An experimental study of the neurophysical mechanisms of photophobia induced by subarachnoid hemorrhage

Neuroscience Letters

Volumn 630, Issue , 2016, Pages 93-100

  Aydin, Nazan ^a   Kotan, Dilcan ^b   Keles, Sadullah ^c   Ondas, Osman ^d   Aydin, Mehmet Dumlu ^c   Baykal, Orhan ^c   Gundogdu, Betul ^c  

^a Psychiatric and Neurological Diseases   (Turkey)

^b SAKARYA UNIVERSITY   (Turkey)

^c ATATURK UNIVERSITY   (Turkey)

^d Opthalmology Clinic of Tokat Erbaa Satate Hospital   (Turkey)

Author keywords

Ciliary ganglion; Photophobia; Rabbit; Subarachnoid hemorrhage; Vasospasm

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BLOOD; CELL DENSITY; CHOLINERGIC SYSTEM; CILIARY GANGLION; CISTERNA MAGNA; CONTROLLED STUDY; DEGENERATION; EXPERIMENTAL STUDY; GANGLION; MYDRIASIS; NERVE CELL; NEUROPHYSIOLOGY; NONHUMAN; PARALYSIS; PHOTOPHOBIA; PRIORITY JOURNAL; PUPIL; PUPIL REFLEX; RABBIT; SHAM PROCEDURE; STEREOLOGY; SUBARACHNOID HEMORRHAGE; SUPERIOR CERVICAL GANGLION; ANIMAL; COMPLICATION; DISEASE MODEL; OCULOMOTOR NERVE; PARASYMPATHETIC GANGLION; PATHOLOGY; PATHOPHYSIOLOGY; RABBITS AND HARES;

ANIMALS; DISEASE MODELS, ANIMAL; GANGLIA, PARASYMPATHETIC; MYDRIASIS; OCULOMOTOR NERVE; PHOTOPHOBIA; RABBITS; SUBARACHNOID HEMORRHAGE;

EID: 84979748471     PISSN: 03043940     EISSN: 18727972     Source Type: Journal    
DOI: 10.1016/j.neulet.2016.07.013     Document Type: Article

References (39)

1. [1] Tessier, L.M., Cadel, E.R., Schwardz, J.R., (eds.) Photoconduction and Information Processing in Retina.) Principles of Neural Science, 1991, Elsevier, New York, 441–466.
2. [2] Kozicz, T., Bittencourt, J.C., May, P.J., Reiner, A., Gamlin, P.D., Palkovits, M., et al. The Edinger-Westphal nucleus: a historical, structural, and functional perspective on a dichotomous terminology. J. Comp. Neurol. 519 (2011), 1413–1434.
3. [3] Kuchiiwa, S., Kuchiiwa, T., Nakagawwa, S., Ushikawa, M., Oculomotor parasympathetic pathway to the accessory cilary ganglion by passing the main ciliary ganglion by way of the trigeminal nerve. Neurosci. Res. 18 (1993), 79–82.
4. [4] Perez, G.M., Keyzer, R.B., Cell body counts in human ciliary ganglia. Invest. Ophthalmol. Vis. Sci. 27 (1986), 1428–1431.
5. [5] Moulton, E.A., Becerra, L., Borsook, D., An fMRI case report of photophobia: activation of the trigeminal nociceptive pathway. Pain 145 (2009), 358–363.
6. [6] Chronicle, E.P., Mulleners, W.M., Visual system dysfunction in migraine: a review of clinical and psychophysical findings. Cephalalgia 16 (1996), 525–535.
7. [7] Cruz-Orive, L.M., Weibel, E.R., Recent stereological methods for cell biology: a brief survey. Am. J. Physiol. 258 (1990), L148–L156.
8. [8] Dolgonos, S., Ayyala, H., Evinger, C., Light-induced trigeminal sensitization without central visual pathways: another mechanism for photophobia. Invest. Ophthalmol. Vis. Sci. 52 (2011), 7852–7858.
9. [9] Aydin, M.D., Akyol-Salman, I., Sahin, O., Histopathological changes in ciliary ganglion of rabbits with subarachnoid hemorrhage. Int. J. Neurosci. 115 (2005), 1595–1602.
10. [10] Aydin, M.D., Onder, S., Ulvi, H., Onder, A., Baykal, O., Histopathological alterations in ciliary ganglions in meningitis: an experimental study. Minim. Invasive Neurosurg. 48 (2005), 297–301.
11. [11] Stroop, W.G., Schaefer, D.C., Severity of experimentally reactivated herpetic eye disease is related to the neurovirulence of the latent virus. Invest. Ophthalmol. Vis. Sci. 28 (1987), 229–237.
12. [12] Sterio, D.C., The unbiased estimation of number and sizes of arbitrary particles using the dissector. J. Microsc. 134 (1984), 127–136.
13. [13] Ahlborn, B.K., Ligt, abundant information. Ahlborn, B.K., (eds.) Zoological Physics. Quantitative Models of Body Design, Actions, and Physical Limitations of Animals, 2006, Springer-Verlag Berlin Heidelberg, New York, 261–307.
14. [14] Kirch, W., Neuhuber, W., Tamm, E.R., Immunohistochemical localisation of neuropeptides in human ciliary ganglion. Brain Res. 681 (1995), 229–234.
15. [15] Suzuki, R., Oso, T., Kobayashi, S., Cholinergic inhibitory response in the bovine iris dilalatatory muscle. Invest. Ophthalmol. Vis. Sci. 24 (1983), 760–765.
16. [16] Paulson, G.W., Kapp, J.P., Dilatation of the pupil in the cat via the oculomotor nerve. Arch. Ophthalmol. 77 (1967), 536–540.
17. [17] Gamlin, P.D., Reiner, A., Erichsen, J.T., Karten, H.J., Cohen, D.H., The neural substrate for the pupillary light reflex in the pigeon (Columba livia). J. Comp. Neurol. 226 (1984), 523–543.
18. [18] Hodos, W., Miller, R.F., Ghim, M.M., Fitzgerald, M.E., Toledo, C., Reiner, A., Visual acuity losses in pigeons with lesions of the nucleus of Edinger-Westphal that disrupt the adaptive regulation of choroidal blood flow. Vis. Neurosci. 15 (1998), 273–287.
19. [19] Jackson, P.C., Reduced activity during development delays the normal rearrangement of synapses in the rabbit ciliary ganglion. J. Physiol. 345 (1983), 319–327.
20. [20] Grozdanic, S.D., Lazic, T., Kuehn, M.H., Harper, M.M., Kardon, R.H., Kwon, Y.H., et al. Exogenous modulation of intrinsic optic nerve neuroprotective activity. Graefes Arch. Clin. Exp. Ophthalmol. 248 (2010), 1105–1106.
21. [21] Jacobson, D.M., Benign episodic unilateral mydriasis Clinical characteristics. Ophthalmology 102 (1995), 1623–1627.
22. [22] Davies, G.E., Shakir, R.A., Giant cell arteritis presenting as oculomotor nerve palsy with pupillary dilatation. Postgrad. Med. J. 70 (1994), 298–299.
23. [23] Micieli, G., Tassorelli, C., Ruiz, L., Sandrini, G., Nappi, G., The trigemino-pupillary response in cluster headache. Cephalalgia 13 (1993), 338–342.
24. [24] Noseda, R., Kainz, V., Jakubowski, M., Gooley, J.J., Saper, C.B., Digre, K., et al. A neural mechanism for exacerbation of headache by light. Nat. Neurosci. 13 (2010), 239–245.
25. [25] McCann, J.D., Gauthier, M., Morschbacher, R., Goldberg, R.A., Anderson, R.L., Fine, P.G., et al. A novel mechanism for benign essential blepharospasm. Ophthal. Plast. Reconstr. Surg. 15 (1999), 384–389.
26. [26] Trobe, J.D., Photophobia in anterior visual pathway disease. J. Neuroophthalmol. 22 (2002), 1–2.
27. [27] Martín, H., del Río, M.S., de Silanes, C.L., Álvarez-Linera, J., Hernández, J.A., Pareja, J.A., Photoreactivity of the occipital cortex measured by functional magnetic resonance imaging-blood oxygenation level dependent in migraine patients and healthy volunteers: pathophysiological implications. Headache 51 (2011), 1520–1528.
28. [28] Okamoto, K., Tashiro, A., Chang, Z., Bereiter, D.A., Bright light activates a trigeminal nociceptive pathway. Pain 149 (2010), 235–242.
29. [29] Alvarez-Linera Prado, J., Ríos-Lago, M., Martín-Alvarez, H., Hernández-Tamames, J.A., Escribano-Vera, J., Sánchez del Río, M., Functional magnetic resonance imaging of the visual cortex: relation between stimulus intensity and bold response. Rev. Neurol. 45 (2007), 147–151.
30. [30] Herz, N.L., Yen, M.T., Modulation of sensory photophobia in essential blepharospasm with chromatic lenses. Ophthalmology 112 (2005), 2208–2211.
31. [31] Stringham, J.M., Fuld, K., Wenzel, A.J., Spatial properties of photophobia. Invest. Ophthalmol. Vis. Sci. 45 (2004), 3838–3848.
32. [32] Aydin, M.D., Serarslan, Y., Gündoğdu, C., Aydın, N., Aygül, R., Kotan, D., et al. The relationship between the neuron density of the trigeminal ganglion and the posterior communicating artery vasospasm in subarachnoid hemorrhage: an experimental study. Neurosurg. Q 22 (2012), 1–6.
33. [33] Kayacı, S., Kanat, A., Aydın, M.D., Müslüman, A.M., Eseoğlu, M., Karalar, M., et al. Role of neuron density of the stellate ganglion on regulation of the basilary artery volume in subarachnoid hemorrhage: an experimental study. Auton. Neurosci. 165 (2011), 163–167.
34. [34] Önder, A., Serarslan, Y., Aydın, M.D., Aydın, N., Ulvi, H., Kotan, D., et al. The role of trigeminal ganglion neuron density in the prevention of subarachnoid hemorrhage-induced basilar artery vasospasm: an experimental study. Neurosurg. Q 19 (2009), 264–269.
35. [35] Cruz-Orive, L.M., Weibel, E.R., Recent stereological methods for cell biology: a brief survey. Am. J. Physiol. 258 (1990), L148–56.
36. [36] Gunderson, H.J., Bendtsen, T.F., Korbo, L., Marcussen, N., Moller, A., Nielsen, K., et al. Some new, simple and efficient stereological methods and their use in pathological research and diagnosis. APMIS 96 (1988), 379–394.
37. [37] Talman, W.T., Corr, J., Nitschke Dragon, D., Wang, D., Parasympathetic stimulation elicits cerebral vasodilatation in rat. Auton. Neurosci. 133 (2007), 153–157.
38. [38] Megyesi, J.F., Vollrath, B., Cook, D.A., Findlay, J.M., In vivo animal models of cerebral vasospasm: a review. Neurosurgery 46 (2000), 448–460.
39. [39] Sehba, F.A., Pluta, R.M., Zhang, J.H., Metamorphosis of subarachnoid hemorrhage research: from delayed vasospasm to early brain injury. Mol. Neurobiol. 43 (2011), 27–40.