• The Korean Journal of Ecology
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• v.28 no.5
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• pp.237-243
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• 2005

To study entering and exiting routes of male and female Hynobius leechii to a breeding site and staying time of them within the breeding site, we monitored a breeding population located in the research forests of Kangwon National University. The breeding site was surrounded by a drift fence associated with nine pitfall traps. The breeding season of this population was about one month, from 16 March to 13 April, 2005. Breeding males arrived earlier at the breeding pond than females did. The operational sex ratio (OSR), defined as the ratio of males to females which are ready to mate, over a breeding season was female-biased as 0.67 male vs 1 female (57 males vs 87 females), but daily OSRs, OSR in a particular day, within the breeding pond were male-biased with $1.36\sim7.5$ male vs f female in six days out of seven investigated days. While breeding males stayed in the breeding pond for about 11 days, breeding females left the pond as soon as they completed oviposition. However, the females stayed at terrestrial areas near the pond for about seven days before completely leaving the breeding site. Entering and exiting routes to the breeding site were different between males and females, and between ovulated and oviposited females. Both males and females arrived earlier at the breeding site stayed longer within the site. Males stayed longer within the breeding site lost more body weight.

• The Korean Journal of Physiology and Pharmacology
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• v.25 no.5
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• pp.449-457
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• 2021

The sleep-wake cycle is regulated by the alternating activity of sleep- and wake-promoting neurons. The dorsal raphe nucleus (DRN) secretes 5-hydroxytryptamine (5-HT, serotonin), promoting wakefulness. Melatonin secreted from the pineal gland also promotes wakefulness in rats. Our laboratory recently demonstrated that daily changes in nitric oxide (NO) production regulates a signaling pathway involving with-no-lysine kinase (WNK), Ste20-related proline alanine rich kinase (SPAK)/oxidative stress response kinase 1 (OSR1), and cation-chloride co-transporters (CCC) in rat DRN serotonergic neurons. This study was designed to investigate the effect of melatonin on NO-regulated WNK-SPAK/OSR1-CCC signaling in wake-inducing DRN neurons to elucidate the mechanism underlying melatonin's wake-promoting actions in rats. Ex vivo treatment of DRN slices with melatonin suppressed neuronal nitric oxide synthase (nNOS) expression and increased WNK4 expression without altering WNK1, 2, or 3. Melatonin increased phosphorylation of OSR1 and the expression of sodium-potassium-chloride co-transporter 1 (NKCC1), while potassium-chloride co-transporter 2 (KCC2) remained unchanged. Melatonin increased the expression of tryptophan hydroxylase 2 (TPH2, serotonin-synthesizing enzyme). The present study suggests that melatonin may promote its wakefulness by modulating NO-regulated WNK-SPAK/OSR1-KNCC1 signaling in rat DRN serotonergic neurons.