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Carprofen rimadyl

Manufactured by Pfizer
Sourced in United Kingdom

Carprofen (Rimadyl) is a non-steroidal anti-inflammatory drug (NSAID) used for the control of pain and inflammation associated with osteoarthritis in dogs. It is available in tablet and injectable formulations for veterinary use.

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6 protocols using carprofen rimadyl

1

Surgical Implantation of Hippocampal Electrodes

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The surgical procedures used here were identical to those described previously (Ainge et al., 2007). Briefly, animals were anaesthetised using Isoflurane inhalation anaesthetic (Abbott Laboratories) delivered using medical oxygen. Hydration was maintained by administration of 2.5 ml 5% glucose and 1 ml 0.9% saline. Animals were also given anti‐inflammatory analgesia (small animal Carprofen/Rimadyl, Pfizer, UK). In a stereotaxic frame, the electrode tips were lowered to the CA1 coordinates (−3.48 mm AP from bregma, +/−2.4 mm ML from the midline, −1.8 mm DV from dura surface). Skull screws were embedded in the skull and the drive assembly was anchored using dental cement mixed with silver sulfate to a 1% concentration (Ag2SO4, Sigma‐Aldrich, St. Louis). At least one week of recovery time passed before screening and recording took place.
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2

Photoconversion of Kaede Transgenic Mice

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Under anaesthesia, the small intestine of Kaede transgenic mice was exposed following laparotomy with a small midline incision. Two- to three-centimetre sections of tissue were exposed to violet light (395 nm UV LED) for 2–3 min each, while PPs and mLN were protected from exposure using high-density black card. Following replacement of the small intestine, the muscle layer was sutured and the skin closed with surgical clips. Zero-hour controls were taken immediately, while mice in 24-h time point were allowed to recover. The small intestine of control mice was exposed to ambient light. Before surgery, the mice received subcutaneous analgesics Carprofen (Rimadyl, Pfizer) and Buprenorphine (Vetergesic, Reckitt Benckiser Healthcare) at 0.1 ml and 0.15 ml per 100 g, respectively.
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3

Adrenalectomized Rats for Corticosterone Studies

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Male Sprague-Dawley rats (250–300 g) (Harlan, Bicester, UK) were individually caged in soundproof rooms under standard conditions with standard chow and water available ad libitum. All CORT infusions were conducted in rats under 14:10 light/dark cycle (lights on at Zt 0 hr) whilst automated blood sampling experiments were under 12:12 light/dark cycle.
Rats were anaesthetised with a combination of Isoflurane (100% w/w liquid vapour (Merial, UK)) and medical air during bilateral adrenalectomy, jugular vein or/ and carotid artery cannulation. The cannula (Smith Medicals, UK) was exteriorised via craniotomy or a vascular access button and attached to a spring and swivel system (S9 Fig). Post-operative analgesic 1 mg of Carprofen (Rimadyl, Pfizer, UK), 25 μg dexamethasone (Sigma, UK) and 2.5 ml of glucose (5%)/ saline (0.9%) were administered subcutaneously. For 5 days post-surgical recovery, 0.9% saline drinking water was supplemented with 0.15 μg/L of corticosterone (Sigma, UK) until 16 hours prior to infusion, whereupon 0.9% saline drinking water was provided ad libitum to ensure complete CORT washout from circulation. Implanted cannula was ‘flushed’ daily via withdrawal of blood and replaced with fresh heparinised saline (1:100) to maintain patency.
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4

Pharmacological Agents in Behavioral Study

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Harmaline hydrochloride dihydrate, 5-MeO-DMT oxalate, and N-N-(2-pyridinyl) cyclohexanecarboxamide trihydrochloride (WAY-100635) were bought from Sigma-Aldrich (St. Louis, MO). (R)-(+)-(2,3-dimethoxyphenyl)-[1-[2-(4-fluorophenyl)ethyl]-4-piperidyl]methanol (MDL-100907) was a generous gift from Sanofi-Aventis (Paris, France). Carprofen (Rimadyl) was purchased from Pfizer Inc. (New York, NY). Isoflurane (AErrane) was bought from Baxter Healthcare (Deerfield, IL). All drugs for injection were dissolved in saline and were administered as their free base weights. An injection volume of 10 ml/kg was used for both intraperitoneal (ip) and subcutaneous (sc) injections.
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5

Standardized Anesthesia and Analgesia Protocol

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For all surgical procedures, animals were anesthetized with 4% isoflurane until unconscious followed by 2% isoflurane during surgery. All animals received analgesia (Temgesic/Buprenorphine, Schering-Plough, 0.1 mg/kg body weight and Rimadyl/Carprofen, Pfizer, 5 mg/kg body weight; subcutaneous injection) for post-operative pain relief and a uniform layer of eye gel (Viscotears/Carbomer, 2 mg/g, Novartis) was applied onto the eye ball to prevent drying. All animals received local anesthesia (Xylocaine/Lidocaine, AstraZeneca, 10 mg/ml and Marcain/Bupivacaine, AstraZeneca, 2 mg/kg body weight) 2–3 min prior to craniotomies and spinal or brain lesions. For recovery from surgery, animals were placed on a heating pad and only returned to their home cage once they were fully awake.
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6

Zoledronate and Vγ9Vδ2 T Cells for Tumor Therapy

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I.t injections were performed as described above and two days post inoculation, tumour growth was assessed by bioluminescence imaging using the IVIS Spectrum. When tumours were established, mice were assigned into four treatment groups (n = 4–6): control, ZOLalone (100 μg/kg s.c), Vγ9Vδ2 T cells alone (1 χ 107 Vγ9Vδ2T cells injected i.v via the tail vein), and ZOL in combination with Vγ9Vδ2 T cells (infusion of Vγ9Vδ2 T cells 24 h after ZOL, treatments as above). If pain relief was required, Rimadyl (carprofen) (Pfizer Animal Health, Australia) was administered at 5 mg/kg s.c every 24 h for a maximum of three days. After 3 weeks treatment, mice were sacrificed and the tumour bearing and non-tumour bearing tibia from each animal were surgically resected for micro-computed tomography (μCT).
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