Experimental Study of the Analgesic Effect of the Antidepressant Escitalopram

Antidepressants have been found to possess antinociceptive and analgesic properties and are prescribed in the treatment of chronic pain. To evaluate the antinociceptive properties of escitalopram after a single administration. Forty Wistar rats were used in the study. They were divided into 5 groups...

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Published in:Folia Medica Vol. 60; no. 3; pp. 433 - 438
Main Authors: Zlatanova, Hristina I, Kandilarov, Ilin K, Kostadinov, Ilia D, Delev, Delian P, Georgieva-Kotetarova, Maria T
Format: Journal Article
Language:English
Published: Bulgaria MEDICAL UNIVERSITY- PLOVDIV 01-09-2018
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Abstract Antidepressants have been found to possess antinociceptive and analgesic properties and are prescribed in the treatment of chronic pain. To evaluate the antinociceptive properties of escitalopram after a single administration. Forty Wistar rats were used in the study. They were divided into 5 groups (n=8) treated with saline solution (control group), metamizole (150 mg/kg b.w.), escitalopram (5, 10 and 20 mg/kg b.w.) intraperitoneally. The nociceptive tests we used employed thermal (hot plate and plantar test), mechanical (analgesimeter) and chemical (formalin test) stimuli. Criteria for analgesic effect were increased latency in hot plate, plantar test, analgesimeter and decreased paw licking time in formalin test. The reference analgesic metamizole showed significant analgesic effect in all tests excluding the first phase with formalin. Escitalopram in doses of 5 and 20 mg/kg b.w. increased paw withdrawal latency in analgesimeter at 2 hours compared to control. Escitalopram in a dose of 5 mg/kg b.w. increased the duration of the stay on the hot plate at 1 hour, while doses of 10 and 20 mg/kg b.w. significantly increased this indicator at 1 and 3 hours in comparison to the saline treated group. In the plantar test, escitalopram in all used doses significantly increased the nociceptive response latency compared to control. A dose of 5 mg/kg b.w. decreased hind paw licking time during phase 1 of the formalin test, whereas doses of 10 and 20 mg/kg b.w. decreased phase 2 licking time compared to the control group. The antidepressant escitalopram has analgesic properties but they are not dose- or time-dependent.
AbstractList Background: Antidepressants have been found to possess antinociceptive and analgesic properties and are prescribed in the treatment of chronic pain.
Antidepressants have been found to possess antinociceptive and analgesic properties and are prescribed in the treatment of chronic pain. To evaluate the antinociceptive properties of escitalopram after a single administration. Forty Wistar rats were used in the study. They were divided into 5 groups (n=8) treated with saline solution (control group), metamizole (150 mg/kg b.w.), escitalopram (5, 10 and 20 mg/kg b.w.) intraperitoneally. The nociceptive tests we used employed thermal (hot plate and plantar test), mechanical (analgesimeter) and chemical (formalin test) stimuli. Criteria for analgesic effect were increased latency in hot plate, plantar test, analgesimeter and decreased paw licking time in formalin test. The reference analgesic metamizole showed significant analgesic effect in all tests excluding the first phase with formalin. Escitalopram in doses of 5 and 20 mg/kg b.w. increased paw withdrawal latency in analgesimeter at 2 hours compared to control. Escitalopram in a dose of 5 mg/kg b.w. increased the duration of the stay on the hot plate at 1 hour, while doses of 10 and 20 mg/kg b.w. significantly increased this indicator at 1 and 3 hours in comparison to the saline treated group. In the plantar test, escitalopram in all used doses significantly increased the nociceptive response latency compared to control. A dose of 5 mg/kg b.w. decreased hind paw licking time during phase 1 of the formalin test, whereas doses of 10 and 20 mg/kg b.w. decreased phase 2 licking time compared to the control group. The antidepressant escitalopram has analgesic properties but they are not dose- or time-dependent.
BACKGROUND In experimental and clinical studies it has been found that antidepressants possess antinociceptive and analgesic properties and are therefore used in the combined therapy of chronic pain.1 The serotoninselective reuptake inhibitors (SSRIs) were first introduced as a new class of antidepressants at the end of 1980s and due to their favorable side-effect profile have since become first-line therapy of depressive disorders.2 Most SSRIs have been found to also possess secondary binding properties - dopamine reuptake inhibition, noradrenaline reuptake inhibition, muscarinic cholinergic antagonism, etc.3 Only citalopram and its S(+)-enantiomer escitalopram are considered highly-selective SSRIs.4 The mechanisms responsible for the antinociceptive and analgesic effects of antidepressants are not entirely clear but it has been hypothesized that their effects are due to, at least partially, their inhibition of reuptake of serotonin.5 The "not so selective" SSRIs (e.g. fluvoxamine, fluoxetine) induce dose-dependent antinociceptive effects.2,6 In a clinical study conducted by Jaracz et al. in 2015, escitalopram shows pain-relieving action7, but in the available scientific literature there is insufficient experimental data on its analgesic effect and the mechanisms by which it is mediated. Subjects A total of 40 adult male Wistar rats were used, randomly divided in 5 groups of 8 animals as follows: group I - control group, treated with saline intraperitoneally (i.p.); group II - positive control, treated with referent analgesic metamizole 150 mg/kg b.w. (i.p.); group III - treated with escitalopram 5 mg/ kg b.w. (i.p.); group IV - treated with escitalopram 10 mg/kg b.w. (i.p.); group V - treated with escitalopram 20 mg/kg b.w. (i.p.). In the hot plate test, escitalopram in a dose of 5 mg/kg b.w. significantly lengthened the duration of the stay on the plate at 1 hour (р<0.05) compared to the control animals. 10 mg/kg b.w. of escitalopram increased the reaction time at one hour (р<0.05) and 3 hours (р<0.05) compared to the saline treated animals. The second phase occurs after a ten minute quiescent period and is attributed to the release of local endogenous mediators, leading to peripheral infl ammatory processes and subsequent sensitization of nociceptive spinal neurons.10 Serotonin is a key modulator of nociceptive transmission primarily at spinal cord level, where 5НТ-2 and 5 НТ-3 receptors mediate its inhibitory effect on pain.11,12 In a formalin test of normal and genetically modified mice lacking central serotonergic neurons (line Lmx1bf/f/p) no significant difference was found in the first phase of the test and enhancement of behavioral responses in Lmx1bf/f/p line in the second phase.13 In our study 10 and 20 mg/kg b.w. of escitalopram showed significant antinociceptive effect in the second phase of the formalin test.
BACKGROUNDAntidepressants have been found to possess antinociceptive and analgesic properties and are prescribed in the treatment of chronic pain. AIMTo evaluate the antinociceptive properties of escitalopram after a single administration. MATERIALS AND METHODSForty Wistar rats were used in the study. They were divided into 5 groups (n=8) treated with saline solution (control group), metamizole (150 mg/kg b.w.), escitalopram (5, 10 and 20 mg/kg b.w.) intraperitoneally. The nociceptive tests we used employed thermal (hot plate and plantar test), mechanical (analgesimeter) and chemical (formalin test) stimuli. Criteria for analgesic effect were increased latency in hot plate, plantar test, analgesimeter and decreased paw licking time in formalin test. RESULTSThe reference analgesic metamizole showed significant analgesic effect in all tests excluding the first phase with formalin. Escitalopram in doses of 5 and 20 mg/kg b.w. increased paw withdrawal latency in analgesimeter at 2 hours compared to control. Escitalopram in a dose of 5 mg/kg b.w. increased the duration of the stay on the hot plate at 1 hour, while doses of 10 and 20 mg/kg b.w. significantly increased this indicator at 1 and 3 hours in comparison to the saline treated group. In the plantar test, escitalopram in all used doses significantly increased the nociceptive response latency compared to control. A dose of 5 mg/kg b.w. decreased hind paw licking time during phase 1 of the formalin test, whereas doses of 10 and 20 mg/kg b.w. decreased phase 2 licking time compared to the control group. CONCLUSIONThe antidepressant escitalopram has analgesic properties but they are not dose- or time-dependent.
Author Zlatanova, Hristina I
Kandilarov, Ilin K
Delev, Delian P
Kostadinov, Ilia D
Georgieva-Kotetarova, Maria T
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/30355833$$D View this record in MEDLINE/PubMed
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escitalopram
SSRIs
analgesia
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Snippet Antidepressants have been found to possess antinociceptive and analgesic properties and are prescribed in the treatment of chronic pain. To evaluate the...
BACKGROUND In experimental and clinical studies it has been found that antidepressants possess antinociceptive and analgesic properties and are therefore used...
BACKGROUNDAntidepressants have been found to possess antinociceptive and analgesic properties and are prescribed in the treatment of chronic pain. AIMTo...
Background: Antidepressants have been found to possess antinociceptive and analgesic properties and are prescribed in the treatment of chronic pain.
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SubjectTerms analgesia
Analgesics
Analgesics - pharmacology
animal pain models
Animals
Antidepressants
Citalopram - pharmacology
Dipyrone - pharmacology
escitalopram
Hot Temperature
Male
Neurosciences
Nociception - drug effects
Pain
Pain Measurement
Physical Stimulation
Random Allocation
Rats
Rats, Wistar
Rodents
Serotonin
Serotonin Uptake Inhibitors - pharmacology
SSRIs
Title Experimental Study of the Analgesic Effect of the Antidepressant Escitalopram
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