2009
DOI: 10.1080/13880200802435754
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Antihyperglycemic and hypoglycemic activities ofPhyllanthus debilisaqueous plant extract in mice

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Cited by 14 publications
(11 citation statements)
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“…It was observed that AEF exerted its hypoglycemic effects through none dose-dependant manner with the mid dose producing pronounced hypoglycaemic effect. Further, the extract did produce a delayed hypoglycemic effect after 4 h and such delayed activity had been reported previously in plants such as Kokoona zeylanica L. [24], Strychnos henningsii L. [25] and Phylanthus debilis L. [26]. High dose of the extract exhibiting less hypoglycemic activity than the mid dose may be due to receptor down regulation activity of the drug thus decreasing the number of receptors for a drug or presence of other phytochemical substances [27].…”
Section: Discussionsupporting
confidence: 75%
“…It was observed that AEF exerted its hypoglycemic effects through none dose-dependant manner with the mid dose producing pronounced hypoglycaemic effect. Further, the extract did produce a delayed hypoglycemic effect after 4 h and such delayed activity had been reported previously in plants such as Kokoona zeylanica L. [24], Strychnos henningsii L. [25] and Phylanthus debilis L. [26]. High dose of the extract exhibiting less hypoglycemic activity than the mid dose may be due to receptor down regulation activity of the drug thus decreasing the number of receptors for a drug or presence of other phytochemical substances [27].…”
Section: Discussionsupporting
confidence: 75%
“…Such delayed effects may be due to active components in the extract that require a lag phase to reach sufficient concentrations at target sites. Similar delayed hypoglycaemic pattern was reported with plants such as Pylanthus debilis L ( Wanniarachchi, Peiris & Ratnasooriya, 2009 ), and Nycanthus arbor-tristis L ( Rangika, Dayananda & Peiris, 2015 ).…”
Section: Discussionsupporting
confidence: 81%
“…Eighteen rats (Wanniarachchi et al, 2009) were weighed, numbered, and randomly divided into 3 groups (NCG1, CME-PM-2000, PCG1) of 6 animals each and each rat was fed with a dosage of 2000 mg/kg body weight for the purpose of evaluation of acute toxicity, anti-hypercholectrolemic activity and 6 rats in five group (NCG2, CME-PM-400, CME-PM-800, CME-PM-1200, PCG2) included in the determinations of dose dependant response ( Table 1).…”
Section: Experimental Designmentioning
confidence: 99%