Abstract:O. stamineus exhibited diuretic activity, but was less potent than furosemide and hydrochlorothiazide. Care should be taken when consuming this herb as slight increase of kidney function enzymes was recorded.
“…The recommended daily dose in folk medicine is at least 6-10 times lower than the highest daily dose tested in mice in this study (i.e., 500-4000 mg/kg body weight po). It is of note that these doses were comparable to or higher than those reported to induce pharmacological effects in rodents such as anti-ulcer effects in rats (125-1000 mg/kg body weight) (Yam et al, 2009), diuretic effects in rats (5-10 mg/kg body weight po) (Adam et al, 2009), and anti-inflammatory and analgesic effects in rats and mice (500-1000 mg/kg body weight po) (Yam et al, 2008).…”
Section: Discussionmentioning
confidence: 62%
“…In Sprague-Dawley rats, an acute oral toxicity study found no mortality and no overt toxicity up to the highest dose of Orthosiphon stamineus extract tested (LD 50 > 5000 mg/kg body weight po) (Abdullah et al, 2009), while a 14-day repeated dose study found no deaths and no other adverse effects on females treated orally with doses of Orthosiphon stamineus extract ranging from 500 up to 5000 mg/kg body weight/day (Chin et al, 2008). In addition, pharmacological studies of Orthosiphon stamineus extracts have not revealed any adverse effect on rats and mice either (Adam et al, 2009;Beaux et al, 1999;Yam et al, 2008Yam et al, , 2009. Considering the lack of overt toxicity in the aforementioned rodent studies and in a preliminary experiment with Swiss Webster mice, 4000 mg/kg of body weight/day (for 3 days) was set as the upper limit of the dose range tested in this study.…”
“…The recommended daily dose in folk medicine is at least 6-10 times lower than the highest daily dose tested in mice in this study (i.e., 500-4000 mg/kg body weight po). It is of note that these doses were comparable to or higher than those reported to induce pharmacological effects in rodents such as anti-ulcer effects in rats (125-1000 mg/kg body weight) (Yam et al, 2009), diuretic effects in rats (5-10 mg/kg body weight po) (Adam et al, 2009), and anti-inflammatory and analgesic effects in rats and mice (500-1000 mg/kg body weight po) (Yam et al, 2008).…”
Section: Discussionmentioning
confidence: 62%
“…In Sprague-Dawley rats, an acute oral toxicity study found no mortality and no overt toxicity up to the highest dose of Orthosiphon stamineus extract tested (LD 50 > 5000 mg/kg body weight po) (Abdullah et al, 2009), while a 14-day repeated dose study found no deaths and no other adverse effects on females treated orally with doses of Orthosiphon stamineus extract ranging from 500 up to 5000 mg/kg body weight/day (Chin et al, 2008). In addition, pharmacological studies of Orthosiphon stamineus extracts have not revealed any adverse effect on rats and mice either (Adam et al, 2009;Beaux et al, 1999;Yam et al, 2008Yam et al, , 2009. Considering the lack of overt toxicity in the aforementioned rodent studies and in a preliminary experiment with Swiss Webster mice, 4000 mg/kg of body weight/day (for 3 days) was set as the upper limit of the dose range tested in this study.…”
“…Increasingly considerable attention has been given to its antioxidant, anti-inflammatory, diuretic, antihyperglycemic, hypouricemic, hepatoprotective and anti-fungal properties (Sriplang et al, 2007;Yam et al, 2007;Yam et al, 2009;Yam et al, 2010;Mohamed et al, 2011a;Pan et al, 2011). OS extracts also exhibited diuretic activity via increase of urine volume and electrolytes (Na þ and K þ ) excretion in hyperuricemic rats (Arafat et al, 2008;Adam et al, 2009). Moreover, aqueous and 50% ethanol extracts of OS are low toxicity (Mohamed et al, 2011b;Muhammad et al, 2011).…”
“…A number of research has also been done to explore the effects of the leave extract of Orthosiphon aristatus (OA) -commonly known as cat whiskers in Malay, or Java tea, on urolithiasis (Yam et al, 2013;Abdelwahab et al, 2011;Adam et al, 2009;Yam et al, 2007). These studies focused on the medicinal properties of OA.…”
The formation of urinary stones is a serious problem worldwide. Struvite (MgNH4PO4.6H2O) is known as one of the main components of the stones. Traditionally, herbal extracts treatment is recommended. This paper discusses the effects of Orthosiphon aristatus Bl.Miq leaves extract (OA) on struvite crystals grown by diffusion gel method. After three weeks the crystals were separated from the gel, air dried and stored for characterisation. The crystals exhibit different morphologies depending upon the location of growth. It was found that OA caused the crystals to have noticeable surface defects, discolorisation and fragmentation. Also, OA (up to 5.0%) decreased the growth rate. XRD analysis confirms struvite crystallinity. Pure crystals and those grown with OA showed identical XRD pattern, indicating that the crystalline nature may be unaffected. For crystals with OA, FTIR spectrum shifted to higher wave numbers, implying that the various organic compounds in OA might be absorbed on the crystal surface. TG-DTA studies showed similar thermal behaviour for both pure crystals and those with OA. However, the later revealed lower endothermic temperature, indicating lower thermal stability. Fragmentation and lower thermal stability of struvite indicated that OA was a potent inhibitor of struvite and could be effective for urinary stone treatment.
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