Furuta S, Toyama S, Miwa M, Itabashi T, Sano H, Yoneta T
Central Research Laboratories, Zeria Pharmaceutical Co., Ltd., Saitama, Japan.
Jpn J Pharmacol. 1995 Apr;67(4):271-8. doi: 10.1254/jjp.67.271.
Polaprezinc, an insoluble zinc complex of L-carnosine, exhibits anti-ulcer effects by acting directly on mucosal lesions. The disposition of polaprezinc in the stomach was studied to clarify the usefulness of its structure as an insoluble complex. The time courses of 14C-radioactivity in the gastric contents and gastric tissues were parallel to those of 65Zn after oral administration of a mixture of 14C-polaprezinc and 65Zn-polaprezinc (14C-, 65Zn-polaprezinc) to rats. The gastric contents of 14C-polaprezinc and 65Zn-polaprezinc were greater than those of 14C-L-carnosine and 65ZnSO4. Mean residence times (MRT) of 14C-polaprezinc and 65Zn-polaprezinc in the stomach were almost the same (ca. 2 hr), and they were double those of 14C-L-carnosine and 65ZnSO4. In gastric tissues, the area under the concentration curves (AUC0-8 hr) of 14C-polaprezinc and 65Zn-polaprezinc were 1.7 times greater than those of 14C-L-carnosine and 65ZnSO4, respectively. After administration of 14C-, 65Zn-polaprezinc to rats with acetic acid-induced ulcers, 14C and 65Zn-radioactivities in the ulcerous sites were very similar and greater than those of 14C-, 65Zn-polaprezinc dissolved in acid. In conclusion, polaprezinc is retained in the stomach longer and adheres to the ulcerous sites more than zinc or L-carnosine. The characteristics of this compound may arise from its insolubility and contribute to its strong pharmacological action.
聚普瑞锌是L-肌肽的一种不溶性锌络合物,通过直接作用于黏膜损伤发挥抗溃疡作用。研究了聚普瑞锌在胃中的处置情况,以阐明其作为不溶性络合物结构的效用。给大鼠口服14C-聚普瑞锌和65Zn-聚普瑞锌(14C-、65Zn-聚普瑞锌)混合物后,胃内容物和胃组织中14C放射性的时间进程与65Zn的相似。14C-聚普瑞锌和65Zn-聚普瑞锌的胃内容物含量高于14C-L-肌肽和65ZnSO4。14C-聚普瑞锌和65Zn-聚普瑞锌在胃中的平均驻留时间(MRT)几乎相同(约2小时),是14C-L-肌肽和65ZnSO4的两倍。在胃组织中,14C-聚普瑞锌和65Zn-聚普瑞锌的浓度曲线下面积(AUC0-8小时)分别比14C-L-肌肽和65ZnSO4大1.7倍。给乙酸诱导溃疡的大鼠施用14C-、65Zn-聚普瑞锌后,溃疡部位的14C和65Zn放射性非常相似,且高于溶解于酸中的14C-、65Zn-聚普瑞锌。总之,聚普瑞锌在胃中保留的时间更长,比锌或L-肌肽更能附着于溃疡部位。该化合物的这些特性可能源于其不溶性,并有助于其强大的药理作用。