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Effect of vagal stimulation and differential densities of M2 receptor and IK,ACh in canine atria.
Int J Cardiol. 2008 Jun 06; 126(3):352-8.IJ

Abstract

OBJECTIVE

We investigated the electrophysiological effect of vagal stimulation (VS) on atrial myocardium in vivo and differential densities of M(2) receptor and acetylcholine-induced inward rectifier K(+) current (I(K,ACh)) to discuss the mechanisms of atrial fibrillation (AF).

METHODS

With the monophasic action potential (MAP) recording technique, data from twenty-four sites, i.e. right atrial appendage (RAA), left atrial appendage (LAA), right atrium (RA) and left atrium (LA) were recorded by electrode probes, which were applied to the epicardial atrial surface of each dog. After cervical vagosympathetic cut, VS(1) (20 Hz, 0.2 ms pulse duration and at a voltage 10 V), VS(2) (20 Hz, 0.2 ms pulse duration and at a voltage 30 V) and sinus node (SN) damage were administrated respectively. MAP, dispersion of action potential duration (dAPD) and AF was recorded. Then, RAA, LAA, RA and LA were dissected. Finally, distribution of M(2) receptors and I(K,ACh) in atrial myocardium were measured by western blot and patch clamp respectively.

RESULTS

During VS(1) and VS(2), AF could be induced at first in right atrial appendage (RAA) and right atrium (RA) without left atrial appendage (LAA) and left atrium (LA). Compared to the parameters in control group and VS(2) group, dAPD was increased significantly by VS(1) and SN damage, but there was no significant difference between control group and VS(2) group. However, AF was not evoked after SN damage. Densities of M(2) receptor and I(K,ACh) were higher in RAA, LAA than those in LA and RA (M(2) receptor: 1 and 1.01 over 0.83 and 0.51, P<0.05; I(K,ACh): 20+/-0.89, 19+/-0.82, 14+/-0.64, 9+/-0.45 pA/pF, P<0.05). Furthermore, densities of M(2) receptor and I(K,ACh) were higher in LA than those in RA (P<0.05).

CONCLUSIONS

Decreased APD is the base in initiation of cholinergic AF by VS and increased dAPD alone can not induce AF. A greater abundance of M(2) receptor and I(KACh) in RAA and LAA imply atrial appendage plays an important role in initiation of cholinergic AF.

Authors+Show Affiliations

Department of Cardiology, Renmin Hospital, Wuhan University School of Medicine, JieFang Road 238, Wuhan 430060, PR China.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

17590455

Citation

Zhao, Qing-Yan, et al. "Effect of Vagal Stimulation and Differential Densities of M2 Receptor and IK,ACh in Canine Atria." International Journal of Cardiology, vol. 126, no. 3, 2008, pp. 352-8.
Zhao QY, Huang CX, Liang JJ, et al. Effect of vagal stimulation and differential densities of M2 receptor and IK,ACh in canine atria. Int J Cardiol. 2008;126(3):352-8.
Zhao, Q. Y., Huang, C. X., Liang, J. J., Chen, H., Yang, B., Jiang, H., & Li, G. S. (2008). Effect of vagal stimulation and differential densities of M2 receptor and IK,ACh in canine atria. International Journal of Cardiology, 126(3), 352-8.
Zhao QY, et al. Effect of Vagal Stimulation and Differential Densities of M2 Receptor and IK,ACh in Canine Atria. Int J Cardiol. 2008 Jun 6;126(3):352-8. PubMed PMID: 17590455.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Effect of vagal stimulation and differential densities of M2 receptor and IK,ACh in canine atria. AU - Zhao,Qing-Yan, AU - Huang,Cong-Xin, AU - Liang,Jin-Jun, AU - Chen,Hui, AU - Yang,Bo, AU - Jiang,Hong, AU - Li,Geng-Shan, Y1 - 2007/06/27/ PY - 2006/03/03/received PY - 2006/08/08/revised PY - 2007/04/02/accepted PY - 2007/6/26/pubmed PY - 2008/7/30/medline PY - 2007/6/26/entrez SP - 352 EP - 8 JF - International journal of cardiology JO - Int J Cardiol VL - 126 IS - 3 N2 - OBJECTIVE: We investigated the electrophysiological effect of vagal stimulation (VS) on atrial myocardium in vivo and differential densities of M(2) receptor and acetylcholine-induced inward rectifier K(+) current (I(K,ACh)) to discuss the mechanisms of atrial fibrillation (AF). METHODS: With the monophasic action potential (MAP) recording technique, data from twenty-four sites, i.e. right atrial appendage (RAA), left atrial appendage (LAA), right atrium (RA) and left atrium (LA) were recorded by electrode probes, which were applied to the epicardial atrial surface of each dog. After cervical vagosympathetic cut, VS(1) (20 Hz, 0.2 ms pulse duration and at a voltage 10 V), VS(2) (20 Hz, 0.2 ms pulse duration and at a voltage 30 V) and sinus node (SN) damage were administrated respectively. MAP, dispersion of action potential duration (dAPD) and AF was recorded. Then, RAA, LAA, RA and LA were dissected. Finally, distribution of M(2) receptors and I(K,ACh) in atrial myocardium were measured by western blot and patch clamp respectively. RESULTS: During VS(1) and VS(2), AF could be induced at first in right atrial appendage (RAA) and right atrium (RA) without left atrial appendage (LAA) and left atrium (LA). Compared to the parameters in control group and VS(2) group, dAPD was increased significantly by VS(1) and SN damage, but there was no significant difference between control group and VS(2) group. However, AF was not evoked after SN damage. Densities of M(2) receptor and I(K,ACh) were higher in RAA, LAA than those in LA and RA (M(2) receptor: 1 and 1.01 over 0.83 and 0.51, P<0.05; I(K,ACh): 20+/-0.89, 19+/-0.82, 14+/-0.64, 9+/-0.45 pA/pF, P<0.05). Furthermore, densities of M(2) receptor and I(K,ACh) were higher in LA than those in RA (P<0.05). CONCLUSIONS: Decreased APD is the base in initiation of cholinergic AF by VS and increased dAPD alone can not induce AF. A greater abundance of M(2) receptor and I(KACh) in RAA and LAA imply atrial appendage plays an important role in initiation of cholinergic AF. SN - 1874-1754 UR - https://www.unboundmedicine.com/medline/citation/17590455/Effect_of_vagal_stimulation_and_differential_densities_of_M2_receptor_and_IKACh_in_canine_atria_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0167-5273(07)00924-2 DB - PRIME DP - Unbound Medicine ER -