Hostname: page-component-cd9895bd7-fscjk Total loading time: 0 Render date: 2024-12-25T02:32:23.962Z Has data issue: false hasContentIssue false

Spectral sensitivity of melatonin synthesis suppression in Xenopus eyecups

Published online by Cambridge University Press:  01 March 1998

GREGORY M. CAHILL
Affiliation:
Department of Biology, University of Houston, Houston
SANDRA E. PARSONS
Affiliation:
Department of Anatomy and Cell Biology, University of Kansas Medical Center, Kansas City
JOSEPH C. BESHARSE
Affiliation:
Department of Anatomy and Cell Biology, University of Kansas Medical Center, Kansas City Present address: Department of Cellular Biology and Anatomy, Medical College of Wisconsin, Milwaukee, WI 53201, USA.

Abstract

Melatonin synthesis in retinal photoreceptors is stimulated at night by a circadian oscillator and suppressed acutely by light. To identify photoreceptor mechanisms involved in the acute suppression of melatonin synthesis, an action spectrum was measured for dark-adapted Xenopus laevis eyecups at night. Intensity–response curves at six wavelengths from 400 to 650 nm were parallel, suggesting that a single photopigment predominates in melatonin suppression. Half-saturating intensities at 400, 440, 480, and 533 nm were not significantly different from one another, at 1–2 × 108 quanta cm−2 s−1. Significantly higher intensities of 580- and 650-nm light were required for melatonin suppression. These results indicate a predominant role for the principal green-absorbing rods in acute regulation of retinal melatonin synthesis in response to light, and argue against an important role for the red-absorbing cones. Higher than expected sensitivity at short wavelengths suggests that photoreceptors sensitive to blue and/or violet light may also contribute to melatonin suppression.

Type
Research Article
Copyright
1998 Cambridge University Press

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)