Abstract:The term Butterfly tea refers to decoction of Mariposa christia vespertilionis leaves which is widely consumed by cancer patients throughout Malaysia and has gained a huge popularity among Malaysians, not only cancer patients but also researchers to discover the real potential of this plant. Herein, the study is aimed at evaluating the possible toxicity in 28-day subacute oral toxicity of ethanolic extract M. christia vespertilionis in male Sprague Dawley rats. The 28-day subacute toxicity study was conducted … Show more
“…Post-mortem was conducted on each of the mouse, liver and kidneys were collected for histopathological evaluation at the histopathology laboratory, Faculty of Veterinary Medicine, Universiti Putra Malaysia. Collected organs were fixed in 10% neutral buffered formalin and processed further for haematoxylin and eosin stain as described by Nurul et al [91] and Aliyu et al [84]. The severity of each of the lesions was also scored according to the method of Nurul et al [91] with modifications.…”
Section: Histopathological Evaluationmentioning
confidence: 99%
“…Collected organs were fixed in 10% neutral buffered formalin and processed further for haematoxylin and eosin stain as described by Nurul et al [91] and Aliyu et al [84]. The severity of each of the lesions was also scored according to the method of Nurul et al [91] with modifications. The scores of each lesion and its interpretation is presented on Table 12.…”
Section: Histopathological Evaluationmentioning
confidence: 99%
“…Interpretation of scores in liver and kidney lesion scoring for the toxicity studies of CELE in ICR mice. Clinacanthus nutans ethanolic leaf extract, * = Modified from Sajjaratul et al[7] and Nurul et al[91].…”
This study investigated the leaves of Clinacanthus nutans for its bioactive compounds and acute and subacute toxicity effects of C. nutans ethanolic leaf extract (CELE) on blood, liver and kidneys of ICR mice. A total of 10 8-week-old female mice were divided into groups A (control) and B (2000 mg/kg) for the acute toxicity study. A single dose of 2000 mg/kg was administered to group B through oral gavage and mice were monitored for 14 days. In the subacute toxicity study, mice were divided into five groups: A (control), B (125 mg/kg), C (250 mg/kg), D (500 mg/kg) and E (1000 mg/kg). The extract was administered daily for 28 days via oral gavage. The mice were sacrificed, and samples were collected for analyses. Myricetin, orientin, isoorientin, vitexin, isovitexin, isookanin, apigenin and ferulic acid were identified in the extract. Twenty-eight days of continuous oral administration revealed significant increases (p < 0.05) in creatinine, ALT and moderate hepatic and renal necrosis in groups D and E. The study concluded that the lethal dose (LD50) of CELE in mice is greater than 2000 mg/kg and that repeated oral administrations of CELE for 28 days induced hepatic and renal toxicities at 1000 mg/kg in female ICR mice.
“…Post-mortem was conducted on each of the mouse, liver and kidneys were collected for histopathological evaluation at the histopathology laboratory, Faculty of Veterinary Medicine, Universiti Putra Malaysia. Collected organs were fixed in 10% neutral buffered formalin and processed further for haematoxylin and eosin stain as described by Nurul et al [91] and Aliyu et al [84]. The severity of each of the lesions was also scored according to the method of Nurul et al [91] with modifications.…”
Section: Histopathological Evaluationmentioning
confidence: 99%
“…Collected organs were fixed in 10% neutral buffered formalin and processed further for haematoxylin and eosin stain as described by Nurul et al [91] and Aliyu et al [84]. The severity of each of the lesions was also scored according to the method of Nurul et al [91] with modifications. The scores of each lesion and its interpretation is presented on Table 12.…”
Section: Histopathological Evaluationmentioning
confidence: 99%
“…Interpretation of scores in liver and kidney lesion scoring for the toxicity studies of CELE in ICR mice. Clinacanthus nutans ethanolic leaf extract, * = Modified from Sajjaratul et al[7] and Nurul et al[91].…”
This study investigated the leaves of Clinacanthus nutans for its bioactive compounds and acute and subacute toxicity effects of C. nutans ethanolic leaf extract (CELE) on blood, liver and kidneys of ICR mice. A total of 10 8-week-old female mice were divided into groups A (control) and B (2000 mg/kg) for the acute toxicity study. A single dose of 2000 mg/kg was administered to group B through oral gavage and mice were monitored for 14 days. In the subacute toxicity study, mice were divided into five groups: A (control), B (125 mg/kg), C (250 mg/kg), D (500 mg/kg) and E (1000 mg/kg). The extract was administered daily for 28 days via oral gavage. The mice were sacrificed, and samples were collected for analyses. Myricetin, orientin, isoorientin, vitexin, isovitexin, isookanin, apigenin and ferulic acid were identified in the extract. Twenty-eight days of continuous oral administration revealed significant increases (p < 0.05) in creatinine, ALT and moderate hepatic and renal necrosis in groups D and E. The study concluded that the lethal dose (LD50) of CELE in mice is greater than 2000 mg/kg and that repeated oral administrations of CELE for 28 days induced hepatic and renal toxicities at 1000 mg/kg in female ICR mice.
“…The blood samples collected were analysed for complete blood count using an automated haematology analyser (ABC Vet ®, ABX Diagnostics, Montpellier, France) for the total red blood cells (RBC), WBC, platelet count, haemoglobin (Hb) concentration, mean corpuscular volume (MCV), mean corpuscular haemoglobin concentration (MCHC) and differential leukocyte counts. Blood smears were prepared and stained with Wright stain and examined under a light microscope [53][54][55].…”
Section: Haematology Analysismentioning
confidence: 99%
“…Selected organs, including the spleen, the lymph nodes, the liver, the kidney and the lungs were collected from each mouse for histopathological analyses. The procedure for analyses was according to Nurul et al [54] as described below:…”
Chemical carcinogens are commonly used to investigate the biology and prognoses of various cancers. This study investigated the mechanism of leukaemogenic effects of n-ethyln-nitrosourea (ENU) in a mouse model. A total of 14 3-week-old male Institute of Cancer Research (ICR)-mice were used for the study. The mice were divided into groups A and B with seven mice each. Group A served as the control while group B received intraperitoneal (IP) injections of 80 mg/kg ENU twice with a one-week interval and were monitored monthly for 3 months for the development of leukaemia via blood smear examination. The mice were sacrificed humanely using a CO 2 chamber. Blood, spleen, lymph nodes, liver, kidney and lung samples were collected for blood smear examination and histopathological evaluation. The expression of angiogenic protein (VEGF), and pro and anti-apoptotic proteins (BCL2 and BAX), was detected and quantified using Western blot technique. Leukaemia was confirmed by the presence of numerous blast cells in the peripheral blood smear in group B. Similarly, the VEGF and BCL2 proteins were significantly (p < 0.05) upregulated in group B compared to A. It is concluded that IP administration of 80 mg/kg ENU induced leukaemia in ICR-mice 12 weeks post administration through upregulation of angiogenic and anti-apoptotic proteins: VEGF and BCL2.
Fermented jackfruit (Artocarpus heterophyllus) extracts were produced using pure symbiotic culture of bacteria and yeast (SCOBY) under controlled fermentation process. Both female and male Sprague‐Dawley rats were orally administrated with 4,000 mg/kg of fermented jackfruit pulp and leaves extracts for 28 consecutive days. Body weight of rats was recorded at 1‐week interval until necropsy day. There was no mortality reported along the experiment with no significant differences (p > .05) record among organ histopathology and blood biochemical parameters in treated groups when compared to control group. Interestingly, there were significant differences (p < .05) in the lower body weight gained of treated rats groups as opposed to control group, indicating the potential anti‐obesity effect of fermented jackfruit extracts. In conclusion, no toxicity symptoms were observed in 28 days oral administration toxicity study of fermented jackfruit pulp and leaves extracts in Sprague‐Dawley rats for both sexes.
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