scholarly journals Improved method for diagnosis of Nerium oleander poisoning in necropsy tissues

2018 ◽  
Vol 38 (5) ◽  
pp. 967-972 ◽  
Author(s):  
Ana F.M. Botelho ◽  
Fabiano A.S. Oliveira ◽  
Aparecida T.L. Fiúza ◽  
Heloísa P. Pedroza ◽  
Stephanie E.M.T. Branco ◽  
...  
Keyword(s):  
Guinea Pigs ◽  
Chromatographic Analysis ◽  
Nerium Oleander ◽  
Control Group ◽  
Improved Method ◽  
Tissue Samples ◽  
Modified Quechers ◽  
The World ◽  
Cardioactive Glycosides

ABSTRACT: Nerium oleander is an ornamental cardiotoxic plant found in tropical and subtropical areas of the World. Its toxicity is related to the content of cardioactive glycosides, mainly oleandrin, found throughout the plant. The present study aimed to describe a new and improved method for oleandrin detection in tissue samples. The determination of oleandrin was made after extraction with a modified QuEChERS technique and measurement by UFLC-MS/MS. A total of 36 guinea pigs (Cavia porcellus) were distributed into 3 groups (n=12): control group that received only water orally (CON), and two treated groups that received hydroalcoholic oleander extract at doses of 150mg.kg-1 (OLE 150) and 300mg.kg-1 (OLE 300) in single oral dose. After three hours, fragments of heart, kidneys, liver and brain were collected for determination of oleandrin levels. The extraction and chromatographic procedures were effective for oleandrin detection and quantification in tissues, with retention time of 1.2 min and detection limit of 0.001μg g-1. The chromatographic analysis of treated guinea pigs indicated that oleandrin is distributed equally among the analyzed tissues. The developed methodology is a reliable, effective and rapid form of diagnosis of N. oleander poisoning based on necropsy tissue samples.

An Ancillary Tool for the Diagnosis of Amyloid A Amyloidosis in a Variety of Domestic and Wild Animals

2005 ◽  
Vol 42 (2) ◽  
pp. 132-139 ◽  
Author(s):  
S. Shtrasburg ◽  
R. Gal ◽  
E. Gruys ◽  
S. Perl ◽  
B. M. Martin ◽  
...  
Keyword(s):  
Guinea Pigs ◽  
Polyacrylamide Gel Electrophoresis ◽  
Amyloid Deposit ◽  
Wild Animals ◽  
Aa Amyloidosis ◽  
Tissue Samples ◽  
Amyloid A ◽  
Congo Red Staining ◽  
Species Specific

Immunohistochemistry, the standard method for diagnosing amyloid A (AA) amyloidosis, is limited in animals because it requires a large array of animal-specific anti-AA antibodies, not commercially available. The Shtrasburg method (SH method) is a highly specific and sensitive technique, helping in the diagnosis and determination of AA amyloidosis in humans. The aim of this study is to determine whether the SH method is applicable in the diagnosis of AA amyloidosis in a variety of animals. Tissue samples were obtained from animals suffering from spontaneous or experimentally induced AA amyloidosis (mice, hamsters, guinea pigs, cheetahs, cats, cows, ducks, a dog, a goose, a chicken, and a turaco). Detection of the amyloid and quantitative evaluation were performed using Congo red staining, and specific AA typing was performed by the potassium permanganate technique. The studied tissues were subjected to the SH method, which confirmed the AA nature of the amyloid deposit, by displaying in polyacrylamide gel electrophoresis protein bands consistent with the molecular weight of the species-specific AA, in all the animals examined, except mice, hamsters, and guinea pigs. N-terminal analysis of these bands corroborated their AA origin. We conclude that the SH method may be used as an ancillary simple tool for the diagnosis of AA amyloidosis in a large number of domestic and wild animals. Moreover, our findings further increase the feasibility of applying this method in humans.

scholarly journals Development of an Improved Method of Sample Extraction and Quantitation of Multi-Mycotoxin in Feed by LC-MS/MS

Toxins ◽  
2020 ◽  
Vol 12 (7) ◽  
pp. 462 ◽  
Author(s):  
Bahar Nakhjavan ◽  
Nighat Sami Ahmed ◽  
Maryam Khosravifard
Keyword(s):  
Proficiency Tests ◽  
Improved Method ◽  
Salting Out ◽  
Modified Quechers ◽  
Sample Extraction ◽  
Z Scores ◽  
Safe Approach ◽  
Preparation Techniques ◽  
Validation Experiments

A multi-mycotoxin chromatographic method was developed and validated for the simultaneous quantitation of aflatoxins (AFB1, AFB2, AFG1 and AFG2), ochratoxin A (OTA), zearalenone (ZON), deoxynivalenol (DON), nivalenol (NIV), diacetoxyscirpenol (DAS), fumonisins (FB1, FB2 and FB3), T-2 toxin (T-2) and HT-2 toxin (HT-2) in feed. The three most popular sample preparation techniques for determination of mycotoxins have been evaluated, and the method with highest recoveries was selected and optimized. This modified QuEChERS (quick, easy, cheap, effective, rugged and safe) approach was based on the extraction with acetonitrile, salting-out and cleanup with lipid removal. A reconstitution process in methanol/water was used to improve the MS responses and then the extracts were analyzed by LC-MS/MS. In this method, the recovery range is 70–100% for DON, DAS, FB1, FB2, FB3, HT-2, T-2, OTA, ZON, AFG1, AFG2, AFB1 and AFB2 and 55% for NIV in the spike range of 2–80 µg/kg. Method robustness was determined with acceptable z-scores in proficiency tests and validation experiments.

scholarly journals Development of Leishmania (Mundinia) in guinea pigs

2019 ◽  
Author(s):  
Tomáš Bečvář ◽  
Padet Siriyasatien ◽  
Paul Bates ◽  
Petr Volf ◽  
Jovana Sádlová
Keyword(s):  
Guinea Pigs ◽  
Model Organism ◽  
Model Organisms ◽  
Control Group ◽  
Post Inoculation ◽  
Sand Flies ◽  
Tissue Samples ◽  
Wild Mammals ◽  
Reservoir Hosts ◽  
Lutzomyia Migonei

Abstract BackgroundLeishmaniasis is a human and animal disease caused by parasites of the genus Leishmania, which is now divided into 4 subgenera – L. (Leishmania), L. (Viannia), L. (Sauroleishmania) and L. (Mundinia). Subgenus Mundinia, established in 2016, is geographically widely dispersed, its distribution covers all continents, except Antarctica. It consists of 5 species - L. enriettii and L. macropodum are parasites of wild mammals while L. martiniquensis, L. orientalis and unnamed L. sp. from Ghana are infectious to humans. There is very little information on natural reservoir hosts and vectors for any Mundinia species. MethodsExperimental infections of guinea-pigs with all five Mundinia species were performed. Animals were injected intradermally with 107 culture-derived promastigotes into both ear pinnae. The courses of infections were monitored weakly; xenodiagnoses were performed at weeks 4 and 8 post infection using Lutzomyia migonei. The distribution of parasites in different tissues was determined post mortem by conventional PCR.ResultsNo significant differences in weight were observed between infected animals and the control group. Animals infected with L. enriettii developed temporary lesions at the site of inoculation and were infectious to Lu. migonei in xenodiagnoses. Animals infected with L. martiniquensis and L. orientalis developed temporary erythema and dry lesions at the site of inoculation, respectively, but were not infectious to sand flies. Guinea pigs infected by L. macropodum and L. sp. from Ghana showed no signs of infection during experiments, were not infectious to sand flies and leishmanial DNA was not detected in their tissue samples at the end of experiments at week 12 post-inoculation.ConclusionsAccording to our results, guinea pigs are not an appropriate model organism for studying Mundinia species other than L. enriettii. We suggest that for better understanding of L. (Mundinia) biology it is necessary to focus on other model organisms.

scholarly journals ОСОБЛИВОСТІ ІМУННОГО ГОМЕОСТАЗУ В ДИНАМІЦІ РОЗВИТКУ ЕКСПЕРИМЕНТАЛЬНОЇ БРОНХІАЛЬНОЇ АСТМИ

2018 ◽  
Author(s):  
M. S. Reheda ◽  
L. A. Lubinets ◽  
B. F. Shchepanskyi
Keyword(s):  
Immune System ◽  
B Lymphocytes ◽  
Immune Complexes ◽  
Guinea Pigs ◽  
Circulating Immune Complexes ◽  
System Response ◽  
Control Group ◽  
Modeling Process ◽  
Immune System Response

In this paper, it is shown that the modeling process of bronchial asthma (BA ) is accompanied by changes, in comparison with the control group, in the indicators of immune system response: T- & B-lymphocytes, circulating immune complexes in blood of guinea pig males on the 4th, 18th, 25th day of experiment.The aim of the study – determination of some indices of immune system in blood of guinea pigs in the modeling process of BA on 4th, 18th, 25th day of the experiment.Materials and Methods. Experiments were conducted on 40 guinea pigs (males), with body weight 0.25–0.27 kg. Animals were divided into four groups of ten animals in each. Intact guinea pigs were the first group. Animals with experimental BA – the second, third, fourth group respectively on the 4th, 18th, 25th day of the experiment. Experimental BA was reproduced by V. I. Babych method. In blood of intact guinea pigs and animals with experimental BA , the number of T- and B-lymphocytes was determined by the method of E. F. Chernushenko, L. S. Kohosov, determination of the level of circulating immune complexes was carried out by the method of V. Haskova and co-authors. The results of the study were processed by the method of variation statistics using Student's criterion.Results and Discussion. The results of the studies showed unidirectional changes in individual parameters of the immune system, depending on the periods of the formation of BA : an increase in the number of B-lymphocytes and circulating immune complexes, a decrease in the number of T-lymphocytes for all of the studied days of the experiment.Conclusions. The obtained results indicate significant changes in the immune system parameters in the blood of experimental animals with BA and are important for understanding the pathogenesis of BA . These studies provide an opportunity to find the more perfect and effective methods of diagnosis of BA.

Role of Plasma miRNA-501 Expression Profile as a Marker of Hepatocellular Carcinoma (HCC) Progression With Hepatitis C Virus Infection

2019 ◽  
Vol 152 (Supplement_1) ◽  
pp. S134-S134
Author(s):  
Mohamed Shedid ◽  
Mohamed Abdelmonem ◽  
Ayman Boraik ◽  
Alaa Elmetwalli ◽  
Ahmed Esmael
Keyword(s):  
Rna Extraction ◽  
Control Group ◽  
Hepatitis C Virus Infection ◽  
Rt Pcr ◽  
The World ◽  
Noninvasive Biomarker ◽  
Biological Aspects ◽  
Plasma Mirna

Abstract Introduction HCV is a health problem that confronts many countries in the world. Those patients will develop complications like cirrhosis and HCC, which is one of the most common cancers in the world, especially in Egypt, and considered the third leading cause of death worldwide. The prognosis of HCC is still dismal due to the late diagnosis. miRNAs are small, short noncoding RNAs, which have roles in the diagnosis of HCC. In our study, we focus on biological aspects of miRNAs. We report that miR-501 is strongly expressed and observed in the process of HCC development. miR-501 regulation is important as an oncofetal relevant to the diagnosis of HCC. Method This study was conducted on 100 adult patients; 25 patients were positive for anti-HCV and 25 patients were negative for HCV and enrolled as a control group. Patients were categorized into three groups: fibrosis (n = 25), CHC (n = 25), and HCC (n = 25) related to HCV evident by CT abdomen. All patients and controls were subjected to full clinical assessment and laboratory investigation. Blood (8 mL) was withdrawn from subjects, and 3 mL was collected in EDTA tubes for processing total RNA extraction and miRNA. The remaining 5 mL was left for determination of biochemical parameters. miRN-501 expression levels were determined by RT-PCR. Results The data revealed a significant increase in levels of AST, ALT, ALP, and CBC in both HCC and CHC groups compared to controls. The results of miRNA expression showed that miR-501 was higher in the HCC group than non-HCC group at P1.1. Conclusion miR-501 can be used as a noninvasive biomarker for early diagnosis of HCC among patients with HCV on account of its affectability for HCC.

Evaluation of intra-testicular injections of calcium chloride and 4-vinylcyclohexene 1,2 monoepoxide for chemical sterilization in guinea pigs

2017 ◽  
Vol 20 (2) ◽  
pp. 251-260 ◽  
Author(s):  
C.C. Sen ◽  
N. Yumusak ◽  
R. Faundez ◽  
F. Temamogullari ◽  
A. Taskin
Keyword(s):  
Calcium Chloride ◽  
Guinea Pigs ◽  
Histopathological Examination ◽  
Sperm Count ◽  
Physiological Saline ◽  
Good Alternative ◽  
Control Group ◽  
Tunel Staining ◽  
Tissue Samples ◽  
Group V

Abstract This study was aimed at investigating the use of intra-testicular calcium chloride (CaCl2) and 4-vinylcyclohexene 1,2-monoepoxide (VCM) injections as a side effect-free alternative method for the control of reproduction in guinea pigs. Fifty male guinea pigs were randomly assigned to five groups. In all groups, the chemical agents were injected into both testes in 1% lidocaine hydrochloride. While Groups I, II and III were administered with a single dose (0.25 mL) of sterile physiological saline, 15 mg/100 g CaCl2, and 240 mg/kg VCM, respectively, Group IV and V received a daily dose of 15 mg/100 g CaCl2, and 240 mg/kg VCM for 3 days, respectively. On day 90 post-administration, all animals were weighed and later decapitated under ether anaesthesia. Blood and tissue (testis, liver, hypophysis and adrenal gland) samples were taken. Sperm samples from the cauda epididymis were examined for spermatological parameters. Blood was used for hormone analyses and tissue samples were examined histopathologically (haematoxylin-eosin) and immunohistochemically (Tunel staining). The epididymal sperm count decreased in all treatment groups. Excluding 2 animals, Group V displayed azoospermia. When compared to the control group, Group V displayed the highest prolactin and lowest testosterone levels, and Group III showed the highest testosterone level. Histopathological examination revealed no intoxication finding. Chemical castration with VCM may be a good alternative to surgical castration as it enables mass sterilization without postoperative risks in guinea pig.

Determination of succinyldicholine in different tissue samples from guinea pigs after injection of a single intravenous dose

1986 ◽  
Vol 32 (3) ◽  
pp. 171-178 ◽  
Author(s):  
D. Malthe-Sørenssen ◽  
E. Odden ◽  
J. Blanch ◽  
A. Bugge ◽  
J. Mørland
Keyword(s):  
Guinea Pigs ◽  
Intravenous Dose ◽  
Single Intravenous Dose ◽  
Tissue Samples

scholarly journals Development of Leishmania (Mundinia) in guinea pigs

2020 ◽  
Author(s):  
Tomáš Bečvář ◽  
Padet Siriyasatien ◽  
Paul Bates ◽  
Petr Volf ◽  
Jovana Sádlová
Keyword(s):  
Guinea Pigs ◽  
Model Organism ◽  
Model Organisms ◽  
Control Group ◽  
Sand Flies ◽  
Animal Disease ◽  
Tissue Samples ◽  
Wild Mammals ◽  
Reservoir Hosts ◽  
Lutzomyia Migonei

Abstract Background: Leishmaniasis is a human and animal disease caused by parasites of the genus Leishmania, which is now divided into 4 subgenera – L. (Leishmania), L. (Viannia), L. (Sauroleishmania) and L. (Mundinia). Subgenus Mundinia, established in 2016, is geographically widely dispersed, its distribution covers all continents, except Antarctica. It consists of 5 species - L. enriettii and L. macropodum are parasites of wild mammals while L. martiniquensis, L. orientalis and unnamed L. sp. from Ghana are infectious to humans. There is very little information on natural reservoir hosts and vectors for any Mundinia species. Methods: Experimental infections of guinea-pigs with all five Mundinia species were performed. Animals were injected intradermally with 107 culture-derived promastigotes into both ear pinnae. The courses of infections were monitored weekly; xenodiagnoses were performed at weeks 4 and 8 post infection using Lutzomyia migonei. The distribution of parasites in different tissues was determined post mortem by conventional PCR.Results: No significant differences in weight were observed between infected animals and the control group. Animals infected with L. enriettii developed temporary lesions at the site of inoculation and were infectious to Lu. migonei in xenodiagnoses. Animals infected with L. martiniquensis and L. orientalis developed temporary erythema and dry lesions at the site of inoculation, respectively, but were not infectious to sand flies. Guinea pigs infected by L. macropodum and L. sp. from Ghana showed no signs of infection during experiments, were not infectious to sand flies and leishmanial DNA was not detected in their tissue samples at the end of experiments at week 12 post-inoculation.Conclusions: According to our results, guinea pigs are not an appropriate model organism for studying Mundinia species other than L. enriettii. We suggest that for better understanding of L. (Mundinia) biology it is necessary to focus on other model organisms.

scholarly journals Coronaphobia in Patients With Fibromyalgia.

2020 ◽  
Author(s):  
Sevinc Kulekcioglu ◽  
Merve Akyüz ◽  
Özenç İnan ◽  
Alp Çetin
Keyword(s):  
Mental Health ◽  
Chronic Disease ◽  
Mental Health Problems ◽  
Daily Life ◽  
Specific Phobia ◽  
Control Group ◽  
Sociodemographic Data ◽  
Global Pandemic ◽  
The World

Abstract Background: Throughout the world, the coronavirus disease (COVID-19) pandemic has had a significant effect on human health and daily life. Recent data in literature showed that the COVID-19 pandemic has increased mental health problems. One of these problems, including specific phobia called as “coronaphobia”. The aim of this study was to measure the level of specific phobia created by the COVID-19 pandemic in fibromyalgia (FMS) patients, and to compare this with levels of coronaphobia in patients without FMS.Results: Sixty-one patients participated in the study. Thirty patients diagnosed with fibromyalgia were included in the fibromyalgia group and 31 patients without a diagnosis of fibromyalgia in the control group. The sociodemographic data of all the patients and the presence of chronic disease were determined. All the patients in both groups were instructed to complete the COVID-19 Phobia Scale (C19P-S). The C19PS total score and psychological, psychosomatic, social, and economic subgroups scores were determined to be statistically significantly higher in the FMS group than in the control group (23.2 vs 16.3, 10.9 vs 7.1, 18.4 vs 12.1, and 10.5 vs 6.5 respectively).Conclusion: The results of this study demonstrated that FMS patients have more concerns in this extraordinary global pandemic situation. Early determination of COVID-19 phobia in individuals predisposed to psychological disorders, such as those with FMS, must be kept in mind in respect of providing timely psychological support and being able to keep the disease under control.

scholarly journals Development of Leishmania (Mundinia) in guinea pigs

2020 ◽  
Author(s):  
Tomáš Bečvář ◽  
Padet Siriyasatien ◽  
Paul Bates ◽  
Petr Volf ◽  
Jovana Sádlová
Keyword(s):  
Guinea Pigs ◽  
Model Organism ◽  
Model Organisms ◽  
Control Group ◽  
Post Inoculation ◽  
Sand Flies ◽  
Tissue Samples ◽  
Wild Mammals ◽  
Reservoir Hosts ◽  
Lutzomyia Migonei

Abstract Background: Leishmaniasis is a human and animal disease caused by parasites of the genus Leishmania , which is now divided into 4 subgenera – L. (Leishmania) , L. (Viannia) , L. (Sauroleishmania) and L. (Mundinia) . Subgenus Mundinia, established in 2016, is geographically widely dispersed, its distribution covers all continents, except Antarctica. It consists of 5 species - L. enriettii and L. macropodum are parasites of wild mammals while L. martiniquensis , L. orientalis and unnamed L . sp. from Ghana are infectious to humans. There is very little information on natural reservoir hosts and vectors for any Mundinia species. Methods: Experimental infections of guinea-pigs with all five Mundinia species were performed. Animals were injected intradermally with 10 7 culture-derived promastigotes into both ear pinnae. The courses of infections were monitored weekly; xenodiagnoses were performed at weeks 4 and 8 post infection using Lutzomyia migonei . The distribution of parasites in different tissues was determined post mortem by conventional PCR. Results: No significant differences in weight were observed between infected animals and the control group. Animals infected with L. enriettii developed temporary lesions at the site of inoculation and were infectious to Lu. migonei in xenodiagnoses. Animals infected with L. martiniquensis and L. orientalis developed temporary erythema and dry lesions at the site of inoculation, respectively, but were not infectious to sand flies. Guinea pigs infected by L. macropodum and L . sp . from Ghana showed no signs of infection during experiments, were not infectious to sand flies and leishmanial DNA was not detected in their tissue samples at the end of experiments at week 12 post-inoculation. Conclusions: According to our results, guinea pigs are not an appropriate model organism for studying Mundinia species other than L. enriettii. We suggest that for better understanding of L. (Mundinia) biology it is necessary to focus on other model organisms.

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