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Tiletamine zolazepam

Manufactured by Virbac
Sourced in France

Tiletamine/zolazepam is a pharmaceutical product used as a general anesthetic for veterinary use. It consists of a combination of two active ingredients, tiletamine and zolazepam, which work together to induce a state of anesthesia in animals. The product is intended for administration by trained veterinary professionals.

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14 protocols using tiletamine zolazepam

1

Murine Unilateral Ureteral Obstruction Model

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Animal welfare and experimental procedures were carried out in accordance with the Guide for the Care and Use of Laboratory Animals (Ministry of Science and Technology of China, 2006), and were approved by the animal ethics committee of Nanjing Medical University. Healthy specific pathogen-free (SPF) purpose-bred domestic C57BL/6 mice (6-weeks-old, 15–23 g body weight) were obtained from the Model Animal Research Center of Nanjing University, Jiangsu, China. Animals had ad libitum access to rodent diet and tap water. The mice were kept in cages with a 12:12-h light–dark cycle, a temperature of 21 °C ±2 °C, and a humidity of 55 % ±5 %.
Mice assigned to the unilateral ureteral obstruction (UUO) model were anesthetized by tiletamine/zolazepam (VIRBAC Laboratories, Carros, France) and placed on a heating pad to maintain their temperature at 37 °C. Left ureters were ligated with silk (4/0). Amoxicillin was given to the animals after surgery for three days. Sham animals underwent the same procedure, except that the ureter was not ligated. The animals were randomly divided into four groups: sham group (n = 10), UUO group (n = 10), UUO + MVs group (n = 10), and UUO + EPO-MVs group (n = 10). The mice were injected in the tail vein with MVs or EPO-MVs (30 μg/mouse) one day after surgery The four groups were killed at 7 days and 14 days after UUO.
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2

Canine Genital Tumor Biopsy and Chemotherapy

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The genital CTVT mass of a 4-year-old mongrel male dog was diagnosed by cytological and polymerase chain reaction (PCR) examination (Supplementary Figure 1), as reported (31 (link)). This dog was intravascularly injected with tiletamine-zolazepam (Zoletil®, Virbac, France) at a dosage of 4 mg/kg body weight (BW). The tumor tissue was aseptically biopsied before commencing chemotherapeutic treatment on the dog, as weekly intravenous injection of vincristine sulfate at 0.025 mg/kg BW. Sampling procedures were approved by the Chulalongkorn University Animal Care and Use Committee (No. 133100077). Biopsied tissue was immediately immersed in Hank's buffered salt solution (HBSS; Gibco Lab, USA) containing 100 IU/ml penicillin and 100 μg/ml streptomycin (Gibco Laboratories, USA). The dog's hematology and serum chemistry profile were in the normal range prior to receiving chemotherapeutic treatment.
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3

Anesthesia and Monitoring for Porcine Organ Procurement

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All the pigs underwent general anesthesia. In the induction phase, tiletamine/zolazepam (5 mg/kg; Virbac, France) was used via intramuscular injection. Endotracheal intubation was executed via laryngoscopy after the onset of anesthesia, which was then connected to a ventilator to maintain breathing during procurement. In the maintenance phase, isoflurane inhalation and intravenous propofol (10 mg/kg/hAstraZeneca, British) were continued throughout the procurement surgery. Meloxicam injection (0.3 mg/kg; Boehringer Ingelheim, Germany) was used as an analgesic.
The heart rate, electrocardiogram and saturation of blood oxygen were monitored during procurement. Invasive arterial blood pressure monitoring in the right femoral artery and right femoral vein catheterization were used for rapid fluid infusion to maintain circulatory stability. Another venous infusion access was the right ear vein. All operations in this research complied with the principle of minimizing suffering.
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4

Bengal Tiger Blood Sampling Protocol

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All procedures with the captive Bengal tigers were approved by the Kasetsart University
Animal Committee (ID number: ACKU59-VET-020). With clients’ informed consent, 30 captive
Bengal tigers in the Sriracha-Tiger Zoo, Chonburi, Thailand, were enrolled in the study
during their routine health examination. Of the 30 tigers, 10 were male, and 20 were
female, with a median age (range) of 8 (1–15) years old. Samples from ten of the tigers
were selected to undergo a crossmatching test. Blood samples from captive Bengal tigers
were drawn by physically restrain or application of general anesthesia using atropine
sulfate (0.02 mg/kg, intramuscular; Atlantic Laboratories Corp., Ltd., Bangkok, Thailand)
and tiletamine/zolazepam (2 mg/kg, intramuscular; Virbac Laboratories, Carros, France) as
premedication and anesthesia induction, respectively. Five ml blood
samples from all of the captive Bengal tigers were collected from the saphenous vein and
immediately transferred into ethylenediaminetetraacetic-acid (EDTA) anti-coagulant
tubes.
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5

Aortic Tissue Sampling from Göttingen Minipigs

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To reduce the number of animals utilized, tissue samples were collected from animals enrolled in an experimental lactation study approved by the Italian Ministry of Health as dictated by D.Lgs 26/2014 (approval n° 32/2021-PR). All procedures were performed in compliance with ARRIVE guidelines. At the end of the experimental trial, sows, acquired by Ellegaard Göttingen Minipigs A/S (Dalmose, Denmark), were group housed with a light/dark cycle of 12:12 and hand fed with a standard commercial diet (Micropigs 9AB20; Mucedola srl, Settimo Milanese Italy). Pens were equipped with both chewable and wooden environmental enrichments. On the day of sacrifice, animals were sedated intramuscularly (IM) with 5 mg/kg of tiletamine/zolazepam (Zoletil, Virbac, Carros, France) and euthanized upon barbiturate overdose (Sodium thiopental 60 mg/kg; Pentothal sodium, MSD Animal Health srl, Madison, NJ, USA). Thoracic aortic traits (11 ± 2 cm; n = 3) were surgically removed and collected from 3 Göttingen Minipigs.
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6

3D-Printed Dental Implant Placement

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The animals were anesthetized by a veterinarian using intravenous injections of tiletamine/zolazepam (5 mg/kg, Virbac, Carros, France), xylazine (2.3 mg/kg, Bayer Korea, Ansan, Korea), and 0.05 mg/kg atropine sulfate for the surgery. Complementary local anesthesia was injected at the mandibular third and fourth premolar area with 2% lidocaine HCl with epinephrine (1:1,000,000, Huons, Seongnam, Korea). The third and fourth premolars were hemisectioned with a diamond fissure bur in the buccolingual direction of the teeth and atraumatically extracted with elevator and forceps without flap reflection. The apical portion of the extraction socket was prepared using a 2.3 mm drill with a motor-driven handpiece (EXPERTsurg LUX, KaVo, Warthausen, Germany) to be 2 mm longer than the corresponding root for single-root 3D-printed implant, and mesial root for double-root 3D-printed implant. The 3D-printed implant heads were directly tapped using a surgical mallet. The protective cap was attached to the adjacent teeth using resin-modified glass ionomer cement (GC FujiCEM2, Tokyo, Japan).
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7

3D-Printed Dental Implant Placement

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The animals were anesthetized using intravenous injections of tiletamine/zolazepam (5 mg/kg, Virbac, Carros, France), xylazine (2.3 mg/kg, Bayer Korea, Ansan, Korea), and 0.05 mg/kg atropine sulfate during the surgical procedures. All procedures related to general anesthesia were performed by a veterinarian. Complementary local anesthesia was conducted at the mandibular third premolar area with 2% lidocaine HCl with epinephrine (1:1,000,000, Huons, Seongnam, Korea). The third premolars were hemisectioned in the buccolingual direction of the teeth with a diamond fissure bur and atraumatically extracted using an elevator and forceps without flap reflection (Figure 1E and F). The apical portion of the extraction socket was prepared at the mesial root site to place the 3D-printed implants, which were 2 mm longer than the corresponding teeth of the mesial root using a 2.3-mm-diameter drill with a motor-driven handpiece (EXPERTsurg™ LUX, KaVo, Warthausen, Germany) (Figure 1G). One of the 2 types of 3D-printed implant (lattice type or solid type) was randomly placed at each of the left or right sides of the mandible according to a random sequence generated before surgery. The 3D-printed implant heads were directly tapped using a surgical mallet. The protective cap was attached to the adjacent teeth using resin-modified glass ionomer cement (GC FujiCEM®2, Tokyo, Japan) (Figure 1).
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8

Beagle model for influenza virus

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One-month-old beagles were shown to be sero-negative by a hemagglutination-inhibition (HI) assay for seasonal influenza viruses (H1N1, H3N2, and influenza B virus) and for avian-origin CIV H3N2. All procedures and animal housing were carried out in the animal laboratory of South China Agricultural University. After the animals were lightly anesthetized using tiletamine–zolazepam (Virbac, Carros, France, 10–15 mg/kg), nine beagles were intranasally inoculated with 107 EID50 (50% egg infectious dose)/animal of H3N2 CIV in a 1mL volume. For the uninfected controls, six additional beagles were inoculated with 1 mL of Phosphate Buffer Saline (PBS) and housed in a separate room. All animals, except for those euthanized for lung tissue collection, were monitored daily for body temperature and virus shedding for 14 days, and serum antibodies were detected at 14 days post-inoculation (dpi). At 3 dpi and 7 dpi, three animals in each inoculated group were euthanized. Lungs were collected to assess viral replication and miRNA expression. This study protocol was reviewed and approved by the Institutional Review Board of South China Agricultural University (identification code: 2014-07).
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9

Evaluating Seal Auditory Thresholds

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The health of each seal was evaluated by an experienced veterinarian prior to measuring auditory thresholds and audiometry was performed only on those animals deemed to be in good health. Animals were sedated with an intramuscular injection of midazolam (0.2 mg/kg; 15 mg/3 ml, HEXAL, Germany) and ketamine (1.5 mg/kg; 100 mg/ml, Albrecht, Germany) or tiletamine/zolazepam (1.5–2 mg/kg; 100 mg/ml, VIRBAC, Germany). Sedation was augmented when the animals showed irregular short latency evoked potentials or signs of awareness. The time given to the hearing measurements did not exceed 90 minutes in duration per individual.
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10

Severe Unilateral Cortical Contusion in Mice

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Adult outbred CD1 mice (Envigo, Indianapolis, IN) 9–10 weeks of age were subjected to a severe unilateral cortical contusion as previously described.16 (link) Mice were anesthetized with a mixture of tiletamine/zolazepam (50 mg/kg; Virbac, Carros, France) and xylazine (20 mg/kg; Troy Laboratories, Glendenning, NSW, Australia). Craniotomy was performed by removing the skullcap 4 mm to the left of the sagittal suture and centered between the bregma and lambda. A CCI injury was delivered by compressing the cortex to a depth of 2.0 mm at a velocity of 5.0 m/s and 100-ms duration with a beveled steel tip 3 mm in diameter (TBI-0310; Precision Systems and Instrumentation, Fairfax, VA). Sham-operated mice received the craniotomy procedure without cortical impact. One hour after brain injury, mice were randomly allocated to receive a single intravenous injection of human plasma-derived C1-INH (15.0 IU of Berinert®; CSL Behring GmbH, Marburg, Germany) or equal volumes of vehicle control (isotonic saline).
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