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直肠绒毛状腺瘤中的分泌性腹泻:生长抑素和吲哚美辛治疗的效果

Secretory diarrhea in villous adenoma of rectum: effect of treatment with somatostatin and indomethacin.

作者信息

Smelt A H, Meinders A E, Hoekman K, Noort W A, Keirse M J

机构信息

Department of General Internal Medicine, Leiden University Hospital, The Netherlands.

出版信息

Prostaglandins. 1992 Jun;43(6):567-72. doi: 10.1016/0090-6980(92)90116-b.

Abstract

The effects of treatment with the synthetic long-acting somatostatin analogue SMS-201-995 were studied in a patient with a fluid and electrolyte secreting villous adenoma of the rectum. The effects of SMS-201-995 on rectal fluid volume and electrolyte loss, and local and general prostanoid production were compared with those of treatment with indomethacin. During treatment with the somatostatin analogue iso-osmolar rectal fluid production increased about 25%; the quantity of prostaglandin E2 in the rectal fluid rose almost 20-fold. Prostaglandin F2 alpha, 6-keto-prostaglandin F1 alpha and 13,14-dihydro-15-keto-prostaglandin F2 alpha output showed similar, though less impressive increments during somatostatin treatment. The somatostatin analogue did not affect urinary prostanoid excretion except for levels of 2,3-dinor-thromboxane B2, which doubled. With indomethacin treatment diurnal rectal fluid production dropped by about 50% and all prostanoids measured in urine and rectal fluid decreased below control values. It appears that the somatostatin analogue SMS-201-995 has a marked stimulatory effect on the in vivo prostanoid production by the villous adenoma. Perhaps this stimulation is not confined to the tumor only, but also affects thromboxane synthesis.

摘要

在一名患有直肠分泌液体和电解质的绒毛状腺瘤患者中,研究了合成长效生长抑素类似物SMS - 201 - 995的治疗效果。将SMS - 201 - 995对直肠液体量和电解质丢失以及局部和全身前列腺素生成的影响与吲哚美辛治疗的效果进行了比较。在使用生长抑素类似物治疗期间,等渗直肠液体生成增加了约25%;直肠液体中前列腺素E2的量增加了近20倍。在生长抑素治疗期间,前列腺素F2α、6 - 酮 - 前列腺素F1α和13,14 - 二氢 - 15 - 酮 - 前列腺素F2α的产量也有类似增加,不过增幅较小。除2,3 - 二去甲血栓素B2水平翻倍外,生长抑素类似物对尿中前列腺素排泄无影响。使用吲哚美辛治疗后,日间直肠液体生成下降约50%,尿液和直肠液体中检测到的所有前列腺素均降至对照值以下。看来生长抑素类似物SMS - 201 - 995对绒毛状腺瘤的体内前列腺素生成有显著的刺激作用。也许这种刺激不仅限于肿瘤,还会影响血栓素的合成。

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