Home Haloperidol-induced parkinsonism is attenuated by varenicline in mice
Article
Licensed
Unlicensed Requires Authentication

Haloperidol-induced parkinsonism is attenuated by varenicline in mice

  • Amit K. Sharma , Sparsh Gupta EMAIL logo , Ranjan K. Patel and Neeta Wardhan
Published/Copyright: April 10, 2018

Abstract

Background

Parkinson’s disease (PD) is a neurodegenerative disorder of the central nervous system (CNS). However, there is no known drug to stop/slow down this neurodegeneration. Varenicline is an anti-smoking drug and has the potential to prevent neurodegeneration. Thus, the present study was designed to evaluate the effect of varenicline in animal models of PD.

Methods

Levodopa and haloperidol were administered in doses of 30 and 1 mg/kg, intraperitoneally (i.p.), respectively. Group 1 was administered haloperidol; groups 2, 3 and 4 were administered haloperidol along with varenicline in doses of 0.5, 1.5 and 2.5 mg/kg, i.p., respectively and group 5 was administered levodopa along with haloperidol. Varenicline was administered daily, 30 min prior to the administration of haloperidol. Varenicline was administered for the first 8 days, and then from the 9th day until the 15th day. Behavioral assessment (rotarod and catalepsy tests) was performed on days 9 and 15. Assessment of striatal dopamine levels and histopathology were also performed.

Results

In the haloperidol-treated groups, significant decrease in latency to fall off (on rotarod) and increase in catalepsy duration (in catalepsy test) were observed as compared to the control group. In the levodopa-treated group, significant increase in latency to fall off the rotarod and significant decrease in catalepsy duration were observed as compared to the haloperidol-treated groups. Further, on day 9, varenicline (2.5 mg/kg) significantly increased the latency to fall off the rotarod, while varenicline (0.5 and 1.5 mg/kg) did not cause any significant change in latency to fall off the rotarod as compared to the haloperidol-treated group. On day 15, significant increase in latency to fall off the rotarod was observed in varenicline (at all doses) as compared to the haloperidol-treated group. In the catalepsy test, the varenicline-treated (at all doses) groups showed significant decrease in duration of catalepsy on day 9 and day 15 as compared to the haloperidol-treated group. Significant decrease in striatal dopamine levels was observed among the haloperidol-treated groups as compared to the control group. Further, varenicline-treated (at all doses) and levodopa-treated groups showed significant increase in striatal dopamine levels when compared with the haloperidol-treated group. In histology, varenicline (0.5 mg/kg) showed moderate decrease in neurons, while varenicline (1.5 and 2.5 mg/kg) showed mild decrease in neurons. However, the levodopa-treated group did not show any significant decrease in neurons. Thus, varenicline has shown promising results and has provided novel strategy for the treatment of PD.


Corresponding author: Dr. Sparsh, Associate Professor, Department of Pharmacology, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi 110029, India, Phone: +91-9818057272

  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: None declared.

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

References

1. Rooke ED, Vesterinen HM, Sena ES, Egan KJ, Macleod MR. Dopamine agonists in animal models of Parkinson’s disease: a systematic review and meta-analysis. Parkinsonism Relat Disord 2011;17:313–20.10.1016/j.parkreldis.2011.02.010Search in Google Scholar

2. Delong MR, Juncos JL. Parkinson’s disease and other extrapyramidal movement disorders. In: Fauci SA, Kasper DL, Longo DL, Braunwald E, Hauser SL, Jameson JL, et al., editors. Harrison’s principles of internal medicine, 17th ed., vol 2. New York: McGraw-Hill Companies Inc, 2008;366:2549.Search in Google Scholar

3. Playfer JR. Parkinson’s disease. Postgrad Med J 1997;73:257–64.10.1136/pgmj.73.859.257Search in Google Scholar

4. Münchau A, Bhatia KP. Pharmacological treatment of Parkinson’s disease. Postgrad Med J 2000;76:602–10.10.1136/pmj.76.900.602Search in Google Scholar

5. Ferré S, Guix T, Prat G, Jane F, Casas M. Is experimental catalepsy properly measured? Pharmacol Biochem Behav 1990;35:753–7.10.1016/0091-3057(90)90354-KSearch in Google Scholar

6. Wang S, Hu LF, Yang Y, Ding JH, Hu G. Studies of ATP-sensitive potassium channels on 6-hydroxydopamine and haloperidol rat models of Parkinson’s disease: implications for treating Parkinson’s disease? Neuropharmacology 2005;48:984–92.10.1016/j.neuropharm.2005.01.009Search in Google Scholar PubMed

7. Scholtissen B, Verhey FR, Steinbusch HW, Leentjens AF. Serotonergic mechanisms in Parkinson’s disease: opposing results from preclinical and clinical data. J Neural Transm 2006;113:59–73.10.1007/s00702-005-0368-3Search in Google Scholar PubMed

8. Gale C, Martyn C. Tobacco, coffee and Parkinson’s disease. Br Med J 2003;326:561–2.10.1136/bmj.326.7389.561Search in Google Scholar PubMed PubMed Central

9. Menzaghi F, Whelan KT, Risbrough VB, Rao TS, Lloyd GK. Interactions between a novel cholinergic ion channel agonist, SIB-1765F and L-DOPA in the reserpine model of Parkinson’s disease in rats. J Pharmacol Exp Ther 1997;280:393–401.10.1016/S0022-3565(24)36404-3Search in Google Scholar

10. Salminen O, Seppä T, Gäddnäs H. The effects of acute nicotine on metabolism of dopamine and the expression of Fos protein in striatal and limbic brain areas of rats during chronic nicotine infusion and its withdrawal. J Neurosci 1999;19:8145–51.10.1523/JNEUROSCI.19-18-08145.1999Search in Google Scholar

11. Quik M, Chen L, Parameswaram N, Xie X, Langston JW, McCallum SE. Chronic oral nicotine normalizes dopaminergic function and synaptic plasticity in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-lesioned primates. J Neurosci 2006;26:4681–9.10.1523/JNEUROSCI.0215-06.2006Search in Google Scholar PubMed PubMed Central

12. Hays JT, Ebbert JO. Varenicline for tobacco dependence. N Engl J Med 2008;359:2018–24.10.1056/NEJMct0800146Search in Google Scholar PubMed PubMed Central

13. Cahill K, Stead LF, Lancaster T. Nicotine receptor partial agonists for smoking cessation. Cochrane Database Syst Rev 2011;4:CD006103.10.1002/14651858.CD006103.pub5Search in Google Scholar PubMed

14. Chang PY, Shiu MN, Yuan YT, Chang HC, Su PY, Lan TH. Comparative effectiveness of varenicline and nicotine replacement therapy for smoking cessation in older and younger smokers: a prospective cohort in Taiwan. Nicotine Tob Res 2017. doi: 10.1093/ntr/ntx275. [Epub ahead of print].10.1093/ntr/ntx275Search in Google Scholar PubMed PubMed Central

15. O’Connor EC, Parker D, Rollema H, Mead AN. The α4β2 nicotinic acetylcholine-receptor partial agonist varenicline inhibits both nicotine self-administration following repeated dosing and reinstatement of nicotine seeking in rats. Psychopharmacology (Berl) 2010;208:365–76.10.1007/s00213-009-1739-5Search in Google Scholar PubMed

16. Wouda JA, Riga D, De Vries W, Stegeman M, van Mourik Y, Schetters D, et al. Varenicline attenuates cue-induced relapse to alcohol, but not nicotine seeking, while reducing inhibitory response control. Psychopharmacology (Berl) 2011;216:267–77.10.1007/s00213-011-2213-8Search in Google Scholar PubMed PubMed Central

17. Costello MR, Reynaga DD, Mojica CY, Zaveri NT, Belluzzi JD, Leslie FM. Comparison of the reinforcing properties of nicotine and cigarette smoke extract in rats. Neuropsychopharmacology 2014;39:1843–51.10.1038/npp.2014.31Search in Google Scholar PubMed PubMed Central

18. Le Foll B, Chakraborty-Chatterjee M, Lev-Ran S, Barnes C, Pushparaj A, Gamaleddin I, et al. Varenicline decreases nicotine self-administration and cue-induced reinstatement of nicotine-seeking behavior in rats when a long pretreatment time is used. Int J Neuropsychopharmacol 2012;15:1265–74.10.1017/S1461145711001398Search in Google Scholar PubMed PubMed Central

19. Hamm RJ, Pike BR, O’Dell DM, Lyeth BG, Jenkins LW. The rotarod test: an evaluation of its effectiveness in assessing motor deficits following traumatic brain injury. J Neurotrauma 1994;11:187–96.10.1089/neu.1994.11.187Search in Google Scholar PubMed

20. Pires JG, Bonikoski V, Futuro-Neto HA. Acute effects of selective serotonin reuptake inhibitors on neuroleptic – induced catalepsy in mice. Braz J Med Biol Res 2005;38:1867–72.10.1590/S0100-879X2005001200015Search in Google Scholar

21. Elliott PJ, Close SP, Walsh DM, Hayes AG, Marriott AS. Neuroleptic-induced catalepsy as a model of Parkinson’s disease. I. Effect of dopaminergic agents. J Neural Transm Park Dis Dement Sect 1990;2:79–89.10.1007/BF02260896Search in Google Scholar PubMed

22. Rang HP, Dale MM, Ritter JM, Flower RJ. Pharmacology, 6th ed. New York: Churchill Livingstone, 2007:512–7.10.1016/B978-0-443-06911-6.50006-2Search in Google Scholar

23. Calne DB, Langston WJ. Etiology of Parkinson’s disease. Lancet 1983;2:1457–9.10.1016/S0140-6736(83)90802-4Search in Google Scholar

24. Kadastik-Eerme L, Taba N, Asser T, Taba P. Factors associated with motor complications in Parkinson’s disease. Brain Behav 2017;7:e00837.10.1002/brb3.837Search in Google Scholar PubMed PubMed Central

25. Mihalak KB, Carroll FI, Luetje CW. Varenicline is a partial agonist at α4β2 and a full agonist at α7 neuronal nicotinic receptors. Mol Pharmacol 2006;70:801–45.10.1124/mol.106.025130Search in Google Scholar PubMed

26. Feduccia AA, Simms JA, Mill D, Yi HY, Bartlett SE. Varenicline decreases ethanol intake and increases dopamine release via neuronal nicotinic acetylcholine receptors in the nucleus accumbens. Br J Pharmacol 2014;171:3420–31.10.1111/bph.12690Search in Google Scholar PubMed PubMed Central

27. Ericson M, Löf E, Stomberg R, Söderpalm B. The smoking cessation medication varenicline attenuates alcohol and nicotine interactions in the rat mesolimbic dopamine system. J Pharmacol Exp Ther 2009;329:225–30.10.1124/jpet.108.147058Search in Google Scholar PubMed

Received: 2017-07-19
Accepted: 2018-01-22
Published Online: 2018-04-10
Published in Print: 2018-07-26

©2018 Walter de Gruyter GmbH, Berlin/Boston

Articles in the same Issue

  1. Frontmatter
  2. Letter to the Editor
  3. Blister-packed levothyroxine sodium or bottle-packed levothyroxine sodium
  4. Metabolism
  5. Comparative hypoglycemic potentials and phytochemical profiles of 12 common leafy culinary vegetables consumed in Nsukka, Southeastern Nigeria
  6. Infection
  7. The effects of oral pregabalin on post-Lichtenstein herniorrhaphic pain: a randomized clinical trial
  8. Cardiovascular Function
  9. Influence of age and gender on blood pressure variability and baroreflex sensitivity in a healthy population in the Indian sub-continent
  10. Autonomic responses during acute myocardial infarction in the rat model: implications for arrhythmogenesis
  11. Phytotherapy
  12. Role of reactive oxygen species–total antioxidant capacity status in Telfairia occidentalis leaves–associated spermatoprotective effect: a pointer to fatty acids benefit
  13. Antidiabetic and renoprotective effect of Anogeissus acuminata leaf extract on experimentally induced diabetic nephropathy
  14. Oxidative Stress
  15. Aged coconut oil with a high peroxide value induces oxidative stress and tissue damage in mercury-treated rats
  16. Anti-ulcerogenic effect of the methanol extract of Chasmanthera dependens (Hochst) stem on male Wistar rats
  17. Hematological Profile
  18. Evaluation of hematological alterations after therapeutic use of dipyrone in healthy adults: a prospective study
  19. Hematology and erythrocyte osmotic fragility of the Franquet’s fruit bat (Epomops franqueti)
  20. Behavior and Neuroprotection
  21. Haloperidol-induced parkinsonism is attenuated by varenicline in mice
  22. Antioxidant-mediated neuroprotection by Allium schoenoprasum L. leaf extract against ischemia reperfusion-induced cerebral injury in mice
  23. Effects of acetone extract of Cola nitida on brain sodium-potassium adenosine triphosphatase activity and spatial memory in healthy and streptozotocin-induced diabetic female Wistar rats
  24. Case Report
  25. Conservative treatment of postoperative chylothorax: a case report
  26. Short Communication
  27. Improved serotonergic neurotransmission by genistein pretreatment regulates symptoms of obsessive-compulsive disorder in streptozotocin-induced diabetic mice
Downloaded on 8.9.2025 from https://www.degruyterbrill.com/document/doi/10.1515/jbcpp-2017-0107/pdf
Scroll to top button