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1.
J Am Vet Med Assoc ; 262(8): 1-7, 2024 Aug 01.
Article in English | MEDLINE | ID: mdl-38503053

ABSTRACT

OBJECTIVE: To describe the effect of different substance combinations administered through mesotherapy in dogs with hip osteoarthritis. ANIMALS: 104 dogs. METHODS: In this retrospective study, 4 groups (dogs treated with a combination of lidocaine, piroxicam, and thiocolchicoside [MG]; dogs treated with lidocaine, piroxicam, and Traumeel [TG]; dogs treated with lidocaine, piroxicam, and glucosamine [GG]; and dogs treated with the same combination as in MG combined with a photobiomodulation session [MPG]) were set. For all groups, the same treatment frequency was followed. Response to treatment was measured with the Canine Brief Pain Inventory (divided into pain interference score and pain severity score), Liverpool Osteoarthritis in Dogs (LOAD), and Canine Orthopedic Index (divided into function, gait, stiffness, and quality of life) before treatment and 15, 30, 60, 90, and 120 days after treatment. Cox proportional hazard regression analysis was used to investigate the influence of treatment, age, sex, body weight, breed, and Orthopedic Foundation for Animals score. RESULTS: Dogs had a mean age of 7.6 ± 3.1 years and body weight of 28.6 ± 5.5 kg. Hip osteoarthritis was classified as mild (4), moderate (70), or severe (30). Greater improvements were observed in MG and MPG. Kaplan-Meier estimators showed MG and MPG had longer periods with clinically significant results. Treatment was the covariable that contributed more frequently to the outcomes observed. CLINICAL RELEVANCE: The combination used in MG, particularly combined with photobiomodulation, produced longer-lasting clinically significant results.


Subject(s)
Dog Diseases , Mesotherapy , Piroxicam , Animals , Dogs , Dog Diseases/drug therapy , Dog Diseases/therapy , Retrospective Studies , Male , Female , Piroxicam/therapeutic use , Piroxicam/administration & dosage , Piroxicam/analogs & derivatives , Mesotherapy/veterinary , Colchicine/therapeutic use , Colchicine/administration & dosage , Lidocaine/therapeutic use , Lidocaine/administration & dosage , Drug Therapy, Combination/veterinary , Osteoarthritis/veterinary , Osteoarthritis/drug therapy , Glucosamine/therapeutic use , Glucosamine/administration & dosage , Plant Extracts/therapeutic use , Plant Extracts/administration & dosage , Osteoarthritis, Hip/veterinary , Osteoarthritis, Hip/drug therapy , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Anti-Inflammatory Agents, Non-Steroidal/administration & dosage , Low-Level Light Therapy/veterinary
2.
J Dairy Res ; 88(1): 64-68, 2021 Feb.
Article in English | MEDLINE | ID: mdl-33731240

ABSTRACT

Our objective was to evaluate the efficacy of intramammary administration, at drying-off, of a Panax ginseng extract (PGe) combined with cephalexin (Ceph) on the post-calving bacteriological cure rate of pre-existing intramammary infections (IMI) and on the occurrence of new IMI during the dry period. In addition, milk yield and somatic cell count (SCC) in the post-treatment lactation were evaluated. One hundred and eight late-lactation cows were randomly divided into two experimental groups and were treated at drying-off with Ceph alone or PGe combined with Ceph.Cure rates for IMI present at drying-off were similar for both treatments (OR = 0.95, 95% CI = 0.33-2.74). Cure rates for Staphylococcus aureus were lower (OR = 15.4, 95% CI = 1.66-142.52) in quarters treated with PGe + Ceph than in those treated with Ceph alone. Intramammary infusion of PGe + Ceph at drying-off had no effect on preventing new dry period IMI (OR = 0.75, 95% CI = 0.38-1.51), compared with infusion of Ceph alone. Milk production and SCC in the ensuing lactation were not affected by PGe + Ceph treatment. In conclusion, addition of PGe to dry cow therapy did not show any advantage over the use of dry cow therapy alone.


Subject(s)
Anti-Bacterial Agents/administration & dosage , Cephalexin/administration & dosage , Mastitis, Bovine/drug therapy , Panax/chemistry , Plant Extracts/administration & dosage , Animals , Cattle , Cell Count/veterinary , Drug Therapy, Combination/veterinary , Female , Lactation , Mammary Glands, Animal/drug effects , Mastitis, Bovine/prevention & control , Milk/cytology , Staphylococcal Infections/drug therapy , Staphylococcal Infections/veterinary , Staphylococcus aureus
3.
Trop Anim Health Prod ; 51(8): 2127-2137, 2019 Nov.
Article in English | MEDLINE | ID: mdl-31076996

ABSTRACT

Therapeutic management of contagious caprine pleuroneumonia (CCPP) involves mostly the use of oxytetracycline followed by enrofloxacin and rarely tylosin. In many parts of the world including India, the former antibiotics are commonly available than the latter. Therefore, prolonged use of the same leads to the development of antibiotic resistance and decreased efficacy of drug. Besides, inflammatory and allergic pathogenesis of CCPP envisages combination therapy. In this study, we evaluated the effectiveness of the combination therapy using different antibiotics (oxytetracycyline @ 10: group I, enrofloxacin @ 5 group II, and tylosin: group III, @ 10 mg/kg body weight), along with anti-inflammatory (meloxicam @ 0.5 mg/kg) and anti-allergic (pheneramine maleate @ 1.0 mg/kg) drugs. These drugs were given intramuscularly at the interval of 48 h for four times in three test groups (n = 10) of Pashmina goats, viz. groups I, II, and III, respectively, affected with CCPP. Group IV (n = 10) was kept as healthy control when group V (n = 10) treated with oxytetracycline @ 10 mg/kg alone was used as positive control. Clinical signs, clinical parameters, pro-inflammatory cytokine (tumor necrosis factor alpha (TNF-α)), and oxidative stress indices (total oxidant status (TOS), total antioxidant status (TAS)) were evaluated at hours 0, 48, 96, and 144 of experimental trial. Tylosin-based combination therapy resulted in a rapid and favorable recovery resulting in restoration of normal body temperature (102.46 ± 0.31 °F), respiration rate (16.30 ± 0.79 per minute), and heart rate (89.50 ± 2.63 per minute) compared to the oxytetracycline (102.95 ± 0.13, 21.30 ± 1.12, 86.00 ± 2.33, respectively) and enrofloxacin (102.97 ± 0.19, 21.00 ± 1.25, 90.00 ± 2.58, respectively) treated groups. By hour 144, all the groups showed restoration of clinical parameters of normal health and diminishing signs of CCPP, viz. fever, dyspnea, coughing, nasal discharge, weakness, and pleurodynia. Significant (P ≤ 0.05) decrease in levels of TNF-α and non-significant (P > 0.05) decrease in levels of TOS and an increase in levels of TAS were noted from hour 0 to 144 in all the test groups. Within the groups, no significant (P > 0.05) change was noted in TNF-α, TOS, and TAS levels; however, TNF-α levels were comparatively lower in group III. Hematological parameters did not differ significantly (P > 0.05). From these findings, it can be inferred that tylosin-based combination therapy is relatively better for early, rapid, and safe recovery besides minimizing inflammatory and oxidative cascade in CCPP affected Pashmina goats compared to oxytetracycline- and enrofloxacin-based therapies.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Goat Diseases/drug therapy , Pleuropneumonia, Contagious/drug therapy , Tylosin/therapeutic use , Animals , Anti-Allergic Agents/therapeutic use , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Drug Therapy, Combination/veterinary , Enrofloxacin/therapeutic use , Female , Goats , India , Meloxicam/therapeutic use , Oxytetracycline/therapeutic use , Pheniramine/therapeutic use , Pleuropneumonia/veterinary , Pneumonia, Mycoplasma
4.
Arq. bras. oftalmol ; 81(4): 293-301, July-Aug. 2018. tab, graf
Article in English | LILACS | ID: biblio-950477

ABSTRACT

ABSTRACT Objective: To compare the efficacy of 0.03% tacrolimus eye drops diluted in two different vehicles (linseed oil and olive oil) for the treatment of keratoconjunctivitis sicca (KCS) in dogs. Methods: This study included 60 dogs. Of this group, 20 were healthy and allocated to the control group, and 40 were diagnosed with bilateral KCS and randomly allocated to either the TO (tacrolimus in olive oil) or the TL (tacrolimus in linseed oil) groups. Ophthalmic examinations, Schirmer Tear Test-1 (STT-1), Tear Film Break-up Time (TBUT) and Fluorescein Test (FT) were carried out monthly, along with cytological and histopathological examinations at the beginning and end of the study. Results: The clinical signs, corneal ulcers, Schirmer Tear Test-1 values, and Tear Film Break-up Time values improved in both groups after one month of treatment. Cytological examination at the end of the study showed decreased lymphocytes, neutrophil, metaplastic, and squamous cell counts in both groups, while the histopathological analysis showed decreases in lymphocytes and neutrophils and an increase in goblet cell density (cells/mm2). The decreases in neutrophil count were more significant (p<0.05) in the TL group for both types of examination. Conclusion: In sum, 0.03% tacrolimus eye drops diluted in olive oil and linseed oil were effective in the treatment of keratoconjunctivitis sicca. None of the evaluated parameters differed significantly between the two groups, except for neutrophil count which was significantly lower in the TL group. Thus, linseed oil may be considered as an alternative diluent for tacrolimus eye drops.


RESUMO Objetivo: Comparar a eficácia do tacrolimus 0,03% colírio, diluído em óleo de linhaça e óleo de oliva, no tratamento de ceratoconjuntivite seca em cães. Métodos: Foram utilizados 60 cães; 20 cães saudáveis como grupo controle, e 40 cães com diagnóstico de ceratoconjuntivite seca bilateral, distribuídos aleatoriamente em dois grupos: Tacrolimus em óleo de oliva (TO) e Tacrolimus em óleo de semente de linhaça (TL). Os animais foram avaliados mensalmente com exames oftálmicos, Teste lacrimal de Schirmer-1 (TLS-1), Tempo de ruptura do filme lacrimal (TRFL) e Teste de Fluoresceína (TF), e mensalmente com citologia conjuntival e com exame histopatológico no início e final do estudo. Resultados: Nos dois grupos de tratamento os sinais clínicos, Teste lacrimal de Schirmer-1, óleo de semente de linhaça e Tempo de ruptura do filme lacrimal apresentaram melhora após um mês de tratamento. E no final do estudo, na análise citológica, ambos apresentaram diminuição de linfócitos, neutrófilos, células metaplásicas e células escamosas, e na análise histopatológica houve diminuição de linfócitos, neutrófilos e o aumento de células caliciformes. No grupo óleo de semente de linhaça, a diminuição de neutrófilos foi mais significativa (p<0,05) em ambas análises. Conclusão: Em suma, tacrolimus 0,03% colírio diluído em óleo de oliva e óleo de linhaça foram eficientes no tratamento de ceratoconjuntivite seca. Nenhum dos parâmetros avaliados diferiu significativamente entre os dois grupos, exceto a contagem de neutrófilos, que foi significativamente menor no grupo TL. Assim, o óleo de linhaça pode ser considerado como um diluente alternativo para o colírio tacrolimus.


Subject(s)
Animals , Male , Female , Linseed Oil/administration & dosage , Keratoconjunctivitis Sicca/veterinary , Tacrolimus/administration & dosage , Olive Oil/administration & dosage , Immunosuppressive Agents/administration & dosage , Keratoconjunctivitis Sicca/drug therapy , Treatment Outcome , Drug Therapy, Combination/veterinary , Administration, Ophthalmic/veterinary
5.
Arq Bras Oftalmol ; 81(4): 293-301, 2018.
Article in English | MEDLINE | ID: mdl-29995121

ABSTRACT

OBJECTIVE: To compare the efficacy of 0.03% tacrolimus eye drops diluted in two different vehicles (linseed oil and olive oil) for the treatment of keratoconjunctivitis sicca (KCS) in dogs. METHODS: This study included 60 dogs. Of this group, 20 were healthy and allocated to the control group, and 40 were diagnosed with bilateral KCS and randomly allocated to either the TO (tacrolimus in olive oil) or the TL (tacrolimus in linseed oil) groups. Ophthalmic examinations, Schirmer Tear Test-1 (STT-1), Tear Film Break-up Time (TBUT) and Fluorescein Test (FT) were carried out monthly, along with cytological and histopathological examinations at the beginning and end of the study. RESULTS: The clinical signs, corneal ulcers, Schirmer Tear Test-1 values, and Tear Film Break-up Time values improved in both groups after one month of treatment. Cytological examination at the end of the study showed decreased lymphocytes, neutrophil, metaplastic, and squamous cell counts in both groups, while the histopathological analysis showed decreases in lymphocytes and neutrophils and an increase in goblet cell density (cells/mm2). The decreases in neutrophil count were more significant (p<0.05) in the TL group for both types of examination. CONCLUSION: In sum, 0.03% tacrolimus eye drops diluted in olive oil and linseed oil were effective in the treatment of keratoconjunctivitis sicca. None of the evaluated parameters differed significantly between the two groups, except for neutrophil count which was significantly lower in the TL group. Thus, linseed oil may be considered as an alternative diluent for tacrolimus eye drops.


Subject(s)
Immunosuppressive Agents/administration & dosage , Keratoconjunctivitis Sicca/veterinary , Linseed Oil/administration & dosage , Olive Oil/administration & dosage , Tacrolimus/administration & dosage , Administration, Ophthalmic/veterinary , Animals , Dogs , Drug Therapy, Combination/veterinary , Female , Keratoconjunctivitis Sicca/drug therapy , Male , Treatment Outcome
6.
Res Vet Sci ; 106: 131-4, 2016 Jun.
Article in English | MEDLINE | ID: mdl-27234550

ABSTRACT

Acarbose (AC) and Sitagliptin (STGP) are oral hypoglycemic agents currently used either alone or in conjunction with human diabetic (Type 2) patients. AC has been used with diabetic cats, but not STGP thus far. Therefore, the objective of this study was to determine the potential use of AC or STGP alone and in combination for diabetic cats, by observing their effect on short-term post-prandial serum glucose, insulin, and incretin hormone (active glucagon-like peptide-1 (GLP-1) and total glucose dependent insulinotropic polypeptide (GIP)) concentrations in five healthy cats, following ingestion of a meal with maltose. All treatments tended (p<0.10; 5-7.5% reduction) to reduce postprandial glucose area under the curve (AUC), with an accompanying significant reduction (p<0.05, 35-45%) in postprandial insulin AUC as compared to no treatment. Meanwhile, a significant increase (p<0.05) in postprandial active GLP-1 AUC was observed with STGP (100% higher) and combined treatment (130% greater), as compared to either AC or no treatment. Lastly, a significant reduction (p<0.05) in postprandial total GIP AUC was observed with STGP (21% reduction) and combined treatment (7% reduction) as compared to control. Overall, AC, STGP, or combined treatment can significantly induce positive post-prandial changes to insulin and incretin hormone levels of healthy cats. Increasing active GLP-1 and reducing postprandial hyperglycemia appear to be the principal mechanisms of combined treatment. Considering the different, but complementary mechanisms of action by which AC and STGP induce lower glucose and insulin levels, combination therapy with both these agents offers great potential for treating diabetic cats in the future.


Subject(s)
Acarbose/adverse effects , Cat Diseases/drug therapy , Hyperglycemia/veterinary , Hypoglycemic Agents/adverse effects , Sitagliptin Phosphate/adverse effects , Animals , Blood Glucose/analysis , Cat Diseases/etiology , Cats , Drug Therapy, Combination/veterinary , Female , Hyperglycemia/drug therapy , Hyperglycemia/etiology , Incretins/blood , Insulin/blood , Male
8.
Vet J ; 210: 77-81, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26975448

ABSTRACT

A randomised, double-blinded, placebo-controlled multicentre trial was conducted in 36 dogs with atopic dermatitis to evaluate the cyclosporine-sparing effect of polyunsaturated fatty acids. Dogs were stable on their individual cyclosporine dosage and received either a mainly omega-3 fatty acid product with a minor omega-6 fatty acid fraction or placebo, orally for 12 weeks. Dogs were examined every 4 weeks and the Canine Atopic Dermatitis Extent and Severity Index (CADESI-03) was determined by a clinician. Pruritus, quality of life, global condition and coat quality were scored by the owner. If the dog's CADESI-03 and/or pruritus score improved by at least 25% compared with the previous visit, the cyclosporine dosage was decreased by approximately 25%. If the scores deteriorated by at least 25%, the cyclosporine dosage was increased by the same percentage. The median daily cyclosporine dosage/kg bodyweight decreased in the active group from 4.1 mg to 2.6 mg and in the placebo group from 3.5 mg to 3.3 mg over the study period. The difference between the two groups was significant (P = 0.009). The improvement in median pruritus score from inclusion to completion was significantly greater in the active group than in the placebo group (P = 0.04). There was no significant difference in CADESI-03 changes between groups (P = 0.38). The results of this study indicate a cyclosporine-sparing effect of a mainly omega-3 fatty acid supplement in dogs with atopic dermatitis.


Subject(s)
Cyclosporine/therapeutic use , Dermatitis, Atopic/veterinary , Dermatologic Agents/therapeutic use , Dog Diseases/drug therapy , Fatty Acids, Omega-6/therapeutic use , Animals , Dermatitis, Atopic/drug therapy , Dogs , Dose-Response Relationship, Drug , Double-Blind Method , Drug Interactions , Drug Therapy, Combination/veterinary , Female , Male
9.
Poult Sci ; 95(8): 1858-68, 2016 Aug 01.
Article in English | MEDLINE | ID: mdl-26976910

ABSTRACT

Essential oil of oregano ( OEO: ) has proven to be a potential candidate for controlling chicken coccidiosis. The aim of the current study is to determine whether OEO and an approved anticoccidial, monensin sodium ( MON: ), as in-feed supplements could create a synergism when combined at low dosages. Day-old broiler chickens were separated into six equal groups with six replicate pens of 36 birds. One of the groups was given a basal diet and served as the control ( CNT: ). The remaining groups received the basal diet supplemented with 100 mg/kg MON, 50 mg/kg MON, 24 mg/kg OEO, 12 mg/kg OEO, or 50 mg/kg MON + 12 mg/kg OEO. All of the chickens were challenged with field-type mixed Eimeria species at 12 d of age. Following the infection (i.e., d 13 to 42), the greatest growth gains and lowest feed conversion ratio values were recorded for the group of birds fed 100 mg/kg MON (P < 0.05), whereas results for the CNT treatment were inferior. Dietary OEO supplementations could not support growth to a level comparable with the MON (100 mg/kg). The MON programs were more efficacious in reducing fecal oocyst numbers compared to CNT and OEO treatments (P < 0.05). Serum malondialdehyde and nitric oxide concentrations were decreased (P < 0.01), whereas superoxide dismutase (P < 0.05) and total antioxidant status (P < 0.01) were increased in response to dietary medication with MON and OEO. All MON and OEO treatments conferred intestinal health benefits to chickens by improving their morphological development and enzymatic activities. The results suggest that OEO supported the intestinal absorptive capacity and antioxidant defense system during Eimeria infection; however, it displayed little direct activity on the reproductive capacity of Eimeria This might be the reason for inferior compensatory growth potential of OEO compared to that MON following the challenge. Combination MON with OEO was not considered to show promise for controlling chicken coccidiosis because of the lack of a synergistic or additive effect.


Subject(s)
Chickens/parasitology , Coccidiosis/veterinary , Coccidiostats/pharmacology , Monensin/pharmacology , Origanum , Plant Oils/pharmacology , Poultry Diseases/prevention & control , Animals , Coccidiosis/drug therapy , Coccidiosis/parasitology , Coccidiosis/prevention & control , Coccidiostats/administration & dosage , Drug Therapy, Combination/veterinary , Eimeria/drug effects , Female , Male , Monensin/administration & dosage , Poultry Diseases/drug therapy , Poultry Diseases/parasitology
10.
Vet Dermatol ; 26(5): 339-44, e72, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26140535

ABSTRACT

BACKGROUND: There is a lack of studies comparing topical antiseptics to systemic antibiotics in the treatment of canine superficial pyoderma. HYPOTHESIS/OBJECTIVES: To compare the efficacy of topical chlorhexidine with systemic amoxicillin-clavulanic acid for the treatment of canine superficial pyoderma. ANIMALS: A randomized controlled trial was conducted in dogs with superficial pyoderma. Group T (n = 31) was treated topically with 4% chlorhexidine digluconate shampoo (twice weekly) and solution (once daily) for 4 weeks. Group S (n = 20) was treated orally with amoxicillin-clavulanic acid (25 mg/kg) twice daily for 4 weeks. METHODS: Bacterial culture and susceptibility testing were performed on clinical specimens collected before treatment. Severity of lesions and number of intracellular bacteria were evaluated using four-point scales to calculate a total pyoderma score for each dog. Pruritus was assessed by owners using a visual analog scale (range 0-10). Scores were analysed for statistical differences between groups T and S. RESULTS: Staphylococcus pseudintermedius was isolated from 48 dogs, including eight meticillin-resistant strains (MRSP). Although the number of dogs was small, no significant differences in pyoderma and pruritus scores were observed between groups throughout the study except for day 1, when group S had a significantly higher total score than group T (P = 0.03). Treatment with chlorhexidine products resulted in resolution of clinical signs in all dogs including those infected with MRSP. CONCLUSION AND CLINICAL IMPORTANCE: Topical therapy with chlorhexidine digluconate products may be as effective as systemic therapy with amoxicillin-clavulanic acid. This finding supports the current recommendations to use topical antiseptics alone for the management of superficial pyoderma.


Subject(s)
Amoxicillin-Potassium Clavulanate Combination/therapeutic use , Chlorhexidine/analogs & derivatives , Chlorhexidine/therapeutic use , Dog Diseases/drug therapy , Methicillin-Resistant Staphylococcus aureus/drug effects , Pyoderma/veterinary , Staphylococcal Skin Infections/veterinary , Administration, Topical , Amoxicillin-Potassium Clavulanate Combination/administration & dosage , Animals , Chlorhexidine/administration & dosage , Dog Diseases/microbiology , Dogs , Drug Therapy, Combination/veterinary , Female , Male , Microbial Sensitivity Tests , Pyoderma/drug therapy , Pyoderma/microbiology , Single-Blind Method , Staphylococcal Skin Infections/drug therapy
11.
Vet Dermatol ; 26(4): 278-e61, 2015 Aug.
Article in English | MEDLINE | ID: mdl-26083147

ABSTRACT

BACKGROUND: Wipes containing chlorhexidine and azole derivates have been recommended for veterinary use. No study has been published about their activity against Malassezia pachydermatis. HYPOTHESIS/OBJECTIVES: To evaluate the in vivo and in vitro activity of wipes soaked in a chlorhexidine, climbazole and Tris-EDTA solution against Malassezia pachydermatis. ANIMALS: Five research colony shar-pei dogs. METHODS: Wipes were applied once daily onto the left axilla, left groin and perianal area (protocol A), and twice daily on the right axilla, right groin and umbilical region (protocol B) for 3 days. In vivo activity was evaluated by quantifying Malassezia colonies through contact plates on the selected body areas before and after wipe application. The activity of the solution in which the wipes were soaked was assessed in vitro by contact tests following the European Standard UNI EN 1275 guidelines. RESULTS: Samples collected after wipe application showed a significant and rapid reduction of Malassezia yeast CFU. No significant difference in the Malassezia reduction was found between protocols A and B. In vitro assay showed 100% activity against Malassezia yeasts after a 15 min contact time with the wipe solution. CONCLUSIONS AND CLINICAL IMPORTANCE: Wipes containing chlorhexidine, climbazole and Tris-EDTA substantially reduced the M. pachydermatis population on the skin of dogs. The results, although this was an uncontrolled study performed on a small number of dogs, suggest that these wipes may be useful for topical therapy of Malassezia dermatitis involving the lips, paws, perianal area and skin folds.


Subject(s)
Antifungal Agents/therapeutic use , Chlorhexidine/therapeutic use , Dermatomycoses/veterinary , Dog Diseases/drug therapy , Edetic Acid/therapeutic use , Imidazoles/therapeutic use , Malassezia , Administration, Cutaneous , Animals , Antifungal Agents/administration & dosage , Chlorhexidine/administration & dosage , Dermatomycoses/drug therapy , Dermatomycoses/microbiology , Dog Diseases/microbiology , Dogs , Drug Therapy, Combination/veterinary , Edetic Acid/administration & dosage , Female , Imidazoles/administration & dosage , Male , Pilot Projects
12.
J Vet Med Sci ; 77(9): 1087-94, 2015 Sep.
Article in English | MEDLINE | ID: mdl-25947887

ABSTRACT

Biotite and bentonite are phyllosilicate minerals that were originally used in industrial applications. Several beneficial activities of them have recently been reported, especially regulation of the immune system and antimicrobial effects. Therefore, we investigated the immune-enhancing and bacterial clearance effects of a biotite and bentonite mixture (BBM) on experimental infection of Salmonella enterica serovar Typhimurium (S. Typhimurium) to determine whether the BBM could be used as an alternative antibiotic. We administered 1% or 2% BBM as a feed supplement. We then evaluated the bacterial clearance effects of the BBM against S. Typhimurium. We also evaluated the immune-enhancing effect of the BBM through several immunological experiments that included examination of the lysozyme activity, CD4(+)/CD8(+) T lymphocyte ratio and the T-helper type 1 (Th 1) cytokine profile. The clinical signs of S. Typhimurium and the number of viable bacteria in feces and tissues were significantly decreased in both BBM groups, especially in the 2% BBM group. The BBM also markedly enhanced the lysozyme activity, CD4(+)/CD8(+) T lymphocyte ratio and expression levels of IFN-γ and IL-12 in S. Typhimurium-challenged pigs. Therefore, the BBM could be a good candidate as an alternative antibiotic that improves Th 1-specific immune responses and the bacterial clearance effect.


Subject(s)
Aluminum Silicates/therapeutic use , Anti-Infective Agents/therapeutic use , Bentonite/therapeutic use , Ferrous Compounds/therapeutic use , Salmonella Infections, Animal/drug therapy , Salmonella typhimurium/drug effects , Swine Diseases/drug therapy , Th1 Cells/drug effects , Aluminum Silicates/administration & dosage , Animals , Anti-Infective Agents/administration & dosage , Bentonite/administration & dosage , Drug Therapy, Combination/veterinary , Ferrous Compounds/administration & dosage , Lymphocyte Subsets/drug effects , Salmonella Infections, Animal/microbiology , Swine , Swine Diseases/microbiology , Up-Regulation/drug effects
13.
J Vet Intern Med ; 28(4): 1221-8, 2014.
Article in English | MEDLINE | ID: mdl-24773179

ABSTRACT

BACKGROUND: Renal fibrosis is common in progressive kidney disease. Transforming growth factors ß (TGF-ß) are important mediators of all types of fibrosis, including renal fibrosis. Chinese rhubarb has been shown to have antifibrotic properties in part because of inhibition of TGF-ß and has slowed the progression of kidney disease in rodent models. HYPOTHESIS: That administration of a Chinese rhubarb supplement will slow the progression of chronic kidney disease (CKD) in cats and the concurrent administration of Chinese rhubarb and benazepril will be more effective than either alone. ANIMALS: Twenty-nine client-owned cats with naturally occurring IRIS Stage 2 or early Stage 3 CKD and without comorbidity such as cancer, urinary tract obstruction, urinary tract infection, poorly controlled hyperthyroidism, or systemic hypertension were enrolled in the study. METHODS: A randomized, positive-controlled, prospective study was performed. Cats received Chinese rhubarb, benazepril, or both in addition to standard treatment for CKD. Repeated measures ANOVA was used to assess changes in serum creatinine concentration, body weight, hematocrit, urine protein: urine creatinine ratio (UPC), and systemic arterial blood pressure over time between and within treatment groups over an average of 22 months. RESULTS: No significant differences were detected in serum creatinine concentration, body weight, hematocrit, UPC, and systemic arterial pressure over time between or within treatment groups. CONCLUSIONS AND CLINICAL IMPORTANCE: This study failed to detect a significant difference in the progression of CKD in cats treated with Chinese rhubarb, benazepril, or both. Further study in specific subsets of cats with CKD is warranted.


Subject(s)
Angiotensin-Converting Enzyme Inhibitors/therapeutic use , Benzazepines/therapeutic use , Cat Diseases/drug therapy , Drugs, Chinese Herbal/therapeutic use , Phytotherapy/veterinary , Renal Insufficiency, Chronic/veterinary , Rheum , Angiotensin-Converting Enzyme Inhibitors/administration & dosage , Animals , Benzazepines/administration & dosage , Blood Pressure/drug effects , Cats , Creatinine/blood , Drug Therapy, Combination/veterinary , Drugs, Chinese Herbal/administration & dosage , Phytotherapy/methods , Proteinuria/drug therapy , Proteinuria/veterinary , Renal Insufficiency, Chronic/drug therapy
14.
Fish Shellfish Immunol ; 35(6): 1813-23, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24041844

ABSTRACT

The aim of the study was to evaluate the effect of micronized ß-1.3/1.6-D-glucan (BG) derived from the oyster mushroom Pleurotus ostreatus Hiratake and tetracycline antibiotic oxytetracycline (OTC) on biometrical, haematological, biochemical, and immunological indices, and histopathological changes in tissues of one- to two-year-old common carp (Cyprinus carpio L.). The fish tested were divided into five experimental groups and one control. Carp in the control group were fed commercial carp feed pellets. Fish in the five experimental groups were fed the same pellets supplemented with either OTC, a combination of OTC and BG, or BG as follows: 75 mg oxytetracycline kg(-1) bw (OTC group), 75 mg oxytetracycline kg(-1) bw and 0.5% ß-glucan (OTC + 0.5% BG group), 75 mg oxytetracycline kg(-1) bw and 2.0% ß-glucan (OTC + 2.0% BG group), 0.5% ß-glucan (0.5% BG group), and 2.0% ß-glucan (2.0% BG group). OTC- and BG-supplemented diets and the control diet were administered to experimental and control carp for 50 days (i.e. samplings 1-3, the exposure period); for the following 14 days, fish were fed only control feed pellets with no OTC or BG supplementation (i.e. sampling 4, the recovery period). Blood and tissue samples were collected both during, and at the end of the study. No significant changes in biometrical indices (i.e. total length, standard length, total weight, hepatosomatic and spleen somatic index, and Fulton's condition factor) were found in experimental carp compared to control in any sampling. In haematological indices, significant changes were found only in sampling 2, in which shifts in PCV (P < 0.01), Hb (P < 0.01), and WBC (P < 0.01), and in the counts of lymphocytes (P < 0.01), monocytes (P < 0.01), and neutrophil granulocytes-segments (P < 0.05) were revealed. As for biochemical profiling, plasma concentrations of glucose, albumins, cholesterol, natrium, and chlorides (all P < 0.01), and total proteins, lactate, phosphorus, and potassium (all P < 0.05) as well as the catalytic activity of ALP (P < 0.05) were altered in common carp. A significant change in induced (opsonizedzymosan particles, OZP) chemiluminescence (P < 0.05) in sampling 3 and no shifts in serum immunoglobulins concentration were found in the immunological analysis. Histopathological examination of skin, gills, liver, spleen, and cranial and caudal kidneys revealed no obvious specific changes in any tissue analysed. The use of ß-glucans in clinically healthy aquaculture remains an issue. Nevertheless, their use in breeding endangered by stress stimuli, infectious disease, or adverse environmental factors is defensible.


Subject(s)
Anti-Bacterial Agents/pharmacology , Carps/physiology , Glucans/pharmacology , Oxytetracycline/pharmacology , Pleurotus/chemistry , Administration, Oral , Animal Feed/analysis , Animals , Anti-Bacterial Agents/administration & dosage , Biomarkers/metabolism , Carps/growth & development , Carps/immunology , Diet/veterinary , Dietary Supplements/analysis , Dose-Response Relationship, Drug , Drug Combinations , Drug Therapy, Combination/veterinary , Glucans/administration & dosage , Hematologic Tests/veterinary , Immunologic Tests/veterinary , Oxytetracycline/administration & dosage
15.
J Anim Sci ; 91(9): 4469-75, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23825328

ABSTRACT

The purpose of this study was to evaluate the efficacy of an oral solution of ketoprofen administered in drinking water at a lower dose as a complement to antimicrobial therapy in a mild outbreak of porcine respiratory disease complex. The study was performed with 120 pigs with rectal temperature between 39.9 and 41°C and at least 1 sign indicating porcine respiratory disease complex (dyspnea, cough, nasal discharge, or depression). Animals were randomly allocated in 2 groups (treated and control group). Animals in both groups received etiological therapy with doxycycline at 10 mg · kg(-1) in drinking water for 5 d. The animals in the treated group also received 1.5 mg · kg(-1) of ketoprofen during the first 3 d. The reduction in rectal temperature in the treated group was significantly greater during the days of ketoprofen administration and up to 1 d after the end of treatment (P < 0.05). The percentage of dyspneic animals was significantly less (P < 0.05) in the treated group from d 2 to 5 of the study. Also, a significant improvement regarding depression and cough was seen in the animals of the treated group. No statistically significant (P > 0.05) differences were evidenced in productive variables. In conclusion, oral treatment with ketoprofen at 1.5 mg · kg(-1) in combination with antimicrobial therapy was found to be a clinically effective approach in outbreaks of mild porcine respiratory disease complex.


Subject(s)
Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Ketoprofen/therapeutic use , Porcine Reproductive and Respiratory Syndrome/drug therapy , Administration, Oral , Animals , Anti-Infective Agents/therapeutic use , Doxycycline/therapeutic use , Drinking Water , Drug Therapy, Combination/veterinary , Female , Male , Porcine Reproductive and Respiratory Syndrome/virology , Swine , Time Factors
16.
Vet Microbiol ; 166(3-4): 655-8, 2013 Oct 25.
Article in English | MEDLINE | ID: mdl-23867084

ABSTRACT

An experiment was performed to compare the microbiological efficacy of four treatments (oxytetracycline, trimethoprim-sulphonamide, amoxicillin (AMX) or enrofloxacin (ENR)) to control experimental colibacillosis induced by an avian pathogenic Escherichia coli (APEC) with reduced susceptibility to fluoroquinolones. The protocol was also developed in order to study resistance gene transfer. Broilers were first orally inoculated with multiresistant E. coli bearing plasmid genes conferring resistance to fluoroquinolones (qnr), cephalosporins (blaCTX-M or blaFOX), tetracycline or trimethoprim-sulphonamide. They were then inoculated in their air sacs with the APEC and treated as soon as symptoms appeared. Internal organs from dead or sacrificed birds were cultivated on non-supplemented or supplemented media. The inoculated O78 APEC was recovered significantly less frequently in ENR treated group (26%) compared to untreated group (47%). This was not true for other treated groups. Isolates obtained on non-supplemented media had the same susceptibility profile as the inoculated APEC. However, one isolate from the AMX-treated group obtained on AMX-supplemented media was resistant to AMX only, and one isolate from the same group obtained on ENR-supplemented media, showed a resistance profile suggesting acquisition of one of the multiresistance plasmids present in the intestinal microbiota. Molecular analysis performed on this multiresistant isolate confirmed the presence of a conjugative plasmid with qnr and blaCTX-M resistance genes. Thus, the experiment illustrated the emergence of resistant isolates in internal organs, probably via acquisition of a plasmid from the intestinal microbiota.


Subject(s)
Anti-Bacterial Agents/administration & dosage , Drug Resistance, Bacterial , Escherichia coli Infections/veterinary , Escherichia coli/drug effects , Poultry Diseases/microbiology , Amoxicillin/administration & dosage , Animals , Chickens , Drug Therapy, Combination/veterinary , Enrofloxacin , Escherichia coli/genetics , Escherichia coli/isolation & purification , Escherichia coli Infections/drug therapy , Escherichia coli Infections/microbiology , Fluoroquinolones/administration & dosage , Oxytetracycline/administration & dosage , Poultry Diseases/drug therapy
17.
Vet Dermatol ; 21(3): 292-6, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20042036

ABSTRACT

The diversity of species of the genus Staphylococcus sp. and the antimicrobial resistance of isolates from 151 unmedicated dogs of both sexes with a clinical diagnosis of otitis were recorded. Ninety-one isolates of Staphylococcus spp. were identified by biochemical reactions and tested for susceptibility to 15 antimicrobials. Coagulase-positive species were most common; S. pseudintermedius (38.4%), S. schleiferi schleiferi (15.4%), S. aureus (14.3%), S. epidermidis (11%), S. simulans (11%), S. schleiferi coagulans (8.8%) and S. saprophyticus (1.1%). All the isolates showed resistance to at least one drug and 89% were multiresistant. Amoxicillin combined with clavulanic acid and oxacillin were the most effective, while resistance was widely observed for neomycin and erythromycin. The results highlight the recognition and the potential need for bacterial culture with species identification and antimicrobial susceptibility tests for appropriate antimicrobial therapy.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Dog Diseases/microbiology , Otitis Externa/veterinary , Staphylococcal Skin Infections/veterinary , Amoxicillin/administration & dosage , Amoxicillin/therapeutic use , Animals , Clavulanic Acid/administration & dosage , Clavulanic Acid/therapeutic use , Dog Diseases/drug therapy , Dogs , Drug Resistance, Bacterial , Drug Therapy, Combination/veterinary , Erythromycin/therapeutic use , Female , Male , Microbial Sensitivity Tests/veterinary , Neomycin/therapeutic use , Otitis Externa/drug therapy , Otitis Externa/microbiology , Oxacillin/administration & dosage , Oxacillin/therapeutic use , Staphylococcal Skin Infections/drug therapy , Staphylococcal Skin Infections/microbiology , Staphylococcus/drug effects
18.
Vet Clin North Am Equine Pract ; 3(1): 145-51, 1987 Apr.
Article in English | MEDLINE | ID: mdl-3555724

ABSTRACT

The clinical significance of drug interactions in animals is often minor, but, in some cases, they may result in a fatal outcome. In the critically ill patient, the temptation to employ relatively large doses, particularly of antimicrobials or corticosteroids, or to use multiple-drug therapy is enhanced. These two factors, combined with a debilitated state of the patient, increase the probability of severe drug interactions that could mean the difference between recovery or death. It would be prudent to consider the possibility of drug interactions when selecting drugs for concomitant use, evaluating adverse reactions, evaluating laboratory test results, or mixing drugs in vitro.


Subject(s)
Drug Incompatibility , Drug Interactions , Drug Therapy, Combination/veterinary , Horse Diseases/drug therapy , Animals , Anti-Infective Agents/adverse effects , Anti-Infective Agents/pharmacology , Anti-Infective Agents/therapeutic use , Horses
19.
Vet Rec ; 112(2): 29-33, 1983 Jan 08.
Article in English | MEDLINE | ID: mdl-6829139

ABSTRACT

Multiple drug therapy is often used in veterinary practice; occasionally, inappropriate combinations of drugs may be administered which interact to produce adverse responses. Such interactions may occur in vitro because of physically or chemically incompatible drugs having been mixed before administration or in vivo. A number of important in vitro incompatibilities concerning parenteral drugs are tabulated, consideration having been given both to problems attending the use of intravenous fluids as vehicles for their administration and to incompatibilities between the drugs themselves. Interactions which occur in vivo are also examined; these have been grouped according to the various mechanisms by which they occur.


Subject(s)
Drug Interactions , Drug Therapy, Combination/veterinary , Absorption , Animals , Drug Incompatibility , Drug Therapy, Combination/adverse effects , Pharmaceutical Preparations/metabolism , Receptors, Drug/drug effects , Tissue Distribution
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