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Volumn 279, Issue 5349, 1998, Pages 396-399

Extraocular circadian phototransduction in humans

Author keywords

[No Author keywords available]

Indexed keywords

MELATONIN;

EID: 0032535952     PISSN: 00368075     EISSN: None     Source Type: Journal    
DOI: 10.1126/science.279.5349.396     Document Type: Article
Times cited : (219)

References (60)
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    • note
    • The protocol was approved by Cornell University Medical College's Committee on Human Rights in Research. All participants gave written consent after being informed of the nature and potential risks of the study. They were paid for their participation.
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    • note
    • The light source was a BiliBlanket Plus (Ohmeda), a fiber optic phototherapy device commonly used for home treatment of hyperbilirubinemia. The device consists of a halogen lamp in a vented metal housing, which also contains a small fan to disperse heat generated by the lamp. Illumination from the halogen bulb leaves the housing through 2400 optic fibers encased in a flexible plastic tube 1 m in length. The optic fibers terminate in a ∼10 cm by ∼15 cm woven pad about ∼0.64 cm thick. Because the light source is remote, the fiber optic pad generates no heat. A Biliblanket pad was placed over the popliteal area of each leg and secured in place with a polyester athletic knee brace. During the 3-hour light exposure interval, participants remained seated in a reclining chair, with a table positioned over their laps. To ensure that the light stimulus did not reach the retina, we draped a 3 m by 3 m black, opaque, double thickness polyester "skirt" over the table that reached the floor on all sides and secured it with Velcro around the participant's waist. The lamp housing was placed beneath the table and under the skirt, so that any light escaping through the housing vents was obscured from the participant's eyes. Illumination at the participant's eye level never exceeded 20 lux. Each BiliBlanket provided ∼13,000 lux to the popliteal region. An exhaust fan (in addition to those in each BiliBlanket housing) was placed beneath the skirt to evacuate any heat produced by the halogen light source.
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    • Saliva samples were collected under dim light from 1800 until 2400 on night 2 (before light exposure) and on night 4. Melatonin concentrations were measured by radioimmunoassay (ALPCO, Windham, NH) with the Kennaway G280 antibody [G. M. Vaughan et al., J. Pineal Res. 15, 88 (1993)]. All samples from a given participant during a given laboratory session were analyzed in the same assay. We have calculated an intra-assay coefficient of variation of 2.1%; the interassay precision has been reported as 10.4% (26).
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    • 2 ≥ 0.8 (variance accounted for); one participant whose baseline temperature curve did not meet this requirement was excluded from the analyses. The nadirs (fitted minima) of the fitted curves were used to determine the phase of the body core temperature rhythm. The DLMO was defined as the time at which salivary melatonin concentrations exceeded 3.33 pg/ml. This threshold was based on a conventional definition of a 10 pg/ml threshold for plasma melatonin concentrations [A. J. Lewy and R. L. Sack, ibid., p. 93] and published evidence that the radioimmunoassay used here yields salivary melatonin concentrations ∼30% of those obtained in plasma (26).
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    • 2 ≥ 0.8 (variance accounted for); one participant whose baseline temperature curve did not meet this requirement was excluded from the analyses. The nadirs (fitted minima) of the fitted curves were used to determine the phase of the body core temperature rhythm. The DLMO was defined as the time at which salivary melatonin concentrations exceeded 3.33 pg/ml. This threshold was based on a conventional definition of a 10 pg/ml threshold for plasma melatonin concentrations [A. J. Lewy and R. L. Sack, ibid., p. 93] and published evidence that the radioimmunoassay used here yields salivary melatonin concentrations ∼30% of those obtained in plasma (26).
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    • note
    • We thank our technical staff for their efforts, A. Barbano for participant recruitment, and R. J. Finney for melatonin assays. Supported by U.S. Public Health Service grants R01 MH45067, R01 MH54617, K02 MH01099, P20 MH49762, R01 AG512112, and R03 AG14197.


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