Repeated Arterial Occlusion, Delta-Opioid Receptor (DOR) Plasticity and Vagal Transmission Within the Sinoatrial Node of the Anesthetized Dog

被引:6
|
作者
Deo, Shekhar H. [1 ]
Barlow, Matthew A. [1 ]
Gonzalez, Leticia [1 ]
Yoshishige, Darice [1 ]
Caffrey, James L. [1 ]
机构
[1] Univ N Texas, Hlth Sci Ctr, Dept Integrat Physiol, Cardiovasc Res Inst, Ft Worth, TX 76107 USA
关键词
DOR phenotypes; opioids; vagal function; GLIBENCLAMIDE-SENSITIVE MECHANISM; CARDIAC ENKEPHALINS; RAT-HEART; MYOCARDIAL-INFARCTION; MESSENGER-RNA; SA NODE; BRADYCARDIA; EXERCISE; MIMICS; CARDIOPROTECTION;
D O I
10.3181/0808-RM-242
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Brief interruptions in coronary blood flow precondition the heart, engage delta-opioid receptor (DOR) mechanisms and reduce the damage that typically accompanies subsequent longer coronary occlusions. Repeated short occlusions of the sinoatrial (SA) node artery progressively raised nodal methionine-enkephalin-arginine-phenylalanine (MEAP) and improved vagal transmission during subsequent long occlusions in anesthetized dogs. The DOR type-1 (DOR-1) antagonist, BNTX reversed the vagotonic effect. Higher doses of enkephalin interrupted vagal transmission through a DOR-2 mechanism. The current study tested whether the preconditioning (PC) protocol, the later occlusion or a combination of both was required for the vagotonic effect. The study also tested whether evolving vagotonic effects included withdrawal of competing DOR-2 vagolytic influences. Vagal transmission progressively improved during successive SA nodal artery occlusions. The vagotonic effect was absent in sham animals and after DOR-1 blockade. After completing the PC protocol, exogenously applied vagolytic doses of MEAP reduced vagal transmission under both normal and occluded conditions. The magnitude of these DOR-2 vagolytic effects was small compared to controls and repeated MEAP challenges rapidly eroded vagolytic responses further. Prior DOR-1 blockade did not alter the PC mediated, progressive loss of DOR-2 vagolytic responses. In conclusion, DOR-1 vagotonic responses evolved from signals earlier in the PC protocol and erosion of competing DOR-2 vagolytic responses may have contributed to an unmasking of vagotonic responses. The data support the hypothesis that PC and DOR-2 stimulation promote DOR trafficking, and down regulation of the vagolytic DOR-2 phenotype in favor of the vagotonic DOR-1 phenotype. DOR-1 blockade may accelerate the process by sequestering newly emerging receptors. Exp Biol Med 234:84-94, 2009
引用
收藏
页码:84 / 94
页数:11
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