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Isoflurane

Manufactured by RWD Life Science
Sourced in China, United States, Canada

Isoflurane is a clear, colorless, and volatile liquid anesthetic agent used in laboratory settings. It is a halogenated ether compound that operates as a general anesthetic, inducing a state of unconsciousness and muscle relaxation in animals. Isoflurane is commonly utilized in the anesthesia of various animal species for medical procedures, surgical operations, and research applications.

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176 protocols using isoflurane

1

Diabetic Wound Model Construction

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Animals that met the blood glucose standard were fed for another month to the next step of wound model construction. Diabetic rats were anesthetized with 5% isoflurane (RWD, Shenzhen, China) and maintained with 2% isoflurane; diabetic mice were anesthetized with 3% isoflurane and maintained with 1% isoflurane, their backs were shaved and disinfected, and full circular wounds of 1.0 cm in diameter were created on the skin 2.0 cm away from the spine on the back of the rats and 0.6 cm in diameter on the skin in the middle of the back of the mice.
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2

Induction and Assessment of Colitis in Mice

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Mice were anesthetized using isoflurane (RWD lifescience, China), which placing the mice in a closed container permeated with a mixture of isoflurane and oxygen vapor. DSS (36,000–50,000 molecular weight; MP Biomedicals) was diluted to 3% with deionized water before use, and the mice were intragastrically administered solution of daily up to 7 days. The mice with free access for sterile food and water were served as control and were euthanized on the 7th day to collect samples. The IBD mouse models were randomly divided into four groups: (1) DSS administered for 7 days and euthanasia (DSS7D group), (2) DSS administered for 7 days and kept for another 7 days without any treatment (DSS14D group), (3) DSS administered for 7 days and followed with hUC-Exos infusion for 7 days (hUC-Exos group) and (4) DSS administered for 7 days and followed with hFP-Exos infusion for 7 days (hFP-Exos group). Dissolve 50 µg exosomes protein in 200 µl of normal saline and injected into mice via tail vein per day. At the end of treatments, the mice in each group were euthanized for subsequent analysis. Briefly, mice were killed using CO2 at 20% chamber replacement rate. Intact colons from the epityphlon to the anus were harvested, and colon lengths were measured. Photographs of the colon were acquired at a vertical angle immediately after the samples were harvested.
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3

Telemetric Monitoring of Cardiovascular Parameters in Mice

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BP and HR were measured in conscious, freely moving TASK−/− mice and the counterparts using telemetry system (Ponemah v6.00, Data Sciences International, USA). In this system, the transmitter (HD-X11) was allowed to transfer the signal to a remote receiver and a data-exchange matrix (PhysioTel Matrix 2.0) connected to a computer. Mice were inhalationally anesthetized with isoflurane (2~3%, RWD Life Science) after initial exposure to a chamber filled with isoflurane for 1~2 min. Depth of anesthesia was assessed by absence of corneal and hindpaw withdrawal reflexes. All surgical procedures were conducted under strict aseptic conditions. After anesthesia, the pressure catheter was inserted into the right common carotid artery and the transmitter body was placed subcutaneously in the abdominal area. After wound closure, the mice received injections of antibiotic ampicillin (125 mg/kg, i.p.) and the analgesic ketorolac (4 mg/kg, i.p.). At least 5 days after recovery, systolic blood pressure (SBP), diastolic blood pressure (DBP), and HR were measured every 1 h for 24 h at a sample rate of 1 kHz.
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4

Laparotomy Protocol for Perioperative Neurological Disorder

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An experimental laparotomy was carried out to mimic clinical perioperative neurological disorder as described previously [15] . Briefly, mice were anesthetized by inhalation of 2 % isoflurane (RWD Life Science, China) through a face mask for 2 min, and anesthesia was maintained by inhalation of 1.4 % isoflurane. A heated surgical table (RWD Life Science, China) was used to maintain the core body temperature at 37.5 °C. The abdominal hair was shaved, followed by thorough sterilization with iodine. Then, a 5-cm segment of the small intestine was gently pulled out from a midline abdominal incision (approximately 1.5 cm), gently kneaded for 10 min in gauze moistened with 0.9 % saline and finally returned to the abdomen. The muscle and skin were closed layer by layer using 4-0 absorbable sutures (VICRYL, Ethicon, USA). The surgical wound was subcutaneously infiltrated with 0.2 % lidocaine in 0.1 ml for postoperative analgesia. The anesthesia duration was fixed at 30 min
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5

Evaluation of Vascular Permeability

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Lipopolysaccharide (LPS), Evans blue, methylcellulose, 70 kDa fluorescein isothiocyanate conjugated dextran were bought from Sigma-Aldrich (St Louis, MO, USA). Propofol (Diprivan®, AstraZeneca, London, British), dexmedetomidine (Yangtze River Pharmaceutical Group, Taizhou, Jiangsu, China), isoflurane (RWD Life Science, Shenzhen, Guangdong, China) and 10% fat emulsion (Intralipid®, Fresenius Kabi, Wuxi, Jiangsu, China) were used in present study.
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6

Transient Middle Cerebral Artery Occlusion in Mice

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tMCAO was carried out owing to previously published research [53 (link)]. Briefly, adult ICR mice (weighing 27 ± 3 g) were anesthetized with 1.5–2% isoflurane (RWD, Shenzhen, China) in a mixture of 30% oxygen and 70% nitrous oxide. The left common carotid artery, along with the internal carotid artery and the external carotid artery, were temporarily ligated. A cut was made between the two ligations on the external carotid artery. Following this, a 6-0 nylon suture (Covidien, Mansfield, MA, USA) coated with silicon (Heraeus Kulzer, Germany) was introduced through the incision and guided toward the ipsilateral middle cerebral artery. The success of middle cerebral artery occlusion was confirmed using laser Doppler flowmetry (Moor Instruments, Devon, UK) to observe a 10% reduction in the surface cerebral blood flow compared to its baseline level. The suture was withdrawn 1.5 h after the occlusion, and successful reperfusion was confirmed by observing the surface cerebral blood flow recovery back to 70% of its baseline level.
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7

Establishing post-traumatic KOA in mice

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The mice were anesthetized with isoflurane (RWD life science, Shenzhen, China) and performed with DMM according to the previous protocol, which was widely accepted to establish post-traumatic KOA [15 (link)]. To relieve the pain and remove the sutures before starting the drug treatment, the mice were administrated with anesthesia one week postoperatively [16 (link),17 ]. Specifically, all mice were treated by subcutaneous injection (S.I) with Teriparatide (PTH (1–34), HY-P0059, MCE, USA) (100 uL ​× ​40 ​μg/kg/day), which was confirmed by Ultimate 3000 U system High Performance Liquid Chromatography (HPLC) (Thermo Scientific) (Fig. S1). The mice were euthanized in the 4th, 8th, and 12th weeks for relevant evaluation.
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8

Low-Intensity Focused Ultrasound Stimulation

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The LIFUS system consists of (1) two function generators (DG4162 and DG822, RIGOL, Beijing, China), (2) a custom-designed radio frequency amplifier (SWA400A, North Star, Shijia zhuang, China), (3) a 0.5MHz single element immersion transducer (V318, Olympus, Tokyo, Japan), and (4) a custom-designed acoustic collimator (Zhang et al., 2019 (link)). The schematic diagram of LIFUS system is shown in Figure 1A. The LIFUS parameters used in this study were as follows (shown in Figure 1B): center frequency = 0.5 MHz; pulse repetition frequency (PRF) = 2.0 kHz; the number of cycles = 150 (0.3 ms tone burst duration, TBD); the sonication duration (SD) = 0.5 s; the interstimulus interval (ISI) = 2 s, and the spatial peak temporal average intensity (Ispta) = 500 mW/cm2. The targets of LIFUS are the bilateral mPFC. In addition, the LIFUS treatment was performed daily for 10 min on each side. During the LIFUS, all rats were mounted on the stereotaxic apparatus (RWD, Shenzhen, China) and anesthetized with 1% isoflurane (RWD, Shenzhen, China). Before applying the LIFUS, the hair on the bilateral mPFC was shaved. The other rats in either CON or VD groups underwent the same procedures including anesthesia but without LIFUS.
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9

6-OHDA Induced Neurodegeneration Protocol

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Isoflurane was purchased from RWD Life Science (Shenzhen, China). Pentobarbital and lidocaine were purchased from Chaohui Pharmaceutical. 6‐OHDA, AP‐5, DNQX, strychnine, muscimol, and gabazine were purchased from Sigma‐Aldrich. CY3 Donkey anti‐rabbit IgG, Mouse and Rabbit Specific HRP/DAB (ABC), Detection IHC kit, and rabbit antityrosine hydroxylase are products of Abcam Corp. 6‐OHDA hydrochloride (Sigma) was dissolved in 0.9% saline containing 0.2% ascorbic acid to avoid decomposition.
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10

Quadriceps and Gastrocnemius Nerve Branching

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The rabbits were anesthetized by isoflurane (RWD Life science Co., Ltd., Shenzhen, Guangdong Province, China) inhalation. After anesthetization, the left lower limb was shaved and sterilized. Then, the left quadriceps, gastrocnemius and their innervating nerves (the muscular branch of the femoral nerve and tibial nerve) were exposed carefully. The number of nerve branches around the neuromuscular junction into the muscle was recorded.
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