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生长抑素类似物SMS 201-995的口服吸收:理论与实际意义。

Oral absorption of the somatostatin analogue SMS 201-995: theoretical and practical implications.

作者信息

Fuessl H S, Domin J, Bloom S R

出版信息

Clin Sci (Lond). 1987 Feb;72(2):255-7. doi: 10.1042/cs0720255.

Abstract

Oral administration of SMS 201-995 (SMS), a subcutaneously injectable somatostatin analogue, was investigated in five healthy volunteers, who drank 2 mg of SMS with 75 g of glucose. Mean maximal plasma SMS concentrations after the 2 mg oral dose were comparable with those after subcutaneous injection of 50 micrograms, although the peak was delayed (90 vs 15 min). Biological activity of absorbed SMS was shown by significant and lasting suppression of plasma insulin concentrations, resulting in significant hyperglycaemia at 90 and 120 min compared with the control study. The feasibility of oral administration of SMS may extend its use in the treatment of acromegaly and gut endocrine tumours. Other peptide hormone analogues, structurally 'protected' against enzymatic degradation, may also be active orally and thus be useful therapeutically.

摘要

在五名健康志愿者中研究了口服SMS 201-995(SMS),一种可皮下注射的生长抑素类似物,这些志愿者饮用了2毫克SMS与75克葡萄糖的混合物。口服2毫克剂量后,血浆SMS的平均最大浓度与皮下注射50微克后的浓度相当,尽管峰值出现延迟(分别为90分钟和15分钟)。吸收的SMS的生物活性表现为血浆胰岛素浓度受到显著且持久的抑制,与对照研究相比,在90分钟和120分钟时导致显著的高血糖。口服SMS的可行性可能会扩大其在肢端肥大症和肠道内分泌肿瘤治疗中的应用。其他在结构上“受保护”免受酶降解的肽激素类似物,也可能口服具有活性,因此在治疗上有用。

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