Calves with arthritis - changes in antioxidant parameters

Background: In a healthy organism, oxidants and antioxidants are in balance. However, in cases such as inflammation, infection, and stress, this balance is disrupted in favor of oxidants, creating oxidative stress that can cause damage to cells or tissues. It is known that oxidative stress plays a role in the pathogenesis of many diseases. Determination of oxidant and antioxidant balance, especially in inflammatory diseases, plays an important role in elucidating the pathogenesis of the disease and developing treatment strategies. This study, it was aimed to reveal the oxidant status in inflammatory disease of calves with septic and aseptic arthritis. Materials, Methods & Results: The material of the study consisted of 21 calves up to 2 months old, of different races and genders, 14 (9 male, 5 female) with arthritis and 7 healthy (control, 5 male, 2 female). Of the calves with arthritis, 11 were septic and 3 were acute aseptic. In the calves with arthritis, the affected joint or joints were determined by clinical examinations. By palpating the joints, swelling, local temperature increase, tension in the joint capsule, presence of pain, and the presence and severity of lameness were examined. The color, clarity, viscosity, odor, and clot formation of the synovial fluid were examined and determined to be septic or aseptic. To determine the antioxidant status, the levels of malondialdehyde (MDA), which is the most important oxidative stress marker, and superoxide dismutase (SOD), gluta-thione peroxidase (GSH-Px), and catalase (CAT), which are the enzymatic antioxidant enzymes, were measured spectro-photometrically in serum samples. Vitamin E, C, and A levels, which are nonenzymatic antioxidants, were also measured colorimetrically. In the clinical examination, lameness was detected in the relevant extremity of all patients with arthritis. In the macroscopic examination of the synovial fluids taken from animals with arthritis, the colors of the synovial fluids varied between yellow and yellow tones in 11 cases; in 3 cases, it was determined that they were red and brown. It was observed that the colors of the synovial fluids were transparent in the subjects in the control group. It was observed that the synovial fluid clarity of the calves with arthritis was lost, with severe turbidity (+++) in 3 cases, moderately turbid (++) in 6 cases, slightly turbid (+) in 2 cases, and clear (-) in 3 cases. It was observed that the viscosity of synovial fluid taken from calves with arthritis decreased in varying degrees according to the severity of the disease, severe (+++) in 5 cases, moderately decreased (++) in 4 cases, slightly decreased (+) in 2 cases, and normal in 3 cases. It was determined that the viscosity of the synovial fluid taken from the calves in the control group was normal. There was a statistically significant difference between the groups in terms of MDA (P < 0.01), SOD (P < 0.01), GSH-Px (P < 0.05), vitamin E (P < 0.001), and vitamin C (P < 0.01), while MDA levels increased in calves with arthritis, SOD and GSH-Px activities and vitamin E and C levels decreased significantly. Although there was no statistically significant difference in CAT (P > 0.05) enzyme activity, it was determined that it was at a lower level in calves with arthritis, and there was no significant difference be-tween the groups in terms of vitamin A (P > 0.05). Discussion: According to the results of the study, there is an increase in oxidative stress and a decrease in antioxidant status in calves with arthritis. It is thought that these changes may be due to efforts to reduce tissue damage by reducing lipid peroxidation. As a result, it was determined that oxidant and antioxidant balance was impaired in calves with arthritis, and oxidative stress and lipid peroxidation developed due to the increase in free radicals. It is thought that giving additional antioxidants to the calves may contribute to the recovery of the disease and reduce treatment costs.

Effects on the lipid peroxidation and the antioxidant defense systems of the use of isoflurane or sevoflurane in calves undergoing surgery

Background: Incoming anaesthesia created by the use of many drugs with different physicochemical properties is a sourceof stress and trauma for the body. This event increases the oxidative response and changes the balance between oxidant/antioxidant capacity in the organism in favor of oxidant capacity. This situation is defined as oxidative stress. For thesereasons, studies are conducted to determine the effects of general anaesthetic agents on oxidant and antioxidant systems inthe organism. In this study, it was aimed to determine the effects of isoflurane and sevoflurane used for general anaesthesiain humans and animals on lipid peroxidation and antioxidant defense system in calves.Materials, Methods & Results: The study included 14 calves of different breeds, ages, sexes, and weighing, average 2 weeksold. The cases randomly were divided into 2 groups, the isoflurane group (group I), and the sevoflurane group (group II),and each group included 7 animals. Before general anaesthesia, 0.04 mg/kg atropine was administered intramuscularly toall animals for premedication. At 15 min after atropine administration, isoflurane was administered at an inspiratory concentration of 3-5% in group I, and sevoflurane was administered at an inspiratory concentration of 5-7% in group II, via aface mask for 15 min for the induction of anaesthesia. Endotracheal intubation was performed in all cases at the 15 min ofthe induction period following the onset of general anaesthesia symptoms. After the induction, anaesthesia was continuedat an inspiratory concentration of 1.5-3% in the isoflurane group and inspiratory concentration of 2.5-4% in the sevofluranegroup. Blood samples were taken just before anaesthesia, just before skin incision, at the end of anaesthesia and surgery,and at the 24 h postoperatively. The malondialdehyde (MDA), superoxide dismutase (SOD), catalase (CAT), glutathione...

Effects on the lipid peroxidation and the antioxidant defense systems of the use of isoflurane or sevoflurane in calves undergoing surgery

Background: Incoming anaesthesia created by the use of many drugs with different physicochemical properties is a sourceof stress and trauma for the body. This event increases the oxidative response and changes the balance between oxidant/antioxidant capacity in the organism in favor of oxidant capacity. This situation is defined as oxidative stress. For thesereasons, studies are conducted to determine the effects of general anaesthetic agents on oxidant and antioxidant systems inthe organism. In this study, it was aimed to determine the effects of isoflurane and sevoflurane used for general anaesthesiain humans and animals on lipid peroxidation and antioxidant defense system in calves.Materials, Methods & Results: The study included 14 calves of different breeds, ages, sexes, and weighing, average 2 weeksold. The cases randomly were divided into 2 groups, the isoflurane group (group I), and the sevoflurane group (group II),and each group included 7 animals. Before general anaesthesia, 0.04 mg/kg atropine was administered intramuscularly toall animals for premedication. At 15 min after atropine administration, isoflurane was administered at an inspiratory concentration of 3-5% in group I, and sevoflurane was administered at an inspiratory concentration of 5-7% in group II, via aface mask for 15 min for the induction of anaesthesia. Endotracheal intubation was performed in all cases at the 15 min ofthe induction period following the onset of general anaesthesia symptoms. After the induction, anaesthesia was continuedat an inspiratory concentration of 1.5-3% in the isoflurane group and inspiratory concentration of 2.5-4% in the sevofluranegroup. Blood samples were taken just before anaesthesia, just before skin incision, at the end of anaesthesia and surgery,and at the 24 h postoperatively. The malondialdehyde (MDA), superoxide dismutase (SOD), catalase (CAT), glutathione...(AU)

Comparison of use of isoflurane or sevoflurane for anaesthesia induced by mask in calves

Background: Inhalation anaesthesia is an effective and reliable general anaesthesia method for inactivity, analgesia, and unconsciousness in extensive surgical procedures. Although widely used, especially in small animals, there are very few studies investigated the reliability and superiority of inhalation anaesthesia in surgical procedures for ruminants. This study intended to evaluate the anaesthetic effects of isoflurane and sevoflurane in different surgical cases with endotracheal intubation following the induction of anaesthesia using a calve-specific facemask, which is not yet a routine option in cattle. Materials, Methods & Results: The study was conducted on 14 calves, from new-born up to 3 months-old, that undergoing various surgical operations. The animals were divided into isoflurane and sevoflurane groups, and each group contained 7 animals. In all cases, atropine (0.04 mg/kg was administered intramusculer as premedication before 15 min from anaesthesia induction. For induction, the anaesthetic agent was given at an inspiratory concentration of 3-5% in the isoflurane group and at an inspiratory concentration of 5 - 7% in the sevoflurane group during 5 min via mask at 15 min after atropine administration. In both groups, endotracheal intubation was performed (about 1-3 min) after of general anaesthesia symptoms starting. At 5 min after induction, anaesthesia was continued at 1.5 - 3% in the isoflurane group and at 2.5 - 4% in the sevoflurane group during operation. The animals were monitored during anaesthesia and, anaesthetic effect, reaction of the calve, pronounced side effects, Heart Rate (HR), Systolic Arterial Blood Pressure (SABP), Diastolic Arterial Blood Pressure (DABP), Mean Arterial Blood Pressure (MABP), Respiration Rate (RR), Pulse Rate (PR), Arterial Oxygen Saturation (SpO2 ) were recorded at before anaesthesia, the premedication period, 5...

Comparison of the effects of isoflurane and sevoflurane general anaesthesia after induction by propofol on clinical and physiological measurements in calves

Background: In veterinary surgical operations for cats and dogs, inhalation anaesthesia is known to be a good option forgeneral anaesthesia in long operations or emergency cases. Studies have revealed that during inhalation anaesthesia, theheart and respiratory functions of the animals are more stable compared to injectable anaesthesia. However, there are fewstudies performed with the use of inhalation anaesthesia in ruminants. In this research, the goal is to evaluate the effectsof isoflurane and sevoflurane after induction with propofol in calves based on clinical and physiological parameters andto find a more reliable strategy for general anaesthesia in ruminants.Materials, Methods & Results: The research was carried out on 30 calves, from new-born up to 3-month-old, undergoingsurgery operation. Each group consisted of 15 animals that were divided as isoflurane and sevoflurane. For premedication,atropine was administered at a dose of 0.04 mg/kg via subcutaneous injection in calves. For induction, 15 min after atropineapplication, propofol was given at 5-6 mg/kg via intravenous infusion. Then, endotracheal intubation was performed andinhalation anaesthesia began at 5 min after induction. In the isoflurane group, the onset of anaesthesia concentration wasset to 3-5% and the maintenance was set to a concentration of 1.5-3%. In the sevoflurane group, the onset of anaesthesiaconcentration was set to 5-7% and the maintenance was set to a concentration of 2.5-4%. To monitor the calves, the heartrate (HR), the pulse rate (PR), the systolic blood pressure (SBP), the diastolic blood pressure (DBP), the respiratory rate(RR), the rectal temperature (RT) and the electrocardiogram (ECG) measurements were recorded before anaesthesia, thepremedication, the induction periods, at 5, 15, 30, 45, 60, and 75 min after the onset of inhalation anaesthesia during theoperation period. Blood samples were taken before anaesthesia, premedication, induction periods...

Comparison of the effects of isoflurane and sevoflurane general anaesthesia after induction by propofol on clinical and physiological measurements in calves

Background: In veterinary surgical operations for cats and dogs, inhalation anaesthesia is known to be a good option forgeneral anaesthesia in long operations or emergency cases. Studies have revealed that during inhalation anaesthesia, theheart and respiratory functions of the animals are more stable compared to injectable anaesthesia. However, there are fewstudies performed with the use of inhalation anaesthesia in ruminants. In this research, the goal is to evaluate the effectsof isoflurane and sevoflurane after induction with propofol in calves based on clinical and physiological parameters andto find a more reliable strategy for general anaesthesia in ruminants.Materials, Methods & Results: The research was carried out on 30 calves, from new-born up to 3-month-old, undergoingsurgery operation. Each group consisted of 15 animals that were divided as isoflurane and sevoflurane. For premedication,atropine was administered at a dose of 0.04 mg/kg via subcutaneous injection in calves. For induction, 15 min after atropineapplication, propofol was given at 5-6 mg/kg via intravenous infusion. Then, endotracheal intubation was performed andinhalation anaesthesia began at 5 min after induction. In the isoflurane group, the onset of anaesthesia concentration wasset to 3-5% and the maintenance was set to a concentration of 1.5-3%. In the sevoflurane group, the onset of anaesthesiaconcentration was set to 5-7% and the maintenance was set to a concentration of 2.5-4%. To monitor the calves, the heartrate (HR), the pulse rate (PR), the systolic blood pressure (SBP), the diastolic blood pressure (DBP), the respiratory rate(RR), the rectal temperature (RT) and the electrocardiogram (ECG) measurements were recorded before anaesthesia, thepremedication, the induction periods, at 5, 15, 30, 45, 60, and 75 min after the onset of inhalation anaesthesia during theoperation period. Blood samples were taken before anaesthesia, premedication, induction periods...(AU)

Effects of flunixin meglumine on oxidant and antioxidant system after disbudding with caustic paste in calves

Background: Disbudding is often practiced in modern farm because of the reasons for the safekeeping of the animal, other animals lessen the risk of injury and less aggressive behavior. Without regard to the method of disbudding leads to disruption behavioral changes, cardiac and endocrine responses related pain of animals. Sedation, local anesthesia and analgesia are performed studies in order to eliminate of cardiac, endocrine, behavioral response which is caused by pain associated with disbudding. In this study, it was aimed to determine the effect on the oxidant and antioxidant system in the calves of disbudding by using the caustic paste with and without painkiller.Materials, Methods & Results: The animal material of the study was created 24 Simmentals calves in different sexes on average 2 weeks (± 2 days) and 50 kg (± 15 kg) live weight. The cases were randomly divided into 2 groups of 12 calves in each group. In the group I (analgesia group); caustic paste+painkiller (2.2 mg-1 flunixin meglumine intravenous, IV) and group II (non-analgesia group); as disbudding applied with caustic pasta application only were divided into 2 groups. In the I group, 15th min before the application, flunixin meglumine at a dose of 2.2 mg-1 was administered IV and the horn blunting was performed by caustic paste method. Blood samples were taken at 15, 30 and 60th min after completion of horn blunting and physiological findings were recorded. In group II, the horns of the calves were disbudding with the same technique (but no analgesia aplication). Blood samples were taken at 15, 30 and 60th min after completion of horn blunting and physiological findings were record. Cortisol, glucose, total oxidant capacity (TOC) and total antioxidant capacity (TAC), 8-hydroxy-2’-deoxyguanosine (8-OHdG), glutathione (GSH), superoxide dismutase (SOD) enzymes measurements (ELISA) were performed in both groups.[...]

Effects of flunixin meglumine on oxidant and antioxidant system after disbudding with caustic paste in calves

Background: Disbudding is often practiced in modern farm because of the reasons for the safekeeping of the animal, other animals lessen the risk of injury and less aggressive behavior. Without regard to the method of disbudding leads to disruption behavioral changes, cardiac and endocrine responses related pain of animals. Sedation, local anesthesia and analgesia are performed studies in order to eliminate of cardiac, endocrine, behavioral response which is caused by pain associated with disbudding. In this study, it was aimed to determine the effect on the oxidant and antioxidant system in the calves of disbudding by using the caustic paste with and without painkiller.Materials, Methods & Results: The animal material of the study was created 24 Simmentals calves in different sexes on average 2 weeks (± 2 days) and 50 kg (± 15 kg) live weight. The cases were randomly divided into 2 groups of 12 calves in each group. In the group I (analgesia group); caustic paste+painkiller (2.2 mg-1 flunixin meglumine intravenous, IV) and group II (non-analgesia group); as disbudding applied with caustic pasta application only were divided into 2 groups. In the I group, 15th min before the application, flunixin meglumine at a dose of 2.2 mg-1 was administered IV and the horn blunting was performed by caustic paste method. Blood samples were taken at 15, 30 and 60th min after completion of horn blunting and physiological findings were recorded. In group II, the horns of the calves were disbudding with the same technique (but no analgesia aplication). Blood samples were taken at 15, 30 and 60th min after completion of horn blunting and physiological findings were record. Cortisol, glucose, total oxidant capacity (TOC) and total antioxidant capacity (TAC), 8-hydroxy-2-deoxyguanosine (8-OHdG), glutathione (GSH), superoxide dismutase (SOD) enzymes measurements (ELISA) were performed in both groups.[...](AU)