Sauter A, Rudin M
Magn Reson Med. 1987 Jan;4(1):1-8. doi: 10.1002/mrm.1910040102.
The effects of various calcium antagonists on the ATP, PCr, and Pi levels as well as intracellular pH in normal and ischemic rat brain were examined by 31P NMR spectroscopy using a surface coil. None of the calcium antagonists tested showed any effect in the nonischemic rat brain. However, when global ischemia was induced by cardiac arrest, the ensuring rapid decrease of ATP and PCr and concomitant increase of Pi were significantly retarded by dihydropyridine calcium antagonists, but not by verapamil. The fall in pH caused by ischemia was not affected by either drug. Barbiturates showed effects similar to calcium antagonists, whereas calcium agonists showed the opposite. These results suggest that dihydropyridine calcium antagonists, similar to barbiturates, decrease the high-energy phosphate consumption of the brain, which might be beneficial in instances where their production is severely hampered, e.g., during ischemia.
使用表面线圈通过31P核磁共振波谱法检测了各种钙拮抗剂对正常和缺血大鼠脑内ATP、磷酸肌酸(PCr)、无机磷酸盐(Pi)水平以及细胞内pH值的影响。所测试的钙拮抗剂在非缺血大鼠脑中均未显示出任何作用。然而,当通过心脏骤停诱导全脑缺血时,二氢吡啶类钙拮抗剂可显著延缓随后出现的ATP和PCr的快速下降以及Pi的伴随增加,但维拉帕米无此作用。缺血引起的pH值下降不受这两种药物中任何一种的影响。巴比妥类药物显示出与钙拮抗剂相似的作用,而钙激动剂则显示出相反的作用。这些结果表明,二氢吡啶类钙拮抗剂与巴比妥类药物类似,可降低脑内高能磷酸盐的消耗,这在其产生严重受阻的情况下可能是有益的,例如在缺血期间。