Differing role of right and left stellate ganglion with respect to coronary artery occlusion induced cardiac arrhythmias R.C. Pandey, R.D. Srivastava and V.M. Bhatnagar. Department of Physiology, G.S.V.M. Medical College, Kanpur, U.P., India

1978 ◽  
Vol 10 ◽  
pp. 75
1991 ◽  
Vol 66 (6) ◽  
pp. 2095-2106 ◽  
Author(s):  
R. W. Blair ◽  
A. R. Evans

1. A total of 59 medullary raphespinal neurons antidromically activated from the T2-T5 segments were tested for responses to coronary artery occlusion, epicardial application of bradykinin, and mechanical probing of the epicardium in cats anesthetized with alpha-chloralose. With the exception of five neurons, only those neurons that were responsive to electrical stimulation of the left stellate ganglion were tested for responses to these stimuli. Neurons in this study are a subset of those in the companion report. 2. Six neurons (12%) responded to epicardial bradykinin. Five cells were excited, and one was inhibited. Nine neurons (18%) had cardiac receptive fields, and one neuron (2%) had a field confined to the pericardium. 3. Neurons were tested for responses to separate occlusions of the left anterior descending (LAD) and circumflex (CX) coronary arteries. Overall, 13/34 (38%) of tested raphespinal neurons were responsive to coronary artery occlusion. Responses to coronary artery occlusion consisted of two major patterns. One pattern consisted of either an increase or decrease in neuronal firing rate after the heart became ischemic; this pattern was termed an ischemic (IS) response. Ten neurons (29%) exhibited an IS response to occlusion of the LAD and/or CX coronary arteries. Because four neurons exhibited IS responses to occlusion of each artery, there were a total of 14 IS responses. Of these, 10 were inhibitory, and 4 were excitatory. The second pattern of response consisted of a rapidly adapting excitation or inhibition at the onset or release of occlusion, but cell activity was unchanged during cardiac ischemia; this pattern was termed an onset (ON) response. Three neurons (9%) exhibited ON responses; two were excited, and one was inhibited. No neurons demonstrated both ON and IS responses during occlusion. 4. Twenty-one neurons were tested for responses to occlusion of each artery. Seventeen neurons (81%) exhibited similar patterns of responses to occlusion of each artery; that is, they either showed the same pattern of response to occlusion of each artery or they were unresponsive to either occlusion. For the 5 of these 17 neurons that were responsive, direction of change in neuronal activity (excitation or inhibition) was the same for occlusion of each artery. 5. All raphespinal neurons tested for responses to epicardial bradykinin and coronary artery occlusion were responsive to electrical stimulation of the left stellate ganglion. In addition, 16/28 (57%) of neurons tested for responses to occlusion were responsive to electrical stimulation of the right cervical vagus nerve.(ABSTRACT TRUNCATED AT 400 WORDS)


1992 ◽  
Vol 12 (6) ◽  
pp. 739-745
Author(s):  
Sadayoshi Komori ◽  
Mituru Osada ◽  
Sohichi Sano ◽  
Tukasa Ishihara ◽  
Takao Sawanobori ◽  
...  

1997 ◽  
Vol 86 (5) ◽  
pp. 1128-1139 ◽  
Author(s):  
Judy R. Kersten ◽  
Karl G. Orth ◽  
Paul S. Pagel ◽  
David A. Mei ◽  
Garrett J. Gross ◽  
...  

Background This investigation tested the hypothesis that adenosine (A1) receptor blockade modulates the cardioprotective effects of isoflurane. Methods Hemodynamics and percentage segment shortening (%SS) in the left anterior descending coronary artery (LAD) perfusion territory were evaluated in barbiturate-anesthetized dogs (n = 31) at selected intervals after pretreatment with the selective A1 receptor antagonist (8-cyclopentyl-1,3,dipropyl-xanthine; DPCPX 0.8 mg/kg, intravenously) or drug vehicle in the presence or absence of 1 minimum alveolar concentration (MAC) isoflurane. Dogs were subjected to five 5-min occlusions and reperfusions of the LAD, followed by 180 min of final reperfusion. Isoflurane was administered for 30 min before and during LAD occlusions and reperfusions and was discontinued at the onset of final reperfusion. Two other groups of dogs (n = 17) were used to measure interstitial concentrations of purines in the LAD region using a microdialysis technique in the presence and absence of isoflurane. Results Dogs receiving drug vehicle or DPCPX exhibited no recovery of %SS after 180 min of reperfusion (-5 +/- 7 and 5 +/- 11% of baseline, respectively, +/- SEM). In contrast, dogs receiving isoflurane alone demonstrated complete recovery of %SS at 60 min after reperfusion. DPCPX pretreatment partially attenuated isoflurane-induced enhancement of recovery of %SS (34 +/- 11% of baseline 180 min after reperfusion; P < 0.05). Interstitial purine concentrations were increased during multiple occlusions and reperfusions of the LAD in dogs not receiving isoflurane, but they were unchanged by coronary artery occlusion and reperfusion in dogs receiving isoflurane. Conclusions The results indicate that isoflurane-induced cardioprotection in stunned myocardium is partially mediated by adenosine type 1 receptor activation and is accompanied by decreases in endogenous adenosine release.


1983 ◽  
Vol 3 (4) ◽  
pp. 401-415 ◽  
Author(s):  
Carlo Vigorito ◽  
Lorenzo De Caprio ◽  
Sergio Poto ◽  
Stefania Maione ◽  
Massimo Chiariello ◽  
...  

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