Background The vestibular system is connected to spinal, cerebellar and cerebral motor control structures and can be selectively activated with external electrodes. The resulting sensation of disturbed balance can be avoided by using stochastic stimulation patterns. Adding noise to the nervous system sometimes improves function. Small clinical trials suggest that stochastic vestibular stimulation (SVS) may improve symptoms in Parkinson's disease. We have investigated this claim and possible mechanisms using the 6-hydroxydopamine (6-OHDA) hemilesion model of Parkinson's disease. Methodology/Principal Findings Animals were tested in the accelerating rod test and the Montoya staircase test of skilled forelimb use. In 6-OHDA hemilesioned animals, SVS improved rod performance by 56±11 s. At group level L-DOPA treatment had no effect, but positive responders improved time on rod by 60±19 s. Skilled forelimb use was not altered by SVS. To investigate how SVS may influence basal ganglia network activity, intracerebral microdialysis was employed in four regions of interest during and after SVS. In presence of the γ-amino buturic acid (GABA) transporter inhibitor NNC 711, SVS induced an increase in GABA to 150±15% of baseline in the substantia nigra (SN) of unlesioned animals, but had no effect in the pedunculopontine nucleus (PPN), the striatum or the ventromedial thalamus (VM). Dopamine release remained stable in all areas, as did GABA and amine concentrations in the SN of unstimulated controls. Following SVS, a sustained increase in GABA concentrations was observed in the ipsilesional, but not in the contralesional SN of 6-OHDA hemilesioned rats. In contrast, L-DOPA treatment produced a similar increase of GABA in the ipsi- and contra-lesional SN. Conclusions/Significance SVS improves rod performance in a rat model of Parkinson's disease, possibly by increasing nigral GABA release in a dopamine independent way. We propose that SVS could be useful for treating symptoms of Parkinson's disease.
References
[1]
Bloem BR, Hausdorff JM, Visser JE, Giladi N (2004) Falls and freezing of gait in Parkinson's disease: a review of two interconnected, episodic phenomena. Mov Disord 19: 871–884.
[2]
Aihara T, Kitajo K, Nozaki D, Yamamoto Y (2010) How does stochastic resonance work within the human brain? - Psychophysics of internal and external noise. Chemical Physics 375: 616–624.
[3]
Hospedales TM, van Rossum MC, Graham BP, Dutia MB (2008) Implications of noise and neural heterogeneity for vestibulo-ocular reflex fidelity. Neural Comput 20: 756–778.
[4]
Li SC, von Oertzen T, Lindenberger U (2006) A neurocomputational model of stochastic resonance and aging. Neurocomputing 69: 1553–1560.
[5]
McDonnell MD, Abbott D (2009) What is stochastic resonance? Definitions, misconceptions, debates, and its relevance to biology. PLoS Comput Biol 5: e1000348.
[6]
Yu XL, Lewis ER (1989) Studies with spike initiators: linearization by noise allows continuous signal modulation in neural networks. IEEE Trans Biomed Eng 36: 36–43.
[7]
Funke K, Kerscher NJ, Worgotter F (2007) Noise-improved signal detection in cat primary visual cortex via a well-balanced stochastic resonance-like procedure. Eur J Neurosci 26: 1322–1332.
[8]
Wells C, Ward LM, Chua R, Timothy Inglis J (2005) Touch noise increases vibrotactile sensitivity in old and young. Psychol Sci 16: 313–320.
[9]
Zeng FG, Fu QJ, Morse R (2000) Human hearing enhanced by noise. Brain Res 869: 251–255.
Kosko B (2006) Noise. New York: Viking Adult. 272 p.
[12]
Smith PF, Geddes LH, Baek JH, Darlington CL, Zheng Y (2010) Modulation of memory by vestibular lesions and galvanic vestibular stimulation. Front Neurol 1: 141.
[13]
Usher M, Feingold M (2000) Stochastic resonance in the speed of memory retrieval. Biological Cybernetics 83: L11-16–L11-16.
[14]
Wilkinson D, Ko P, Kilduff P, McGlinchey R, Milberg W (2005) Improvement of a face perception deficit via subsensory galvanic vestibular stimulation. Journal of the International Neuropsychological Society: JINS 11: 925–929.
Wilkinson D, Zubko O, Degutis J, Milberg W, Potter J (2010) Improvement of a figure copying deficit during subsensory galvanic vestibular stimulation. J Neuropsychol 4: 107–118.
[17]
Lobel E, Kleine JF, Bihan DL, Leroy-Willig A, Berthoz A (1998) Functional MRI of galvanic vestibular stimulation. J Neurophysiol 80: 2699–2709.
[18]
Mian OS, Day BL (2009) Determining the direction of vestibular-evoked balance responses using stochastic vestibular stimulation. J Physiol 587: 2869–2873.
[19]
Yamamoto Y, Struzik ZR, Soma R, Ohashi K, Kwak S (2005) Noisy vestibular stimulation improves autonomic and motor responsiveness in central neurodegenerative disorders. Ann Neurol 58: 175–181.
[20]
Pavlik AE, Inglis JT, Lauk M, Oddsson L, Collins JJ (1999) The effects of stochastic galvanic vestibular stimulation on human postural sway. Exp Brain Res 124: 273–280.
[21]
Scinicariello AP, Inglis JT, Collins JJ (2002) The effects of stochastic monopolar galvanic vestibular stimulation on human postural sway. J Vestib Res 12: 77–85.
[22]
Mulavara AP, Fiedler MJ, Kofman IS, Wood SJ, Serrador JM, et al. (2011) Improving balance function using vestibular stochastic resonance: optimizing stimulus characteristics. Exp Brain Res 210: 303–312.
[23]
Scinicariello AP, Eaton K, Inglis JT, Collins JJ (2001) Enhancing human balance control with galvanic vestibular stimulation. Biol Cybern 84: 475–480.
[24]
Pan W, Soma R, Kwak S, Yamamoto Y (2008) Improvement of motor functions by noisy vestibular stimulation in central neurodegenerative disorders. J Neurol 255: 1657–1661.
[25]
Pal S, Rosengren SM, Colebatch JG (2009) Stochastic galvanic vestibular stimulation produces a small reduction in sway in Parkinson's disease. J Vestib Res 19: 137–142.
[26]
Sikstr?m S, S?derlund G (2007) Stimulus-dependent dopamine release in attention-deficit/hyperactivity disorder. Psychol Rev 114: 1047–1075.
[27]
P?lsson E, S?derlund G, Klamer D, Bergquist F (2010) Noise benefit in prepulse inhibition of the acoustic startle reflex. Psychopharmacol 214: 675–685.
[28]
Andersson D, Nissbrandt H, Bergquist F (2006) Partial depletion of dopamine in substantia nigra impairs motor performance without altering striatal dopamine neurotransmission. Eur J Neurosci 24: 617–624.
[29]
Bergquist F, Shahabi HN, Nissbrandt H (2003) Somatodendritic dopamine release in rat substantia nigra influences motor performance on the accelerating rod. Brain Res 973: 81–91.
[30]
Lappin JM, Reeves SJ, Mehta MA, Egerton A, Coulson M, et al. (2009) Dopamine release in the human striatum: motor and cognitive tasks revisited. J Cereb Blood Flow Metab 29: 554–564.
[31]
Winn P (2008) Experimental studies of pedunculopontine functions: are they motor, sensory or integrative? Parkinsonism Rel Disord 14: Suppl 2S194-198–S194-198.
[32]
Andersson DR, Bjornsson E, Bergquist F, Nissbrandt H (2010) Motor activity-induced dopamine release in the substantia nigra is regulated by muscarinic receptors. Exp Neurol 221: 251–259.
[33]
Bergquist F, Ludwig M, Dutia MB (2008) Role of the commissural inhibitory system in vestibular compensation in the rat. J Physiol 586: 4441–4452.
[34]
Lindgren HS, Andersson DR, Lagerkvist S, Nissbrandt H, Cenci MA (2010) L-DOPA-induced dopamine efflux in the striatum and the substantia nigra in a rat model of Parkinson's disease: temporal and quantitative relationship to the expression of dyskinesia. J Neurochem 112: 1465–1476.
[35]
Dakin CJ, Son GML, Inglis JT, Blouin J-S (2007) Frequency response of human vestibular reflexes characterized by stochastic stimuli. J Physiol 583: 1117–1127.
[36]
Gravelle DC, Laughton CA, Dhruv NT, Katdare KD, Niemi JB, et al. (2002) Noise-enhanced balance control in older adults. Neuroreport 13: 1853–1856.
[37]
Priplata AA, Patritti BL, Niemi JB, Hughes R, Gravelle DC, et al. (2006) Noise-enhanced balance control in patients with diabetes and patients with stroke. Ann Neurol 59: 4–12.
[38]
Manjarrez E, Mendez I, Martinez L, Flores A, Mirasso CR (2007) Effects of auditory noise on the psychophysical detection of visual signals: cross-modal stochastic resonance. Neurosci lett 415: 231–236.
[39]
Baker KB, Lee JY, Mavinkurve G, Russo GS, Walter B, et al. (2010) Somatotopic organization in the internal segment of the globus pallidus in Parkinson's disease. Exp Neurol 222: 219–225.
[40]
Ostergaard K, Sunde NA (2006) Evolution of Parkinson's disease during 4 years of bilateral deep brain stimulation of the subthalamic nucleus. Mov Disord 21: 624–631.
[41]
Umemura A, Oka Y, Okita K, Toyoda T, Matsukawa N, et al. (2010) Predictive factors affecting early deterioration of axial symptoms after subthalamic nucleus stimulation in Parkinson's disease. Parkinsonism Rel Disord 16: 582–584.
[42]
Timmerman W, Westerink B (1997) Brain microdialysis of GABA and glutamate: what does it signify? Synapse 27: 242–261.
[43]
DeLong MR, Wichmann T (2007) Circuits and Circuit Disorders of the Basal Ganglia. Arch Neurol 64: 20–24.
[44]
Kravitz AV, Freeze BS, Parker PR, Kay K, Thwin MT, et al. (2010) Regulation of parkinsonian motor behaviours by optogenetic control of basal ganglia circuitry. Nature 466: 622–626.
[45]
Windels F, Bruet N, Poupard A, Urbain N, Chouvet G, et al. (2000) Effects of high frequency stimulation of subthalamic nucleus on extracellular glutamate and GABA in substantia nigra and globus pallidus in the normal rat. Eur J Neurosci 12: 4141–4146.
[46]
Paxinos G, Watson C (1998) The Rat Brain in Stereotaxic Coordinates, Fourth Edition. Waltham, MA: Academic Press. 256 p.
[47]
Bergquist F, Jonason J, Pileblad E, Nissbrandt H (1998) Effects of local administration of L-, N-, and P/Q-type calcium channel blockers on spontaneous dopamine release in the striatum and the substantia nigra: a microdialysis study in rat. J Neurochem 70: 1532–1540.
[48]
Bostan AC, Dum RP, Strick PL (2010) The basal ganglia communicate with the cerebellum. Proc Natl Acad Sci U S A 107: 8452–8456.
[49]
Hoshi E, Tremblay L, Feger J, Carras PL, Strick PL (2005) The cerebellum communicates with the basal ganglia. Nat Neurosci 8: 1491–1493.