Pharmacokinetic and pharmacodynamic evidence for developing an oral formulation of octreotide against gastric mucosal injury

• 来源期刊: 中国药理学报（英文版）
• 关键词: somatostatin somatostatin receptors 2 octreotide CYN-154806 oral formulation pharmacokinetics pharmacodynamics gastric mucosal injury gastrin gastric acid
• 年，卷（期）: 2018,（8）
• 页码范围: 1373-1385
• 页数: 13页
• 语种: 英文
• DOI: 10.1038/aps.2017.159

摘要

Among the somatostatin analogues,octreotide (OCT) is the most commonly used in clinic via intravenous or subcutaneous injection to treat various diseases caused by increased secretion of growth hormone,gastrin or insulin.In order to assesse the feasibility of developing oral formulations of OCT,we conducted systematical pharmacokinetic and pharmacodynamic analyses of OCT in several animal models.The pharmacokinetic studies in rats showed that intragastric administration of OCT had extremely low bioavailability (＜0.5％),but it could specifically distribute to the gastric mucosa due to the high expression of somatostatin receptor 2 (SSTR2) in the rat stomach.The pharmacodynamic studies revealed that intragastric administration of OCT dose-dependently protected against gastric mucosal injury (GMI) in mice with WIRS-induced mouse gastric ulcers,which were comparable to those achieved by intravenous injection of OCT,and this effect was markedly attenuated by co-administration of CYN-154806,an antagonist of SSTR2.In pyloric ligation-induced ulcer mice,we further demonstrated that OCT significantly reduced the secretion of gastric acid via down-regulating the level of gastrin,which was responsible for the protective effect of OCT against GMI.Overall,we have provided pharmacokinetic and pharmacodynamic evidence for the feasibility of developing an oral formulation of OCT.Most importantly,the influence of SSTR2 on the pharmacokinetics and pharmacodynamics of OCT suggested that an oral formulation of OCT might be applicable for other clinical indications,including neuroendocrine neoplasms and pituitary adenoma due to the overexpression of SSTR2 on these tumor cells.