Jonassen T E, Christensen S, Sørensen A M, Marcussen N, Flyvbjerg A, Andreasen F, Petersen J S
Department of Pharmacology, The Panum Institute, University of Copenhagen, Denmark.
Hepatology. 1999 May;29(5):1387-95. doi: 10.1002/hep.510290532.
We examined the effect of a new long-acting release formula (LAR) of the somatostatin analogue, octreotide, on development of sodium retention and functional and structural changes in the thick ascending limb of Henle's loop (TAL) in rats with cirrhosis induced by common bile duct ligation (CBL). CBL and sham-operated control rats were treated with octreotide-LAR (10 mg/kg body weight subcutaneously, as a single dose) or vehicle at the time of CBL or sham-CBL. The rats were instrumented with chronic catheters, and sodium balance and renal function were examined 4 weeks after CBL or sham operation. Octreotide-LAR treatment significantly inhibited sodium retention in CBL rats and prevented renal vasodilatation without changes in glomerular filtration rate (GFR). The natriuretic response to a test dose of furosemide (7.5 mg/kg body weight intravenously) was significantly increased in CBL rats, and when expressed in terms of natriuretic efficiency (mmol Na/mg furosemide in urine), the natriuretic response was increased by 57% relative to sham-operated controls. Stereological examination of kidneys demonstrated a 53% increase in the volume of the inner stripe of the outer medulla and a 108% increase in the volume of TAL epithelium in cirrhotic rats relative to controls. The increased natriuretic efficiency of furosemide as well as the hypertrophy of the inner stripe and the TAL in this renal zone were absent in CBL rats treated with octreotide-LAR. These results suggest that octreotide-LAR treatment inhibits sodium retention in cirrhotic rats, partly by inhibition of increased furosemide-sensitive sodium reabsorption in the TAL.
我们研究了生长抑素类似物奥曲肽的一种新型长效释放制剂(LAR),对胆总管结扎(CBL)诱导的肝硬化大鼠钠潴留的发展以及髓袢升支粗段(TAL)功能和结构变化的影响。CBL大鼠和假手术对照大鼠在CBL或假CBL时,皮下注射奥曲肽-LAR(10 mg/kg体重,单剂量)或赋形剂。给大鼠植入慢性导管,并在CBL或假手术后4周检查钠平衡和肾功能。奥曲肽-LAR治疗显著抑制了CBL大鼠的钠潴留,并防止了肾血管舒张,而肾小球滤过率(GFR)无变化。CBL大鼠对静脉注射速尿试验剂量(7.5 mg/kg体重)的利钠反应显著增加,以利钠效率(尿中Na/毫克速尿的毫摩尔数)表示时,利钠反应相对于假手术对照增加了57%。肾脏的体视学检查显示,与对照相比,肝硬化大鼠外髓质内带体积增加53%,TAL上皮体积增加108%。用奥曲肽-LAR治疗的CBL大鼠中,速尿利钠效率的增加以及该肾区TAL和内带的肥大均未出现。这些结果表明,奥曲肽-LAR治疗抑制肝硬化大鼠的钠潴留,部分是通过抑制TAL中速尿敏感性钠重吸收增加来实现的。