scholarly journals Acute Toxicity Study of Porang (Amorphophallus oncophyllus) Flour Macerated with Strobilanthes crispus in Wistar Rats

2021 ◽  
Vol 9 (A) ◽  
pp. 976-981
Author(s):  
Rizka Qurrota A’yun ◽  
Uswatun Hasanah ◽  
Hamam Hadi ◽  
Mustofa Mustofa ◽  
Eva Nurinda ◽  
...  
Keyword(s):  
Acute Toxicity ◽  
Bioactive Compound ◽  
Urinary Protein ◽  
Toxicity Study ◽  
Fixed Dose ◽  
Oral Toxicity ◽  
Biochemical Tests ◽  
Serum Glutamic Oxaloacetic Transaminase ◽  
Acute Toxicity Study ◽  
Strobilanthes Crispus

BACKGROUND: Porang (Amorphophallus oncophyllus) is a local tuber food that high in bioactive compound glucomannan. It uses are limited due to oxalate acid content which poses health risks. Strobilanthes crispus leaves could reduce the level of calcium oxalate in porang. However, there is still no study to prove its safety. AIM: This study aimed to investigate the acute oral toxicity study of porang (A. oncophyllus) macerated with S. crispus based on observation of mortality rate (LD50), the changes in behavior during 72 h, renal and hepatic function such as urinary protein, serum glutamic oxaloacetic transaminase (SGOT), and serum glutamic pyruvic transaminase (SGPT) levels of Wistar rat (Rattus norvegicus) METHODS: An acute toxicity test was conducted based on the Organization of Economic Co-Operation and Development 420 Fixed-Dose Procedure Guideline that consists of preliminary and main studies. For the preliminary study, rats were divided into control and five treatment groups with the dosage of 50, 300, 2000, and 5000 mg/kg body weight (BW) for each natural porang flour (NPF) and S. crispus-macerated porang flour (SPF). For the main study, rats were divided into four groups, those were NPF and SPF with the dosage of 2000 and 5000 mg/kg BW. Levels of urinary protein and blood serum SGOT and SGPT levels were measured at 0, 24, and 72 after treatment. RESULTS: The acute toxicity study showed that porang and porang macerated with S. crispus were not toxic until the highest dose of 5000 mg/kg BW. It was proved by the absence of LD50, no change in behavior, no weight losses, and also the results of biochemical tests, such as urinary protein, SGOT, and SGPT which were still in the normal range. CONCLUSIONS: Porang flour and SPF were concluded as non-toxic food based on acute toxicity study.

scholarly journals Acute Oral Toxicity of Pinnatoxin G in Mice

Toxins ◽  
2020 ◽  
Vol 12 (2) ◽  
pp. 87 ◽  
Author(s):  
Silvio Sosa ◽  
Marco Pelin ◽  
Federica Cavion ◽  
Fabienne Hervé ◽  
Philipp Hess ◽  
...  
Keyword(s):  
Acute Toxicity ◽  
Nicotinic Acetylcholine Receptors ◽  
Morphological Changes ◽  
Clinical Signs ◽  
Rapid Onset ◽  
Toxicity Study ◽  
Oral Exposure ◽  
Acute Oral Toxicity ◽  
Oral Toxicity ◽  
Acute Toxicity Study

Pinnatoxin G (PnTx-G) is a marine cyclic imine toxin produced by the dinoflagellate Vulcanodinium rugosum, frequently detected in edible shellfish from Ingril Lagoon (France). As other pinnatoxins, to date, no human poisonings ascribed to consumption of PnTx-G contaminated seafood have been reported, despite its potent antagonism at nicotinic acetylcholine receptors and its high and fast-acting toxicity after intraperitoneal or oral administration in mice. The hazard characterization of PnTx-G by oral exposure is limited to a single acute toxicity study recording lethality and clinical signs in non-fasted mice treated by gavage or through voluntary food ingestion, which showed differences in PnTx-G toxic potency. Thus, an acute toxicity study was carried out using 3 h-fasted CD-1 female mice, administered by gavage with PnTx-G (8–450 µg kg−1). At the dose of 220 µg kg−1 and above, the toxin induced a rapid onset of clinical signs (piloerection, prostration, hypothermia, abdominal breathing, paralysis of the hind limbs, and cyanosis), leading to the death of mice within 30 min. Except for moderate mucosal degeneration in the small intestine recorded at doses of 300 µg kg−1, the toxin did not induce significant morphological changes in the other main organs and tissues, or alterations in blood chemistry parameters. This acute oral toxicity study allowed to calculate an oral LD50 for PnTx-G equal to 208 μg kg−1 (95% confidence limits: 155–281 µg kg−1) and to estimate a provisional NOEL of 120 µg kg−1.

scholarly journals Acute and Subchronic (28-day) Oral Toxicity Studies on the Film Formulation of k-Carrageenan and Konjac Glucomannan for Soft Capsule Application

2019 ◽  
Vol 87 (2) ◽  
pp. 9 ◽  
Author(s):  
Ni Sutrisni ◽  
Sundani Soewandhi ◽  
I Adnyana ◽  
Lucy Sasongko
Keyword(s):  
Acute Toxicity ◽  
Experimental Period ◽  
Konjac Glucomannan ◽  
Toxicity Study ◽  
Oral Toxicity ◽  
Subchronic Toxicity ◽  
Acute Toxicity Study ◽  
Relative Organ Weight ◽  
Film Formulation ◽  
Safe Dose

The aim of this study was to investigate the acute and subchronic toxicity of a film formulation that combines κ-Carrageenan and konjac glucomannan for soft capsule application. For the acute toxicity study, a dose of 2000 mg/kg body weight (bw) of the film suspension was administered orally to rats. The animals were observed for toxic symptoms and mortality daily for 14 days. In a subchronic toxicity study, the film suspension, at doses of 10, 30 and 75 mg/kg bw for 28 days, were orally administered to rats. After 28 days, the rats were sacrificed for hematological, biochemical and histological examination. In the acute toxicity study, neither signs of toxicity nor death among the rats were observed for up to 14 days of the experimental period. The results of the subchronic toxicity study show that there were no significant changes observed in the hematology and organ histology. Some alterations to the relative organ weight and blood biochemistry were observed, but they were considered to be temporary effects and not an indication of toxic effects. The overall findings of this study indicate that the film formulation of κ-Carrageenan and konjac glucomannan is non-toxic up to a dose of 75 mg/kg bw, which could be considered a safe dose for soft capsule application.

scholarly journals Withania frutescens. L Extract: Phytochemical Characterization and Acute and Repeated Dose 28-Day Oral Toxicity Studies in Mice

2020 ◽  
Vol 2020 ◽  
pp. 1-7
Author(s):  
Abdelfattah EL Moussaoui ◽  
Mohammed Bourhia ◽  
Fatima Zahra Jawhari ◽  
Imane Es-safi ◽  
Syed Saeed Ali ◽  
...  
Keyword(s):  
Acute Toxicity ◽  
Oral Administration ◽  
Biochemical Parameters ◽  
Clinical Symptoms ◽  
Toxicity Study ◽  
Control Group ◽  
Oral Toxicity ◽  
Traditional Use ◽  
Subacute Toxicity ◽  
Acute Toxicity Study

Background. Withania frutescens. L (W. frutescens) is a perennial woody medicinal plant belonging to family Solanaceae largely used by the indigenous population to Morocco for the treatment of disease. Objective. The purpose of this study was to investigate the chemical composition, acute, and subacute toxicity of W. frutescens extract in mice. Materials and Methods. The phytochemical composition of W. frutescens extract was determined using a gas chromatograph (GC/MS). Acute toxicity study was carried out in mice through oral administration of single doses 500 mg/kg, 1000 mg/kg, and 2000 mg/kg for 14 days. Subacute toxicity was performed with oral administration of repeated doses 500 and 2000 mg/kg/day for 28 days. Biochemical parameters (alanine aminotransferase, aspartate aminotransferase, urea, and creatinine), as well as histopathological changes potentially occurred in organs, (liver, kidney, and spleen) were evaluated. Results. The results of chromatographic analysis showed the richness of W. frutescens extract in interesting phytochemical compounds majorly constituted of bicyclo[3.1.1]heptane, 6,6-dimethyl-2-methylene-(C10H16). Regarding acute toxicity study, the results showed no clinical symptoms occurred in treated mice compared to the control group and no histological changes detected in analyzed organs of treated mice with dose put to 2000 mg/kg nor adverse effect on biochemical parameters. Conclusion. The outcome of this work showed no toxic effect of W. frutescens in mice up to dose 2000 mg/kg bodyweight. Therefore, this study could scientifically validate further traditional use with safety in the range of tested doses.

An experiemental study to evaluate the principle Trini Dravyani Nati Upayunjita w.s.r. to Kshara (Alkali)

2019 ◽  
Vol 4 (04) ◽  
Author(s):  
Amrita Paul ◽  
Umapati C. Baragi ◽  
Kashinath Hadimur ◽  
R. A. Deshmukh
Keyword(s):  
Acute Toxicity ◽  
Adverse Effects ◽  
Dose Level ◽  
Behavioral Changes ◽  
Toxicity Study ◽  
Fixed Dose ◽  
Albino Rats ◽  
Acute Administration ◽  
Acute Toxicity Study ◽  
Acute Study

Background: In Charaka Samhita it has been mentioned that three medicinal substances viz. Pippali (Piper longum), Kshara (alkali) and Lavana (salt) can be used as emergency medicine, but they should not be consumed in excess (Ati Upayunjita). If they are consumed in excess quantity they will cause several adverse effects in the body. Hence in the present study Kshara has been evaluated in experimental animals in two different phases viz. acute administration at graded doses as part of acute toxicity study and sub-acute administration at fixed dose level, as part of sub-acute toxicity study, to assess the possible adverse effects if any. Objectives: To evaluate the acute and sub-acute toxic effect of Kshara in albino rats to establish the principle of Trini Dravyani Nati Upayunjita. Materials and Methods: Wister strain albino rats of either sex weighing between 150 - 200g body weights were used for experimental study. The experiment was carried out as per ‘Ayush Guidelines’ after the IAEC clearance. For Acute Toxicity - 9 Albino rats were used and for Sub-Acute Toxicity - 12 Albino rats were used. The dose calculation was done on the basis of body surface area ratio using the table of ‘Paget and Barnes rule’. Results: In Acute toxicity study no mortality and behavioral changes were observed when the drug Kshara was studied after two dose level i.e. TED X 5 and TED X 10. In Sub-acute study some behavioral changes (including cage side behavior) were observed. No mortality was observed in any of the groups. Discussion: Acute toxicity study of Kshara showed no immediate and evident toxic signs and mortality within 24 hours of observation. In Sub-acute toxicity study in all four groups, no mortality or evident toxic effects were observed, however some mild histopathological changes were observed in sub-acute study.

Absence of Detectable Toxicity in Rats Fed Partially Hydrolyzed Guar Gum (K-13) for 13 Weeks

1997 ◽  
Vol 16 (6) ◽  
pp. 611-623 ◽  
Author(s):  
Takatoshi Koujitani ◽  
Hidetoshi Oishi ◽  
Yuji Kubo ◽  
Toshihiro Maeda ◽  
Keiji Sekiya ◽  
...  
Keyword(s):  
Acute Toxicity ◽  
Guar Gum ◽  
Toxicity Study ◽  
Oral Toxicity ◽  
Subchronic Toxicity ◽  
Mutagenic Potential ◽  
Reverse Mutation ◽  
Acute Toxicity Study ◽  
K 13 ◽  
Partially Hydrolyzed Guar Gum

Toxicity studies were conducted to evaluate acute and subchronic oral toxicity and mutagenicity of partially hydrolyzed guar gum (K-13). In an acute toxicity study, mice and rats were treated with K-13 at a dose of 6000 mg/ kg. There were no deaths, so the LD50s were >6000 mg/ kg in both species. In a subchronic toxicity study, K-13 was given to rats as a dietary admixture at concentrations of 0.2. 1.0 and 5.0% for 13 weeks. There were no effects attributable to K-13 in any examinations. K-13 proved to have no mutagenic potential in a reverse mutation test using bacteria.

scholarly journals Hepatoprotective effect of Helicanthus elastica

2016 ◽  
Vol 11 (2) ◽  
pp. 525 ◽  
Author(s):  
K.N. Sunil Kumar ◽  
R. Rajakrishnan ◽  
J. Thomas ◽  
G. Aadinaath Reddy
Keyword(s):  
Body Weight ◽  
Acute Toxicity ◽  
Dose Level ◽  
Video Clip ◽  
Ethanolic Extract ◽  
Ethanol Extract ◽  
Toxicity Study ◽  
Oral Toxicity ◽  
Acute Toxicity Study ◽  
Whole Plant

<p class="Abstract">Search for medicinal plants to treat liver disorders is an important research topic on herbs. Acute toxicity study is a prerequisite for safety and dose fixation for further pharmacological actions. In the present study, aqueous and 95% ethanolic extract of whole plant of <em>Helicanthus elastica</em> were subjected to acute oral toxicity. The aqueous and ethanolic extract revealed no observable changes in the rats up to the dose level of 2,000 mg /kg body weight. The extracts were then screened for paracetamol-induced hepatic injury at dose levels of 200 and 400 mg/kg body weight (1/10 and 1/5 LD<sub>50 </sub>based on toxicity study). The aqueous extract of whole plant of <em>H. elastica</em> was found to produce significant (p&lt;0.05) reversal of the paracetamol-induced changes in the measured biochemical and histopathological parameters at lower dose of 200 mg/kg which was found to be better than ethanol extract at the same dose level.</p><p class="Abstract"><strong>Video Clip:</strong></p><p class="Abstract"><a href="https://www.youtube.com/v/cO6HI1Kikxs">Acute toxicity study and others:</a> 5 min 38 sec</p><p> </p>

Comparative Study of different Solvent Extract of Plectranthus amboinicus Stem for their Diuretic Activity

2021 ◽  
pp. 4727-4730
Author(s):  
Noor Salma ◽  
Chandra Prakash K ◽  
Syed Sagheer Ahmed ◽  
Saba Tabassum ◽  
Ahalya Devi K H
Keyword(s):  
Acute Toxicity ◽  
Urine Volume ◽  
Chloride Concentration ◽  
The Body ◽  
Toxicity Study ◽  
Fixed Dose ◽  
Diuretic Activity ◽  
Solvent Extract ◽  
Acute Toxicity Study ◽  
Plectranthus Amboinicus

Diuresis can be beneficial in removing toxins from the body. Globally traditional and folklore medicines plays a vital role in health care services. Plectranthus amboinicus belongs to Lamiaceae family is an Indian medicinal plant which has been utilized traditionally to treat various diseases. However, there is no systematic methodology for the use of Plectranthus amboinicus stem as a diuretic. Hence the present study is proposed to evaluate the diuretic activity of various solvent extract of Plectranthus amboinicus stem in the rat model. The acute toxicity study was performed in albino mice by fixed-dose method (OECD guidelines number 425) of CPCSEA. The diuretic activity was carried out using the Lipschitz method. The total urine volume collected in 24hours was observed. Sodium, potassium and chloride concentration in urine were also recorded. The ionic concentrations were recorded calorimetrically. Acute toxicity study proved no toxicity and mortality in any of the animal up to the dose of 2000mg/kg bodyweight. All three extracts of Plectranthus amboinicus have exhibited dose-dependent diuretic activity by increasing urine volume and excreting sodium ions in urine. The urine pH was also elevated. From the study, it can be concluded that the plant Plectranthus amboinicus could be considered as a diuretic agent. This current study encourages the use of this plant in folk medicine. Further study is required for isolation, characterization and formulation of the active constituents responsible for its diuretic activity.

An experimental study to evaluate the concept of Trividha Atisevana Varjya Dravya w.s.r. to Lavana

2019 ◽  
Vol 4 (04) ◽  
Author(s):  
Shilpa Nimbal ◽  
Umapati C. Baragi ◽  
Kashinath Hadimur ◽  
Jyothi Alias Jyostna
Keyword(s):  
Acute Toxicity ◽  
Dose Level ◽  
Equivalent Dose ◽  
Toxicity Study ◽  
Fixed Dose ◽  
Albino Rats ◽  
Acute Administration ◽  
Acute Toxicity Study ◽  
Wistar Strain ◽  
Acute Study

Background: Lavana is used as medicine as well as Ahara since ancient times. In Caraka Samhita it has been mentioned that three Dravyas viz. Pippali, Kshara (alkali) and Lavana (salt) can be used as emergency medicine, but they should not be consumed in excess (Ati Upayunjita). Hence in the present study Lavana has been evaluated in experimental animals in two different phases’ viz. Acute administration at graded doses as part of acute toxicity study and Sub-Acute administration at fixed dose level, as part of toxic Sub-Acute toxicity study, to assess the possible adverse effects. Materials andamp; Methods: Wistar strain albino rats of either sex weighing between 150 - 200g. body weights were used, The experiment was carried out in accordance with the direction of the Institutional animal ethics committee (IAEC) after obtaining its permission (Approval number IAEC – 138/k/2018). Results: Results were drawn based on histopathological reports and biochemical reports of each group of toxicity study. Acute toxicity study has been carried out in albino rats receiving the 2 dose level maximum at up to 10 times higher (855mg/kg) then the therapeutic equivalent dose (427.5mg/kg). In Sub-Chronic toxicity: dose given was five times higher than therapeutic equivalent dose and ten times the equivalent to human therapeutic dose for duration of 30 days. Discussion: Toxicity is not found in Acute study and in Sub-Acute study moderate to high toxicity is found.

PHARMACOGNOSTIC, ANTIOXIDANT AND ACUTE TOXICITY STUDY OF Ficus sycomorus (Linn) (Moraceae) ROOT AND STEM BARK

2020 ◽  
Vol 4 (2) ◽  
pp. 605-614
Author(s):  
Murtala M. Namadina ◽  
H. Haruna ◽  
U. Sanusi
Keyword(s):  
Acute Toxicity ◽  
Radical Scavenging ◽  
Stem Bark ◽  
The Body ◽  
Toxicity Study ◽  
Bark Extract ◽  
Root Extract ◽  
Acute Toxicity Study ◽  
Radical Scavenging Ability ◽  
Phytochemical Components

Most of biochemical reactions in the body generates Reactive Oxygen Species (ROS), which are involved in the pathogenesis of oxidative stress-related disorders like diabetes, nephrotoxicity, cancer, cardiovascular disorders, inflammation and neurological disorders when they attack biochemical molecules like proteins, lipids and nucleic acid. Antioxidants are used to protect the cells or tissues against potential attack by ROS. Most medicinal plants possess a rich source of antioxidants such as flavonoids, phenols, tannins, alkaloids among others. These phytochemicals are currently pursued as an alternative and complimentary drug. In this study, phytochemical components, antioxidant and acute toxicity study of the methanol extract of stem bark and root of F. sycomorus were carried out using standard methods. Findings from this study revealed the presence of some diagnostic microscopical features such as calcium oxalate, starch, gum/mucilage, lignin, Aleurone grain, suberized/Cuticular cell wall and inulin but calcium carbonate was absent in stem bark but present in the powdered root. Quantitative physical constants include moisture contents (6.40% and 7.82%), ash value (7.20% and 9.30 %) in stem bark and root respectively. Carbohydrates, alkaloid, flavonoids, saponins, tannins, glycoside, steroid, triterpenes and phenols were present in all the extracts. They were found to exhibit potent 1,1,-diphenyl 2-picryl hydrazyl (DPPH) free scavenging activity. The DPPH radical scavenging ability of the extracts showed the following trend Ascorbic acid < stem bark extract˃ root extract. The LD50 of the methanolic stem bark and root extracts were found to be greater than 5000 mg /kg and is considered safe for use. Nonetheless, further

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