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Male wistar kyoto wky rats

Manufactured by Charles River Laboratories
Sourced in United States, China

Male Wistar-Kyoto (WKY) rats are an inbred strain of laboratory rats. They are commonly used as a reference or control strain in research studies. The WKY rat is characterized by its genetic uniformity and stability, making it a reliable model for various scientific investigations.

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8 protocols using male wistar kyoto wky rats

1

Wistar-Kyoto Rat Stress Study

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Male Wistar-Kyoto (WKY) rats 12-week-old for pilot study and 4-week-old for main study were purchased from Charles River Laboratories, Inc, Raleigh, NC. During 1-week acclimation, animals were double-housed in cages with hardwood chip bedding and EnviroDryR enrichment material. The animal rooms were maintained at 21-22°C, ~55% relative humidity, and 12h light/dark cycle. Throughout acclimation and experimentation period, animals were fed Purina 5001 rat chow (Brentwood, MO) and drank tap water, ad libitum unless noted. At the beginning of experimentation, rats were randomized by body weight and allocated to each stress condition. EPA animal facility is approved by the Association for Assessment and Accreditation of Laboratory Animal Care. All procedures were approved by U.S. EPA’s Institutional Animal Care and Use Committee following the experimental protocol and guidelines of the National Institutes of Health for the care and use of rats (NIH Publications No. 8023).
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2

Rat Brain Homogenate Preparation

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Male Wistar Kyoto (WKY) rats (200–250 g; Charles River, Maastricht, The Netherlands) were sacrificed by CO2 inhalation, and brains were rapidly removed and put into the assay buffer. The brains were obtained from untreated control animals of animal studies with other objectives. These studies were conducted according to the ethical guidelines (EEC Council directives 86/609) after the animal experiments were approved by the University Animal Ethical Committee. This use of rest materials from other studies is encouraged to reduce the number of experimental animals (2014-110, 15 January 2015). The homogenization of rat Brains were carried out by using a Potter tube. The Brain homogenate was first centrifuged at 500× g for 10 min to remove unwanted pieces. Then this homogenate was centrifuged at a higher speed at 20,000× g for 15 min. All the centrifugations are carried out at 4 °C to protect the protein and aimed to remove all the substances that may interfere with solubility and radioligand binding assay. The final precipitated material was resuspended in assay buffer and diluted to reach the concentration of 1 mg of protein per 0.25 mL. The final brain homogenate was stored at −20 °C.
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3

Wistar-Kyoto and Hypertensive Rat Study

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Male Wistar–Kyoto (WKY) rats or spontaneously hypertensive rats (SHR) 19–20 weeks of age (Charles River Laboratories) were used in the study. All animals were housed in a temperature-controlled animal facility with a 12-h light/dark cycle, with water and rodent chow provided ad libitum. All animals received humane care in compliance with the Principles of Laboratory Animal Care formulated by the National Society of Medical Research and the Guide for the Care and Use of Laboratory Animals published by the NIH (8th Edition, Revised 2011). The LSUHSC New Orleans IACUC approved all animal procedures.
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4

Evaluating Cisplatin-Induced Nephrotoxicity

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Male Wistar-Kyoto (WKY) rats weighing 180–200 g (Charles River, Wilmington, MA, USA) were used. Rats were assigned into groups (n = 6 in each group). Treatments were given i.p. in an osmotic pump (2ML, Alzet, Cupertino, CA, USA) starting two days prior to cisplatin injection and included vehicle (20% DMSO in PEG-400 v/v), EET analog A (EET-A in double distilled water, 10 mg/kg/d), or EET-F01 at 2 mg/kg/d and 20 mg/kg/d doses (prepared in a mixture of 20% DMSO in PEG400), respectively. The control-vehicle rat group received drinking water ad libitum and were administered the same DMSO (300–500 µL i.p.) that was used to prepare cisplatin solutions. Rats in the treatment groups were administered a single dose of cisplatin (7 mg/kg i.p.). One day prior to euthanasia, rat urine was collected over a 24 h period. Five days after cisplatin or vehicle administration, rats were anesthetized for blood and kidney sample collection followed by euthanasia.
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5

Standardized Male Wistar Kyoto Rat Housing

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Male Wistar Kyoto (WKY) rats for all studies were purchased from Charles River Laboratories, Inc., at 10–12 wk of age and maintained in our Association for Assessment and Accreditation of Laboratory Animal Care–approved U.S. Environmental Protection Agency (U.S. EPA) animal facility. Animals were pair-housed in polycarbonate cages with hard wood chips or pine-shavings bedding and EnviroDry enrichment material (Lab Supply), except when stated. Animal rooms were maintained on a 12-h light/dark cycle [0600–1800 hours (6 A.M.–6 P.M.)] at 22°C and 50% relative humidity. They were provided free access to Purina (5001) pellet rat chow and water ad libitum, unless stated during experimental procedures. All animal protocols were approved by the U.S. EPA’s Institutional Animal Care and Use Committee prior to starting studies, and we followed National Institutes of Health guide for the care and use of rats (National Institutes of Health Publication No. 8023; ncbi.nlm.nih.gov/books/NBK54050/).
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6

Hypertension Protocol in Rodents

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Male SHRs and male Wistar-Kyoto (WKY) rats 19 to 20 weeks of age (Charles River Laboratories) were used in the present study. All animals were housed in a temperature-controlled animal facility with a 12-hour light/dark cycle, with water and rodent chow provided ad libitum. All animals received humane care in compliance with the Principles of Laboratory Animal Care formulated by the National Society of Medical Research and the Guide for the Care and Use of Laboratory Animals published by the National Institutes of Health (Publication No 85-23, Revised 1996). The Louisiana State University Health Sciences Center New Orleans Institutional Animal Care and Use Committee approved all animal procedures.
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7

Chronic Predator Stress Induces Depression-like Behaviors in Rats

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All experiments were conducted according to the Health Guide for the Use and Care of Laboratory Animals of Shanghai Jiao Tong University. Male Wistar rats (3 weeks old) and male Wistar Kyoto (WKY) rats (3 weeks old) were purchased from Vital River Laboratory Animal Technology Co., Ltd., in Beijing. All rats were maintained on a 12-hr light-dark cycle with lights on at 12 a.m. and lights off at 12 p.m., at room temperature 22 ± 2°C, and at room humidity around 40%. Each rat was housed in a separate cage. WKY rats are required to be housed separately to induce the depression-like behavior; in order to reduce the effect caused by housing conditions, we housed Wistar rats separately as well. After one-week adaptation, rats (4 weeks old) were randomly divided into four groups: Wistar control, Wistar predator stress, WKY control, and WKY predator stress groups; each group consisted of 5 rats. The mean body weights of each group were 113.9 ± 2.3 g, 118.9 ± 4.6 g, 98.2 ± 2.5 g, and 96.8 ± 3.6 g, respectively. All the animals were treated alike except for the predator exposure between the control and stress groups. During the experiment, we recorded the body weight of each rat, both before and after predator stress. The percentage of weight change was calculated as (weight after predator stress—weight before predator stress)/weight before predator stress ∗ 100%.
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8

Hypertension Model in Wistar-Kyoto Rats

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Male Wistar-Kyoto (WKY) rats and spontaneously hypertensive rats (SHRs) (7 - 8 weeks old, weighting 200 - 230 g) were purchased from Beijing Vital River Laboratory Animal Technology Co., Ltd. (China). Rats were housed under (specific pathogen free) SPF conditions with a constant temperature (20 - 24 °C) and humidity (40-60%). After 4 weeks of adaptation, the experiment protocol started when rats were at 11 - 12 weeks.
All protocols were approved by the Ethics Committee of the Second Hospital of Hebei Medical University (No. 2022-AE154). Animal experiments were followed the Guidelines for the Ethical Review of Laboratory Animal Welfare (China National Standard GB/T 35892-2018).
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