scholarly journals TOXICITY PROFILE OF CELASTRUS PANICULATUS SEEDS: A PRECLINICAL STUDY

2020 ◽  
pp. 115-118
Author(s):  
BHARAT MISHRA ◽  
ELEZABETH JOHN ◽  
KRUPAMOL JOY ◽  
BADMANABAN R ◽  
ALEESHA R
Keyword(s):  
Seed Oil ◽  
Preclinical Study ◽  
Tween 20 ◽  
Toxicity Profile ◽  
Swiss Albino Mice ◽  
Subacute Toxicity ◽  
Toxicity Studies ◽  
Group I ◽  
Celastrus Paniculatus ◽  
Albino Mice

Objective: The objective of the study was to evaluate the toxicity profile of Celastrus paniculatus (CP) by performing a preclinical study on Swiss albino mice and demonstrate a safety description through monitoring their autonomic, neurological, behavioral, physical, and biochemistry profiles. Methods: The toxicity profiles (acute and subacute) of CP were evaluated using Swiss albino mice in which they were divided into four groups: Group I received 1% Tween 20 and dimethyl sulfoxide. Group II, III, and IV received CP seed oil orally, at doses of 300, 2000, and 5000 mg/kg body weight for both acute and subacute toxicity studies in accordance with Organization for Economic Cooperation and Development guidelines No. 423. Special attention was given during the first 4 h and daily thereafter for a total of 14 days. Behavioral profile, physical state changes, and other parameters such as tremors, convulsion, lethargy were noted. Clinical signs were observed daily during the 28 days of the treatment period. Body weights were measured once a week. On the 29th day, the animals were kept to overnight and blood samples were collected through retro-orbital puncture for biochemical analysis. Results: In both acute and subacute toxicity studies, the treatment with CP did not affect the normal health status of animals. It is suggestive that CP is considered practically non-toxic. Conclusion: The toxicity profile of CP seed oil was evaluated and found to be safe until 2000 mg/kg dose.

scholarly journals Effect of aqueous Extract of Terminalia bellirica fruit pulp on Alcohol affected learning in swiss albino mice

2021 ◽  
Vol 6 (2) ◽  
pp. 76-78
Author(s):  
Sowmya ◽  
Manohar VR ◽  
Mohandas Rai ◽  
H N Gopalakrishna ◽  
Chandrashekar R
Keyword(s):  
Aqueous Extract ◽  
Protective Action ◽  
Negative Control ◽  
Control Group ◽  
Acute Administration ◽  
Aqueous Extracts ◽  
Swiss Albino Mice ◽  
Alcohol Administration ◽  
Group I ◽  
Albino Mice

To evaluate the effect of Aqueous extract of Terminalia belliricafruit pulp (AETB) on learning by Hebb William maze model in mice with acute alcohol consumption.Swiss albino mice (n=48) of either sex weighing 20-30g will be divided into eight groups of six mice each. Drugs were given orally after 12 hours of fasting. Group I mice received 10ml/kg of Normal Saline, Group II mice received Piracetam 200mg/kg, Group III received AETB 36mg/kg, Group IV received ethanol 1.5g/kg orally, Group V received ethanol(1.5g/kg )+ piracetam (200mg/kg), Group VI mice received ethanol(1.5g/kg) +AETB(9mg/kg), Group VII mice received ethanol(1.5g/kg) +AETB (18mg/kg), Group VIII mice received ethanol(1.5g/kg) +AETB(36mg/kg). Time taken by the animal to reach the reward chamber from the start chamber (TRC) in Hebb-William maze was used as a parameterto evaluate the learning.Acute alcohol administration showed increase in TRC. Whereas, acute administration of Aqueous extracts of Terminalia belliricafruit pulp showed a decrease in TRC when compared to the control group. The TRC values for the groups that were administered AETB along with acute alcohol administration showed decrease in TRC values compared to the negative control.Current study showed acute alcohol administration caused impairment of thelearning ability in mice. Whereas, acute administration of Aqueous extracts of Terminalia belliricafruit pulp (AETB)caused enhancement of learning. Pre-treatment with AETB before acute alcohol administration indicated protective action of AETB on alcohol affected learning in mice.

scholarly journals The Effect of Piracetam on Valproic Acid Induced Congenital Malformations in Swiss Albino Mice

2019 ◽  
Vol 21 (3) ◽  
pp. 204-209
Author(s):  
Shamsher Shrestha ◽  
M. Singh ◽  
S.P. Mishra
Keyword(s):  
Valproic Acid ◽  
Brain Injuries ◽  
Treated Group ◽  
Aging Brain ◽  
Teratogenic Effects ◽  
Swiss Albino Mice ◽  
Group Iii ◽  
Group I ◽  
Albino Mice ◽  
Higher Doses

Valproic acid (VPA) is an antiepileptic drug which is widely used in humans and is a well known teratogenic agent when used during pregnancy. Piracetam is a nootropic or cognitive enhancer drug used to treat cognitive impairment in aging, brain injuries as well as dementia. In the present study, these two drugs VPA and Piracetam were administered orally to Swiss albino mice in the doses of400 mg/kg and 800 mg/kg body weight respectively from gestational day (GD) 6-11 in order to see the protective effect of Piracetam against VPA induced teratogenesis. The fetuses were collected on GD 18 after uterotomy and observed for gross malformations if any. In VPA treated group the malformations observed were exencephaly, cranioschisis, limb and tail defects, haemorrhage, resorptions and retardation. No such anomalies were observed in control and Piracetam treated groups. However,in VPA+ Piracetam treated group some resorptions and growth retardation were noted. This group showed highly significant (p < 0.001) protection against the teratogenic effects of VPA treated group though the developmental parameters were significantly reduced (p < 0.001) in comparison to those of group I (control) and group III (receiving piracetam). These findings suggest that Piracetam, if given in higher doses might protect the development in utero against the teratogenic effects of VPA.

Effect of Pesticide Indoxacarb on the Thyroid Gland in Swiss Albino Mice

2021 ◽  
pp. 23-30
Author(s):  
Salma Abusrer ◽  
Zainab EL Mabrouk ◽  
Habiba El Jaafari ◽  
Naema Shibani ◽  
Sassia Regeai
Keyword(s):  
Thyroid Gland ◽  
Control Group ◽  
Epithelial Tissue ◽  
Female Group ◽  
Male And Female ◽  
Swiss Albino Mice ◽  
Group I ◽  
Significant Difference ◽  
Albino Mice ◽  
Tsh Levels

Background and objectives: Pesticides play an essential role in crop protection, but their overuse caused environmental pollution and harmful effect on different animal body systems, including the endocrine system. The thyroid gland is one of the homeostatic regulators of metabolic activities, which is affected by the elements of the external environment. There are very limited studies on the effect of indoxacarb on the histological architecture and functions of thyroid gland. Therefore, this study was conducted with the aim of examining functionally and histologically of the thyroid gland exposed to indoxacarb. Method: 24 Swiss albino mice male and female were randomly divided into two groups, each group male and female; group I is a control group given orally with 1ml of distilled water and group II orally treated with 120 mg/kg Bw. of indoxacarb daily for 3 weeks. Blood samples were collected from each mouse under anesthetic to determine the thyroid-stimulating hormone (TSH), thyroxine (T4) levels. Thyroid gland histopathology was attained for the evaluation of the indoxacarb effect. Results: The treated mice showed non-significant increase in T4 levels and a significant decrease in TSH levels but there was no significant difference recorded in T4 and TSH levels between sexes. Histologically, the sections of the thyroid gland of the treated group showed empty and irregular follicles, degeneration of the follicular epithelial tissue, and hyperplasia in the lining of some follicles, the capsule with congestion blood vessels. Conclusion: This study concluded that indoxacarb may act as a thyroid gland toxicant.

scholarly journals Neuroprotective effects of Zingerone against carbon tetrachloride (CCl4) induced brain mitochondrial toxicity in Swiss albino mice

2018 ◽  
Vol 10 (2) ◽  
pp. 548-552
Author(s):  
Mohammad Firoz Alam
Keyword(s):  
Oxidative Stress ◽  
Carbon Tetrachloride ◽  
Antioxidant Enzyme ◽  
Brain Mitochondria ◽  
Control Group ◽  
Mitochondrial Toxicity ◽  
Swiss Albino Mice ◽  
Group I ◽  
Albino Mice ◽  
Group Ii

The present study targeted the brain mitochondria dysfunction in Swiss albino mice through carbon tetrachloride intoxication and its treatment with Zingerone. It is proposed that brain mitochondria is the main organelle responsible for oxidative stress by producing  reactive oxygen species (ROS). Swiss albino mice were divided into four groups; Group-1 was control; Group-2 was carbon tetrachloride (CCl4) toxic (1.5mg kg-1 bm i.p two days in a week.); Group-3 was pretreated with Zingerone (100 mg kg-1 b.m)  a day before  the administration of CCl4 and Group-4 was only Zingerone (100 mg kg-1 bm) given orally for 15days once in a day. At the end of the experiment mice were sacrificed and mitochondria were isolated from brain. Isolated brain mitochondria were further analyzed for oxidative stress marker. Thiobarbituric acid reactive substance (TBARS) content was increased significantly by CCl4 administration in Group-II as compared to the control Group-I, while the antioxidant (GSH) and other antioxidant enzyme GPx , GR, and CAT was depleted significantly in CCl4 treated Group-II as compare to control Group-I. Zingerone protected the  toxicity of brain mitochondria by reducing the lipid peroxidation and enhancing the antioxidant enzyme in Group-III and there was no significant changes were noticed in Group-IV as  compared to Group-I. Overall results showed the potential effects of Zingerone in protecting the neuronal cell loss by oxidative stress. Thus, the  present study indicated that the Zingerone may be used as the potential therapeutic tools for the prevention of CCl4 induced brain mitochondrial toxicity.  

scholarly journals EVALUATION OF GENOTOXICITY PROFILE OF JASADA BHASMA (A ZINC-BASED MINERAL FORMULATION) IN SWISS ALBINO MICE

2019 ◽  
Vol 12 (1) ◽  
pp. 305
Author(s):  
Ravi Bhasker ◽  
Megha A Doshi ◽  
Anjana S ◽  
Ravi M ◽  
Naveen Kumar ◽  
...  
Keyword(s):  
Comet Assay ◽  
Chromosomal Aberrations ◽  
Mutagenic Activity ◽  
Genetic Material ◽  
Safety Data ◽  
Vehicle Group ◽  
Swiss Albino Mice ◽  
Group I ◽  
Potential Risk Factors ◽  
Albino Mice

  Objective: Genotoxicity is regarded as one of the potential risk factors for causing pathological diseases. It was confirmed that many chemicals have the mutagenic activity which leads to cancer. A compound which interacts with genetic material DNA and shows adverse effects by altering its structure or function is referred to as genotoxic.Methods: The present study involved 40 Swiss albino mice weighing between 25 and 30 g body weights categorized into four different groups. Group-I (normal control) received 0.5% carboxymethyl cellulose as vehicle. Group-II (toxicant control) received 40 mg/kg/body weight cyclophosphamide on the 28th day. Group-III and IV received test drug JB 15.6 mg/kg and 78 mg/kg, respectively, for 28 consecutive days. Blood samples were collected and processed for evaluating by comet assay. The animals were sacrificed and collected the bone marrow from both the femur for chromosomal aberration and micronuclei assay.Results: JB administered at two different dose levels did not show any significant changes in the comet assay parameters, no micronucleus was found and did not produce any chromosomal aberrations both numerically and structurally when compared to positive test control group.Conclusion: The genotoxicity evaluation of JB did not show any chromosomal aberrations and presence of micronucleus. Thus, the safety data will refine therapeutic utility of JB encouraging their rationale use and translate into greater and broader utilization of JB.

Evaluation of acute and sub-acute oral toxicity of ethanolic root extract of Tetracera akara (Burm. f.) Merr., an ethnomedicinal plant used by the Kani tribe of Kerala

2018 ◽  
Vol 5 (2) ◽  
Author(s):  
Ragesh R Nair
Keyword(s):  
Acute Toxicity ◽  
Wistar Rats ◽  
Body Weight Gain ◽  
Root Extract ◽  
Oral Toxicity ◽  
Swiss Albino Mice ◽  
Toxicity Studies ◽  
Biochemical Profiles ◽  
Albino Mice ◽  
Group Sex

The aim of the study was to evaluate the acute oral and sub-acute toxicity of ethanolic root extract of Tetracera akara in Swiss albino mice and Wistar rats. Tetracera akara (Burm. f.) Merr. has been used as traditional medicine by the Kani tribe of Kerala to cure liver diseases. In acute toxicity studies, four groups of mice (n = 5/group/sex) were orally treated with doses of 0.625 g, 1.25 g, 2.5 g and 5.0 g/kg and mortality were recorded. In the sub-acute toxicity study, animals received T. akara extract at the doses of 0.1 g, 0.5 g and 2.5 g/kg/day (n = 5/group/sex) for 28 days, biochemical, hematological, morphological and histopathological parameters were determined. T. akara did not produce any mortality in the acute toxicity studies, showing LD50 higher than 5 g/kg. Sub-acute treatment with T. akara didn’t cause any changes in body weight gain, hematological, biochemical profiles when compared to normal control. In addition, no changes in morphological and histopathological aspect of organs were observed in the animals. Taking all factors into consideration, administration of Tetracera akara does not produce acute toxicity in Swiss albino mice or sub-acute toxicity in Wistar rats, suggesting it’s safe use by humans.

scholarly journals EVALUATION OF ANTIDEPRESSANT ACTIVITY OF TAPENTADOL IN SWISS ALBINO MICE

2017 ◽  
Vol 10 (8) ◽  
pp. 103
Author(s):  
Pradeep Be ◽  
Narendranath S ◽  
Shruthi Ks ◽  
Shashikala Gh ◽  
Krishnagouda Patil ◽  
...  
Keyword(s):  
Animal Studies ◽  
Antidepressant Activity ◽  
Tail Suspension Test ◽  
Experimental Models ◽  
Control Group ◽  
Swiss Albino Mice ◽  
Group I ◽  
Antidepressant Efficacy ◽  
Albino Mice ◽  
Post Hoc

Objective: The aim of this study is to evaluate the antidepressant activity of tapentadol using forced swimming test (FST) and tail suspension test (TST) experimental models.Methods: A total of 36 Swiss albino mice (18 for each experimental model) were divided into 3 groups of 6 animals each. In both the experimental models, Group I received normal saline – 10 ml/kg (Control group), Groups II and III given tapentadol 20 mg/kg and tapentadol 40 mg/kg, respectively, for 7 days, intraperitoneally. On day 7, the drugs were given 40 minutes before conducting the experiment. The duration of immobility was noted and compared among all the 3 groups. The observations were analyzed using analysis of variance and Tukey’s post-hoc test.Results: The duration of immobility was significantly decreased in both the experimental models. Tapentadol groups when compared to control group showed statistically significant values, and better results were obtained with tapentadol 20 mg/kg groups in both the models. The mean duration of Immobility was 34.67 seconds in FST model and 101.00 seconds in TST model when treated with tapentadol 20 mg/kg compared to 102.33 seconds in FST control and 141 seconds in TST control groups. FST model demonstrates greater antidepressant efficacy of tapentadol (p<0.00) than with TST model (p<0.04).Conclusion: Tapentadol showed significant antidepressant activity at the dose of 20 mg/kg. The results should be further confirmed by animal studies with different experimental models for the evaluation of depression and by human clinical studies, and if found effective, tapentadol can be preferred for patients with chronic pain, such as cancer pain.

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