Effects of Acute Toxicity of Chlorpyrifos (EC 50%) and Associated Histological Alterations in Gills, Liver and Kidney of Mozambique Tilapia, Oreochromis mossambicus (Peters, 1852)

2020 ◽  
Author(s):  
N. Jayakumar ◽  
A. Subburaj ◽  
P. Jawahar ◽  
A. Srinivasan ◽  
B. Ahilan
Keyword(s):  
Acute Toxicity ◽  
Oreochromis Mossambicus ◽  
The Body ◽  
Dependent Manner ◽  
Histopathological Changes ◽  
Aquatic Life ◽  
Histological Changes ◽  
Mozambique Tilapia ◽  
Secondary Lamellae ◽  
Liver And Kidney

Background: The pesticides are known to adversely affect the quality of water and create hazards for aquatic life that results in severe damage to non-target freshwater organisms including fish. Among them, the organophosphorus pesticide, chlorpyrifos (CPF) is one of the most commonly used pesticides for controlling various kinds of pests in agriculture. Pesticides after entering in to the body of fish bring about histopathological and biochemical changes in different target and non-target organs. Hence, the present study aimed to investigate the toxicity effects of Chlorpyrifos (CPF) and associated histopathological changes in the gill, liver and kidney of the Mozambique Tilapia, Oreochromis mossambicus under the acute toxicity concentrations. Methods: Static bioassay was carried out for Chlorpyrifos with Oreochromis mossambicus as test animal for a period of 96 hrs as per standard methods and LC50 values were calculated through Probit analysis. The fishes were exposed to five acute concentrations (0.033, 0.066, 0.132, 0.264 and 0.528 ppb). The gill, liver and kidney tissues were collected from the fishes exposed to the pesticide and standard histology protocol was followed to investigate the histopathological changes. Result: The histological changes observed in the gill included lamellar aneurysm, curling of secondary lamellae, shortening of the secondary lamellae, hypertrophy of epithelial cell, fusion of secondary lamellae, deformation of the cartilage core, blood congestion, collapsed secondary lamellae, excessive mucus secretion, disorganization of the secondary lamellae, haemorrhage at primary lamellae, necrosis, haemorrhage at secondary lamellae. The most common histopathological changes in the liver were characterized by cellular necrosis, degeneration of hepatocytes, nuclear degeneration, fat deposition, rupture of nucleus, hypertrophied hepatocytes, blood congestion, blood sinusoids, cellular hypertrophy, increased pycnotic nucleus, cirrhosis and hemosiderosis. Further, histological changes like appearance of dilated lumen, hypertrophied epithelial cells, severe haemorrhage, blood congestion, melanomacrophage aggregation, narrowing of lumen, degenerated tubule, degenerated glomerulus, shrunken glomerulus and distended glomerulus were observed in the kidney. Thus, it is evident from the present study that Chlorpyrifos can be a potential toxicant affecting the fishes at tissue level on dose and time dependent manner which are expected to affect the other physiological processes in the long run.

scholarly journals Effect of saponin on mortality and histopathological changes in mice

2000 ◽  
Vol 6 (2-3) ◽  
pp. 345-351
Author(s):  
F. H. Diwan ◽  
I. A. Abdel Hassan ◽  
S. T. Mohammed
Keyword(s):  
Small Intestine ◽  
Acute Toxicity ◽  
Large Intestine ◽  
Lethal Dose ◽  
Renal Tubules ◽  
Histopathological Changes ◽  
Citrullus Colocynthis ◽  
Histological Changes ◽  
Liver And Kidney ◽  
Histopathological Effects

We evaluated the acute toxicity and histopathological effects of saponin [extracted from the plant Citrullus colocynthis] on mice in order to assess its safety. The median lethal dose [LD50]of the saponin was 200 mg/kg. The histological changes were confined to the small intestine, liver and kidney, whereas the stomach, large intestine and heart appeared normal. The changes in the small intestine included haemorrhage and erosion of the mucosa. In addition, hepatorenal damage resulted from necrosis of liver cells and renal tubules

Toxic effects of sub lethal concentration of dioctyl phthalate on the histology of liver of Clarias batrachus (Linn.).

2016 ◽  
Vol 5 (09) ◽  
pp. 4874
Author(s):  
Manisha Satpathi* ◽  
Ravinder Singh
Keyword(s):  
Acute Toxicity ◽  
Light Microscopy ◽  
Dioctyl Phthalate ◽  
Clarias Batrachus ◽  
Fresh Water Fish ◽  
Histopathological Changes ◽  
Histological Changes ◽  
Water Fish ◽  
Toxicity Effects ◽  
Plastic Products

Dioctyl phthalate (DOP) commonly used as plasticizer enters into aquatic environment from the industries manufacturing plastic products, PVC resins, cosmetics and many other commercial products. Therefore, this study was designed to evaluate the acute toxicity effects of Dioctyl phthalate on fresh water fish Clarias batrachus. The 96 hour LC50 of Dioctyl phthalate in Clarias batrachus was estimated as 14.5ml/L. Histopathological changes in liver of Clarias batrachus were determined by exposing them to a fraction of LC50(1/5th) dose with every change of water for 30 days.The liver of Clarias batrachus was excised at every interval of 30 days and histological changes of liver were studied under light microscopy. Liver tissues showed abnormalities. Centrilobular vacuolation, necrosis, eccentric nuclei and enlarged nuclei, Centrilobular degeneration of hepatocytes were observed in liver tissue of fish.

scholarly journals Arsenic induced genotoxic and histopathological changes in male Swiss albino mice, Mus musculus

2011 ◽  
Vol 3 (2) ◽  
pp. 329-339
Author(s):  
Animesh K. Mohapatra ◽  
Deepika Rai ◽  
Anika Tyagi
Keyword(s):  
Arsenic Trioxide ◽  
Mus Musculus ◽  
Seminiferous Tubules ◽  
Histopathological Changes ◽  
Histological Changes ◽  
Hydropic Degeneration ◽  
Swiss Albino Mice ◽  
Cytoplasmic Vacuolization ◽  
Liver And Kidney ◽  
Albino Mice

The present study was carried out to investigate the effect of arsenic trioxide on the DNA and histomorphology of testis, liver and kidney of Swiss albino mice, Mus musculus. Oral administration of arsenic trioxide induced DNA damage in the testis, liver and kidney marked by light pink staining of nuclei after Feulgen’s reaction with reduced fine chromatin. Simultaneously severe histological changes were noted like distortion of seminiferous tubules, disorganization of spermatogonia, spermatocytes and spermatids with cytoplasmic vacuolization and nuclear pycnosis in testis. There was almost disappearance of sinusoids due to disruption of hepatic plates, inflammatory cellular infiltration around central veins and cytoplasmic vacuolization in hepatocytes with large irregular nuclei in liver of treated mice. Disorganized glomeruli with distorted Bowman’s capsules and mild to severe multifocal cloudy and hydropic degeneration with necrosis of tubules were observed in the kidney of treated mice. Inference drawn from the study indicated that arsenic induced both genotoxic histotoxic lesions.

scholarly journals Prophylactic effect of vitamin E against hepatotoxicity, nephrotoxicity, haematological indices and histopathology induced by diazinon insecticide in mice

2009 ◽  
Vol 55 (3) ◽  
pp. 219-226 ◽  
Author(s):  
Nahla S. El-Shenawy ◽  
Rasha A. Al-Eisa ◽  
Fawzia El-Salmy ◽  
Omema Salah
Keyword(s):  
Body Weight ◽  
Vitamin E ◽  
Kidney Function ◽  
Kidney Tissue ◽  
The Body ◽  
High Dose ◽  
Protective Effects ◽  
Histopathological Changes ◽  
Liver And Kidney ◽  
Haematological Indices

Abstract Considering that the involvement of reactive oxygen species (ROS) has been implicated in the toxicity of various pesticides, this study was designed to study the ameliorative effect of Vitamin E (100 mg/kg body weight) on mice (25 - 30 mg) treated with diazinon (32.5 or 16.25 mg/kg body weight) organophosphate insecticide for 14 days. Subchronic DZN exposure and the protective effects of vitamins E (vitE) were evaluated for their effects on haematological indices, the enzymes concerning liver damage [plasma alanine aminotransferase (ALT), aspartate aminotaransferase (AST), alkaline phosphatise (AIP), and some parameters of kidney function (urea and creatinine) in mice. Additionally, the histopathological changes in liver and kidney tissue were examined. The high dose of diazinon (DZNH) decreased the body weight significantly at the end of experiment. Additionally, the liver and kidney were examines for histopathological changes. The high dose of diazinon decreased body weight significantly. Moreover, there was a statistically significant decrease in haemoglobin (Hb), red blood cell (RBC) and hematocrit (Hct) in diazinon-treated mice compared to controls. This decrease was partially remedied in the diazinon-treated group that also received vitE. Damage in the liver and kidney tissues was also evident as elevated plasma ALT, AST, ALP, urea and creatinine. VitE partially counteracts the toxic effect of DZN and repairs tissue damage in the liver and kidney, especially when supplemented to 1/4 LD50 intoxicated animals. Histopathological changes in liver and kidney were observed only in 32.5 mg/kg DZN given group. These results suggest that the effects of DZN are dose dependent. No pathological findings were observed in vitE + DZN treated groups. According to the present study, we conclude that vitE can reduce the detrimental impacts of diazinon on haematological indicies, as well as liver and kidney function.

scholarly journals Histopathological changes in gills and liver of Clarias gariepinus fingerlings exposed to acute concentrations of dry cell battery

2021 ◽  
Vol 19 (1) ◽  
pp. 26-33
Author(s):  
B.S. Audu ◽  
M. Damshit ◽  
J.O. Omirinde ◽  
I.A. Wakawa ◽  
Y. Sulaiman ◽  
...  
Keyword(s):  
Acute Toxicity ◽  
Clarias Gariepinus ◽  
Water Soluble ◽  
African Catfish ◽  
Histopathological Changes ◽  
Secondary Lamellae ◽  
Freshwater Habitats ◽  
Indiscriminate Disposal ◽  
Dry Cell ◽  
Soluble Fractions

Waste dry cell batteries are frequently improperly disposed and subsequently washed into water bodies-- causing deleterious effects on fish particularly Clarias gariepinus which inhabits diverse freshwater habitats. Acute toxicity of water-soluble fractions of waste dry cell batteries was investigated on C. gariepinus fingerlings under laboratory conditions in 96 hours. Ten (10) C. gariepinus fingerlings were exposed to acute concentrations (0.31, 0.63, 1.25, 2.50, and 5.00 g/L) of waste dry cell batteries and a control (0.00 g/L), each duplicate replicated. Histopathological alterations  evident in the gills were lamellar fusion, hyperplasia, inter-lamella space occlusion, hypertrophy and erosion of secondary lamellae. The liver showed nuclear and hepatocytes degeneration, vacuolation and portal congestion. Acute concentrations of water-soluble fractions of waste dry cell batteries caused significant (P<0.05) changes in the histomorphology of the gills and liver of C. gariepinus fingerlings, therefore indiscriminate disposal of waste dry cell batteries around riparian ecosystem should be safeguarded to reduce the declining diversity and abundance of freshwater fish species. Keywords: African catfish, 96 hr.LC50, Fingerlings, Histopathology Zinc-carbon battery

scholarly journals Single Oral Acute Toxicity of Banhasasim-Tang and Its Antiobesity Effect on Diet-Induced Obese Mice and 3T3-L1 Adipocytes

2018 ◽  
Vol 2018 ◽  
pp. 1-9 ◽  
Author(s):  
Sae-Rom Yoo ◽  
Soo-Jin Jeong ◽  
Mee-young Lee ◽  
Hyeun-Kyoo Shin ◽  
Chang-Seob Seo ◽  
...  
Keyword(s):  
Body Weight ◽  
Weight Gain ◽  
Acute Toxicity ◽  
Body Weight Gain ◽  
Clinical Signs ◽  
The Body ◽  
Dependent Manner ◽  
Obese Mice ◽  
Triglyceride Accumulation ◽  
Sd Rats

We had tested antiobesity effect of 52 traditional herbal formulas in 3T3-L1 adipocyte, and Banhasasim-tang (BHSST) was chosen as one of the effective medications to inhibit triglyceride accumulation. We investigated the antiobesity effect of BHSST on 3T3-L1 adipocytes and high-fat diet- (HFD-) induced obese mice. In addition, we evaluated the acute toxicity of BHSST in Sprague Dawley (SD) rats. Differentiated 3T3-L1 cells were treated with various concentrations of BHSST for 8 days. Accumulated triglyceride level and the expressions of adipogenesis-related genes and proteins were subsequently investigated. To evaluate the single oral toxicity of BHSST, the SD rats of each sex were administered a single dose (5000 mg/kg) of BHSST via oral gavage; the control group received vehicle only. After a single administration, the mortality, clinical signs, gross findings, and body weight were monitored for 15 days. Male C57BL/6J mice were fed HFD for 4 weeks to induce obesity and randomly received 50 mg/kg of Orlistat (n=12, OR), 200 mg/kg of BHSST (n=12, B200), and 1000 mg/kg of BHSST (n=12, B1000) for another 8 weeks. BHSST suppressed the triglyceride contents and lipid accumulation in a dose-dependent manner in 3T3-L1 adipocytes. BHSST also downregulated the adipogenesis-related gene levels and protein expression compared with those in undifferentiated adipocytes. In a single oral dose toxicity study, there was no adverse effect on mortality, clinical signs, body weight changes, and gross findings in the treatment group. HFD-fed mice treated with BHSST showed significantly reduced body weight gain, food efficiency ratio, and white adipose tissue weight. The medial lethal dose (LD50) of BHSST was 5000 mg/kg/day body weight for each sex in the rats. BHSST decreased the body weight gain in HFD-fed obese mice and inhibited triglyceride accumulation via a cascade of multiple factors at the mRNA and protein levels in 3T3-L1 adipocytes.

scholarly journals Differential effects of cortisol and 11-deoxycorticosterone on ion transport protein mRNA levels in gills of two euryhaline teleosts, Mozambique tilapia (Oreochromis mossambicus) and striped bass (Morone saxatilis)

2011 ◽  
Vol 209 (1) ◽  
pp. 115-126 ◽  
Author(s):  
Pia Kiilerich ◽  
Christian K Tipsmark ◽  
Russell J Borski ◽  
Steffen S Madsen
Keyword(s):  
Striped Bass ◽  
Morone Saxatilis ◽  
Oreochromis Mossambicus ◽  
Mitogen Activated Protein Kinase ◽  
Mrna Levels ◽  
Dependent Manner ◽  
Ion Regulation ◽  
Transcript Levels ◽  
Mozambique Tilapia

The role of cortisol as the only corticosteroid in fish osmoregulation has recently been challenged with the discovery of a mineralocorticoid-like hormone, 11-deoxycorticosterone (DOC), and necessitates new studies of the endocrinology of osmoregulation in fish. Using an in vitro gill explant incubation approach, DOC-mediated regulation of selected osmoregulatory target genes in the gill was investigated and compared with that of cortisol in two euryhaline teleosts, Mozambique tilapia (Oreochromis mossambicus) and striped bass (Morone saxatilis). The effects were tested in gills from both fresh water (FW)- and seawater (SW)-acclimated fish. Both cortisol and DOC caused an up-regulation of the Na+,K+-ATPase α1 subunit in SW-acclimated tilapia but had no effect in FW-acclimated fish. Cortisol conferred an increase in Na+,K+,2Cl− cotransporter (NKCC) isoform 1a transcript levels in FW- and SW-acclimated tilapia, whereas DOC had a stimulatory effect only in SW-acclimated fish. Cortisol had no effect on NKCC isoform 1b mRNA levels at both salinities, while DOC stimulated this isoform in SW-acclimated fish. In striped bass, cortisol conferred an up-regulation of Na+,K+-ATPase α1 and NKCC transcript levels in FW- and SW-acclimated fish, whereas DOC resulted in down-regulation of these transcripts in FW-acclimated fish. It was also found that both corticosteroids may rapidly (30 min) alter the mitogen-activated protein kinase signalling pathway in gill, inducing phosphorylation of extracellular signal-regulated kinase 1 (ERK1) and ERK2 in a salinity-dependent manner. The study shows a disparate organisation of corticosteroid signalling mechanisms involved in ion regulation in the two species and adds new evidence to a role of DOC as a mineralocorticoid hormone in teleosts.

Effect of sub-acute exposure to nickel nanoparticles on oxidative stress and histopathological changes in Mozambique tilapia, Oreochromis mossambicus

2014 ◽  
Vol 107 ◽  
pp. 220-228 ◽  
Author(s):  
Chidambaram Jayaseelan ◽  
Abdul Abdul Rahuman ◽  
Rajendiran Ramkumar ◽  
Pachiappan Perumal ◽  
Govindasamy Rajakumar ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Nickel Nanoparticles ◽  
Oreochromis Mossambicus ◽  
Acute Exposure ◽  
Histopathological Changes ◽  
Mozambique Tilapia

scholarly journals Curdione Induces Antiproliferation Effect on Human Uterine Leiomyosarcoma via Targeting IDO1

2021 ◽  
Vol 11 ◽  
Author(s):  
Chao Wei ◽  
Donghua Li ◽  
Yu Liu ◽  
Wenna Wang ◽  
Tiantian Qiu
Keyword(s):  
Xenograft Model ◽  
The Body ◽  
Uterine Leiomyosarcoma ◽  
Dependent Manner ◽  
Tumor Weight ◽  
Indoleamine 2 ◽  
Traditional Chinese Herbal Medicine ◽  
Liver And Kidney

ObjectivesCurdione is one of the active ingredients of a traditional Chinese herbal medicine-Curcuma zedoary and established anti-tumor effects. Uterine leiomyosarcoma (uLMS) is a rare gynecological malignancy, with no standard therapeutic regimen at present. The aim of this study was to explore the potential anti-tumor impact of curdione in uLMS and elucidate the underlying mechanisms.MethodsIn vitro functional assays were performed in the SK-UT-1 and SK-LMS-1 cell lines. The in vivo model of uLMS was established by subcutaneously injecting SK-UT-1 cells, and the tumor-bearing mice were intraperitoneally injected with curdione. Tumor weight and volume were measured at specific time points. The biosafety was evaluated by monitoring changes of body weight and the histopathology in the liver and kidney. The expression levels of relevant proteins were analyzed by western blotting and immunohistochemistry.ResultsCurdione decreased the viability and proliferation of uLMS cells in a concentration and time-dependent manner. In addition, the curdione-treated cells exhibited significantly higher rates of apoptosis and autophagic death. Curdione also decreased the tumor weight and volume in the SK-UT-1 xenograft model compared to the untreated control without affecting the body bodyweight or pathological injury of liver and kidney tissues. At the molecular level, the anti-tumor effects of curdione were mediated by indoleamine-2, 3-dioxygenase-1 (IDO1).ConclusionCurdione exhibited an anti-uLMS effect in vitro and in vivo; the underlying mechanism involved in IDO1 mediate apoptosis, autophagy, and G2/M phase arrest.

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