Toxicity Study of Potash Extract, “jar Kanwa”: An Earthy Material Consumed for Remedy of various Ailments in Northern Nigeria

Potash comprises potassium bearing minerals. These minerals are traditionally used for treatments of many ailments in Northern Nigeria with little knowledge of their safety profile. Acute toxicity (LD50) study of the potash extract was carried out on adults Wistar rats. Based on the result of LD50; four groups of Wistar rats; Group I, II, III and IV, each containing six males were formed. Group I was administered distilled water while group II was administered 20% (1,000 mg/kg) of the highest non-lethal dose. Group III and IV were administered 10% (500 mg/kg) and 5% (250 mg/kg) of the highest non-lethal dose respectively. These were done continuously for 28 days. Intakes of food and water were recorded daily while weights of animals were recorded weekly. There was no mortality at both phase 1& 2 of the LD50. Results of chronic toxicity revealed two mortalities recorded in group II. Acute toxicity studies of potash extract showed that it is generally safe but in sub-chronic toxicity study, the extract was lethal on the experimental animals at higher doses. Therefore, consumption of this earthy material on a long term basis should be discouraged due to its lethal effects on animal studies

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Impact of Neem Oil on Malathion in the Fish Oreochromis mossambicus

Current World Environment ◽

10.12944/cwe.15.2.19 ◽

2020 ◽

pp. 314-322

Author(s):

Jothigayathri D ◽

Amthul Azeez ◽

Akthari Begum F ◽

Lubna Ghazia C M

Keyword(s):

Acute Toxicity ◽

Chronic Toxicity ◽

Oreochromis Mossambicus ◽

Toxicity Study ◽

Free Sugar ◽

Fresh Water Fish ◽

Negative Consequences ◽

Neem Oil ◽

Cell Degeneration ◽

Group I

The far reaching dissemination and toxic nature of pesticides and their elements seriously affects the aquatic surroundings, and exerts negative consequences on the related organisms. The present study was carried out to investigate the effect of malathion and neem oil individually and also in combination on the fresh water fish, Oreochromis mossambicus to elucidate the change in the different target organs like liver and kidney with reference to biochemical and histopathological studies. Median lethal concentration (LC50) of neem oil and malathion was maintained for acute toxicity (96 hours) and chronic toxicity (21 days) studies. Further the fishes were segregated into 4 groups where in each group contained 6 fishes. Group I fishes were maintained in tap water, Group II in neem oil, Group III fishes were maintained in malathion , Group IV fishes were maintained in both neem oil and malathion. The LC50 dose of neem oil and malathion was found to be 0.9 ml/L and 3.52 mg/L respectively. The results of biochemical analysis revealed that total protein and lipid increased in combination of neem oil and malathion which was comparatively more than that of the neem oil and malathion maintained individually. The total free sugar showed a decrease in combination as well as individually in acute toxicity study .However there is an increase in total free sugar as observed in chronic toxicity study. Histopathological study in acute and chronic toxicity (i) in liver, fishes exposed to neem oil showed normal hepatocellular architecture while fishes exposed to malathion only and those of malathion combined with neem oil showed hepatocellular degeneration while the latter showed the signs of recovery (ii) in kidney the neem oil exposed fishes showed normal renal architecture , malathion exposed fishes showed epithelial cell degeneration and necrosis, while those exposed to neem oil and malathion combined showed mild degeneration. This study indicated the action of neem oil which has interacted with malathion and reveals a protective influence on harmful effects of the toxicant.

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GAMBARAN HISTOLOGIK AORTA TIKUS WISTAR DENGAN DIET LEMAK BABI SETELAH PEMBERIAN EKSTRAK DAUN PEPAYA

JURNAL BIOMEDIK (JBM) ◽

10.35790/jbm.5.1.2013.2610 ◽

2013 ◽

Vol 5 (1) ◽

Author(s):

Friska W. F. Panjaitan ◽

Marie M. Kaseke ◽

George N. Tanudjaja

Keyword(s):

Wistar Rats ◽

Leaf Extract ◽

Foam Cells ◽

Group Iv ◽

Control Group ◽

Histological Features ◽

Group I ◽

Group Ii ◽

Lard Diet ◽

Control Group Group

Abstract: Papaya leaves contain several antioxidants (flavonoid, tanin, and vitamin C) which have antiatherogenic effects that may inhibit the progression of an atherosclerotic lesion. One of the risk factors causing atherosclerosis is the consumption of food containing highly saturated fatty acids e.g. lard. Low density lipoproteins (LDL) accumulate within the intima and then are oxidized (LDL-ox). This LDL-ox is ingested by macrophages, resulting in foam-cell formation (early lesion of atherosclerosis). This study aimed to find out the histological features of the aorta of wistar rats having lard diets without the addition of the papaya leaf extract; having lard diets along with the papaya leaf extract; and having lard diets followed by papaya leaf extract. This was an experimental study on 16 wistar rats divided into 4 groups: group I without treatment (negative control group), group II lard diet for 14 days (positive control group), group III lard diet with papaya leaf extract for 14 days (treatment group I), and group IV lard diet for 14 days, and then followed by papaya leaf extract for 14 days (treatment group II). It was found that the aorta of group I showed adipose cells in the intima and media layers; group II and III showed foam cells in both layers; and group IV showed foam cells in fewer numbers than group II. Conclusion: The aorta histological features of wistar rats given lard diets for 14 days, with or without papaya leaf extract, showed foam cells in the intima and media layers. Papaya leaf extraxt added to lard diets had no effect on decreasing foam cells (no protective effect), meanwhile papaya leaf extract following lard diets showed a reduction of foam cells (therapeutic effect). Keywords: papaya leaf, lard dietary, foam cells, wistar rat. Abstrak: Daun pepaya mengandung antioksidan (flavonoid, vitamin C) yang berefek anti-aterogenik, sehingga diharapkan dapat menghambat perkembangan lesi aterosklerosis. Salah satu faktor risiko penyebab aterosklerosis yaitu makanan yang berkandungan tinggi asam lemak jenuh, antara lain lemak babi. Konsumsi lemak jenuh berlebihan dapat mengganggu fungsi sel endotel, sehingga lipoprotein berdensitas rendah (LDL) dapat masuk dan menjadi LDL teroksidasi (LDL-oks). Makrofag menangkap LDL-oks dan menjadi sel busa (lesi dini aterosklerosis). Penelitian ini bertujuan untuk mengetahui gambaran histologik aorta tikus wistar dengan diet lemak babi tanpa pemberian ekstrak daun pepaya, diet lemak babi bersamaan pemberian ekstrak daun pepaya, dan setelah diet lemak babi dilanjutkan pemberian ekstrak daun pepaya. Penelitian ini bersifat eksperimental. Subyek penelitian terdiri dari 16 ekor tikus wistar yang dibagi menjadi empat kelompok: kelompok I tanpa perlakuan (kelompok kontrol negatif); kelompok II dengan diet lemak babi selama 14 hari (kelompok kontrol positif); kelompok III dengan diet lemak babi serta pemberian ekstrak daun pepaya selama 14 hari (kelompok perlakuan I); dan kelompok IV dengan diet lemak babi selama 14 hari, dilanjutkan pemberian ekstrak daun pepaya selama 14 hari (kelompok perlakuan II). Hasil penelitian memperlihatkan gambaran histologi aorta kelompok I tampak perlemakan; pada kelompok II terdapat sel-sel busa; pada kelompok III masih terdapat sel-sel busa; dan pada kelompok IV terdapat sel-sel busa, namun dalam jumlah yang lebih sedikit dibandingkan pada gambaran kelompok II. Simpulan: Tikus wistar dengan diet lemak babi selama 14 hari, baik dengan maupun tanpa ekstrak daun pepaya, memperlihatkan gambaran histologik adanya sel-sel busa pada tunika intima dan tunika media aorta. Pemberian ekstrak daun pepaya bersamaan dengan diet lemak babi tidak berefek menurunkan jumlah sel busa (tidak ada efek protektif) sedangkan pemberian ekstrak daun pepaya setelah diet lemak babi berefek mengurangi jumlah sel-sel busa yang terbentuk (efek terapi). Kata kunci: daun pepaya, diet lemak babi, sel-sel busa, tikus wistar.

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GAMBARAN MIKROSKOPIK GINJAL TIKUS WISTAR (RATTUS NORVEGICUS) SETELAH DIINDUKSI DENGAN GENTAMISIN

JURNAL BIOMEDIK (JBM) ◽

10.35790/jbm.4.3.2012.800 ◽

2013 ◽

Vol 4 (3) ◽

Author(s):

Poppy M Lintong ◽

Carla F Kairupan ◽

Priska L N Sondakh

Keyword(s):

Body Weight ◽

Epithelial Cells ◽

Wistar Rats ◽

Periodic Acid ◽

Basal Membrane ◽

Tubular Epithelial Cells ◽

Periodic Acid Schiff ◽

Group Iii ◽

Group I ◽

Group Ii

Abstract: Gentamycin, a frequently used aminoglycoside antibiotics, has a nephrotoxic effect to human beings and animals. The purpose of this research was to find out the microscopic changes of wistar rat kidneys after gentamycin induction. This was an experimental study, using five adult wistar rats, divided into three groups. Group I was the control group; group II consisted of two rats, injected with gentamycin 0,3 ml/day (dose of 60 mg/kg body weight/day) intraperitoneally for seven days; and group III consisted of two rats, injected with gentamycin 0,3 ml/day intraperitoneally for 10 days. Group I and II were terminated at day-8, and group III at day-11. Their kidneys were processed for microscopic slides, stained with hematoxylin eosin and Periodic Acid Schiff. In microscopic evaluation, group II and III showed oedema, necrosis, apoptosis, and basal membrane destruction of tubular epithelial cells. Group III also showed fat vacuoles in these epithelial cells (macrovesicular fatty changes). Conclusion: wistar rats injected with gentamycin 60 mg/kg body weight/day for 7 and 10 days showed oedema, necrosis, apoptosis, and basal membrane destruction of tubular epithelial cells; and macrovesicular fatty changes after 10 days of gentamycin.Key words: gentamycin, necrosis tubular epithelial cells, fatty changesAbstrak: Gentamisin termasuk antibiotik golongan aminoglikosida berspektrum luas yang bersifat nefrotoksik terhadap manusia dan hewan. Tujuan penelitian ini untuk melihat perubahan mikroskopik struktur ginjal tikus Wistar setelah diberikan gentamisin. Metode penelitian eksperimental dengan menggunakan lima ekor tikus Wistar dewasa yang dibagi atas tiga kelompok. Kelompok I tanpa perlakuan; kelompok II terdiri dari dua ekor tikus perlakuan yang diinjeksi dengan gentamisin 0,3 ml/hari (dosis 60 mg/kgBB/hari) secara intraperitonial selama tujuh hari; dan kelompok III terdiri dari dua ekor tikus perlakuan yang diinjeksi dengan gentamisin 0,3 ml/hari secara intraperitonial selama 10 hari. Tikus Wistar kelompok I dan II diteminasi hari ke-8, sedangkan kelompok III diterminasi hari ke-11. Ginjal tikus kelompok I -III kemudian dibuat preparat histopatologik dengan pengecatan rutin hematoksilin eosin dan Periodic Acid Schiff (PAS). Hasil penelitian menunjukkan tikus Wistar perlakuan yang diberikan gentamisin 0,3 ml/hari selama 7 sampai 10 hari secara mikroskopik memperlihatkan pembengkakan, nekrosis, apoptosis, dan destruksi membrana basalis sel epitel tubulus; dan pada hari ke-10 terlihat vakuol-vakuol lemak pada sel epitel sehingga inti terdesak ke tepi (perlemakan makrovesikuler). Simpulan: pemberian gentamisin pada tikus Wistar dengan dosis 60 mg/kg BB/hari selama 7-10 hari menunjukkan pembengkakan, nekrosis, apoptosis sel epitel tubulus, dan membrana basalis tubulus rusak; dan setelah hari ke-10 juga terlihat perlemakan makrovesikuler.Kata kunci: gentamisin, nekrosis sel epitel tubulus, perlemakan makrovesikuler

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SUB-CHRONIC TOXICITY STUDY OF THE RAMBUTAN RIND EXTRACT IN MALE WISTAR RATS

Reviews on Clinical Pharmacology and Drug Therapy ◽

10.17816/rcf102101_1 ◽

2012 ◽

Vol 10 (2) ◽

pp. 101-1

Author(s):

Aree Thinkratok ◽

Parin Suwannaprapha ◽

Rungrudee Srisawat

Keyword(s):

Wistar Rats ◽

Chronic Toxicity ◽

Toxicity Study ◽

Male Wistar Rats

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Antidiarrhoeal activity of aqueous leaf extract of Olea europaea var. sylvestris in albino Wistar rats

Journal of Biological Research - Bollettino della Società Italiana di Biologia Sperimentale ◽

10.4081/jbr.2018.7614 ◽

2018 ◽

Vol 91 (2) ◽

Cited By ~ 1

Author(s):

Mohamed Zaouani ◽

Fatima Yahiaoui ◽

Nazli Nacer Bey ◽

Meriem Hind Ben-Mahdi

Keyword(s):

Body Weight ◽

Acute Toxicity ◽

Aqueous Extract ◽

Olea Europaea ◽

Castor Oil ◽

Wistar Rats ◽

Toxicity Study ◽

Motility Assay ◽

Phytochemical Screening ◽

Leaf Aqueous Extract

Olea europaea var. sylvestris, also named oleaster, is widely used by traditional medicine practitioners in Algeria to treat high blood pressure and diabetes. However, the antidiarrhoeal activity of this plant has not been scientifically evaluated. The main aim of the study deals with an investigation of three topics: the phytochemical screening, the acute toxicity, and antidiarrhoeal activity of the oleaster leaf aqueous extract. Acute oral toxicity study was carried out based on Organization for Economic Cooperation and Development 423 guideline. The extract was orally administered in wistar rats at a single dose of 2000 mg/kg body weight and the animals were observed for mortality, behavioral changes and other abnormal signs. Qualitative analysis of phytochemical constituents was carried out using standard methods developed by Harborne, Trease and Evans. Castor oil-induced diarrhoea tests and gastro intestinal motility assay were evaluated in rats to determine the antidiarrhoeal activity of the extract. In the acute toxicity study, the extract did not induce death or any sign of toxicity in treated rats. The preliminary phytochemical screening of the extract revealed the presence of saponins, flavonoids, and triterpenoids. The oleaster extract at oral doses of 100, 200 and 400 mg/kg body weight showed a significant (P<0.05) antidiarrhoeal activity compared to the control group treated with castor oil induced diarrhoea, enteropooling and gastrointestinal motility assay, after charcoal meal administration. The oleaster leaf aqueous extract has shown a gradual response with increasing dose. The present study indicates that the oleaster leaf aqueous extract is safe with antidiarrhoeal property.

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Effects of sodium hyaluronate and carboxymethylcellulose membrane on collagen and fibroblast formation in bowel suture healing: experimental study in rats

Acta Cirurgica Brasileira ◽

10.1590/s0102-86502005000100004 ◽

2005 ◽

Vol 20 (1) ◽

pp. 15-21 ◽

Cited By ~ 1

Author(s):

Antônio Carlos Perez ◽

Delcio Matos ◽

Edna Frasson de Souza Montero ◽

Heitor Soares de Souza ◽

Fábio Colagrossi Paes Barbosa ◽

...

Keyword(s):

Experimental Study ◽

Wistar Rats ◽

Sodium Hyaluronate ◽

Morbidity And Mortality ◽

Collagen Formation ◽

Significant Variance ◽

Group I ◽

Male Wistar Rats ◽

Group Ii ◽

Observation Period

PURPOSE: To analyze the effects of sodium hyaluronate and carboxymethylcellulose membrane on collagen and fibroblast formation in bowel suture healing in rats. METHODS: 48 male Wistar rats, weighing 250 to 343g, were randomized into two groups: group I - bowel suture without applying a biologically absorbable membrane and group II - bowel suture with application of an absorbable membrane. The two groups were divided into subgroups of 3, 14 and 30 days of observation, with 8 rats in each subgroup. All were sacrificed after the end of the observation period. RESULTS: No morbidity or mortality was observed during the experiment. The amounts of collagen in group I were 23.4%, 72.1% and 67.6% and in group II were 22.5%, 52.5% and 51.6%, for the subgroups of 3, 14 and 30 days, respectively. Comparison between groups showed that the 14-day (p=0.0013) and 30-day (p=0.0587) subgroups had significant variance, with larger collagen zones in animals in which the membrane was not applied. However, with regard to fibroblasts, group I had 2%, 13% and 8% and group II had 2%, 10% and 8%, for the 3-day (p=1.0), 14-day (p=0.3184) and 30-day (p=0.5995) subgroups, respectively, showing no significant variance. CONCLUSION: The use of the biologically absorbable membrane cause a decrease in collagen formation, while not altering the number of fibroblasts, in bowel suture healing in rats, without increased morbidity and mortality.

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Acute, Subacute, and Genotoxicity Assessments of a Proprietary Blend of Garcinia mangostana Fruit Rind and Cinnamomum tamala Leaf Extracts (CinDura®)

Journal of Toxicology ◽

10.1155/2020/1435891 ◽

2020 ◽

Vol 2020 ◽

pp. 1-15

Author(s):

Sundararaju Dodda ◽

Venkata Krishnaraju Alluri ◽

Trimurtulu Golakoti ◽

Krishanu Sengupta

Keyword(s):

Body Weight ◽

Wistar Rats ◽

Lethal Dose ◽

Toxicity Study ◽

Mouse Bone Marrow ◽

Acute Oral Toxicity ◽

Oral Toxicity ◽

Garcinia Mangostana ◽

Cinnamomum Tamala ◽

Fruit Rind

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.

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Acute and Subacute Toxicity Studies of the Ethyl Acetate Soluble Proanthocyanidins of the Immature Inflorescence of Cocos nucifera L. in Female Wistar Rats

BioMed Research International ◽

10.1155/2019/8428304 ◽

2019 ◽

Vol 2019 ◽

pp. 1-12

Author(s):

C. P. Ekanayake ◽

M. G. Thammitiyagodage ◽

S. Padumadasa ◽

B. Seneviratne ◽

C. Padumadasa ◽

...

Keyword(s):

Body Weight ◽

Acute Toxicity ◽

Ethyl Acetate ◽

Wistar Rats ◽

Cocos Nucifera ◽

Toxicity Study ◽

Immature Inflorescence ◽

Subacute Toxicity ◽

Toxicity Studies ◽

Female Wistar Rats

Ayurvedic and traditional medical practitioners of Sri Lanka use the decoction of the immature inflorescence of Cocos nucifera L. (IC) variety aurantiaca for the treatment of menorrhagia. The progestogenic effect of the ethyl acetate soluble proanthocyanidins (EASPA) of the IC in female rats at a dose of 3.5 mg/kg body weight has been reported. Acute and subacute toxicity studies of EASPA of the IC carried out using female Wistar rats according to Organization for Economic Co-operation and Development (OECD) guidelines 423 and 407, respectively, are reported herein. In the acute toxicity study, a single dose of EASPA (2000 mg/kg body weight) was orally administered to rats, which were monitored for 14 days. In the subacute toxicity study, rats were orally administered with EASPA daily for 28 days at doses of 1.75, 3.5, 7, and 14 mg/kg body weight. No rat in either the acute or subacute toxicity study exhibited mortality or clinical signs of toxicity. Further, these rats did not show any significant change in their mean body weight, food, and water intake, haematological and biochemical parameters as well as in the results of their histopathological examinations compared to those of control group rats. According to results of the acute toxicity, the LD50 of EASPA is estimated to be greater than 2000 mg/kg body weight. Considering the results of the subacute toxicity study, the oral administration of EASPA daily for 28 days was well tolerated up to the dose, 14 mg/kg by rats. These results will be useful in the development of a novel therapeutic agent from EASPA of the IC for the treatment of menorrhagia, which incapacitates a considerable proportion of women worldwide.

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