Nicorandil, a hybrid between nitrate and ATP-sensitive potassium channel opener, preconditions human heart to ischemia during percutaneous transluminal coronary angioplasty

Citation
T. Yasuda et al., Nicorandil, a hybrid between nitrate and ATP-sensitive potassium channel opener, preconditions human heart to ischemia during percutaneous transluminal coronary angioplasty, JPN CIRC J, 65(6), 2001, pp. 526-530
Citations number
40
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
JAPANESE CIRCULATION JOURNAL-ENGLISH EDITION
ISSN journal
00471828 → ACNP
Volume
65
Issue
6
Year of publication
2001
Pages
526 - 530
Database
ISI
SICI code
0047-1828(200106)65:6<526:NAHBNA>2.0.ZU;2-C
Abstract
The human heart progressively becomes more tolerant to ischemia after repea ted balloon inflations during percutaneous transluminal coronary angioplast y (PTCA). The present study investigated whether nicorandil, a hybrid betwe en nitrate and an ATP-sensitive potassium channel opener, affects this isch emic preconditioning. Sixteen patients with stable angina pectoris caused b y left anterior descending artery lesions were subjected to 2 balloon infla tions of 2-min duration with a 3-min reperfusion period. Seven of these pat ients served as the control group and in the remaining 9 patients, nicorand il was administered intravenously (6 mg/h) throughout the PTCA procedure (n icorandil group). The lactate extraction ratio (LER) was obtained at 30s af ter each ischemic event (LERpost-1 and LERpost-2) in both groups. In the co ntrol group, LERpost-1 was more negative than LERpost-2 (-185.7 +/- 74.2 vs -98 +/- 37.3%, p < 0.01). The ratio of the sum of the ST elevation in the precordial leads during the second inflation (<Sigma>ST-2, 0.94 +/- 0.66 mV ) to that during the first inflation (Sigma ST-1, 1.43 +/- 1.17 mV) was 0.7 2 +/- 0.16 in the control group; which was less than the ratio in the nicor andil group (1.06 +/- 0.13, p < 0.01). Nicorandil abolished the difference between the 2 ischemic events (LERpost-1, -45.1 <plus/minus> 41.6 vs LERpos t-2, -43.5 +/- 51.1%; Sigma ST-1, 1.38 +/- 0.80 vs Sigma ST-2, 1.46 +/- 0.9 0 mV). LER was less negative in the nicorandil group than that in the contr ol group (LERpost-1, -45.1 +/- 41.6 vs -185.7 +/- 74.2%, p < 0.01; LERpost- 2, -43.5 <plus/minus> 51.1 vs -98.0 +/- 37.3%, p < 0.05). Thus, nicorandil improved lactate metabolism during PTCA without significantly influencing S T-elevation In conclusion, intravenous pre-administration of nicorandil app ears to precondition the human heart during PTCA.