“…The presence of 5-HT in DCV varies in different species, depending upon the quantity of remaining 5-HT (which is not rapidly metabolized) and probably also, in a given species, upon daily changes ; the circadian rhythm of 5-HT and its related indoleamines is well known (Quay, 1974 ;Wurtman et al, 1968 ;Axelrod, 1974Axelrod and Zatz, 1977 (Roux et al, 1977) and after blinding and continuous darkness in hamsters (Sheridan, 1975) (Romijn, 1975), hamsters (Lin et al, 1975 ;Sheridan, 1975) and mice (Pellegrino de Iraidi, 1969) ; administration of parasympatholytic drugs in rabbits (Romijn, 1976) ; surgical castration in rats (Karasek et a/., 1976) ; injection of human chorionic gonadotropin (HCG) and pregnant mare serum gonadotropin (PMSG) in rats (Karasek and Marek, 1978) ; in the presence of norepinephrine (NE) or dibutyryl-cyclic-adenosine 3'-5'-monophosphate (db-c-AMP) in rat pineals cultured in vitro (Karasek, 1974) or in rabbits (Romijn and Gelsema, 1976). It has also been shown that a mean number of DCV in rabbits (Quay, 1974 ;Ebels, 1976 ;Benson et al, 1976 Finally, taking into account the detailed discussions of previous papers on reptiles, birds and mammals (Collin and Meiniel, 1971 ;Collin, , 1979Collin et al, 1977a, b ;Juillard and Collin, 1978) …”