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首页> 外文期刊>Japanese Journal of Pharmacology >Residence Time of Polaprezinc (Zinc L-Carnosine Complex) in the Rat Stomach and Adhesiveness to Ulcerous Sites
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Residence Time of Polaprezinc (Zinc L-Carnosine Complex) in the Rat Stomach and Adhesiveness to Ulcerous Sites

机译:Polaprezinc(锌左旋肌氨酸复合物)在大鼠胃中的停留时间和对溃疡部位的粘附性

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References(32) Cited-By(8) 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 14-Cpolaprezinc 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.
机译:参考文献(32)Cited-By(8)Polaprezinc,一种不溶的L-肌肽锌配合物,通过直接作用于粘膜病变而表现出抗溃疡作用。研究了泊拉普嗪在胃中的分布,以阐明其结构作为不溶性复合物的有用性。大鼠口服14-Cpolaprezinc和65Zn-polaprezinc(14C-,65Zn-polaprezinc)混合物后,胃内容物和胃组织中14C放射性的时程与65Zn的时程平行。 14C-polaprezinc和65Zn-polaprezinc的胃液含量高于14C-L-肌肽和65ZnSO4的胃液含量。 14C-polaprezinc和65Zn-polaprezinc在胃中的平均停留时间(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-polaprezinc和65Zn-polaprezinc的浓度曲线下面积(AUC0-8 hr)分别是14C-L-肌肽和65ZnSO4的1.7倍。向患有乙酸诱发的溃疡的大鼠施用14C-,65Zn-泊拉普锌后,溃疡部位的14C和65Zn放射性非常相似,大于溶解在酸中的14C-,65Zn-泊拉普锌。总之,与锌或左旋肌肽相比,波拉前锌在胃中的保留时间更长,并且更能粘附在溃疡部位。该化合物的特性可能源于其不溶性,并有助于其强大的药理作用。

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