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Infusion pump

Manufactured by Med Associates
Sourced in United States

Infusion pumps are medical devices used to deliver fluids, such as medications, nutrients, or blood, into a patient's body in a controlled and precise manner. They are designed to accurately and consistently administer these fluids at predetermined rates, volumes, and time intervals, ensuring the safe and effective delivery of the prescribed treatment.

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23 protocols using infusion pump

1

Operant Conditioning Chambers for Self-Administration

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The operant conditioning chambers (Med Associates, VT, USA) contained an active and inactive lever, a cue light, and a tone generator as previously described in Pentkowski et al.16 . The chambers contained either an infusion pump (Med Associates) connected to a liquid swivel (Instech, PA, USA) and attached to a polyethylene tubing sheltered within a metal leash (PlasticsOne, VA, USA) or contained pellet dispensers (Med Associates). All operant conditioning chambers were housed within sound attenuating boxes that contained a ventilation fan. Male and female rats underwent self-administration in different rooms to avoid potential confounding influences of sex on behavior.
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2

Oxycodone Self-Administration in Mice

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The self-administration chamber, ENV-307W (21.6 cm × 17.8 cm × 12.7 cm, Med. Associates, St. Albans, VT, USA), was located inside a larger sound attenuation chamber (Med. Associates). Each chamber contained a wall with two small holes (0.9-cm diameter, 4.2 cm apart, 1.5 cm from the floor of the chamber). One hole was defined as active, the other was inactive. When the photocell in the active hole was triggered by a nose-poke, an infusion pump (Med. Associates) delivered an oxycodone infusion of 20 μl/3 s from a 5-ml syringe. The syringe was connected by a swivel via Tygon tubing. The infusion pump and syringe were outside the chamber. During infusion, a cue light above the active hole was illuminated. Each injection was followed by a 20-s “time-out” period during which poking responses were recorded but had no programed consequences. All responses at the inactive hole were also recorded. Mice were tested during the dark phase of the diurnal cycle (all experiments were performed between 8:00 am and 12:00 pm).
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3

Operant Conditioning and Cue-Induced Relapse

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Behavioral sessions took place in eight operant boxes (MedAssociates, VT), as described previously (Exton-McGuinness and Lee, 2015 (link)). Prior to each session catheters were flushed with heparinized saline (0.1 ml, 30 IU/ml). Catheters were then connected to an infusion pump (MedAssociates, VT, USA) and secured with a spring tether. The study consisted of five experiments each with the same training and reactivation protocols, however, testing was conducted in one of five conditions: (1) spontaneous seeking; (2) CS-induced relapse; (3) yohimbine-induced stress; (4) cocaine priming; and (5) yohimbine + CS relapse.
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4

Operant Conditioning Chamber Setup for Intravenous Self-Administration

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Testing was conducted in 16 standard operant response chambers (32 x 25 x 34 cm; Med Associates, St Albans, VT, USA), which were housed in sound-attenuating boxes (41 x 56 x 56 cm) equipped with a fan for masking noise and to provide ventilation. Each chamber was equipped with two retractable levers (1 active, 1 inactive) and a house light. The chambers also contained a metal arm with an adjustable weight and a spring connector, which were attached to a swivel. Polyethylene tubing threaded through the spring connector was connected to a 10 ml syringe attached to an infusion pump (Med Associates) located outside of the sound-attenuating chamber. The tubing exiting from the base of the spring connector was connected to the back mount of the intravenous catheter.
Four infrared photobeam detectors were also positioned on the sidewall of each operant chamber to measure locomotor activity. Active and inactive lever presses, number of infusions and locomotor activity was collected and recorded using MED-PC software.
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5

Operant Conditioning for Oral MA Reinforcement

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Operant conditioning for oral MA reinforcement was conducted in cohorts of 12 mice of the same sex during the dark phase of the circadian cycle. On each self-administration day, mice were relocated in their home cages to a non-colony procedural room, approximately 30 min before testing. Mice were tested in 59.69 cm × 40.64 cm operant chambers (Med Associates, St. Albans, VT, USA), housed in a sound-attenuated cabinet and equipped with two nose-poke holes (one inactive and one active/MA-reinforced) and a liquid receptacle attached to an infusion pump (Med Associates, St. Albans, VT, USA), which delivered 20 µL of the assigned MA solution (0.8, 1.6, or 3.2 g/L) into the receptacle (respectively, MA-0.8, MA-1.6, and MA-3.2). MA-naïve controls responded to potable water only (MA-0). Mice were trained to self-administer water/MA for 7 consecutive days under a fixed ratio (FR) 1 schedule of reinforcement. As in our prior study [17 (link)], each reinforcer delivery was signaled by a compound light/tone cue and 20 s time-out period. At the end of each self-administration session, mice were returned to their home cages and relocated to the colony room. At twenty-four hours following the 7th self-administration session, mice underwent a behavioral test battery to assay the effects of oral MA on the indices of negative affect and sensorimotor processing.
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6

Operant Conditioning Self-Administration Chamber

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The self-administration chamber (ENV-307W: 21.6 cm × 17.8 cm × 12.7 cm; Med Associates, St. Albans, VT) was located inside a sound attenuating chamber (Med Associates). The front, back and top were constructed of 5.6 mm polycarbonate. Each chamber contained a wall with two small holes (0.9 cm diameter, 4.2 cm apart, 1.5 cm from the floor of the chamber). One hole was defined as active, the other was inactive. When the photocell in the active hole was triggered by a nose-poke, the infusion pump (Med Associates) delivered an infusion of 20 μl/3 s from a 5 ml syringe connected by a swivel via Tygon tubing. The infusion pump and syringe were located outside the chamber. During infusion, a cue light above the active hole was illuminated. Each injection was followed by a 20-sec “time-out” period during which poking responses were recorded but had no programmed consequences. All responses at the inactive hole were also recorded. Mice were tested during the dark phase of the diurnal cycle (all experiments were performed between 8:00 a.m. and 2:00 p.m.).
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7

Operant Chambers for Fentanyl Self-Administration

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Standard rat operant chambers (Med Associates, St Albans, VT, USA) were used for IV fentanyl self-administration. Each operant chamber had plexiglass front and back walls, metal side walls, a metal grid floor, and a removable tray below the grid floor filled with bedding. The chambers contained two retractable levers with a cue light located above each lever. Fentanyl was delivered through Tygon tubing (Cole-Parmer, Vernon Hills, IL, USA) that connected to the rat’s catheter and a 30 ml BD luer lock syringe (Mckesson, USA) attached to an infusion pump (Med Associates) outside of the operant chamber. The tubing was protected by a modified leash (Med Associates) and held in place by a drug delivery arm (Med Associates) and swivel (Med Associates), which allowed the animals to move freely in the chambers. For all operant sessions, we provided animals with hard plastic chew toys (Bio-Serv Nylon Bones, Fisher Scientific) to minimize destructive chewing or self-injury.
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8

Operant Conditioning Methamphetamine Self-administration

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The experiments were conducted in operant chamber boxes (25 × 27 × 30 cm). Each box has two levers located 9 cm above the floor, but only one lever (an “active”, retractable lever) activates the infusion pump (Med Associates Inc., St. Albans, VT, USA). METH-HCL was dissolved in sterile saline at a concentration 0.1 mg/kg/infusion and loaded into syringes. Each syringe was mounted above infusion pumps and connected via a rotating “swivel” to a back mounted cannula, which finally led to the jugular catheter of the rat. Swivel apparatuses are sufficiently long enough to allow rats to move freely in the behavioral chamber. Data collection and programming were conducted using PC computers with a Med-PC interface (Med Associates, Inc., St. Albans, VT, USA).
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9

Operant Conditioning Chamber Protocol

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Behavioural testing was conducted in 16 standard operant response chambers (32 × 25 × 34 cm: Med Associates, St Albans, VT, USA). Operant response chambers were housed in sound-attenuating boxes (41 × 56 × 56 cm) equipped with a fan for ventilation. Each chamber was equipped with two retractable levers, two cue lights and a house light. Chambers also contained a metal arm and a spring connector which was attached to the animal’s catheter. Polyethylene tubing was attached to a 10-mL syringe, driven by an infusion pump (Med Associates). Four infrared detectors were used to measure locomotor activity during test sessions. Active and inactive lever presses, number of infusions and locomotor activity were recorded using MED-PC software (Med Associates).
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10

Operant Conditioning with Ketamine Infusions

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Ketamine or vehicle infusions were delivered in operant chambers encased in sound-insulated cubicles, equipped with ventilation fans (Med Associates Inc., St Albans, Vermont, USA). Each chamber contained two levers.
In the S/A group, right lever (ketamine-paired lever) presses corresponding to Fixed-Ratio (FR) value of 1 produced the activation of the infusion pump (Med Associates Inc.). Lever pressing during the Time-Out (TO) period was recorded, although it did not have any consequence. Left lever presses did not have any consequence. All types of lever presses were recorded for all the groups. A 2 W house light located on the back panel near the chamber ceiling provides ambient illumination during the entire session duration, except during infusions and TO periods. The house light indicated the availability of the drug. Data acquisition and schedule parameters were controlled by Med-PC software (Med Associates Inc.).
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