Harris A G
Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, California.
Gut. 1994;35(3 Suppl):S1-4. doi: 10.1136/gut.35.3_suppl.s1.
Somatostatin is a 14 amino acid peptide that inhibits pancreatic exocrine and endocrine secretion. Its clinical application has been limited by its very short half life, necessitating continuous intravenous infusion. Octreotide is an 8 amino acid synthetic analogue of somatostatin that possesses similar pharmacological effects. It has a much longer duration of action, however, and can be given subcutaneously. Both the intravenous and subcutaneous routes of injection of octreotide are well tolerated. Peak serum concentrations occur within 30 minutes after subcutaneous administration and within four minutes of a three minute intravenous infusion. Serum concentration increases linearly with dose. Octreotide is distributed rapidly, mainly in the plasma, where it is 65% protein bound. The elimination half life is about 1.5 hours and about 32% of a subcutaneous dose is excreted in the urine as unchanged octreotide. Octreotide inhibits gastroenteropancreatic secretion, especially of insulin, glucagon, pancreatic polypeptide, gastric inhibitory polypeptide, and gastrin. It also inhibits both release of thyroid stimulating hormone and growth hormone secretion in response to exercise, insulin induced hypoglycaemia, and argenine stimulation. Octreotide reduces splanchnic blood flow in healthy volunteers and hepatic venous pressure in cirrhotic patients. It can accelerate or delay gastric emptying, prolong transit time at moderate to high doses, stimulate motility at low doses, and inhibit gall bladder emptying. Octreotide considerably inhibits pentagastrin stimulated gastric acid secretion and significantly diminishes exocrine pancreatic function (amylase, trypsin, lipase). Octreotide increases intestinal transit time and decreases endogenous fluid secretion in the jejunum and ileum, thus increasing the absorption of water and electrolytes. These pharmacological effects of the analogue point to its therapeutic role in a variety of endocrine and gastrointestinal disorders.
生长抑素是一种由14个氨基酸组成的肽,可抑制胰腺外分泌和内分泌分泌。其临床应用因半衰期极短而受到限制,需要持续静脉输注。奥曲肽是生长抑素的一种由8个氨基酸组成的合成类似物,具有相似的药理作用。然而,它的作用持续时间长得多,可以皮下给药。奥曲肽的静脉注射和皮下注射途径耐受性良好。皮下给药后30分钟内以及3分钟静脉输注后4分钟内出现血清峰值浓度。血清浓度随剂量呈线性增加。奥曲肽分布迅速,主要分布在血浆中,其中65%与蛋白质结合。消除半衰期约为1.5小时,皮下剂量的约32%以未改变的奥曲肽形式经尿液排泄。奥曲肽抑制胃肠胰分泌,尤其是胰岛素、胰高血糖素、胰多肽、胃抑制多肽和胃泌素的分泌。它还抑制运动、胰岛素诱导的低血糖和精氨酸刺激后促甲状腺激素的释放以及生长激素的分泌。奥曲肽可降低健康志愿者的内脏血流量和肝硬化患者的肝静脉压力。它可以加速或延迟胃排空,在中高剂量时延长转运时间,在低剂量时刺激蠕动,并抑制胆囊排空。奥曲肽可显著抑制五肽胃泌素刺激的胃酸分泌,并显著降低胰腺外分泌功能(淀粉酶、胰蛋白酶、脂肪酶)。奥曲肽可增加肠道转运时间,并减少空肠和回肠的内源性液体分泌,从而增加水和电解质的吸收。该类似物的这些药理作用表明其在多种内分泌和胃肠道疾病中的治疗作用。