scholarly journals Safety Profile of Meswak Root Extract on Liver, Kidney, Sexual Hormones and Hematological Parameters of Rats

2012 ◽  
Vol 4 (1) ◽  
pp. 18-23
Author(s):  
Abeer Y. IBRAHIM ◽  
Souad E. El-GENGAIHI
Keyword(s):  
Acute Toxicity ◽  
Safety Profile ◽  
Toxicity Test ◽  
Biochemical Parameters ◽  
Chronic Toxicity ◽  
Female Rats ◽  
Root Extract ◽  
Acute Toxicity Test ◽  
Sexual Hormones ◽  
Delayed Toxicity

This study was conducted to investigate the safety profile of Salvadora persica (Salvadoraceae) aqueous alcoholic root extract by carrying out acute and sub-chronic toxicity assessment in order to find out any side effect of the traditionally using of these root sticks. Regarding to acute toxicity test, mice were administered the extract up to 5 g kg-1, intraperitoneally. Animals were then observed for behavioural changes; signs of toxicity, and mortality within 24 h. Surviving mice were monitored for 7 days for signs of delayed toxicity. In the sub-chronic toxicity test, rats were daily treated with the extract at a dose of 400 mg kg-1 intraperitoneally, for 30 days. At the end of the test period, hematological and biochemical parameters were determined in blood and serum samples with determination of vital organs weights. In the acute toxicity test, the extract was practically non-toxic showing no mortality and visible signs of delayed toxicity. The LD50, given intraperitoneally, was estimated to be 4 g kg-1. Administration of extract (at a dose of 400 mg Kg-1 b.wt.) to male and female rats for 30 days did not produce any significant (P < 0.05) effect on hematological and most biochemical parameters also vital organs weights. The root extract showed adverse effects on sexual hormones, by increasing estrogen secretion and reducing testosterone level in male rats. At the same time, the extract reduces progesterone level in female satellite group. Overall, Meswak aqueous extract is safe concerning liver and kidney functions and hematological assessments; however, it induces reversal effect on sexual hormones levels determined in sera.

Effects of atrazine and alachlor on self-purification processes in receiving streams

1996 ◽  
Vol 33 (6) ◽  
pp. 181-187 ◽  
Author(s):  
Jana Zagorc-Koncan
Keyword(s):  
Adverse Effect ◽  
Acute Toxicity ◽  
Toxicity Test ◽  
Chronic Toxicity ◽  
Acute Toxicity Test ◽  
Organic Substances ◽  
Inhibiting Effect ◽  
Scenedesmus Subspicatus ◽  
Net Assimilation ◽  
Chlorophyll A Content

In recent years many waterways in Slovenia have been subjected to an increased loading with pesticides due to intensification of agriculture. The most widely used herbicides are atrazine and alachlor and they were detected in some rivers and even in ground water. Therefore the effects of atrazine and alachlor on selfpurification processes were investigated. The basic selfpurification processes studied were biodegradation of organic substances and photosynthesis and growth of algae. The inhibiting effect of pesticides on the process of biodegradation of organic pollutants was evaluated by the use of laboratory river model and mathematical modelling. The harmful impacts of pesticides on aquatic autotrophic organisms were assessed by measurement of net assimilation inhibition (24-h acute toxicity test) as well as growth inhibition - chlorophyll- a content (72-h chronic toxicity test) of algae Scenedesmus subspicatus. The results obtained demonstrate that atrazine and alachlor in concentrations found in our rivers have practically no effect on biodegrading heterotrophic organisms, while their adverse effect on algae is quite considerable.

Safety Evaluation of an Apitherapy Formulation, Bao-Yuan-Ling: Acute and Sub-acute Oral Toxicity in Wistar Rats

2017 ◽  
Vol 17 (1) ◽  
pp. 85-92
Author(s):  
Sun Yanru ◽  
Shen Zhenhuang ◽  
Jia Zhe ◽  
Miao Xiaoqing
Keyword(s):  
Acute Toxicity ◽  
Toxicity Test ◽  
Wistar Rats ◽  
Lethal Dose ◽  
Drug Effects ◽  
Female Rats ◽  
Male Rats ◽  
Acute Toxicity Test ◽  
Weight Changes ◽  
Oral Toxicity

Bao-Yuan-Ling (BYL) is an apitherapy formulation which is composed of royal jelly, propolis and bee venom. Cardioprotective effects of BYL has been demonstrated, while the toxicity of BYL was not clear. In this study, acute and sub-acute toxicity test of BYL was processed following Organization for Economic Co-operation and Development (OECD) 423 and OECD 407, respectively, in Wistar rats. In acute toxicity test, rats were orally treated with BYL at the single dose of 2000 mg/kg and 5000 mg/kg. No death occurred in the acute toxicity test for 7 days, which indicated the lethal dose 50% value exceeded 5000 mg/kg. In sub-acute toxicity study, rats were treated with BYL at the dose of 250 mg/kg, 500 mg/kg and 1000 mg/kg in a daily base for continuous 28 days. Results showed that female rats were more likely to be affected by BYL in body weight changes, while biochemical indicators of blood serum in male rats were more susceptible to drug effects. However, neither female nor male rats were affected by BYL administration significantly on the organs via hematoxylin-eosin staining analysis. Results suggested that BYL was slightly toxic and clinical use was safe and reliable.

scholarly journals ACUTE TOXICITY TEST OF ETHANOLIC EXTRACT OF Acalypha hispida LEAVES IN FEMALE RATS: A PHYSIOLOGICAL AND HISTOLOGICAL STUDY

2020 ◽  
Vol 14 (3) ◽  
Author(s):  
Hamzah Alfarisi ◽  
Mawar Subangkit ◽  
Siti Sa’diah ◽  
Tutik Wresdiyati
Keyword(s):  
Body Weight ◽  
Acute Toxicity ◽  
Toxicity Test ◽  
Clinical Signs ◽  
Ethanolic Extract ◽  
Female Rats ◽  
Control Group ◽  
Acute Toxicity Test ◽  
Glomerular Cell ◽  
Eosinophilic Cytoplasm

This research aims to evaluate the safety of ethanolic extract of Acalypha hispida (A. hispida) leaves with acute toxicity test using 15 female rats strain Sprague-Dawley. A single dose of different doses of extract (2, 4, 8, and 16 g/kg body weight) was administrated orally, and theobservation was conducted for 14 days. The results revealed that the ethanolic extract of A. hispida leaves was relatively harmless (LD50 16 g/kg BW), did not affect body weight, and did not show clinical signs of toxicity during the observation periods. The parameters of blood serumbiochemistry of all extract-treated groups (alanine aminotransferase, aspartate aminotransferase, creatinine, and urea) did not change significantly  compared to the control group. The histological observation of the liver showed a significant increase in eosinophilic cytoplasm and basophilic nuclei at all doses. However, the ethanolic extract of A. hispida leaves did not significantly affect glomerulus/Bowman’s capsule ratio, glomerular cell density, and the proportion of normal cell tubule. In conclusion, the ethanolic extract of A. hispida leaves was relatively harmless with LD5016 g/kg BW and seems to be safe in low doses (2 g/kg BW).

scholarly journals Acute Toxicity Test of Ethanolic Extract of Dayak Onion Leaves (Eleutherine americana Merr.) Toward Wistar Female Rats Using OECD 425 Method

2019 ◽  
Vol 18 (2) ◽  
pp. 171-177
Author(s):  
Sri Wahdaningsih ◽  
Eka Kartika Untari ◽  
Robiyanto
Keyword(s):  
Acute Toxicity ◽  
Toxicity Test ◽  
Ethanolic Extract ◽  
Test Dose ◽  
Female Rats ◽  
Acute Toxicity Test ◽  
Safety Level ◽  
Ld50 Value ◽  
Eleutherine Americana ◽  
Single Dosage

Pre-clinically, the potential of Eleutherine americana Merr. as antioxidant has been studied, but it’s safety level of its safety has not been widely known. Safety level of ethanolic extract of E. americana Merr leaves (EEEaL) can be detected by acute toxicity test using OECD 425. The aim of this study was to investigate the acute toxicity of EEEaL as the guideline of its safe dose for therapy. This test was performed through OECD 425 (Up and Down Procedure) method with two doses (2000 and 5000 mg/kgbw) of EEEaL administration orally which observed for two weeks toward Wistar rats. The results of the test dose showed no toxic symptoms and they did not cause death in the test animals. Single dosage up to 5000 mg/kgbw also did not show any symptoms of toxicity, and did not cause weight loss until the 14th day of test. The LD50 value of EEEaL is more than 5000 mg/kgbw, suggesting that the plants is practically non toxic according to Loomis classification. Phytochemical screening showed that EEEaL contains compounds such as alkaloids, flavonoids, triterpenoids, steroids, and saponins. Dhaka Univ. J. Pharm. Sci. 18(2): 171-177, 2019 (December)

scholarly journals ACUTE TOXICITY TEST OF LOW CALCIUM OXALATE PORANG (Amorphophallus mueleri BLUME) FLOUR

2021 ◽  
Vol 52 (1) ◽  
pp. 218-231
Author(s):  
I. Donowarti ◽  
S. B. Widjanarko ◽  
Y. Yunianta ◽  
P. Pudjiastuti
Keyword(s):  
Acute Toxicity ◽  
Calcium Oxalate ◽  
Toxicity Test ◽  
Cell Damage ◽  
Female Rats ◽  
Laboratory Animals ◽  
Acute Toxicity Test ◽  
Food Ingredient ◽  
White Rats ◽  
Significant Difference

A field experiment Porang (Amorphophallus mueleri Blume) has the potential to be developed as a functional food ingredient because it contains high levels of glucomannan. Research on the acute toxicity test of macerated porang flour has been carried out. The results of research showed a toxic effect which was characterized by high SGOT and sodium levels. The purpose of this study was to find out the safety level of consuming porang flour with lowered calcium oxalate content. This research was an experimental study designed in one directional-pattern Completely Randomized Design using 5 treatments of porang flour administration with doses of 0; 5; 50; 500; 5000 and 15000 mg/kgbw and 6 repetitions for 60 days using Wistar-strain white rats (Rattus norvegicus) as laboratory animals. The results showed that during the treatment, the administration up to a dose of 500 mg/kgbw did not give a significant difference to all observed variables. The administration of 5000 and 15000 mg/kgbw gave a significant difference on the changes in body weight, the addition of the amount of water drunk, the levels of Calcium, Potassium and Sodium in the blood, SGOT and SGPT values, and observation on necrotic cells in the kidneys. The administration of the highest porang flour dosage, namely 15000 mg/kgbw did not cause any rat mortality and did not cause any real cell damage to the liver, but caused hyperactive behavior in female rats.

THE HEMATOLOGIC PROFILE IN THE ACUTE TOXICITY TEST OF COGON GRASS ROOTS ETHANOL EXTRACT IN WISTAR RATS

2020 ◽  
pp. 72-75
Author(s):  
VANESSA AYU SUMIRAT ◽  
IRMA MELYANI PUSPITASARI ◽  
NENI ANGGRAENI ◽  
MAS RIZKY ANGGUN ADIPURNA SYAMSUNARNO
Keyword(s):  
Acute Toxicity ◽  
Toxicity Test ◽  
Wistar Rats ◽  
Ethanol Extract ◽  
Female Rats ◽  
Control Group ◽  
High Dose ◽  
Acute Toxicity Test ◽  
Grass Roots ◽  
Hematologic Profile

Objective: This study aimed to investigate the hematologic profile of Wistar rats in the acute toxicity test of Cogon grass roots ethanol extract (CGEE). Methods: Cogon grass roots were dissolved in 70% ethanol. An acute toxicity test was conducted based on The National Agency of Drug and Food Control of the Republic of Indonesia. Five female rats in the treatment group were administered a single high dose of 5000 mg/kg body weight (BW) of CGEE in 200 μl of 0.5% carboxymethyl cellulose (CMC), and the 5 female rats in the control group were administered 200 μl of 0.5% CMC. After 14 d, blood samples were collected, and 18 hematologic parameters were measured with a hematology analyzer. Statistical analyses were performed to compare the parameters between the two groups with the independent t-test for normally distributed data and the Mann Whitney test for non-normally distributed data. Results: None of the hematologic parameters in the treatment group significantly differed from those in the control group after 14 d of observation (P>0.05). Conclusion: A single high dose of 5000 mg/kg BW of CGEE did not change the hematologic profile of Wistar rats. These results indicate that CGEE does not have an acute hemotoxic effect, at least for hematologic parameters.

scholarly journals Toxicity Study of 1-(2, 5-Dihidroxyphenil)-3-Pyridine-2-Il-Propenone In Adult Female Mice

2021 ◽  
Author(s):  
Ika Puspitasari ◽  
Ratna Asmah Susidarti
Keyword(s):  
Body Weight ◽  
Acute Toxicity ◽  
Toxicity Test ◽  
Biochemical Parameters ◽  
Chronic Toxicity ◽  
Histological Analysis ◽  
Lymphocytic Infiltration ◽  
Experimental Animals ◽  
Female Mice ◽  
Chronic Toxicity Test

This research aimed to evaluate the toxicity of 1-(2, 5-dihidroxyphenil)-3-pyridine-2-il-propenone (DPP) after 24 hours and 90-day administration in female mice. Acute toxicity test was performed using the OECD 423 method, and DPP was administered once a day at doses of 300, 2000, and 5000 mg/kg body weight (BW). Toxic symptoms were observed after 24 hours of administration, and this continued until the 14th day. The experimental animals were dissected and examined for histological organs on the 15th day. The sub-chronic toxicity test was performed using the OECD 408 method, and DPP at 14, 28, and 56 mg/kg/day was administered for 90 days. Toxic symptoms were observed every day, and the amount of food and water intakes were also measured. Furthermore, statistical analysis was performed, and changes in body weight as well as routine blood checks and biochemistry were observed. At the end of the study, experimental animals were killed and the vital organs' weights were examined before their histological analysis. The results showed that DPP at 300-5000 mg/kg/day and 14-56 mg/kg/day for 90 days did not show any toxic symptom respectively. In the sub-chronic toxicity test, no change was observed in blood and urine biochemical parameters (p≥0.05). However, lymphocytic infiltration in the liver and congested vessel in the kidney occurred after administration at 56 mg/kg / day. The results showed that the acute toxicity of DPP is at category 5 according to Globally Harmonized Classification System and sub-chronic toxicity is at a dose below 56 mg/kg/day.

scholarly journals Dying for change: A roadmap to refine the fish acute toxicity test after 40 years of applying a lethal endpoint

2021 ◽  
Vol 223 ◽  
pp. 112585
Author(s):  
Ioanna Katsiadaki ◽  
Tim Ellis ◽  
Linda Andersen ◽  
Philipp Antczak ◽  
Ellen Blaker ◽  
...  
Keyword(s):  
Acute Toxicity ◽  
Toxicity Test ◽  
Acute Toxicity Test

Ceriofast™: An acute toxicity test based onCeriodaphnia dubiafeeding behavior

1996 ◽  
Vol 15 (2) ◽  
pp. 123-125
Author(s):  
Gabriel Bitton ◽  
Kimberly Rhodes ◽  
Ben Koopman
Keyword(s):  
Acute Toxicity ◽  
Toxicity Test ◽  
Acute Toxicity Test

Study on the Safety of Mineral and Synthetic Oil Added Commonly Used Extreme Pressure Additives

2012 ◽  
Vol 430-432 ◽  
pp. 1386-1389
Author(s):  
Zhuo Jun Chen ◽  
Long Long Feng ◽  
Bao Liang Li ◽  
Jin Jin Yue ◽  
Ying Liang Wu ◽  
...  
Keyword(s):  
Acute Toxicity ◽  
Toxicity Test ◽  
Mineral Oil ◽  
Stimulation Test ◽  
Toxicity Tests ◽  
Acute Toxicity Test ◽  
Base Oil ◽  
Synthetic Oil ◽  
Four Levels ◽  
Oral Acute Toxicity

This article use the Sulphide Isobutene (T321), Five Sufides Dialkyl(RC2540) and Star of Phosphorus(P110) as the additives,Neopentyl Polyol Ester(NPE) and mineral oil N32 as base oil. Compound above additives and base oil for the four levels. A sample: adding 4% T321 additive in NPE. B sample: adding 4% T321 additive in N32. C sample: adding 4% RC2540 additive in NPE. D sample: adding RC2540, T321 and P110 additives in NPE (all is mass fraction). The oral acute toxicity test, eye mucous stimulation test, skin hypersensitive test, soaking tail toxicity tests were conducted in above samples. The test results show that. The mineral oil, it’s not only toxic then synthetic oil but also has a poor lubricating ability compare with the same percent additive in synthetic oil. In oral acute toxicity test, eye mucous stimulation test, skin hypersensitive test, soaking tail toxicity tests, Toxic reaction of mineral N32+4%wt Sulphide Isobutene (T321) obviously from other oil samples.

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