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Imipramine imi

Manufactured by Merck Group
Sourced in United States

Imipramine (IMI) is a tricyclic antidepressant medication used for the treatment of depression. It is a laboratory compound utilized in research and development for pharmaceutical applications. IMI functions as a serotonin-norepinephrine reuptake inhibitor (SNRI), which helps regulate neurotransmitter levels in the brain.

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4 protocols using imipramine imi

1

Antidepressant Effects of Melatonin, Fluoxetine, and Imipramine

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All drugs were intraperitoneally (i.p.) administered in a total volume of 10.0 mL/kg (body weight). Doses are expressed as milligrams per kilogram of mouse body weight. Melatonin (MEL) (Sigma-Aldrich Corp., St. Louis, MO, USA) was dissolved in the minimum amount of absolute ethanol and then in isotonic (0.9%) saline solution. Ethanol concentration in that solution was 0.006%, so the vehicle (VEH) tested had that same amount of ethanol. Fluoxetine (FLX) and imipramine (IMI) (Sigma-Aldrich Corp., St. Louis, MO, USA) were dissolved in isotonic saline solution. Experiment series comprised independent groups of 8 animals for each specified drug treatment and behavioral test.
Single administration at ZT11 was as follows: Either MEL or its VEH were administered at ZT11 (1 h before the lights were off), and behavioral tests were assessed 7.5 h later (ZT18.5).
Single administration at ZT18 was as follows: Drugs were administered at ZT18 (the middle of the dark phase), 30 min before the behavioral tests.
Triple scheme administration (for the FST only) was as follows: First administration of the drugs was at 24.5 h before the test (ZT18; immediately after the pre-test session); the second injection was applied one hour before lights were off (ZT11; 7.5 h before the test); finally, the third administration was at ZT18, 30 min before the test [39 (link)].
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2

Pharmacological Modulation of P2X Receptors

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The following drugs were freshly prepared before use and administered intraperitoneally (ip): BBG (#B0770; Sigma Aldrich, St. Louis, MO, USA), a P2RX7/P2RX4 antagonist (Jiang et al., 2000 (link)), diluted in sterile isotonic saline and 2% tween 80, administered at 25 or 50 mg/kg/day doses (Csölle et al., 2013a (link); Carmo et al., 2014 (link)). Imipramine (IMI; #I7379; Sigma Aldrich, St. Louis, MO, USA), a tricyclic antidepressant, diluted in sterile isotonic saline, administered at 15 mg/kg/day dose (Stanquini et al., 2017 (link)). Chloral hydrate (Vetec) was used as a sedative for sample collection, at 5% concentration and administered at one ml/100g volume.
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3

N2a Cell Culture and Treatment

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Mouse neuroblastoma 2A (N2a) cell line was obtained from the China Biological Part Stock Center (Beijing, China) and cryopreserved after subculturing different passages. N2a cells were routinely propagated using Dulbecco's Modified Eagle Medium (DMSO, Gibco Laboratories, Grand Island, NY, USA), supplemented with 10% fetal bovine serum (Gibco Laboratories, Grand Island, NY, USA) and 100 U/mL penicillin and 100 μg/mL streptomycin (Gibco Laboratories, Grand Island, NY, USA) in a humidified incubator of 5% CO2 at 37 °C. Cultured cells were incubated for 48 h with pharmacological agents at the following concentrations: 0.1% DMSO (vehicle), 10 μM imipramine (IMI; Sigma-Aldrich, St. Louis, MO, USA), 10 μM amitriptyline (AMT; Aladdin, Shanghai, China), 10 μM mirtazapine (TCI, Tokyo, Japan), 10 μM fluoxetine (Sigma-Aldrich, St. Louis, MO, USA). Then, RNA was extracted from the N2a cells with Trizol (Takara Bio, Tokyo, Japan).
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4

Antidepressant Effects on Prenatal Stress

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After the behavioral verification, the control and prenatally stressed offspring were randomly divided into 8 experimental groups (CONTROL + Veh, CONTROL + Imi, CONTROL + Flu, CONTROL + Tia, STRESS + Veh, STRESS + Imi, STRESS + Flu, and STRESS + Tia; 6 animals per group) and were treated for 14 days with antidepressant drugs. Imipramine (Imi; Sigma Aldrich, St. Louis, MO, USA), fluoxetine (Flu; Eli Lilly, Indianapolis, USA), or tianeptine (Tia; Tocris Bioscience, United Kingdom) were injected intraperitoneally, once daily between 09.00 and 10.00 h at a dose of 10 mg/kg in a volume of 2 ml/kg (diluted in 0.9 % saline). The CONTROL + VEH and STRESS + VEH groups received 0.9 % saline (Polpharma, Poland) in a volume of 2 ml/kg b.w. In the last 2 days of antidepressants treatment, the behavioral parameters in the forced swim test were measured (Fig. 1). The behavioral study was not blinded.

Schematic diagram representing the schedule of the experiment. *2 h after pretest (13th day) or Porsolt (14th day) tests animals were treated with the antidepressants

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