2010
DOI: 10.1016/j.jep.2010.07.013
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Acute toxicity study of the standardized methanolic extract of Mitragyna speciosa Korth in Rodent

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Cited by 132 publications
(104 citation statements)
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“…Murine models fed doses as low as 100 mg/kg and as high as 1 g/kg of MG were noted to have multiorgan changes including elevation of transaminases with simultaneous lobular destruction, dilated biliary systems, and hemorrhagic hepatocytes demonstrated on biopsy [12,13]. …”
Section: Discussionmentioning
confidence: 99%
“…Murine models fed doses as low as 100 mg/kg and as high as 1 g/kg of MG were noted to have multiorgan changes including elevation of transaminases with simultaneous lobular destruction, dilated biliary systems, and hemorrhagic hepatocytes demonstrated on biopsy [12,13]. …”
Section: Discussionmentioning
confidence: 99%
“…This research also highlights the need for regulations to prevent boosting the concentration of addictive Kratom is sold on the internet and in specialty stores (i.e., head shops) as capsules, tablets, powder, concentrated extract, gum, or raw leaves for chewing or brewing tea [6,13,31]. Reported benefits include anticancer and antioxidant effects [32,33], antiinflammatory properties [34], appetite reduction, glycemic control, treatment of chronic pain [35,36], antidepressant actions [37], antidiarrheal and antimalarial properties [1,38], treatment of ethanol [36,39] or opioid withdrawal [1,40,41], and antibacterial activity [33]. Due to its stimulant and opioid-like properties, Kratom is also consumed for analgesic and recreational purposes [26].…”
Section: Discussionmentioning
confidence: 99%
“…Chronic use results in insomnia, anorexia, weight loss, facial hyperpigmentation, dry mouth, polyuria, psychosis, or addiction [1,45,46]. Infrequent findings associated with chronic Kratom use include seizure or coma [10,24,47,48], acute respiratory distress syndrome [49], hypothyroidism [50], intrahepatic cholestasis or toxic hepatitis [38,48,51], cardiotoxicity or dysrhythmia [52], and hypertension or nephrotoxicity [38]. Fatalities have been reported in the setting of therapeutic or supratherapeutic levels of coingestants such as sympathomimetics [53,54], benzodiazepines and over the counter cold medications [55], antidepressants [56], muscle relaxers, and opioids [57,58].…”
Section: Discussionmentioning
confidence: 99%
“…General toxicity can be accessed through organ weight measurements, in which changes in the body weight and organ weight is a sensitive indicator of toxicity in their respective studies reported that toxicity indication can be seen in organ weights rather than absolute weight of rats [10][11][12]. The study reveals that following the oral administration of leaf extract of Erytherina senegalensis that there was a significant difference in the body weight of the albino rats at doses of 8000 mg/kg (Group iv) from the 4th week to 8th week (Table 3), this may show that the extract may not be toxic, although there was a decline in the fluid and food intakes from week 2 (Tables 1 and 2), The weights and relative organ weights of the ovaries of experimental rats showed no significant difference when compared with the control, which signifies that the leaf extract of Erytherina senegalensis may be nutritional and not toxic on the albino rats and the research agreed with that there were no significant changes in the relative weights of organs between the control and treated rats [13].…”
Section: Discussionmentioning
confidence: 99%