scholarly journals IN VIVO ACUTE AND SUB-ACUTE TOXICITY STUDY OF ROOT EXTRACT OF CARISSA SPINARUM LINN. IN SWISS ALBINO MICE

Author(s):  
SIBHATU GEBREHIWOT

Objective: The objective of the present research work had been done to evaluate the toxicity of crude extract of Carissa spinarum in Swiss albino mice. Methods: In studying the toxicity, the Organization for Economic Cooperation and Development (OECD) guidelines were used. Experimental animals (mice), five mice in each, were grouped into four groups; three experimental groups and one negative control. In studying the acute toxicity, 2000, 3000 up to 5000 mg/kg crude plant extract was given orally using standard intragastric oral gavages. For acute toxicity, a single dose was given and gross behavioral changes were recorded. In sub-acute oral toxicity test, Carissa spinarum crude extract was given to the mice by standard intragastric oral gavages at doses of 500, 750 and 1000 mg/kg body weight of hydro-methanolic extract and 200, 600 and 1000 mg/kg of body weight of chloroform extract in every single to 28 d and various hematological and physical parameters were recorded. Results: In acute toxicity, the given dose of the plant extract did not produce significant physical and behavior changes up to the dose of 5000 mg/kg extracts. In addition, no death was occurred in the given doses. In sub-acute toxicity studies of the hydro-methanolic and chloroform extracts, there was no recorded significant change (p>0.05) of hematological and physical parameters in the treated groups when compared to the control groups. Conclusion: from the present study it was revealed that the crude extract of the plant did not produce any significant toxicological effect in the experimental animals and this supports the use of the plant in folk medicines.

2019 ◽  
Vol 10 (4) ◽  
pp. 3750-3754
Author(s):  
Siva Ganesh M ◽  
Radhika J

The recent study was planned to determine the acute toxicity study of Apium leptophyllum pers. A single dose of 400,1200,2000 mg/ kg of ethanolic extract of Apium leptophyllum pers according to the OECD guidelines and the dose level was administrated orally into swiss albino mice. Oral administration of maximum level of ethanolic extract of Apium leptophyllum pers upto 2000 mg/kg body weight to experimental group of albino mice was evaluated. Biochemical, haematological  and histopathological parameters were checked throughout the study. Signs of toxicity, mortality and body weight were monitored for 14 days post treatment of Apium leptophyllum pers . There is no substantial variations were noticed in control and treated groups. Result revealed that the ethanolic extract of Apium leptophyllum is safe and no toxicity was caused. 


2021 ◽  
Vol 15 (3) ◽  
pp. 135-142
Author(s):  
Manoharan Karuppiah Pillai ◽  

Background: Polygonum bistorta has been used as a remedy for jaundice, smallpox, pimples, measles, cholera, diarrhoea, dysentery, expelling worms, insect stings and snakebites. In this study, the crude extract from P. bistorta and two fractions viz. hexane and chloroform obtained from the crude extract were studied for their median Lethal Dosages (LD50) in Swiss albino mice. Methods: Powdered rhizomes of P. bistorta was macerated with chloroform and the crude extract was dissolved in a solvent mixture of methanol/water (95:5). The mixture was then subjected to solvent-solvent partition, first with hexane followed by chloroform. The crude extract and the hexane and chloroform fractions were evaluated for their LD50 in Swiss albino mice of both sexes. Results: The LD50 of the crude extract and the hexane and chloroform fractions were determined to be 142.82, 200 and 200.17mg per kg of the mice body weight, respectively. Conclusion: The LD50 values of the crude extract and the hexane and chloroform fractions from P. bistorta were determined. The crude extract of P. bistorta had greater lethality than the hexane and chloroform fractions. This is the first report on the LD50 values of Swiss albino mice for P. bistorta.


Author(s):  
Surekha D. Shetty ◽  
Laxminarayana Bairy K. ◽  
AM Prasad ◽  
Satheesha Nayak B. ◽  
Ashwini Aithal P.

Background: Hormones play a vital role in initiating and maintenance of male reproductive or testicular function which includes the production of androgens and spermatozoa. Testosterone is essential for the initiation and maintenance of spermatogenesis. FSH is responsible for the stimulation of spermatogenesis. Semen analysis and hormone evaluation are essential parameters in the diagnosis of infertility in males. Objective: The aim of the present study is to evaluate the effect of sorafenib on FSH and intratesticular testosterone levels in male Swiss albino mice. Materials and Methods: The animals were segregated into control, positive control, and treatment groups (n=6). Treatment group received 25, 50 and 100 mg/kg body weight of sorafenib orally for seven consecutive days at intervals of 24 hours between two administrations. Positive control group received 100 mg/kg body weight of imatinib. The animals were sacrificed at the end of 1st, 2nd, 4th, 5th, 7th and 10th week after the last exposure to sorafenib. Results: The intratesticular testosterone level was significantly (P<0.05) reduced in treated groups and severe effect was observed on week 4th and 5th weeks. FSH level was increased significantly (P<0.05) in sorafenib treated groups of mice. Conclusion: The administration of sorafenib does affect testosterone and FSH level significantly, but this effect is reversible once the drug is withdrawn. This finding may help the clinicians to plan and address the fertility-related issues in young patients of reproductive age who are being treated with sorafenib for advanced renal cell carcinoma, hepatocellular carcinoma and differentiated thyroid carcinoma.


Author(s):  
Mishra N. ◽  
Joshi S. ◽  
Tandon V. L. ◽  
Munjal A.

Population explosion is a major problem it is raising tremendously; this may affect drastically the economic growth. So family planning has been promoted through several methods of contraception. A wide variety of synthetic contraceptive agents are available, but these cannot be used continuously due to their side effects. Thus the present study was to evaluate the effect of Bougainvillea spectabilis on fertility of male and female mice. Swiss Albino mice were orally administered with aqueous crude extract of the leaves of Bougainvillea spectabilis (800 mg/kg of body weight/day, for 30 days), and effect of crude extract on reproductive organs and fertility was investigated. The treatment Caused decrease in weight of testis, sperm count and the histological examination revealed a reduction in the size of seminiferous tubules along with the thickness of germinal epithelial cells, though some of the epithelial cells and interstitial cells of leydig showed hypertrophy. Moreover, the lumen of the tubules was found to be devoid of sperms. On the other hand, in treated females no histological changes could be observed. The only marked change, which could be visualized, was the slight disruption of estrous cycle having prolonged metaestrus phase, which has been increased by 145.28 %. The overall duration of estrous cycle had been extended by more than one day. The hormonal profile was also influenced by the Bougainvillea spectabilis extract. The testosterone and estrogen levels were significantly decreased.


2022 ◽  
Author(s):  
Joseph Tchamgoue ◽  
Amelework N. Eyado ◽  
Boniface P. Kamdem Kamdem ◽  
Yvan Anderson T. Ngandjui Ngandjui ◽  
Jean Claude Tchouankeu ◽  
...  

Malaria is regarded as one of the most lethal diseases. Resistance to artemisinin and its derivatives jeopardises effective malaria treatment. Finding novel antimalarial chemicals is critical given the existing treatment situation. This work aimed to examine the antiplasmodial capabilities of <i>Pseudarthria hookeri</i> fractions and flavonoids in vivo. The fractions and compounds antiplasmodial activity were evaluated on male Swiss albino mice infected with <i>Plasmodium berghei</i>, and on healthy female Swiss albino mice, the crude extract's acute toxicity was assessed. The EtOAc fraction had significant antiplasmodial activity (32.53 percent suppression at 500 mg/kg BW) and considerably prolonged the survival period of infected mice (9.8 days) compared to control mice (7.8 days). Parasitaemia was dramatically reduced (85.01, 59.41, and 70.39 percent), and the mean survival time extended (11.33, 10.00, and 9.33 days) with 15, 20 and 35 mg/kg of quercetin (<b>1</b>), 7-O-benzyl-6-prenylpinocembrin (<b>6</b>) and 6,8-diprenyleriodictyol (<b>11</b>) (isolates of the EtOAc fraction), respectively. BW loss and PCV reduction were also averted. Moreover, at 2500 mg/kg, the crude extract of <i>P. hookeri</i> showed no acute toxicity in mice. LC-MS analysis of the EtOAc fraction enabled the identification of nine flavonoids, with <b>8</b> and <b>11</b> being the main components. The present investigation confirmed <i>P. hookeri</i>'s antiplasmodial action, substantiating its ethnomedicinal application for malaria treatment.


2021 ◽  
Vol Volume 14 ◽  
pp. 2583-2596
Author(s):  
Dejen Nureye ◽  
Eyob Tekalign ◽  
Nebeyi Fisseha ◽  
Tarekegn Tesfaye ◽  
Workineh Woldeselassie Hammeso

Heliyon ◽  
2020 ◽  
Vol 6 (1) ◽  
pp. e03108
Author(s):  
Jairaman Chitra ◽  
Syed Ali Mohamed Yacoob ◽  
Sivanesan Senthil Kumar ◽  
Anuradha Venkataraman ◽  
Rajagopalan Vijayaraghavan ◽  
...  

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