» Articles » PMID: 20148284

Circadian Variation in the Electroretinogram and the Presence of Central Melatonin

Overview
Journal Doc Ophthalmol
Specialty Ophthalmology
Date 2010 Feb 12
PMID 20148284
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

The light/dark cycle is the most important circadian clock synchronizer for mammals and humans. Circadian rhythms of dopamine and melatonin production in the retina have been reported to follow the light and dark cycle, but their impact on rod and cone functioning is not clear. The purpose of this study was to assess diurnal variations (morning vs. evening) in retinal function as measured with the photopic and scotopic electroretinogram (ERG). We also tried to correlate our results with the presence or absence of melatonin secretion in the saliva. Photopic and scotopic luminance-response functions were obtained in 29 participants at 11:00 (when melatonin should not be present) and 23:00 (when melatonin should be present). From the luminance-response function, Vmax, log K and slope parameters were derived. In scotopic condition, a significant increase of 6% in Vmax amplitude was observed in evening compared to morning (P = 0.03) along with a prolonged b-wave implicit time of 8% (P = 0.01) and an increase in rod sensitivity in evening compared to morning (P = 0.02). As expected, these changes in rod function were accompanied by a higher concentration of melatonin in saliva samples in the evening (P = 0.01). In photopic condition, only a prolonged a-wave implicit time of 5% was observed in evening when compared to morning (P = 0.02). Our findings suggest that the rod system is favored during night time, when circulating melatonin is present. Although statistically significant changes were observed, the day vs. night difference observed in the present study appears to be too small to impact significantly upon clinical assessment of retinal function.

Citing Articles

Developing a clinical decision tool based on electroretinogram to monitor the risk of severe mental illness.

Peredo R, Hebert M, Merette C BMC Psychiatry. 2022; 22(1):718.

PMID: 36401192 PMC: 9673390. DOI: 10.1186/s12888-022-04375-3.


Therapeutic Effects of Melatonin on Ocular Diseases: Knowledge Map and Perspective.

Yu H, Wang Q, Wu W, Zeng W, Feng Y Front Pharmacol. 2021; 12:721869.

PMID: 34795578 PMC: 8593251. DOI: 10.3389/fphar.2021.721869.


Electoretinographic evidence of retinal ganglion cell-dependent function in schizophrenia.

Moghimi P, Torres Jimenez N, McLoon L, Netoff T, Lee M, MacDonald 3rd A Schizophr Res. 2019; 219:34-46.

PMID: 31615740 PMC: 7442157. DOI: 10.1016/j.schres.2019.09.005.


Diabetes Alters Diurnal Rhythm of Electroretinogram in db/db Mice.

Di R, Luo Q, Mathew D, Bhatwadekar A Yale J Biol Med. 2019; 92(2):155-167.

PMID: 31249476 PMC: 6585529.


ISCEV extended protocol for the stimulus-response series for the dark-adapted full-field ERG b-wave.

Johnson M, Jeffrey B, Messias A, Robson A Doc Ophthalmol. 2019; 138(3):217-227.

PMID: 30929109 PMC: 11332362. DOI: 10.1007/s10633-019-09687-6.


References
1.
Miranda-Anaya M, Bartell P, Menaker M . Circadian rhythm of iguana electroretinogram: the role of dopamine and melatonin. J Biol Rhythms. 2002; 17(6):526-38. DOI: 10.1177/0748730402238235. View

2.
Peachey N, Alexander K, Fishman G, Derlacki D . Properties of the human cone system electroretinogram during light adaptation. Appl Opt. 2010; 28(6):1145-50. DOI: 10.1364/AO.28.001145. View

3.
Zawilska J, Nowak J . Regulatory mechanisms in melatonin biosynthesis in retina. Neurochem Int. 1992; 20(1):23-36. DOI: 10.1016/0197-0186(92)90122-8. View

4.
Tosini G, Menaker M . Circadian rhythms in cultured mammalian retina. Science. 1996; 272(5260):419-21. DOI: 10.1126/science.272.5260.419. View

5.
Schneider T, Zrenner E . Effects of D-1 and D-2 dopamine antagonists on ERG and optic nerve response of the cat. Exp Eye Res. 1991; 52(4):425-30. DOI: 10.1016/0014-4835(91)90038-g. View