Kessel D
Department of Medicine (Hematology/Oncology), Wayne State University School of Medicine, Detroit, MI.
Cancer Lett. 1988 Mar;39(2):193-8. doi: 10.1016/0304-3835(88)90104-8.
Dicarboxylic porphyrins were reported to be potent inhibitors of the binding of benzodiazepines to peripheral drug receptors in mitochondria, but the reverse does not appear to be true. Moreover, the photosensitization of mitochondria by the tumor-localizing porphyrin dimer/oligomer fraction of 'HPD' was not inhibited by benzodiazepines in cell culture.
据报道,二羧酸卟啉是苯二氮䓬类药物与线粒体中周围药物受体结合的有效抑制剂,但反之似乎不成立。此外,在细胞培养中,苯二氮䓬类药物并不能抑制由 “血卟啉衍生物”(HPD)的肿瘤定位卟啉二聚体/寡聚体部分引起的线粒体光敏化作用。