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Rompun ts

Manufactured by Bayer
Sourced in Germany

Rompun TS is a veterinary drug used as a sedative and analgesic for various animal species. It contains the active ingredient xylazine hydrochloride. The core function of Rompun TS is to provide a safe and effective means of sedation and pain relief for animals during veterinary procedures or transportation.

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5 protocols using rompun ts

1

Anesthesia and Euthanasia Protocol for Animal Imaging

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Prior to tomography, animals were fasted for 24 hours with water ad libitum. Premedication consisted of an intramuscular injection of 0.5 mg atropine (Atropinum sulfuricum, 1 mg/ml, Eifelfango, Bad Neuenahr-Ahrweiler, Germany). For the induction of anaesthesia, an intramuscular injection of ketamine (27 mg/kg, Ursotamin, 100 mg/ml, Serumwerk Bernburg, Germany), xylazine (3.5 mg/kg, Rompun TS, 20 mg/ml, Bayer Vital GmbH, Leverkusen, Germany) and 3 ml azaperone (Stresnil, 40 mg/ml, Janssen Animal Health, Neuss, Germany) was administered. Throughout the entire procedure, an isotonic electrolyte solution was infused intravenously (Ionosteril, Fresenius, Bad Homburg v. d. H., Germany) [51 ]. For separate studies on the vascular distribution of the whole body [49 ] and further histologic examination, all animals were euthanised when in deep anaesthesia by a 15 ml intravenous injection of T61 (Intervet Deutschland GmbH, Unterschleißheim, Germany).
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2

Anesthesia and Euthanasia in Animal Studies

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Prior to tomography, animals were fasted for 24 hours with water ad libitum. Then the animals were premedicated by intramuscular injection of 0.5 mg atropine (Atropinum sulfuricum, 1 mg/ml, Eifelfango, Bad Neuenahr-Ahrweiler, Germany). Anaesthesia was induced by intramuscular injection of ketamine (27 mg/kg, Ursotamin®, 100 mg/ml, Serumwerk Bernburg, Germany), xylazine (3.5 mg/kg, Rompun® TS, 20 mg/ml, Bayer Vital GmbH, Leverkusen, Germany) and 3 ml azaperone (Stresnil®, 40 mg/ml, Janssen Animal Health, Neuss, Germany). An electrolyte solution was infused intravenously throughout the entire procedure (Ionosteril®, Fresenius, Bad Homburg v.d.H., Germany) [28 ]. At the end of the experiment all animals were euthanised in deep anaesthesia by intravenous injection of 15 ml T 61 (Intervet Deutschland GmbH, Unterschleißheim, Germany) for separate studies of the vascular distribution of the whole body [26 ] and histologic experiments.
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3

Diabetic Mouse and Rat Models

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All experiments were approved by the Institutional Animal Care and Use Committee of Yonsei University Wonju College of Medicine, Wonju, Korea, and the methods were performed in accordance with the relevant guidelines and regulations. Male diabetic db/db mice (C57BLKS/J- Leprdb/Leprdb, n = 10) and male nondiabetic db/m mice (C57BLKS/J- Leprdb/+, n = 10) were purchased at 6 to 7 weeks of age from Jackson Laboratory (Bar Harbor, MA, USA). Long-Evans Tokushima Otsuka (LETO, nondiabetic control model, n = 10) and OLETF (Type 2 diabetic mellitus model, n = 10) rats were purchased from Otsuka Pharmaceutical Co., Ltd. (Tokushima, Japan). The animals were anesthetized with Zoletil (Virvac Laboratories, Carros, France) and xylazine hydrochloride (Rompun TS, Bayer AG, Leverkusen, Germany) by intraperitoneal injection at 16 and 46 weeks of age, respectively.
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4

Anesthesia and Hemodynamic Monitoring in Rats

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All rats were anesthetized with an intraperitoneal (ip) injection of a mixture of zoletil (40 mg/kg; Virbac, Carros, France) and xylazine (Rompun TS, Bayer, Leverkusen, Germany) and were placed in a supine position. The right carotid artery was cannulated with a polyethylene (PE-50) catheter for continuous hemodynamic monitoring and blood drawing. A tracheostomy was performed and a 16-gauge angiocatheter was inserted as a tracheostomy tube. Blood pressure and respiratory rate were continuously monitored throughout the experiments. Supplemental doses of zoletil/xylazine mixture (13/3 mg/kg, ip) were given every 30–60 minutes until the end of the study to ensure and maintain adequate anesthesia.
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5

Rodent models for diabetes research

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We purchased diabetic db/db mice (n = 9) and nondiabetic db/m mice (n = 9) at 6 to 7 weeks of age from Jackson Laboratory (Bar Harbor, MA, USA). We purchased LETO (n = 9) and OLETF (n = 8) rats from Otsuka Pharmaceutical Co., Ltd. (Tokushima, Japan). We anesthetized all experimental animals at the age of 16 to 46 weeks with Zoletil (Virbac Laboratories, Carros, France) and xylazine hydrochloride (Rompun TS, Bayer AG, Leverkusen, Germany) by intraperitoneal injection.
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