Chronic Nasal Administration of Kisspeptin-54 Regulates Mood-Related Disorders Via Amygdaloid GABA in Hemi-Parkinsonian Rats

Osman Sinen, Ayşegül Gemici Sinen, Narin Derin, Mutay Aydın Aslan
Author Information
  1. Osman Sinen: Department of Physiology, Akdeniz University Faculty of Medicine, Antalya, Türkiye ORCID
  2. Ayşegül Gemici Sinen: Department of Biophysics, Akdeniz University Faculty of Medicine, Antalya, Türkiye ORCID
  3. Narin Derin: Department of Biophysics, Akdeniz University Faculty of Medicine, Antalya, Türkiye ORCID
  4. Mutay Aydın Aslan: Department of Medical Biochemistry, Akdeniz University Faculty of Medicine, Antalya, Türkiye ORCID

Abstract

Background: Depression and anxiety, the most prevalent neuropsychiatric manifestations in Parkinson’s disease (PD), negatively impact their quality of life.
Aims: To determine whether the chronic nasal administration of kisspeptin-54 (KP-54) could. Alleviate symptoms of anxiety and depression in hemi-Parkinsonian rats.
Study Design: Experimental study.
Methods: This study included adult Sprague Dawley male rats who were administered either a vehicle (artificial cerebrospinal fluid) or 6-hydroxydopamine (6-OHDA) unilaterally into the medial forebrain bundle. The vehicle, or KP-54 (3 nmol/kg, applied topically to the rhinarium), was administered daily for a seven-day period. The sucrose preference test (SPT), elevated plus maze test (EPMT), and open field test (OFT) were implemented to evaluate depression- and anxiety-like behaviors, respectively, seven days following the lesion surgery. Gamma-aminobutyric acid (GABA) concentrations in the amygdala were quantified using mass spectrometry. Tyrosine hydroxylase in substantia nigra was analyzed using immunohistochemistry.
Results: The nasal delivery of KP-54 significantly reduced depressionand anxiety-like behaviors that were induced by 6-OHDA, as indicated by the results of the SPT, OFT, and EPMT. Moreover, it was observed that nasal KP-54 effectively mitigated 6-OHDA-induced motor deficits and the loss of nigral dopaminergic neurons. The nasal administration of KP-54 augmented the decline in GABA levels in the amygdala induced by 6-OHDA. Furthermore, effective correlations were established between GABA concentrations and behavioral parameters.
Conclusion: The nasal delivery of KP-54 could function as a viable therapeutic alternative for treating mood-related disorders in PD.

References

  1. Int J Neurosci. 2021 Aug;131(8):765-774 [PMID: 32441169]
  2. Neurochem Res. 2022 Nov;47(11):3331-3343 [PMID: 35895153]
  3. Nat Protoc. 2007;2(2):322-8 [PMID: 17406592]
  4. Neurogastroenterol Motil. 2024 Jan;36(1):e14719 [PMID: 38105366]
  5. Nat Rev Neurosci. 2017 Jul;18(7):435-450 [PMID: 28592904]
  6. Peptides. 2006 May;27(5):1073-86 [PMID: 16500002]
  7. Brain Res. 2009 Apr 24;1267:65-76 [PMID: 19268657]
  8. Neuropharmacology. 2012 Jan;62(1):398-405 [PMID: 21871467]
  9. Biol Mood Anxiety Disord. 2012 Nov 20;2:20 [PMID: 23168129]
  10. Biomedicines. 2021 Jan 25;9(2): [PMID: 33503835]
  11. Front Neurosci. 2016 Jun 09;10:269 [PMID: 27375426]
  12. Regul Pept. 2013 Jan 10;180:1-4 [PMID: 22999921]
  13. JCI Insight. 2018 Oct 18;3(20): [PMID: 30333302]
  14. J Affect Disord. 1995 Aug 18;34(4):275-81 [PMID: 8550953]
  15. Nat Rev Neurol. 2011 Dec 26;8(1):35-47 [PMID: 22198405]
  16. Med J Aust. 2010 Feb 1;192(3):144-9 [PMID: 20121682]
  17. Neuroendocrinology. 2018;106(2):195-202 [PMID: 28866668]
  18. J Biol Chem. 2001 Sep 14;276(37):34631-6 [PMID: 11457843]
  19. Toxins (Basel). 2021 Jul 20;13(7): [PMID: 34357977]
  20. Front Neuroendocrinol. 2022 Apr;65:100977 [PMID: 34999056]
  21. Sci Rep. 2018 Feb 12;8(1):2794 [PMID: 29434234]
  22. Pharmacol Biochem Behav. 1995 Dec;52(4):701-6 [PMID: 8587908]
  23. Behav Brain Res. 2013 Mar 15;241:56-61 [PMID: 23219969]
  24. Mol Psychiatry. 2011 Apr;16(4):383-406 [PMID: 21079608]
  25. Neuropsychiatr Dis Treat. 2015 Jan 17;11:165-75 [PMID: 25653526]
  26. Physiol Behav. 2021 Nov 1;241:113593 [PMID: 34536434]
  27. Front Behav Neurosci. 2014 Sep 16;8:321 [PMID: 25278855]
  28. Proc Natl Acad Sci U S A. 2014 Mar 11;111(10):3841-6 [PMID: 24567386]
  29. Mol Psychiatry. 2003 Aug;8(8):721-37, 715 [PMID: 12888801]
  30. J Neuroendocrinol. 2018 Mar;30(3):e12572 [PMID: 29356147]
  31. Transl Psychiatry. 2012 Nov 13;2:e181 [PMID: 23149445]
  32. J Clin Psychiatry. 2003;64 Suppl 3:21-7 [PMID: 12662130]
  33. Talanta. 2013 Sep 30;114:79-89 [PMID: 23953445]

MeSH Term

Animals
Administration, Intranasal
Rats
Rats, Sprague-Dawley
Male
gamma-Aminobutyric Acid
Amygdala
Disease Models, Animal
Kisspeptins
Mood Disorders
Parkinson Disease
Anxiety
Oxidopamine
Depression

Chemicals

gamma-Aminobutyric Acid
Kisspeptins
Oxidopamine

Word Cloud

Created with Highcharts 10.0.0KP-54nasalGABA6-OHDAtestanxietyPDadministrationratsstudyadministeredvehicleSPTEPMTOFTanxiety-likebehaviorsconcentrationsamygdalausingdeliveryinducedBackground:DepressionprevalentneuropsychiatricmanifestationsParkinson’sdiseasenegativelyimpactqualitylifeAims:determinewhetherchronickisspeptin-54Alleviatesymptomsdepressionhemi-ParkinsonianStudyDesign:ExperimentalMethods:includedadultSpragueDawleymaleeitherartificialcerebrospinalfluid6-hydroxydopamineunilaterallymedialforebrainbundle3nmol/kgappliedtopicallyrhinariumdailyseven-dayperiodsucrosepreferenceelevatedplusmazeopenfieldimplementedevaluatedepression-respectivelysevendaysfollowinglesionsurgeryGamma-aminobutyricacidquantifiedmassspectrometryTyrosinehydroxylasesubstantianigraanalyzedimmunohistochemistryResults:significantlyreduceddepressionandindicatedresultsMoreoverobservedeffectivelymitigated6-OHDA-inducedmotordeficitslossnigraldopaminergicneuronsaugmenteddeclinelevelsFurthermoreeffectivecorrelationsestablishedbehavioralparametersConclusion:functionviabletherapeuticalternativetreatingmood-relateddisordersChronicNasalAdministrationKisspeptin-54RegulatesMood-RelatedDisordersViaAmygdaloidHemi-ParkinsonianRats

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