Acute Oral Toxicity Evaluation of Some Polyherbal Formulations in Albino Wistar Rats

2008 ◽  
Vol 4 (5) ◽  
pp. 388-392 ◽  
Author(s):  
A.J. Joshua ◽  
K.S. Goudar ◽  
A. Damodaran ◽  
N. Sameera ◽  
A. Amit
2018 ◽  
Vol 24 (1) ◽  
pp. 23-30 ◽  
Author(s):  
Mohammadmehdi Hassanzadeh-Taheri ◽  
Mehran Hosseini ◽  
Mojtaba Salimi ◽  
Hesam Moodi ◽  
Davood Dorranpour

2022 ◽  
Vol 22 (1) ◽  
Author(s):  
Florence Nalimu ◽  
Joseph Oloro ◽  
Emanuel L. Peter ◽  
Patrick Engeu Ogwang

Abstract Background Several local communities in Central, Western, Eastern, and Northern regions of Uganda have been using the whole leaf extracts of Aloe vera (L.) Burm. f. (Asphodelaceae) in the treatment of various ailments. Also, several commercial companies sell A. vera as soft drinks in Uganda. However, there are inadequate reports on the toxicities of such preparations. This paper reports the acute and sub-acute oral toxicity of aqueous extracts of whole leaf and green rind of A. vera in Wistar rats. Methods Acute oral toxicity test was carried out in female Wistar rats at doses of 175, 550, 1750, and 5000 mg/kg, p.o. The animals were observed for signs of toxicity for 14 days. Similarly, a sub-acute oral toxicity test was performed in both sexes of rats at doses of 200, 400, and 800 mg/kg, p.o. daily for 28 days. All the groups of animals were monitored for behavioral, morphological, biochemical, and physiological changes, including mortality and compared with respective controls. Body weights were measured weekly while the animals’ relative organ weights, hematological, biochemical, gross, and microscopic pathology were examined on day 29. Results There was no mortality or apparent behavioral changes at the doses tested in acute and sub-acute oral toxicity tests. Thus, the Median Lethal Dose (LD50) of green rind and whole leaf aqueous extracts was above 5000 mg/kg. Gross anatomy revealed that the rats’ relative spleen weight in green rind extract at 200 mg/kg significantly decreased compared to the control group. The creatinine levels in female rats that received green rind extract and the chloride ion levels in male rats administered whole leaf extract were significantly elevated. Conversely, Mean Corpuscular Hemoglobin Concentration (MCHC) levels significantly decreased at lower doses of the green rind extract compared to the control. Histopathology of the kidney revealed the renal interstitium’s inflammation at doses of 200 and 800 mg/kg of the whole leaf extract. Conclusion The findings demonstrated that A. vera green rind and whole leaf extracts are non-toxic at relatively high doses when used for a short duration. Prolonged use of the aqueous whole leaf extract might be associated with kidney toxicity.


2019 ◽  
Vol Volume 14 ◽  
pp. 10035-10046 ◽  
Author(s):  
Muhammad Ahmad Mahmood ◽  
Asadullah Madni ◽  
Mubashar Rehman ◽  
Muhammad Abdur Rahim ◽  
Abdul Jabar

2019 ◽  
Vol 108 ◽  
pp. 104443 ◽  
Author(s):  
M. Clemente ◽  
M.D. Miguel ◽  
K.B. Felipe ◽  
C. Gribner ◽  
P.F. Moura ◽  
...  

2020 ◽  
Vol 2020 ◽  
pp. 1-15
Author(s):  
Sundararaju Dodda ◽  
Venkata Krishnaraju Alluri ◽  
Trimurtulu Golakoti ◽  
Krishanu Sengupta

The present communication describes a battery of toxicity studies that include an acute oral toxicity, a subacute twenty-eight-day repeated oral dose toxicity, and genotoxicity studies on a herbal formulation CinDura® (GMCT). This proprietary herbal composition contains the extracts of the Garcinia mangostana fruit rind (GM) and the Cinnamomum tamala leaf (CT). The toxicological evaluations were performed following the Organization for Economic Cooperation and Development (OECD) guidelines. The acute oral toxicity study in Wistar rats suggests that the median lethal dose of CinDura® is at least 2000 mg/kg body weight. Acute dermal and eye irritation tests in New Zealand white rabbits indicate that the test item is nonirritant to the skin and eyes. A twenty-eight-day repeated dose oral toxicity study was conducted in male and female Wistar rats using daily doses of 250, 500, and 1000 mg/kg body weight, followed by a fourteen-day reversal period for two satellite groups. The CinDura®-supplemented animals did not show any sign of toxicity on their body weights, organ weights, and on the hematobiochemical parameters. The gross pathology and histopathological examinations indicated no treatment-related changes in the experimental animals. Overall, the no-observed-adverse-effect level (NOAEL) of the herbal blend is 1000 mg/kg body weight, the highest tested dose. Also, the results of the bacterial reverse mutation test and the erythrocyte micronucleus assay in mouse bone marrow suggest that CinDura® (GMCT) is neither mutagenic nor clastogenic.


2019 ◽  
Vol 6 ◽  
pp. 426-430 ◽  
Author(s):  
Luksamee Worasuttayangkurn ◽  
Watanyoo Nakareangrit ◽  
Jackapun Kwangjai ◽  
Pishyaporn Sritangos ◽  
Nanthanit Pholphana ◽  
...  

1993 ◽  
Vol 12 (6) ◽  
pp. 584-585
Author(s):  
L. D. Brown ◽  
D. W. Korte ◽  
J. D. Justus ◽  
C. R. Wheeler ◽  
E. W. Morgan ◽  
...  

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