Effect of formaldehyde inhalation on rat livers: A light and electron microscopic study

2010 ◽  
Vol 26 (2) ◽  
pp. 113-119 ◽  
Author(s):  
Selman Cikmaz ◽  
Tunc Kutoglu ◽  
Mehmet Kanter ◽  
Recep Mesut
Keyword(s):  
Liver Tissue ◽  
Exposure Period ◽  
Electron Microscopic Level ◽  
Albino Rats ◽  
Electron Microscopic ◽  
Tissue Samples ◽  
Microscopic Evaluation ◽  
Microscopic Studies ◽  
Wistar Albino Rats ◽  
The Individual

It is well known that formaldehyde (FA) is cytotoxic and potentially carcinogenic. Although the individual effects of this reactant on cells has been investigated, the cytotoxicity exerted by the coexistence of FA is poorly understood. The aim of this study was to investigate the effects of FA on the liver in rats, by light and electron microscopic level. We used 18 Wistar albino rats divided into three groups, exposed to 0 (control), 19.7 ppm FA gas for a total of 4 weeks, 8 h/day, 5 days a week (subacute) and 20.3 parts per million (ppm) FA gas for a total of 13 weeks, 8 h/day, 5 days a week (subchronic). After the completion of the exposure period, they were sacrificed by decapitation and their liver tissue samples were taken in order to be processed for light and electron microscopic studies. Light microscopic evaluation of liver tissue samples of FA-exposed rats revealed enlarged sinusoids filled with blood and mononuclear cell infiltration in the portal areas and around the central veins. In addition, some of the hepatocytes showed loss of cytoplasm, and some had a hyperchromatic nucleus. The cells of FA-exposed livers, on the other hand, showed an electron-lucent ground-cytoplasm and a hypertrophy of the smooth-surfaced endoplasmic reticulum. In conclusion, we observed that exposure FA caused diverse histopathological changes indicating the destruction in the liver tissue and this destruction has direct relationship with the length of the exposure period.

scholarly journals Analytical electron microscopic evaluation of the effects of paraformaldehyde pretreatment on the reaction of glutaraldehyde with biogenic amines.

1982 ◽  
Vol 30 (5) ◽  
pp. 481-486 ◽  
Author(s):  
R E McClung ◽  
J Wood
Keyword(s):  
Electron Microscopy ◽  
Analytical Electron Microscopy ◽  
Microscopic Level ◽  
Electron Microscopic Level ◽  
Spectrographic Analysis ◽  
Electron Microscopic ◽  
X Ray ◽  
Microscopic Evaluation ◽  
Analytical Electron ◽  
Dense Product

Analytical electron microscopy was used to determine the quantitative effects of paraformaldehyde pretreatment on the formation of the biogenic amine-glutaraldehyde-chrome complex. Pretreatment with paraformaldehyde prevented the glutaraldehyde-chrome reaction with norepinephrine in the rat adrenal medulla. In contrast to the effect of paraformaldehyde on norepinephrine, pretreatment did not prevent the chrome reaction in serotonin-containing argentaffin cells of the gut. X-Ray energy spectrographic analysis revealed a significant decrease in chrome content in the paraformaldehyde treated tissue, but sufficient chrome did react to produce an electron-dense product. Thus by treating tissue with paraformaldehyde prior to the glutaraldehyde chrome procedure, serotonergic sites may be differentiated from catecholaminergic areas at the electron microscopic level.

Protective effects of erdosteine on rotenone-induced oxidant injury in liver tissue

2004 ◽  
Vol 20 (6-10) ◽  
pp. 141-147 ◽  
Author(s):  
Alpaslan Terzi ◽  
Mustafa Iraz ◽  
Semsettin Sahin ◽  
Atilla Ilhan ◽  
Nuri Idiz ◽  
...  
Keyword(s):  
Lipid Peroxidation ◽  
Liver Tissue ◽  
Antioxidant Properties ◽  
Albino Rats ◽  
Protective Agent ◽  
Protective Effects ◽  
Oxidant Injury ◽  
Sod Activity ◽  
Significant Difference ◽  
Wistar Albino Rats

Rotenone, an insecticide of botanical origin, causes toxicity through inhibition of complex I of the respiratory chain in mitochondria. This study was undertaken to determine whether rotenone-induced liver oxidant injury is prevented by erdosteine, a mucolytic agent showing antioxidant properties. There were four groups of Male Wistar Albino rats: group one was untreated as control; the other groups were treated with erdosteine (50 mg/kg per day, orally), rotenone (2.5 mg/mL once and 1 mL/kg per day for 60 days, i.p.) or rotenone plus erdosteine, respectively. Rotenone treatment without erdosteine increased xanthine oxidase (XO) enzyme activity and also increased lipid peroxidation in liver tissue P < 0.05). The rats treated with rotenone plus erdosteine produced a significant decrease in lipid peroxidation and XO activities in comparison with rotenone group PB / 0.05). Erdosteine treatment with rotenone led to an increase in catalase (CAT) and superoxide dismutase (SOD) activities in comparison with the rotenone group PB / 0.05). There was no significant difference in nitric oxide (NO) level between groups. There were negative correlations between CAT activity and malondialdehyde (MDA) level (r= -0.934, P <0.05) with between CAT and SOD activities (r= -0.714, P <0.05), and a positive correlation between SOD activity and MDA level (r= 0.828, P <0.05) in rotenone group. In the rotenone plus erdosteine group, there was a negative correlation between XO activity and NO level in liver tissue (r= -0.833, P -0.05). In the light of these findings, erdosteine may be a protective agent for rotenone-induced liver oxidative injury in rats.

The Ultrastructure of Crystalliferous Cells in Some Lecythidaceae With a Discussion of Their Terminology

IAWA Journal ◽  
1984 ◽  
Vol 5 (3) ◽  
pp. 229-236 ◽  
Author(s):  
N. Parameswaran ◽  
H.-G. Richter
Keyword(s):  
Electron Microscopic ◽  
Axial Parenchyma ◽  
Individual Crystal ◽  
Microscopic Studies ◽  
Per Se ◽  
The Individual

On the basis of a light microscopic c1assification of the genera of the Lecythidaceae according to the presence of crystalliferous cells in the axial wood parenchyma an attempt was made to characterise these cells at the fine structurallevel. Electron microscopic studies of the genera Allantoma, Grias and Gustavia revealed normal cross walls, as well as septumIike walls separating the individual crystal-containing units in the axial parenchyma strand. Based on these findings the terminology of the crystalliferous cells per se is discussed at some length.

scholarly journals Differential localizations of and requirements for the two Drosophila ninaC kinase/myosins in photoreceptor cells.

1992 ◽  
Vol 116 (3) ◽  
pp. 683-693 ◽  
Author(s):  
J A Porter ◽  
J L Hicks ◽  
D S Williams ◽  
C Montell
Keyword(s):  
Retinal Degeneration ◽  
Photoreceptor Cells ◽  
Kinase Domain ◽  
Electron Microscopic Level ◽  
Head Region ◽  
Electron Microscopic ◽  
Myosin I ◽  
Microvillar Structure ◽  
The Difference ◽  
The Individual

The ninaC gene encodes two retinal specific proteins (p132 and p174) consisting of a protein kinase domain joined to a domain homologous to the head region of the myosin heavy chain. The putative myosin domain of p174 is linked at the COOH-terminus to a tail which has some similarities to myosin-I tails. In the current report, we demonstrate that the ninaC mutation results in light- and age-dependent retinal degeneration. We also show that ninaC flies display an electrophysiological phenotype before any discernible retinal degeneration indicating that the electrophysiological defect is the primary effect of the mutation. This suggests that ninaC has a role in phototransduction and that the retinal degeneration is a secondary effect resulting from the defect in phototransduction. To examine the requirements for the individual ninaC isoforms, mutant alleles were generated which express only p132 or p174. Elimination of p174 resulted in a ninaC phenotype as strong as the null allele; however, elimination of p132 had little if any effect. As a first step in investigating the basis for the difference in requirements for p174 and p132 we performed immuno-localization at the electron microscopic level and found that the two isoforms display different subcellular distributions in the photoreceptor cells. The p132 protein is restricted primarily to the cytoplasm and p174 to the rhabdomeres, the microvillar structure which is the site of action of many of the steps in phototransduction. This suggests that the p174 myosin-I type tail is the domain responsible for association with the rhabdomeres and that the substrate for the p174 putative kinase may be a rhabdomeric protein important in photo-transduction.

scholarly journals Scanning Electron Microscopic Studies of the Lingual Papillae in the English Horse

2016 ◽  
Vol 66 (2) ◽  
pp. 257-264 ◽  
Author(s):  
Mehmet Can ◽  
Şükrü Hakan Atalgin ◽  
Mehmet Faruk Aydin
Keyword(s):  
Electron Microscopic ◽  
Male Adult ◽  
Tissue Samples ◽  
Lingual Papillae ◽  
Cylindrical Form ◽  
Scanning Electron Microscopic ◽  
Microscopic Studies ◽  
Vallate Papillae ◽  
Filiform Papillae ◽  
Scanning Electron

Abstract The purpose of this study was to describe the distribution and surface structure of the lingual papillary system in four male adult English horses by scanning electron microscopy. The animals were supplied from the Jockey Club of Turkey (TJK). Tissue samples were taken from the dorsal, ventral and lateral surface of the apex, corpus and radix of the tongue. Filiform papillae were distributed mainly on the dorsum, being abundant, very long and with a slim cylindrical form with pointed endings or multi-bifurcated terminations at the apex. These papillae were typically conical in shape with a wider base in the corpus of the lingua and absent on the radix of the lingua. Fungiform papillae were mainly on the lateral surfaces and lobulated forms were also observed. The horses have two large vallate papillae, located on the dorsum close to the caudal part of the tongue. These papillae were surrounded by a prominent gustatory groove. The vallate papillae had many taste pores opening into the papillary groove. The foliate papillae were observed just rostral to the palatoglossal arches. These papillae have many variable sized taste pores which open into the grooves between the papillary leaves. The papillary leaves were covered with concentrically arranged cornified cells of variable appearance. However, there were no lingual papillae on the ventral aspect of the horse’s tongue.

scholarly journals Immuno-electron-microscopic studies on the subcellular distribution of rat liver epoxide hydrolase and the effect of phenobarbitone and 2-acetamidofluorene treatment

1982 ◽  
Vol 202 (3) ◽  
pp. 677-686 ◽  
Author(s):  
F Waechter ◽  
P Bentley ◽  
M Germann ◽  
F Oesch ◽  
W Stäubli
Keyword(s):  
Electron Microscopy ◽  
Rat Liver ◽  
Subcellular Distribution ◽  
Epoxide Hydrolase ◽  
Specific Binding ◽  
Subcellular Fractions ◽  
Electron Microscopic ◽  
Immuno Electron Microscopy ◽  
Microscopic Studies ◽  
The Individual

The distribution of rat liver epoxide hydrolase in various subcellular fractions was investigated by immuno-electron-microscopy. Ferritin-linked monospecific anti-(epoxide hydrolase) immunoglobulins bound specifically to the cytoplasmic surfaces of total microsomal preparations and smooth and rough microsomal fractions as well as the nuclear envelope. Specific binding was not observed when the ferritin conjugates were incubated with peroxisomes, lysosomes and mitochondria. The average specific ferritin load of the individual subcellular fractions correlated well with the measured epoxide hydrolase activities. This correlation was observed with fractions prepared from control, phenobarbitone-treated and 2-acetamidofluorene-treated rats.

scholarly journals A low direct electrical signal attenuates oxidative stress and inflammation in septic rats

PLoS ONE ◽  
2021 ◽  
Vol 16 (9) ◽  
pp. e0257177
Author(s):  
Savas Ustunova ◽  
Ebru Haciosmanoglu ◽  
Huri Bulut ◽  
Birsen Elibol ◽  
Aysu Kilic ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Antibacterial Effect ◽  
Antimicrobial Effect ◽  
Electrical Signal ◽  
Albino Rats ◽  
Histological Structure ◽  
Tissue Samples ◽  
Blood Ph ◽  
Healthy Control ◽  
Wistar Albino Rats

Electrical stimulation is proposed to exert an antimicrobial effect according to studies performed using bacterial and cell cultures. Therefore, we investigated the effects of electrification on inflammation in septic rats. Twenty-eight male Wistar albino rats were divided into 4 groups: healthy control (C), electrified healthy (E), sepsis (S), and electrified sepsis (SE) groups. Staphylococcus aureus (1 x 109 colonies) in 1 ml of medium was intraperitoneally injected into rats to produce a sepsis model. The rats in the E and SE groups were exposed to a low direct electrical signal (300 Hz and 2.5 volts) for 40 min and 1 and 6 h after bacterial infection. Immediately after the second electrical signal application, blood and tissue samples of the heart, lung, and liver were collected. An antibacterial effect of a low direct electrical signal was observed in the blood of rats. The effects of electrical signals on ameliorating changes in the histological structure of tissues, blood pH, gases, viscosity and cell count, activities of some important enzymes, oxidative stress parameters, inflammation and tissue apoptosis were observed in the SE group compared to the S group. Low direct electrical signal application exerts antibacterial, antioxidant, anti-inflammatory and antiapoptotic effects on septic rats due to the induction of electrolysis in body fluids without producing any tissue damage.

scholarly journals Ethanolic Extract of Syzygium cumini Causes Toxic Effects on Ethanol-induced Liver and Kidney Damage in Albino Wistar Rats: A Biochemical and Histological Study

2022 ◽  
Vol 16 (1) ◽  
pp. 63-72
Author(s):  
Abba Aji Manu ◽  
◽  
Bello Muhammad Musa ◽  
Martha Orendu Oche Attah ◽  
Helga Ishaya Bedan ◽  
...  
Keyword(s):  
Histological Study ◽  
Kidney Tissue ◽  
Ethanolic Extract ◽  
Albino Rats ◽  
Syzygium Cumini ◽  
Tissue Samples ◽  
Inflammatory Conditions ◽  
Therapeutic Value ◽  
Liver And Kidney ◽  
Wistar Albino Rats

Background: The therapeutic value of Syzygium cumini (S. cumini) has been documented in traditional medicine for the treatment of many diseases and ailments. Various preparations of this plant have been made and used especially for liver inflammatory conditions in livestock. Further, many liver diseases in humans are inflammatory conditions, which are caused by alcohol intake. This study sought to examine the effect of S. cumini on ethanol-induced hepatotoxicity in Wistar albino rats. Methods: Twenty-five rats were divided into five groups of five rats each. The first group was control and the other four were administered ethanol at varying doses to induce liver and kidney damages. Two doses of the S. cumini extract were administered at a concentration of 200 mg/kg or 400 mg/kg. Silymarin was administered to the last group at 10 mg/kg. The liver and kidney tissue samples were collected and preserved for histological analyses and the rat sera were analyzed for the associated biochemical biomarkers. Results: Histopathological analyses revealed pyknotic nuclei and distortion in the arrangement of the hepatocytes in extract-treated groups. The kidney tissue samples showed signs of interstitial bleeding and aggregation of lymphocytes in the peri-glomerular areas. The analyses of the biochemical parameters revealed that there were significant increases in the aspartate aminotransferase (AST), alanine transaminase (ALT), Urea and creatinine in the sera of the groups treated with the extract compared to those of the controls (P<0.05). Conclusion: The S. cumini extract caused elevation of serum hepatic and renal biomarkers at 400 mg/kg and did not have a hepatoprotective effect.

scholarly journals THE EFFECT OF PRETREATMENT WITH TOLL-LIKE RECEPTOR 4 ANTAGONIST RESATORVID ON METHOTREXATE-INDUCED LIVER INJURY IN RATS: HISTOPATHOLOGICAL STUDY

2018 ◽  
Vol 11 (12) ◽  
pp. 560
Author(s):  
Bassim I Mohammad ◽  
Bassim S Ahmed ◽  
Alaa F Hassan ◽  
Samer F Hassan
Keyword(s):  
Liver Tissue ◽  
Inflammatory Cells ◽  
Fatty Degeneration ◽  
Treated Group ◽  
Control Group ◽  
Histopathological Study ◽  
Tissue Samples ◽  
Alcoholic Fatty Liver ◽  
Tissue Sections ◽  
Microscopic Evaluation

Objective: This research aims to evaluate the histopathological changes after pretreatment with resatorvid against methotrexate induced-liver injury.Methods: 28 male albino-wistar rats divided into random 4 groups (7 rats in each). Control group: Rats left untreated. Vehicle pre-treated group: Rats were administered dimethyl sulfoxide (DMSO) followed by methotrexate (MTX). Methotrexate treated group: Rats left untreated then administered MTX. Resatorvid pre-treated group: Rats were administered resatorvid followed by MTX. 24 h after the end of treatment, the animals were sacrificed. Liver tissue samples dissected out immediately and fixed in 10% formalin. The traditional procedures (paraffin-embedded method) was used to prepare liver tissue for microscopic evaluation by none alcoholic fatty liver disease (NAFLD) Activity Score Components.Results: Liver tissue sections of MTX-treated group show moderate-to-severe steatosis of hepatic cells and micro- and macro- hepatocellular fatty degeneration and giant fatty cysts with chronic inflammatory cells infiltration. While liver tissue sections of the resatorvid pre-treated group show moderate hepatic cellular fatty degeneration, with a decreased number of fatty cysts chains and the inflammation disappeared.Conclusion: Resatorvid hepatoprotective effect against MTX-induced injury was promising throughout resolving the accompanying inflammation and partial restoring histopathological fatty alterations.

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