.01.015