TY - JOUR
T1 - Antiurolithic effect of Bergenia ligulata rhizome
T2 - An explanation of the underlying mechanisms
AU - Bashir, Samra
AU - Gilani, Anwar H.
N1 - Funding Information:
This study was financed in part by the Higher Education Commission of Pakistan and the University Research Council of the Aga Khan University, Karachi, Pakistan. Samra Bashir was on study leave from Bahauddin Zakariya University, Multan.
PY - 2009/2/25
Y1 - 2009/2/25
N2 - Ethnopharmacological relevance: Bergenia ligulata is widely used plant in South Asia, mainly India and Pakistan, as a traditional medicine for treatment of urolithiasis. Aim of the study: To rationalize the Bergenia ligulata use in kidney stones and to explain the underlying mechanisms. Materials and methods: The crude aqueous-methanolic extract of Bergenia ligulata rhizome (BLR) was studied using in vitro and in vivo methods. Results: BLR inhibited calcium oxalate (CaC2O4) crystal aggregation as well as crystal formation in the metastable solutions and exhibited antioxidant effect against 1,1-diphenyl-2-picrylhydrazyl free radical and lipid peroxidation in the in vitro. BLR caused diuresis in rats accompanied by a saluretic effect. In an animal model of urolithiasis, developed in male Wistar rats by adding 0.75% ethylene glycol (EG) in drinking water, BLR (5-10 mg/kg) prevented CaC2O4 crystal deposition in the renal tubules. The lithogenic treatment caused polyuria, weight loss, impairment of renal function and oxidative stress, manifested as increased malondialdehyde and protein carbonyl contents, depleted reduced glutathione and decreased antioxidant enzyme activities of the kidneys, which were prevented by BLR. Unlike the untreated animals, EG intake did not cause excessive hyperoxaluria and hypocalciuria in BLR treated groups and there was a significant increase in the urinary Mg2+, instead of a slight decrease. Conclusions: These data indicate the antiurolithic activity in Bergenia ligulata mediated possibly through CaC2O4 crystal inhibition, diuretic, hypermagneseuric and antioxidant effects and this study rationalizes its medicinal use in urolithiasis.
AB - Ethnopharmacological relevance: Bergenia ligulata is widely used plant in South Asia, mainly India and Pakistan, as a traditional medicine for treatment of urolithiasis. Aim of the study: To rationalize the Bergenia ligulata use in kidney stones and to explain the underlying mechanisms. Materials and methods: The crude aqueous-methanolic extract of Bergenia ligulata rhizome (BLR) was studied using in vitro and in vivo methods. Results: BLR inhibited calcium oxalate (CaC2O4) crystal aggregation as well as crystal formation in the metastable solutions and exhibited antioxidant effect against 1,1-diphenyl-2-picrylhydrazyl free radical and lipid peroxidation in the in vitro. BLR caused diuresis in rats accompanied by a saluretic effect. In an animal model of urolithiasis, developed in male Wistar rats by adding 0.75% ethylene glycol (EG) in drinking water, BLR (5-10 mg/kg) prevented CaC2O4 crystal deposition in the renal tubules. The lithogenic treatment caused polyuria, weight loss, impairment of renal function and oxidative stress, manifested as increased malondialdehyde and protein carbonyl contents, depleted reduced glutathione and decreased antioxidant enzyme activities of the kidneys, which were prevented by BLR. Unlike the untreated animals, EG intake did not cause excessive hyperoxaluria and hypocalciuria in BLR treated groups and there was a significant increase in the urinary Mg2+, instead of a slight decrease. Conclusions: These data indicate the antiurolithic activity in Bergenia ligulata mediated possibly through CaC2O4 crystal inhibition, diuretic, hypermagneseuric and antioxidant effects and this study rationalizes its medicinal use in urolithiasis.
KW - Animal model
KW - Antioxidant
KW - Bergenia ligulata
KW - Calcium oxalate crystallization
KW - Diuretic
KW - Urolithiasis
UR - http://www.scopus.com/inward/record.url?scp=59849129889&partnerID=8YFLogxK
U2 - 10.1016/j.jep.2008.12.004
DO - 10.1016/j.jep.2008.12.004
M3 - Article
C2 - 19118615
AN - SCOPUS:59849129889
SN - 0378-8741
VL - 122
SP - 106
EP - 116
JO - Journal of Ethnopharmacology
JF - Journal of Ethnopharmacology
IS - 1
ER -