Prevention of renal crystal deposition by an extract of Ammi visnaga L. and its constituents khellin and visnagin in hyperoxaluric rats

• Published in: Urological research 2011-06, Vol.39 (3), p.189-195
• Main Authors: Vanachayangkul, P., Chow, N., Khan, S. R., Butterweck, Veronika
• Format: Article
• Language: English
• Subjects: Administration, Oral; Ammi; Animals; Calcium Oxalate - metabolism; Disease Models, Animal; Hyperoxaluria - complications; Hyperoxaluria - metabolism; Hyperoxaluria - pathology; Khellin - administration & dosage; Khellin - analogs & derivatives; Khellin - pharmacology; Khellin - therapeutic use; Kidney - drug effects; Kidney - metabolism; Kidney - pathology; Kidney Calculi - etiology; Kidney Calculi - prevention & control; Male; Medical Biochemistry; Medicine; Medicine & Public Health; Nephrology; Original Paper; Plant Extracts - administration & dosage; Plant Extracts - pharmacology; Plant Extracts - therapeutic use; Rats; Rats, Sprague-Dawley; Treatment Outcome; Urology
• ISSN: 0300-5623; 1434-0879
• DOI: 10.1007/s00240-010-0333-y

In Egypt, teas prepared from the fruits of Ammi visnaga L. (syn. “Khella”) are traditionally used by patients with urolithiasis. The aim of this study was to evaluate whether oral administration of an aqueous extract prepared from the fruits of A. visnaga as well as two major constituents khellin and visnagin could prevent crystal deposition in stone-forming rats. Hyperoxaluria was induced in male Sprague-Dawley rats by giving 0.75% ethylene glycol and 1% ammonium chloride via the drinking water. The Khella extract (KE; 125, 250 or 500 mg/kg) was orally administered for 14 days. The histopathological examination of the kidneys revealed that KE significantly reduced the incidence of calcium oxalate (CaOx) crystal deposition. In addition, KE significantly increased urinary excretion of citrate along with a decrease of oxalate excretion. Comparable to the extract, khellin and visnagin significantly reduced the incidence of CaOx deposition in the kidneys. However, both compounds did not affect urinary citrate or oxalate excretion indicating a mechanism of action that differs from that of the extract. For KE, a reasonably good correlation was observed between the incidence of crystal deposition, the increase in citrate excretion and urine pH suggesting a mechanisms that may interfere with citrate reabsorption. In conclusion, our data suggest that KE and its compounds, khellin and visnagin, may be beneficial in the management of kidney stone disease caused by hyperoxaluria but that it is likely that different mechanism of action are involved in mediating these effects.