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 »  Abstract
 » Introduction
 »  Materials and Me...
 » Results
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 Table of Contents    
Year : 2015  |  Volume : 47  |  Issue : 2  |  Page : 199-201

Enhancement of nootropic effect of duloxetine and bupropion by caffeine in mice

1 Department of Pharmacology, SPP SPTM, SVKM'S NMIMS; Department of Pharmacology, Dr. Bhanuben Nanavati College of Pharmacy, Mumbai, Maharashtra, India
2 Department of Pharmacology, SPP SPTM, SVKM'S NMIMS, Mumbai, Maharashtra, India

Date of Submission29-Jun-2014
Date of Decision18-Jan-2015
Date of Acceptance26-Feb-2015
Date of Web Publication17-Mar-2015

Correspondence Address:
Veeranjaneyulu Addepalli
Department of Pharmacology, SPP SPTM, SVKM'S NMIMS, Mumbai, Maharashtra
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Source of Support: None, Conflict of Interest: None

DOI: 10.4103/0253-7613.153430

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 » Abstract 

Objective: The existing evidence suggests an association between depression and memory impairment. The objective of present study was to assess the effect of low dose caffeine with duloxetine and bupropion on memory.
Materials and Methods: Mice were divided randomly into seven groups. Intra-peritoneal treatment of normal saline (10 ml/kg), caffeine (10 mg/kg), duloxetine (10 mg/kg), bupropion alone (10 mg/kg), caffeine + duloxetine (5 mg/kg, each), caffeine + bupropion (5 mg/kg, each), and bupropion + duloxetine (5 mg/kg, each) were given to groups I-VII, respectively. Elevated plus maze was used to evaluate transfer latency (TL) and Morris water maze was used to estimate the time spent in target quadrant.
Results: Caffeine with duloxetine treated group was better than other combination treated groups in terms of a significant decrease in TL and increase in the time spent in target quadrant recorded.
Conclusion: Combining lower dose of caffeine with duloxetine may enhance cognitive benefits than respective monotherapies.

Keywords: And bupropion, caffeine, duloxetine, memory

How to cite this article:
Kale PP, Addepalli V. Enhancement of nootropic effect of duloxetine and bupropion by caffeine in mice. Indian J Pharmacol 2015;47:199-201

How to cite this URL:
Kale PP, Addepalli V. Enhancement of nootropic effect of duloxetine and bupropion by caffeine in mice. Indian J Pharmacol [serial online] 2015 [cited 2023 Oct 1];47:199-201. Available from: https://www.ijp-online.com/text.asp?2015/47/2/199/153430

 » Introduction Top

The association between depression and memory impairment is well-established. [1],[2] Kim et al. reported memory impairment in 22% of depressed patients. [3] Modulation of neurotransmitters such as serotonin (5-HT), norepinephrine (NE), and dopamine (DA) through hippocampus and cerebral cortex play a vital role in cognition. [1] Antidepressant treatment resulted in relieving short-term memory deficit. [4],[5] Duloxetine is a potent and selective reuptake inhibitor of 5-HT and NE, and a weak reuptake inhibitor of DA. Eight weeks of duloxetine treatment showed significant improvement in cognition and depression in depressed patients. [6] Bupropion is another preferred antidepressant, inhibits reuptake of NE and DA. [7] It showed better cognitive improvement than selective serotonin reuptake inhibitors in depressed patients. [8] The low dose of caffeine (5 mg/kg) produced augmentation of antidepressant effects of duloxetine/bupropion. [9] Therefore, the present study is designed to evaluate the nootropic effect of low dose of caffeine combination with duloxetine or bupropion.

 » Materials and Methods Top


Male Swiss albino mice were procured from Bharat Serum Ltd., Thane. The weight range was 25-30 g. Animals had free access to standard food and water. Experiments were performed between 10.00 and 16.00 h. Animals were randomly distributed into seven groups (n = 6/group). The arena of elevated plus maze (EPM) was wiped with 70% ethyl alcohol solution before placing each mouse. Study protocols were approved by the Institutional Animal Ethics Committee (Project approval number CPCSEA/IAEC/SPTM/P-46/2011), New Delhi, Government of India.

Drug Solutions and Treatment

Drugs were administered through intra-peritoneal route. Normal saline (0.9% w/v NaCl) was used to prepare drug solutions. EPM was performed first and Morris water maze (MWM) later in separate sets of animals consisting seven groups each. Each animal received treatment 30 min before test session in EPM on 1 st and 2 nd day. In MWM, treatments were given to mice 30 min before the test on each trial day. Selection of doses was done on the basis of in-house study. [9] Control group received vehicle treatment (Group I) that is, normal saline (10 ml/kg). Treatment of caffeine (10 mg/kg; Elders Pharmaceutical Pvt. Ltd.), duloxetine (10 mg/kg; Dr. Reddy's Laboratories Ltd.), and caffeine (5 mg/kg) + duloxetine (5 mg/kg) were given to groups II-IV, respectively. Groups V-VII received treatment of bupropion (10 mg/kg; Aurobindo Pharma Ltd.), caffeine (5 mg/kg) + bupropion (5 mg/kg), and bupropion (5 mg/kg) + duloxetine (5 mg/kg), respectively.

Spatial Memory Tests

In the present study, the protocol described by Dhingra et al. [10] was used to evaluate the transfer latency (TL). Apparatus consists of two open arms (30 cm × 5 cm) and two closed arms (30 cm × 5 cm × 12 cm). Arms were arranged so that the two closed arms kept opposite to each other without roof. Each mouse was placed at the end of open arm facing away from the central platform (5 cm × 5 cm). The acquisition session (1 st day) consists of 90 s exposure interval. Time taken by animal to reach the closed arm is recorded as the TL. If the animal fails to enter in closed arm in 90 s, it was excluded from the study. Animal was put on the open arm in retention session (2 nd day) and the recorded video was used to evaluate TL by the single trained person.

The protocol of MWM described by Bromley-Brits et al. [11] was used to determine percent time spent in target quadrant. The pool (150 cm diameter and 50 cm depth) was constructed of seamless black polyethylene. The escape platform (10 cm diameter, 31 cm high) was fabricated using clear plastic. The platform positions (visible) on 1 st day were South-West, North-West, North-East, Centre, and South-East on trial 1-5, respectively. On 2-5 days, platform position was South-West (hidden) and the starting positions of animal in five different trials were West-South-North-East-South, North-West-East-West-South, North-East-West-South-North, and East-South-West-East-North, respectively. In this black colored pool, clear water (22°C-24°C) and a clear plexiglass platform was used. On 6 th day, platform was removed and starting position of animals was north. The time spent by each animal in target quadrant, that is, South-West was determined from video of each animal by the single trained person.

Statistical Analysis

Statistical analysis was performed using the Graphpad InStat for 32 bit Windows version 3.06 (GraphPad Software, Inc). The statistical significance was estimated using ANOVA, followed by Tukey's honest significant difference post-hoc test.

 » Results Top

Caffeine plus duloxetine combination treated group showed a significant decrease in TL [Table 1], as compared to the control group. All other comparisons showed a slight decrease in TL, which were statistically not significant. In training and acquisition stage of MWM, the escape latency was decreased from 1 st to 5 th day. The differences between groups were not statistically significant [Table 2]. On 6 th day, the observed time spent in target quadrant was significantly increased in caffeine plus duloxetine-treated group, as compared to the control group [Table 2].
Table 1: Elevated plus maze-transfer latency (on 2nd day) in mice

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Table 2: Escape latency (time required to reach hidden platform in seconds) observed on day 1-5 and time spent (s) in target quadrant on 6th day in MWM in mice

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 » Discussion Top

Nehlig concluded no benefits in short-term and long-term memory with caffeine in a review. [12] The present study has focused on the short-term (EPM) and long-term (MWM) memory assessment. The results of caffeine, bupropion, and duloxetine-treated groups were in conformity with available reports. [13],[14],[15] Although the acute or sub-acute treatment of duloxetine was not beneficial in cognition, [14] a clinical study reported cognition related benefits with 8 and 12 weeks treatment period in depressed patients. [6],[16] Gualtieri and Johnson reported improvement in cognitive performance with bupropion treatment in depressed patients. [8] Caffeine also showed benefits in reducing Alzheimer's disease. [17] It has been reported that CYP1A2 plays a vital role in the metabolism of caffeine. [18] Duloxetine may not increase the retention of drugs metabolized by CYP1A2. [19] Therefore, caffeine plus duloxetine may have lower potential of drug interaction. Bupropion inhibits CYP2D6, which plays an important role in duloxetine metabolism. This indicates higher potential of interaction between duloxetine and bupropion. Caffeine plus bupropion combination may have lower potential of interaction because the enzymes involved in caffeine and bupropion metabolism are separate (i.e. CYP1A2 and CYP2B6). [20] Thus, the combination of duloxetine and caffeine at half of their monotherapy doses (5 mg/kg, each) may have better safety profile than other combinations. However, there is a need to study the impact of caffeine (low dose) combination with duloxetine/bupropion on their metabolism in acute and chronic dosing, which may enable us to understand the results of present study.

Hippocampus and cerebral cortex regions play a vital role in cognition and emotions. [1] The in vivo findings of the present study are in-line with the in vitro data of brain monoamines analyzed in-house. [9] Caffeine plus duloxetine group was better among all groups in terms of a significant increase in NE, DA, and 5-HT levels in hippocampi and cerebral cortices. The present study consists of chronic dosing, whereas the changes observed in brain monoamines were after single dosing as per in-house study. [9] The present study findings can be further probed in different preclinical models and clinical setting as a future endeavor.

 » References Top

Eriksson TM, Delagrange P, Spedding M, Popoli M, Mathé AA, Ögren SO, et al. Emotional memory impairments in a genetic rat model of depression: Involvement of 5-HT/MEK/Arc signaling in restoration. Mol Psychiatry 2012;17:173-84.  Back to cited text no. 1
Burt DB, Zembar MJ, Niederehe G. Depression and memory impairment: A meta-analysis of the association, its pattern, and specificity. Psychol Bull 1995;117:285-305.  Back to cited text no. 2
Kim JM, Stewart R, Shin IS, Choi SK, Yoon JS. Subjective memory impairment, cognitive function and depression - A community study in older Koreans. Dement Geriatr Cogn Disord 2003;15:218-25.  Back to cited text no. 3
Sternberg DE, Jarvik ME. Memory functions in depression. Arch Gen Psychiatry 1976;33:219-24.  Back to cited text no. 4
Glass RM, Uhlenhuth EH, Hartel FW, Matuzas W, Fischman MW. Cognitive dysfunction and imipramine in outpatient depressive. Arch Gen Psychiatry 1981;38:1048-51.  Back to cited text no. 5
Raskin J, Wiltse CG, Siegal A, Sheikh J, Xu J, Dinkel JJ, et al. Efficacy of duloxetine on cognition, depression, and pain in elderly patients with major depressive disorder: An 8-week, double-blind, placebo-controlled trial. Am J Psychiatry 2007;164:900-9.  Back to cited text no. 6
Bystritsky A, Kerwin L, Feusner JD, Vapnik T. A pilot controlled trial of bupropion XL versus escitalopram in generalized anxiety disorder. Psychopharmacol Bull 2008;41:46-51.  Back to cited text no. 7
Gualtieri CT, Johnson LG. Bupropion normalizes cognitive performance in patients with depression. MedGenMed 2007;9:22.  Back to cited text no. 8
Kale PP, Addepalli V. Augmentation of antidepressant effects of duloxetine and bupropion by caffeine in mice. Pharmacol Biochem Behav 2014;124:238-44.  Back to cited text no. 9
Dhingra D, Parle M, Kulkarni SK. Memory enhancing activity of Glycyrrhiza glabra in mice. J Ethnopharmacol 2004;91:361-5.  Back to cited text no. 10
Bromley-Brits K, Deng Y, Song W. Morris water maze test for learning and memory deficits in Alzheimer's disease model mice. J Vis Exp 2011;53:2920.  Back to cited text no. 11
Nehlig A. Is caffeine a cognitive enhancer? J Alzheimers Dis 2010;20 Suppl 1:S85-94.  Back to cited text no. 12
Biala G, Kruk M. Influence of bupropion and calcium channel antagonists on the nicotine-induced memory-related response of mice in the elevated plus maze. Pharmacol Rep 2009;61:236-44.  Back to cited text no. 13
Pereira P, Gianesini J, da Silva Barbosa C, Cassol GF, Von Borowski RG, Kahl VF, et al. Neurobehavioral and genotoxic parameters of duloxetine in mice using the inhibitory avoidance task and comet assay as experimental models. Pharmacol Res 2009;59:57-61.  Back to cited text no. 14
Singh N, Parle M. Sildenafil improves acquisition and retention of memory in mice. Indian J Physiol Pharmacol 2003;47:318-24.  Back to cited text no. 15
Greer TL, Sunderajan P, Grannemann BD, Kurian BT, Trivedi MH. Does duloxetine improve cognitive function independently of its antidepressant effect in patients with major depressive disorder and subjective reports of cognitive dysfunction? Depress Res Treat 2014;2014:627863.  Back to cited text no. 16
Carman AJ, Dacks PA, Lane RF, Shineman DW, Fillit HM. Current evidence for the use of coffee and caffeine to prevent age-related cognitive decline and Alzheimer's disease. J Nutr Health Aging 2014;18:383-92.  Back to cited text no. 17
Daniel WA, Kot M, Wójcikowski J. Effects of classic and newer antidepressants on the oxidation pathways of caffeine in rat liver. In vitro study. Pol J Pharmacol 2003;55:1045-53.  Back to cited text no. 18
Knadler MP, Lobo E, Chappell J, Bergstrom R. Duloxetine: Clinical pharmacokinetics and drug interactions. Clin Pharmacokinet 2011;50:281-94.  Back to cited text no. 19
Jefferson JW, Pradko JF, Muir KT. Bupropion for major depressive disorder: Pharmacokinetic and formulation considerations. Clin Ther 2005;27:1685-95.  Back to cited text no. 20


  [Table 1], [Table 2]


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