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米索前列醇、西咪替丁和乙醇对大鼠胃血浆容量及形态的影响。

Effects of misoprostol, cimetidine, and ethanol on rat gastric plasma volume and morphology.

作者信息

Lacy E R, Hund P, Tietge J

机构信息

Department of Anatomy and Cell Biology, Medical University of South Carolina, Charleston 29425.

出版信息

J Clin Gastroenterol. 1990;12 Suppl 1:S158-69. doi: 10.1097/00004836-199001001-00026.

Abstract

Prostaglandins have effects on the gastric vasculature and blood flow that may be related to the phenomenon of "cytoprotection." We evaluated the effects of two potent antiulcer compounds--misoprostol, a prostaglandin E1 analog, and cimetidine, an H2-receptor antagonist--as well as a necrotizing agent, absolute ethanol (EtOH), on gastric plasma volume using the Evans blue-albumin binding technique. In addition, the effects of these two drugs on the morphology of the gastric mucosa were evaluated by light microscopy of epoxy resin sections. Fasted rats were given one of the following oral doses: (a) misoprostol, subantisecretory (100 micrograms/kg) or antisecretory (1 mg/kg); (b) cimetidine, subantisecretory (100 micrograms/kg, or 1 mg/kg) or antisecretory (50 mg/kg); or (c) EtOH only or EtOH following 30 min of pretreatment with one of the above doses of misoprostol or cimetidine. Animals were killed 30 or 90 min after a single dose or 30 min after two doses that were 60 min apart. The stomachs were then removed and processed for biochemical determination of Evans blue concentration. For morphology, rat stomachs were fixed and processed after exposure to each of the above concentrations of misoprostol and cimetidine. Results were as follows: (i) Misoprostol (but not cimetidine) caused a significant increase in stomach weight (subantisecretory dose = +15%, antisecretory dose = +21%) independent of changes in plasma volume. (ii) Misoprostol at both doses caused a transient (30-min) reduction in plasma volume (subantisecretory dose = -12%, antisecretory dose = -14%) that rebounded to slightly elevated levels within the following 60 min. (iii) Antisecretory doses of cimetidine caused an increase in plasma volume 30 min after a single dose (+37%) and at 90 min after two doses (+46%). (iv) EtOH only at 30 or 90 min produced elevated stomach weights (+25 and +28%, respectively) and plasma volumes (+300 and +250%, respectively), the latter of which was due in part to hemorrhagic lesions. (v) Cimetidine pretreatment (30 min) followed by EtOH did not significantly reduce plasma volume, stomach weight, or the gross hemorrhagic lesions compared to EtOH alone, but (vi) misoprostol pretreatment followed by EtOH significantly protected against hemorrhagic lesions and elevated tissue plasma volumes. Both drugs at all concentrations caused expansion of the mucosal interstitial space (lamina propria), but this edema was greater with misoprostol. Severe interfoveolar cell stretching and even epithelial breaks were found with misoprostol treatment. Cimetidine showed moderate mucosal edema and a "collapse" of interfoveolar epithelial cells so the intercellular spaces were reduced.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

前列腺素对胃血管系统和血流有影响,这可能与“细胞保护”现象有关。我们使用伊文思蓝 - 白蛋白结合技术评估了两种强效抗溃疡化合物——米索前列醇(一种前列腺素E1类似物)和西咪替丁(一种H2受体拮抗剂)以及一种坏死剂无水乙醇(EtOH)对胃血浆容量的影响。此外,通过环氧树脂切片的光学显微镜检查评估了这两种药物对胃黏膜形态的影响。给禁食的大鼠口服以下剂量之一:(a) 米索前列醇,亚抑酸剂量(100微克/千克)或抑酸剂量(1毫克/千克);(b) 西咪替丁,亚抑酸剂量(100微克/千克或1毫克/千克)或抑酸剂量(50毫克/千克);或(c) 仅给予乙醇,或在给予上述剂量的米索前列醇或西咪替丁之一预处理30分钟后给予乙醇。单次给药后30或90分钟或两次间隔60分钟给药后30分钟处死动物。然后取出胃并进行处理,以生化方式测定伊文思蓝浓度。为观察形态,在暴露于上述浓度的米索前列醇和西咪替丁后,对大鼠胃进行固定和处理。结果如下:(i) 米索前列醇(而非西咪替丁)导致胃重量显著增加(亚抑酸剂量 = +15%,抑酸剂量 = +21%),与血浆容量变化无关。(ii) 两种剂量的米索前列醇均导致血浆容量短暂(30分钟)减少(亚抑酸剂量 = -12%,抑酸剂量 = -14%),并在随后60分钟内反弹至略高于正常水平。(iii) 抑酸剂量的西咪替丁在单次给药后30分钟(+37%)和两次给药后90分钟(+46%)导致血浆容量增加。(iv) 仅乙醇在30或90分钟时导致胃重量增加(分别为 +25% 和 +28%)和血浆容量增加(分别为 +300% 和 +250%),后者部分归因于出血性病变。(v) 与单独给予乙醇相比,西咪替丁预处理(30分钟)后再给予乙醇并未显著降低血浆容量、胃重量或明显的出血性病变,但(vi) 米索前列醇预处理后再给予乙醇可显著预防出血性病变并降低组织血浆容量。所有浓度的两种药物均导致黏膜间质间隙(固有层)扩张,但米索前列醇引起的这种水肿更严重。米索前列醇治疗可见严重的腺窝间细胞拉伸甚至上皮破裂。西咪替丁表现为中度黏膜水肿和腺窝间上皮细胞“塌陷”,因此细胞间隙减小。(摘要截断于400字)

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