scholarly journals Effect of Analgesics on Monoclonal Antibody Ascites Production in Mice Administered Upon Recognition of Pain

2014 ◽  
Vol 2014 ◽  
pp. 1-8
Author(s):  
Shannon T. Marko ◽  
Stephen F. Little ◽  
Carrie G. Benton ◽  
Richard Kelly ◽  
Amy E. Field ◽  
...  
Keyword(s):  
Monoclonal Antibody ◽  
Protective Antigen ◽  
Fluid Collection ◽  
Clinical Signs ◽  
Saline Group ◽  
Ascites Fluid ◽  
Control Group ◽  
Antibody Concentration ◽  
Fluid Production ◽  
Group B

Monoclonal antibody (mAb) ascites fluid production in mice is a well described method of antibody production, although ethical questions regarding the pain and distress of the animals utilized in this process have been raised. In this study, mice were injected with pristane to initiate granuloma formation, followed by an injection of murine hybridoma PA 2II 2F9-1-1 (2F9) to produce IgG1 subclass mAb directed against protective antigen (PA) protein of Bacillus anthracis. Upon the recognition of pain or distress, characterized by well accepted clinical signs, analgesics were administered by treatment group. The control group (A) received saline, group (B) received meloxicam, group (C) received buprenorphine, and group (D) received both meloxicam and buprenorphine. Analgesics were administered by group for a total of 36–48 hours prior to the second ascites fluid collection. There was no statistical difference in the antibody titer or functionality (P>0.05) between treatment groups at the first or the second collection time points. As reported here, analgesics may be administered upon recognition of pain in mice used for mAb ascites fluid production without affecting antibody concentration or quality and may warrant further evaluation as a refinement in other hybridoma cell lines.

Histopathologic lesions in conventional pigs experimentally infected with Haemophilus parasuis serovar 5

2015 ◽  
Vol 43 (02) ◽  
pp. 91-96 ◽  
Author(s):  
R.-L. Austin-Busse ◽  
A. Ladinig ◽  
G. Balka ◽  
S. Zoels ◽  
M. Ritzmann ◽  
...  
Keyword(s):  
Clinical Signs ◽  
Control Group ◽  
Post Inoculation ◽  
Haemophilus Parasuis ◽  
Tissue Samples ◽  
Group A ◽  
Pathologic Lesions ◽  
Group B ◽  
Kidney Lesions ◽  
Challenge Group

Summary Objective: In the present study various tissues of pigs were investigated for the presence of histopathologic lesions after an experimental infection with Haemophilus (H.) parasuis serovar 5. Material and methods: Conventional pigs (n = 36) were divided into a control group B (n = 9) and a challenge group A (n = 27), which was infected intratracheally. Pigs that did not die prior to study termination were euthanized on day 14 post inoculation. Postmortem samples of the lung, heart, liver, kidney, spleen, left tarsal joint capsule and brain were collected. Results: All but one pig with detectable histopathologic lesions (n = 11) showed typical macroscopic changes. Histopatho logic examination of all tissue samples identified pyelitis (n = 10), synovitis (n = 7) and meningitis (n = 7) and all those animals were euthanized prior to study termination. No histopathologic lesions were found in pigs of the control group. The correlations between pyelitis and meningitis, pyelitis and synovitis and synovitis and meningitis were significant (p < 0.001). No significant correlation could be observed between the histopathologic and the clinical examination of the joints. The investigation of samples from the joints by PCR was not significantly correlated with the observed synovitis. The clinical observation of neurologic signs was significantly correlated with meningitis (p = 0.03). A significant correlation (p < 0.001) could be detected between meningitis and the detection of H. parasuis by PCR in brain samples. Conclusions: H. parasuis constantly causes clinical signs and pathologic lesions as soon as it infects the brain while it can infect the joints without causing histopathologic lesions. Pigs with histopathologic lesions do not always show typical clinical signs. Only few studies described the finding of kidney lesions in pigs with Glässer’s disease and this is the first study to describe a pyelitis in pigs experimentally infected with H. parasuis. The observed pyelitis mainly occurred in acute cases.

scholarly journals Study on antihyperglycemic effect of bromocriptine in dexamethasone induced hyperglycemic wistar rats

2021 ◽  
Vol 10 (6) ◽  
pp. 699
Author(s):  
Rekha M. B. ◽  
Basavaraj Bhandare ◽  
Satyanarayana V. ◽  
Hemamalini M. B.
Keyword(s):  
Diabetes Mellitus ◽  
Normal Saline ◽  
Wistar Rats ◽  
Saline Group ◽  
Control Group ◽  
Normal Saline Group ◽  
Male Wistar Rats ◽  
Group B ◽  
Control Group Group

Background: Diabetes mellitus is a chronic metabolic disorder that develops due to insulin deficiency or insulin resistance. Recent animal and human studies have reported bromocriptine to be effective in the management of type 2 diabetes mellitus. The present study was done to evaluate the antihyperglycemic effect of bromocriptine in dexamethasone induced hyperglycemic rats.Methods: Male wistar rats were used and divided into 5 groups. Dexamethosone was used to induce hyperglycemia in group B-E. Group A was the untreated control group, group B was the standard control group, group C was the oral 10 mg/kg of bromocriptine dissolved in 0.9% normal saline, group D was the oral 20 mg/kg metformin dissolved in 0.9% normal saline, group E was the oral 10 mg/kg bromocriptine+20 mg/kg metformin dissolved in 0.9% normal saline. Fasting blood glucose, post prandial blood glucose and body weight was estimated on day 1, 15, 30.Results: It was seen that dexamethasone induced hyperglycemia and increase in body weight in male wistar rats, which were significantly controlled by oral bromocriptine and bromocriptine with metformin combination.Conclusions: Results obtained from this study showed that bromocriptine can be a promising drug with novel mechanism to treat type 2 diabetes mellitus.

A Recombinant Humanized Monoclonal Antibody for Treatment of Endometriosis in a Rat Model

2011 ◽  
Vol 3 (3) ◽  
pp. 143-150
Author(s):  
Hatice Işık ◽  
Ozlem Moraloglu ◽  
Sevtap Kilic ◽  
Ali Seven ◽  
Muzaffer Caydere ◽  
...  
Keyword(s):  
Monoclonal Antibody ◽  
Rat Model ◽  
Female Rats ◽  
Control Group ◽  
Ki 67 ◽  
Beneficial Effects ◽  
Anti Vegf ◽  
Humanized Monoclonal Antibody ◽  
Group A ◽  
Group B

Aim Angiogenesis plays an important role in the pathogenesis of endometriosis. Thus, the inhibition of angiogenesis may prevent endometriosis. Bevacizumab is a recombinant humanized monoclonal antibody against VEGF. The aim of this study is to investigate the efficacy of anti-VEGF therapy on the prophylaxis and treatment of endometriotic foci in a rat model. Methods This experimental study is prospective, randomized, and placebo-controlled. Thirty-six Wistar-Albino female rats were divided into 3 groups. Experimental endometriosis was induced by the implantation of autologous endometrial tissue. The bevacizumab administration route was intraperitoneal. Group A was the prophylaxis group; Group B was the treatment group, and Group C was the control group. The volumes of the implants as well as their VEGF and Ki-67 immunohistochemical staining are main outcome measures. Results The volumes of the lesions were smaller in Group A than Group C [P<.05]. The volumes of endometriotic foci in Group B were smaller than in Group C [P<.05]. Bevacizumab caused regression and atrophy of the endometriotic lesions. After the treatment the histopathologic and immunohistochemical scores in Group B were less than before treatment and less than the scores in Group C. Conclusions Bevacizumab treatment had a regressive effect on the endometriotic implants. As an anti-VEGF agent, bevacizumab has beneficial effects on the prophylaxis and treatment of endometriosis.

PREPARATION AND EVALUATION OF AVIAN INFLUENZA (H9) AND NEWCASTLE DISEASE (THERMOSTABLE I-2 STRAIN) BIVALENT VACCINE FOR COMMERCIAL POULTRY

2020 ◽  
Vol 3 ◽  
pp. 17-23
Author(s):  
Rabia Sabir
Keyword(s):  
Avian Influenza ◽  
Newcastle Disease ◽  
Geometric Mean ◽  
Clinical Signs ◽  
Control Group ◽  
Broiler Chicks ◽  
Group A ◽  
Commercial Poultry ◽  
Group B ◽  
Preparation And Evaluation

The goal of current research was production of bivalent adjuvant based inactivated I-2 strain of Newcastle Disease (ND) and Avian Influenza (AI) vaccine and to compare efficacy with commercially available bivalent inactivated vaccine. Experiment was carried out on one-day-old broiler chicks by dividing them into 3 groups A, B & C. Vaccine was injected on 7, 14, 21 and 28 day. Blood samples were collected on 7, 14, 21, 28 and 35 day. Results of Hemagglutination Inhibition (HI) test presented the geometric mean titers of group A and B were <1:4, 1:18.8, 1:115.2, 1:358.4, 1:128 & <1:4, 1:8.4, 1:36.8, 1:56, 1:22.4 respectively for AI. Similarly the geometric mean titers of group A and B were <1:4, 1:19.6, 1:89.6, 1:320, 1:115.2 & <1:4, 1:9.2, 1:25.6, 1:36.8, 1:22.4, respectively for ND. However, control group showed <1:4 geometric mean titer. The challenge was given on 28th day and birds were monitored for next 7 days for clinical signs. The chicks of group A showed no clinical signs of diseases (AI, ND). However, in group B 60% morbidity and 90% mortality was recorded on 4th and 6th day of post challenge, respectively. While 100% mortality was recorded in control group.

scholarly journals Development of an Inhalational Bacillus anthracis Exposure Therapeutic Model in Cynomolgus Macaques

2012 ◽  
Vol 19 (11) ◽  
pp. 1765-1775 ◽  
Author(s):  
Lisa N. Henning ◽  
Jason E. Comer ◽  
Gregory V. Stark ◽  
Bryan D. Ray ◽  
Kevin P. Tordoff ◽  
...  
Keyword(s):  
Monoclonal Antibody ◽  
Bacillus Anthracis ◽  
Protective Antigen ◽  
Lethal Dose ◽  
Clinical Signs ◽  
Cynomolgus Macaque ◽  
Content Type ◽  
Clinical Observations ◽  
Medical Countermeasures ◽  
Therapeutic Model

ABSTRACTAppropriate animal models are required to test medical countermeasures to bioterrorist threats. To that end, we characterized a nonhuman primate (NHP) inhalational anthrax therapeutic model for use in testing anthrax therapeutic medical countermeasures according to the U.S. Food and Drug Administration Animal Rule. A clinical profile was recorded for each NHP exposed to a lethal dose ofBacillus anthracisAmes spores. Specific diagnostic parameters were detected relatively early in disease progression, i.e., by blood culture (∼37 h postchallenge) and the presence of circulating protective antigen (PA) detected by electrochemiluminescence (ECL) ∼38 h postchallenge, whereas nonspecific clinical signs of disease, i.e., changes in body temperature, hematologic parameters (ca. 52 to 66 h), and clinical observations, were delayed. To determine whether the presentation of antigenemia (PA in the blood) was an appropriate trigger for therapeutic intervention, a monoclonal antibody specific for PA was administered to 12 additional animals after the circulating levels of PA were detected by ECL. Seventy-five percent of the monoclonal antibody-treated animals survived compared to 17% of the untreated controls, suggesting that intervention at the onset of antigenemia is an appropriate treatment trigger for this model. Moreover, the onset of antigenemia correlated with bacteremia, and NHPs were treated in a therapeutic manner. Interestingly, brain lesions were observed by histopathology in the treated nonsurviving animals, whereas this observation was absent from 90% of the nonsurviving untreated animals. Our results support the use of the cynomolgus macaque as an appropriate therapeutic animal model for assessing the efficacy of medical countermeasures developed against anthrax when administered after a confirmation of infection.

scholarly journals Time-Dependent Testicular and Epididymal Damage in Rabbit Bucks Experimentally Infected with Trypanosoma brucei brucei

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Adewale Ayodeji Adeyeye ◽  
Musbaudeen Olayinka Alayande ◽  
Monsurat Bansima Adio ◽  
Lauratu Lawal Haliru ◽  
Aliyu Abdulrafiu
Keyword(s):  
Trypanosoma Brucei ◽  
Clinical Signs ◽  
Control Group ◽  
Pathological Changes ◽  
Epididymal Sperm ◽  
Trypanosoma Brucei Brucei ◽  
Group A ◽  
Time Of Infection ◽  
Gross Lesions ◽  
Group B

Abstract This study was designed to determine the progressive pathological changes in the testis and epididymis of rabbit bucks experimentally infected with Trypanosoma brucei brucei (T. brucei). Fifteen local rabbit bucks were divided into 2 groups comprising 8 bucks in group A and 7 bucks in group B. Bucks in group A were infected intraperitoneally with approximately 1.0x106 of T. brucei while bucks in group B served as the uninfected control. The bucks were closely monitored for clinical signs of trypanosomosis from the time of infection till the end of the study. One buck from each group was humanely sacrificed on days 9, 19, 29 and 38 post-infection (pi) and its testis and epididymis were examined for pathological changes. At post mortem, no gross lesions were observed in the infected bucks except for adhesion of the testis and epididymis to the scrotum on days 29 and 38 pi. There were no histological changes in the testis and epididymis of the infected buck sacrificed on day 9 pi apart from mild depletion of the epididymal sperm reserve. The buck infected on day 19 pi had moderate testicular degeneration but the epididymis was devoid of sperm reserve. Severe testicular and epididymal degeneration was observed in the buck on days 29 and 38 pi. The testis and epididymis of bucks from the control group were normal with evidence of spermatogenic activities and full epididymal sperm reserve throughout. The study shows that infected bucks were unfit for breeding from day 19 pi.

scholarly journals Catalase and Glutathione Peroxidase in Dogs Naturally Infected by Leishmania infantum

2018 ◽  
Vol 44 (1) ◽  
pp. 6 ◽  
Author(s):  
Belarmino Eugênio Lopes-Neto ◽  
Glauco Jonas Lemos Santos ◽  
Adam Leal Lima ◽  
Maritza Cavalcante Barbosa ◽  
Talya Ellen Jesus dos Santos ◽  
...  
Keyword(s):  
Glutathione Peroxidase ◽  
Pearson Correlation ◽  
Clinical Signs ◽  
Erythrocyte Count ◽  
Control Group ◽  
Positive Correlation ◽  
Antioxidant Agents ◽  
Group A ◽  
Group B ◽  
Gpx Activity

Background: Canine leishmaniasis (CanL) is caused by an obligatory intracellular parasite of Leishmania genus that  affects organs and tissues. Several studies evaluate the role of reactive oxygen species (ROS) in the pathogenesis of many diseases. The overproduction of ROS on infectious diseases can induce an imbalance between oxidants and antioxidants at cellular or systemic level. Thus, the aim of this study was to evaluate the activity of antioxidant enzymes in CanL.Materials, Methods & Results: Females (n = 17) and males (n = 10), at different ages and with different weight, were selected for this study. Dogs were divided into two groups according classical clinical signs and sorological test to CanL. Animals were considered infected based on indirect immunofluorescent assay and ELISA titration ≥ 1:40.  Group B (n = 15) composed by positive dogs to CanL from Zoonosis Control Center of Fortaleza (Ceará, Brazil) and group A (n = 12) was composed by dogs from private kennel that were serologically negative to L. infantum and had absence of clinical signs to CanL. Blood sample were collected for evaluation of hematological and biochemical parameters and glutathione peroxidase (GPx) and catalase (CAT) enzymatic activity. Data were analyzed by Student’s t-test and Pearson correlation coefficient (P < 0.05). Total proteins (TP, mg/dL) and alkaline phosphatase (ALP, U/L) were increased (P < 0.05) on group B (8.2 ± 1.2; 165.4 ± 46.4) when compared to group A (6.5 ± 1.1; 109.1 ± 38.3), respectively. Hemoglobin (Hb; g/dL) and hematocrit (Hct; %) were decreased (P < 0.05) on Group B (14.7 ± 1.8; 48.2 ± 5.7) when compared to group A (16.5 ± 1.3; 52.1 ± 2.4), respectively. Group B presented CAT (U/g Hb) and GPx (mU/mg Hb) lower (189.4 ± 90.4; 3,609.6 ± 1,569.1) than group A (326.6 ± 104.5; 5,055.6 ±1,569.1), respectively (P < 0.001). Positive correlation was observed between RBC and CAT; however, it was not significant.Discussion: Organisms require a good defense system in order to revert the overproduction of free radicals and consequently the injuries caused by them. This is possible through the production of antioxidant agents, which act on oxidative prevention and on tissue and cellular regeneration, by taking the reduced glutathione (GSH), superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPx) enzymes in the frontline. Erythrocyte changes promoted by CanL suggest possible correlation between anemia and the appearance of clinical signs, which in many cases is not seen. Erythrocytes contain SOD, CAT and GPx enzymes, thus, changes in these cells will reflect on the activity of these enzymes. In our results only CAT showed positive correlation with erythrocyte count, however it was not significant. GPx activity was lower (P < 0.001) in infected dogs than control group. This result agrees with another study, which showed a decrease in GPx levels in CanL, although it was not significant. However, it was found a positive correlation (P < 0.001) between erythrocytes and GPx activity and between hemoglobin and GPx activity in animals with leishmaniasis. These results suggest that the reduction in detoxification activity can be related to the decrease in erythrocyte count and that the GPx activity depends on the control mechanism of the antioxidant system in CanL. Furthermore, this result could be associated with decrease of blood cell count in animals with CanL, once GPx is an erythrocyte enzyme, which plays an important role in hemoglobin protection against oxidative damage. This study was carried out in naturally infected dogs with L. infantum. In conclusion, CAT and GPx activities are relate to oxidative stress induced by L. infantum infection and can be used as biomarkers on CanL.

scholarly journals Sensory Neuropathy in Hypothyroidism: Electrophysiological and Clinical Findings

1970 ◽  
Vol 2 ◽  
pp. 1-6 ◽  
Author(s):  
Sabina Yeasmin ◽  
Noorzahan Begum ◽  
Shelina Begum ◽  
Shah M Hafizur Rahman
Keyword(s):  
Healthy Subjects ◽  
Hormone Replacement ◽  
Clinical Signs ◽  
Sensory Neuropathy ◽  
Clinical Findings ◽  
Ultra Sound ◽  
Personal Contact ◽  
Control Group ◽  
Group B ◽  
Hypothyroid Patients

Peripheral neuropathy may be a manifestation of hypothyroidism which usually develops insidiously over a long period of time due to irregular taking of drugs or lack of thyroid hormone replacement. The present study was designed to observe the clinical and electro-physiological findings in hypothyroid patients in order to evaluate the neuromuscular dysfunction as well as sensory neuropathy. For this purpose, 70 subjects with the age range of 20 to 50 years of both sexes were included in the study. Among them, 40 hypothyroid patients were taken in study group (Group B) and 30 aparently healthy subjects were taken as control (Group A). On the basis of their TSH levels, group B was further divided into group B1 with TSH <60 MIU /L or (less severe) and group B2 with TSH >60 MIU /L (severe group). The duration of the disease ranged from 6 months to 5 years. All the hypothyroid patients were selected from Thyroid Clinic, Center of Nuclear Medicine and Ultra sound, Dhaka Medical College and Hospital, Dhaka, during the period from January 2005 to December 2005. Healthy subjects were selected from personal contact. Most of the hypothyroid patients were under hormone replacement therapy. Diagnosis of hypothyroidism was done by serum levels of TT3, TT4 and the TSH. In this study, both TT3, TT4 levels were significantly (P<0.01) lower in hypothyroids in comparison to those of control. The patients were searched for the clinical signs of sensory neuropathy. Clinical findings revealed diminished or absence of most of the deep tendon reflexes. The nerve conduction studies for sensory nerve function were done in all the subjects by electrophysiological technique. All the tests were done in median and ulnar nerve for upper limb and in sural nerve for lower limb and these parameters were measured on the day 1 (one) of their first visit. Data were compared among the different groups. Most of the patients had higher sensory distal latencies (SDL) with lower conduction velocities (SNCV) which were more marked in severe cases. About 67.5% of hypothyroid patients had shown abnormal sensory NCV when compared to that of euthyroids. Therefore, this study concludes that sensory neuropathy may be a consequence of hypothyroidism. Key Words: Hypothyroidism; Neuropathy; ElectrophysiologyDOI:10.3329/jbsp.v2i0.975  J Bangladesh Soc Physiol. 2007 Dec;(2): 1-6.

scholarly journals Evaluation and comparison of analgesic activity of essential oil of Rosmarinus officinalis and Thymus vulgaris: an experimental study

2017 ◽  
Vol 6 (7) ◽  
pp. 1718
Author(s):  
Asha R. Jha ◽  
Srimanti Paul
Keyword(s):  
Body Weight ◽  
Essential Oil ◽  
Analgesic Activity ◽  
Analgesic Effect ◽  
Saline Group ◽  
Rosmarinus Officinalis ◽  
Thymus Vulgaris ◽  
Control Group ◽  
Natural Forms ◽  
Group B

Background: Since the time of stone age herbs in its natural forms are used for a variety of medicinal purposes including the treatment of pain. Research in herbal medicine is in a relatively early phase. Herbal approaches usually have been pursued because of the perception that these therapies are gentler and cause fewer side effects than allopathic treatment. The aim was to evaluate and compare the analgesic activity of essential oil of Rosmarinus officinalis and Thymus vulgaris in wistar rats.Methods: Wistar rats and hot plate method was used for this study. Control group (Group A) of 6 animals was given normal saline. Group B of 6 animals was given standard analgesic drug, aspirin (200mg/kg body weight). Group C of 6 rats was given REO at 100, 200, 300 and 400 mg/kg body weight on day 1, 2, 3 and 4 while Group D of 6 animals was given TEO at doses of 100, 200 and 300 mg/kg body wt. The analgesic activity of REO and TEO in terms of Response Time were noted and depicted in tabular form.Results: Results were analyzed by one-way-Anova and Tukey tests. Analgesic effect of Rosemary oil found to be statistically significant at all four doses, 100, 200, 300 and 400mg/kg body wt compared to control group. TEO was found significantly analgesic at 100 and 200mg/kg body wt compared to control group but at 300mg/kg body it was found lethal. REO was found superior.Conclusions: Analgesic effect of REO and TEO was not comparable to aspirin even at higher concentration like 400mg/kg (REO) but it was significantly more compare to control group.

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