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Tcat 2lv

Manufactured by Physitemp
Sourced in United States

The TCAT-2LV is a temperature control and monitoring device designed for laboratory applications. It provides precise temperature control and monitoring functionality for various experimental and research purposes. The device's core function is to accurately maintain and monitor temperature within a defined range.

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26 protocols using tcat 2lv

1

Carotid Artery Exposure Surgery in Mice

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We performed the right carotid artery exposure surgery as previously described [22 (link), 23 (link)]. Briefly, mice were anesthetized by 2.5% sevoflurane delivered with anesthetic-specific vaporizer. The anesthetic concentrations were monitored with a DATex-Ohmeda monitor. During the procedure, the mouse was kept spontaneous respiration. A 1.5-cm midline neck incision was made after the mouse was exposed to volatile anesthetics at least for 15 min. The soft tissues over the trachea were retracted gently. One centimeter of right common carotid artery was dissected free from adjacent tissues without damaging vagus nerve. The wound was then irrigated and closed using surgical suture. The surgical procedure was performed under sterile conditions and lasted about 15 min. No response to toe pinching was observed throughout the anesthetic and surgical process. Rectal temperature was monitored and maintained at 37 °C with the servo-controlled warming blanket (TCAT-2LV, Physitemp instruments, Clifton, NJ, USA). MouseOX Murine Plus Oximeter System (Starr Life Sciences Corporation, Oakmont, PA, USA) was used to continuously monitor animal’s heart rate and pulse oxygen saturation. After the surgery, all animals received a subcutaneous injection of 0.003 mg/kg bupivacaine. Animals in the control group did not receive anesthesia, surgery or bupivacaine.
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2

Stereotactic Injections in Anesthetized Mice

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Adult mice were anesthetized with isoflurane (3–4% for induction, 1.5% for maintenance) for retrobead and adeno-associated virus injections, or by intraperitoneal injection of ketamine (65 mg/kg) and xylazine (13 mg/kg) for rabies virus injections, or with urethane (1.6 g/kg) for pharmacological injections. Anesthetized mice were placed in a stereotactic instrument (David Kopf Instruments, Model 940), with body temperature maintained at 36°C using a feedback-controlled heating pad (Physitemp, TCAT-2LV). The following coordinates were used for injection: LHA, −1.40 mm posterior to bregma, −5.25 mm ventral from surface, ±0.95 mm from midline; RTN, −6.0 mm, −5.25 mm ventral from surface, ±1.3 mm from midline; preBötC, −6.85 mm, −4.65 mm ventral from surface, ±1.25 mm from midline. For retrobead and viral injections, animals were recovered from the stereotactic injection and subcutaneous injections of carprofen were administered (5 mg/kg) for pain alleviation.
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3

Right Carotid Artery Exposure in Rats

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The surgery was right carotid artery exposure. Briefly, as described before [1 (link)], P7 rats were anesthetized by 3% sevoflurane. During the procedure, the rats maintained spontaneous respiration with a facemask supplied with 100% oxygen. The rectal temperature was maintained at 37°C with the aid of a heating blanket (TCAT-2LV, Physitemp Instruments Inc., Clifton, NJ). A 1.5-cm midline neck incision was made after the rats had been anesthetized for at least 30 min. Soft tissues above the trachea were separated gently. One-centimeter-long right common carotid artery was carefully dissected from adjacent tissues without any damage to the vagus nerve. The wound was then irrigated and closed by using surgical clips. The surgical procedure was performed for around 10 min under sterile conditions. The total duration of general anesthesia was 2 h. This length of anesthesia was provided to simulate the duration of anesthesia often applied to pediatric patients with surgery and was part of the model in the previous studies [1 (link), 3 (link)]. Because this procedure was minimally invasive, no additional medication was needed for postoperative pain control based on the observations of animal activity and performance.
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4

Simultaneous Binocular PERG Recording in Mice

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Anesthetized mice were placed on a feedback-controlled heating pad (TCAT-2LV, Physitemp Instruments Inc, Clifton, NJ) to maintain body temperate at 37°C. Simultaneous binocular PERG recording was completed with the Miami PERG system (Intelligent Hearing Systems, Miami, FL) according to published protocol (Chou et al., 2018 (link)). Eye drops were added as needed to prevent corneal drying (Systane Ultra Lubricant Eye Drops, Alcon Laboratories, Ft Worth, TX). The reference electrode was placed subcutaneously on the back of the head between the two ears and the ground electrode was placed at the root of the tail. The signal electrode was placed subcutaneously on the snout for the simultaneous acquisition of left and right eye responses. Two 14 cm × 14 cm LED-based screens were placed 10 cm in front of each eye. The pattern remained at a contrast of 85% and a luminance of 800 cd/m2, and consisted of four cycles of black-gray elements, with a spatial frequency of 0.052 c/d. Upon stimulation, the PERG signals were recorded by asynchronous binocular acquisition. Two consecutive recordings of 200 traces were averaged to achieve one readout. The first positive peak in the waveform was designated as P50 and the second negative peak as N95. The investigators who measured the amplitudes were blinded to the treatment of the samples.
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5

Exploratory Laparotomy in Mice for Clinical Mimicry

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The surgery was an exploratory laparotomy. Briefly, mice were anesthetized with 3% sevoflurane. During the procedure, spontaneous respiration was maintained. Rectal temperature was monitored and maintained at 37°C with the aid of a heating blanket (TCAT-2LV, Physitemp instruments Inc., Clifton, NJ). After sterilization, local analgesia at the abdominal incision site was achieved by infiltrating 0.25% bupivacaine (3 mg/kg). An incision was made in the middle abdomen from low processus xiphoideus to superior margin of pubic symphysis. A cotton tip wet with normal saline (NS) was used to explore the abdominal cavity to see the diaphragmatic surface of the liver and spleen, and to identify the kidneys and bladder to mimic clinical exploratory laparotomy. After rinsing the abdominal cavity with NS, the peritoneum and skin were closed with surgical suture. The total duration of anesthesia was 2 h. The depth of anesthesia was maintained to have no response to toe pinching. After the surgery, all mice received a subcutaneous injection of 3 mg/kg bupivacaine into the wound area for three days, once every day.
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6

Right Carotid Artery Exposure in Rats

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The surgery was right carotid artery exposure [3 (link)]. Briefly, PND7 rats were anesthetized by 3% sevoflurane. During the procedure, the rat was breathing spontaneously with a facemask supplied with 100% oxygen. Rectal temperature was monitored and maintained at 37°C with the aid of a heating blanket (TCAT-2LV, Physitemp Instruments Inc., Clifton, NJ) during the anesthesia. A 1.5-cm midline neck incision was made after the rat was exposed to sevoflurane for at least 30 min. Soft tissues over the trachea were retracted gently to allow dissection of 1-cm long right common carotid artery free from adjacent tissues with no damage to the vagus nerve. The wound was then irrigated and closed by using surgical suture. The surgery was done under sterile conditions and lasted for about 15 min. After the surgery, all rats had a subcutaneous injection of 6 mg/kg bupivacaine. Additional medication for postoperative pain control was not needed based on the observation of animal activity and presentation. The total duration of general anesthesia was 2 h. The anesthesia level was maintained to abolish the response to toe pinching.
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7

Carotid Artery Exploration Surgery in Mice

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The animals were subjected to right carotid artery exploration surgery [3 (link), 9 , 10 (link)]. Briefly, mice were anesthetized with 2% isoflurane and mechanically ventilated. A servo-controlled warming blanket (TCAT-2LV, Physitemp instruments Inc., Clifton, NJ) was used to maintain the rectal temperature at 37°C. Mouse's heart rate and pulse oxygen saturation were monitored continuously by MouseOX Murine Plus Oximeter System (Starr Life Sciences Corporation, Oakmont, PA). A 1-cm long neck incision was made in the midline after 0.25% bupivacaine was injected subcutaneously. The soft tissues were retracted to expose the trachea. A 0.5 cm long right common carotid artery was dissected out from surrounding tissues with care to avoid damage to the vagus nerve. Isoflurane anesthesia was stopped once the wound was closed with skin staple. The surgical procedure was performed under sterile conditions and lasted for 10 min.
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8

Right Carotid Artery Exposure in Mice

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The surgery was a right carotid artery exposure [22 (link)]. Briefly, mice were anesthetized by 2.5% sevoflurane (the first and second experiments) or 1.5% isoflurane (the third and fourth experiments) in oxygen. During the procedure, spontaneous respiration was maintained and rectal temperature was monitored and maintained at 37 °C with the aid of a heating blanket (TCAT-2LV, Physitemp Instruments Inc., Clifton, NJ, USA). A 1.5-cm midline neck incision was made after the mouse was exposed to sevoflurane or isoflurane for at least 30 min. Soft tissues over the trachea were retracted gently. One-centimeter-long right common carotid artery was carefully dissected free from adjacent tissues without any damage on the vagus nerve. The wound was then irrigated and closed by using surgical suture. The surgical procedure was performed under sterile conditions and lasted approximately 10 min. After the surgery, all animals received a subcutaneous injection of 3 mg/kg bupivacaine. The total duration of anesthesia was 2 h. No response to toe pinching was observed during the anesthesia. Our previous studies had shown that animals maintained good arterial blood oxygen saturation and heart rates under these surgery and anesthesia conditions [23 (link),24 (link)].
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9

Exploratory Laparotomy Procedure in Mice

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All mice were anesthetized by 1.5% isoflurane for exploratory laparotomy as we did before [19 (link)]. Briefly, mouse was kept at spontaneous respiration with an inspiration of 50% O2. Rectal temperature was monitored and maintained at 37 °C with the aid of a heating blanket (TCAT-2LV, Physitemp instruments Inc., Clifton, NJ, USA). The hair in the abdomen was shaved and the abdominal area was sterilized with iodine. Bupivacaine (0.25%, 3 mg/kg) was infiltrated to the incision site before surgery. The abdominal cavity was opened by an incision from the xiphoid process to the superior margin of the pubic symphysis. The right colon, diaphragmatic surface of the liver, spleen, kidneys, and bladder were explored by a cotton tip wetted with NS to mimic clinical exploratory laparotomy. To ensure similar degree of stimulation, every mouse was explored by the same set of procedure. After the peritoneum and skin were closed separately, all animals received a subcutaneous injection of 3 mg/kg bupivacaine to the wound again for postoperative analgesia. The total duration of anesthesia was 2 h.
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10

Mouse Model of Myocardial Infarction

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The left anterior descending (LAD) coronary artery was occluded to induce MI in an acute open chest, in situ mouse model as described previously17 (link) to assess the effects of AR-C141990 on I/R injury. Briefly, mice were anaesthetized by administration of sodium pentobarbital (70 mg/kg intraperitoneally), endotracheally intubated, ventilated with 3 cm H2O positive end expiratory pressure and kept at 37 °C using a rectal thermometer-controlled heatpad (TCAT-2LV, Physitemp, USA). Ventilation frequency was maintained at 110 breaths/min, with tidal volume between 125 and 150 μl. The heart was exposed and a suture was placed around the prominent branch of the LAD and passed through a small plastic tube used to initiate ischemia by pressing the tube against the heart surface to occlude the LAD. Mice were subjected to 30 min of ischemia and 120 min of reperfusion, after reperfusion, hearts were stained with Evans Blue and 2% triphenyltetrazolium chloride (TTC) and blindly analyzed by an independent researcher.
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