Shoji Kitamura

The involvement of sex steroid hormones in downstream and upstream migratory behavior of masu salmon.

From May through July when masu salmon, Oncorhynchus masou, commence downstream migration under natural conditions, yearling precocious male masu salmon (resident form) showed higher GSI and plasma levels of testosterone (T) and 11-ketotestosterone (11-KT) in contrast to immature smolts (migratory form). From March through September coinciding with the upstream migration period, 2-year-old male and female adults also showed higher GSI and plasma levels of T, estradiol-17beta (E(2)) 11-KT, 17alpha-hydroxyprogesterone and 17alpha,20beta-dihydroxy-4-pregnene-3-one (DHP). In order to test the effects of steroid hormones on migratory behaviors, silascone tube capsules containing 500 microg of T, E(2), 11-KT, DHP, or a vehicle was implanted into smolts, castrated precocious males, or immature parr, and downstream and upstream behavior were observed in artificial raceways in spring and autumn. Downstream behavior of smolts was inhibited significantly by T, E(2) and 11-KT. Upstream behavior was stimulated by T and 11-KT in castrated precocious males and stimulated by T, E(2) and 11-KT in immature parr. These results indicate that T, E(2) and 11-KT are the factors regulating downstream and upstream migratory behavior. In particular, because of its changing patterns in plasma and significant effects, T, the common precursor hormone of E(2) (female) and 11-KT (male), is considered to play central roles in both types of behavior.

Ontogenic development of salmon GnRH and chicken GnRH-II systems in the brain of masu salmon (Oncorhynchus masou)

Abstractu2002Ontogenic development of salmon gonadotropin-releasing hormone (GnRH) and chicken GnRH-II systems in masu salmon (Oncorhynchus masou) was examined. Salmon GnRH was first detected by radioimmunoassay in the embryo on day 36 after fertilization. Salmon GnRH-immunoreactive fibers were detected initially by immunocytochemistry in the vicinity of the olfactory placode of the embryo (day 36) and were distributed widely in the brain as well as in the pituitary gland of fish just after hatching (day 80). Salmon GnRH-immunoreactive neuronal somata were first detected about 6 months after fertilization in the rostroventral brain area, ranging from the olfactory nerve to the preoptic area. Salmon GnRH neuronal somata were detected earlier by in situ hybridization than by immunocytochemistry. Neuronal somata expressing salmon GnRH mRNA were first detected in the vicinity of the olfactory epithelium on day 40 and then were seen to be migrating from the olfactory epithelium, along the olfactory nerve, on day 60 and in the transitional area between olfactory nerve and olfactory bulb on day 80. In the brain, these neurons were first detected in the ventral olfactory bulb on day 80, and thereafter they were also detected in the caudal brain regions. The chicken GnRH-II system was detected later than the salmon GnRH system; chicken GnRH-II was first detected by radioimmunoassay on day 57, and chicken GnRH-II-immunoreactive fibers were first detected on day 67. Chicken GnRH-II-immunoreactive neuronal somata were not detected during the observation period. These results suggest that salmon GnRH neurons derive from the olfactory placode and then migrate into the brain and that salmon GnRH is synthesized before chicken GnRH-II.

Disturbance of plasma melatonin profile by high dose melatonin administration inhibits testicular maturation of precocious male masu salmon.

Abstract We have previously shown that the testicular development of underyearling male masu salmon Oncorhynchus masou reared under a long photoperiod was accelerated by oral melatonin treatment (0.5mg melatonin/kg body weight/day), suggesting that melatonin mediates photoperiodic signaling. In this study, we further examined the effects of a disturbance in the plasma melatonin profile on gonadal development in underyearling male masu salmon by administering a higher dose of melatonin. Fish randomly selected in June were divided into two groups. They were reared under a light:dark (LD) cycle of 16:8 (lights on 04:00–20:00 hr) and fed with pellets sprayed with melatonin or vehicle twice a day at 08:30 and at 15:30 hr (7.5mg melatonin/kg body weight/day) until October. Fish were sampled on Day 0, 25, 60, 90 and 120. The plasma melatonin levels were high in the dark phase and low in the light phase in the control group, while they were constantly high with no significant change in the melatonin-treated group. Melatonin treatment had inhibitory effects on the gonadosomatic index and plasma testosterone levels. Pituitary salmon gonadotropin-releasing hormone content and luteinizing hormone content were significantly lower in the melatonin-treated group on Day 60 and 90, respectively. These results indicate that the plasma melatonin profile is important for mediating photoperiodic signals that regulate brain-pituitarygonadal axis in underyearling precocious male masu salmon.

Inhibitory effects of testosterone on downstream migratory behavior in masu salmon, Oncorhynchus masou.

Abstract The effects of testosterone (T) on downstream migratory behavior of yearling masu salmon, Oncorhynchus masou, were studied during its downstream migratory period using artificial raceways. In experiment 1, 22 and 19 smolts were implanted with a medical silicone tube capsules containing 500μg of T or vehicle only. These groups were transferred together to the upper pond of artificial raceway which was connected to the lower pond through fish-way. Downstream migratory behavior was then observed for 1 week. In experiment 2, T500μg-, T50μg-, and T5μg-treated smolts, control smolts, and precociously mature males were transferred to the upper pond of the raceway and downstream migratory behavior was observed for 2 months. In experiment 3, 40 smolts were implanted with capsules containing 500μg of T or vehicle only. These groups were transferred separately to the upper ponds of raceways and downstream migratory behavior was observed for 3 weeks. In each experiment, injection of T caused increases in plasma T levels within physiological levels. In experiment 1, frequency of downstream migratory behavior was 89.5% in the control group and 31.8% in the T500μg-treated group. In experiment 2, the frequency was lower in the T500μg- and T50μg-treated groups than in the control group. T5μg implantation failed to inhibit downstream migratory behavior. Precocious males were not observed to go down the raceway. In experiment 3, frequency of downstream migratory behavior of the control group and the T500μg-treated group was 100 and 40%, respectively. In each experiment, plasma levels of T in T500μg-treated smolts which did not show downstream migratory behavior was higher than those of migrants. These results indicate that the downstream migratory behavior of masu salmon smolts is inhibited by physiological levels of T.

Acidification severely suppresses spawning of hime salmon (land-locked sockeye salmon, Oncorhynchus nerka)

A laboratory study was conducted to investigate the effects of an acidic environment on the female sexual behavior of hime salmon (land-locked sockeye salmon, Oncorhynchus nerka). Spawning hime salmon were extremely sensitive to the acidity of ambient water. Nest-digging behavior was severely inhibited (P<0.05) by very slight acidification (pH below 6.4) of the water. Below pH 6.0, females showed almost no diggings. When the ambient water was returned to nearly neutral (pH 6.6), diggings reappeared in four of the six fish tested, whereas in two individuals, none was observed. Avoidance of slightly acidic water in selection of spawning site or cessation of spawning behavior in weakly acidic environments may be the most potent cause of the reduction of salmonid populations in the early stages of acidification.

Effects of low pH on the reproductive behavior of salmonid fishes

In northern Europe and America, the acidification of lakes and rivers induced by acid precipitation has damaged fish populations. At present, rapidly expanding industrial activities in East Asia have led to continuous increases in the quantity of emission of acidic pollutants, and rain of acidic levels of pH4 has precipitated throughout Japan. In this way, the effects of acid rain on fish populations have also been manifested in Japan. In order to examine the effects of low pH on the reproductive behavior of salmonids which are known to be acid-sensitive species, changes in the frequency of upstream behavior and spawning-related female nest-digging behavior in response to changes in pH were observed in mature hime salmon (land-locked sockeye salmon) Oncorhynchus nerka, brown trout Salmo trutta and Japanese char Salvelinus leucomaenis. Digging and upstream behavior were significantly inhibited in weakly acidic water of pHxa05.8–6.4 formulated using sulfuric acid. Land-locked sockeye salmon was the most sensitive to changes in pH among the three species.

Ontogenic origin of salmon GnRH neurons in the ventral telencephalon and the preoptic area in masu salmon

During the ontogeny of masu salmon Oncorhynchus masou, neurons producing the salmon type of gonadotropin-releasing hormone (sGnRH) were first detected in the olfactory epithelium of the eyed egg and, subsequently, in the brain, suggesting a migration of these cells. Among sGnRH neurons distributed from the olfactory nerve (ON) through the preoptic area (POA), those in the ventral telencephalon (VT) and the POA are indicated to regulate gonadotropin secretion. Thus, it is of interest to know whether all the sGnRH neurons originate from the olfactory epithelium. In the present study, we examined by in situ hybridization whether sGnRH neurons are present in the VT-POA of fish, whose olfactory epithelia including sGnRH clusters were cauterized just after hatching (44 days after fertilization). Fish were sampled in June (212 days after the operation). Neurons expressing sGnRH mRNA were detected in the VT-POA as well as in the ON, ventral olfactory bulb, and transitional area between the olfactory bulb and telencephalon (which is considered to correspond to the terminal nerve ganglion) in the control group. In contrast, neurons expressing sGnRH mRNA were not detected in the VT-POA in the olfactory epithelium lesioned (OEL) group. Furthermore, pituitary sGnRH content in the OEL group was just above the detectable limit and was significantly lower than that in the corresponding control group in both sexes. These results indicate that sGnRH neurons in the VT-POA are derived from the olfactory epithelium in masu salmon, although the possibility cannot be ruled out that sGnRH neurons in the VT-POA arise from the VT-POA, but were delayed in expressing sGnRH because of the trauma of cauterization.

Effects of Acidification on Salmonid Spawning Behavior

We studied the effects of acidification on female sexual behavior in brown trout (Salmo trutta) and compared the results with those in hime (land-locked sockeye) salmon (Oncorhynchus nerka) (Kitamura and Ikuta, 2000). The results were similar to those of sockeye salmon. Spawning brown trout were extremely sensitive to the acidity of ambient water, and nest-digging behavior was severely inhibited (p<0.05) by very slight acidification (pH below 6.4). However, there were some differences between the two species. Female trout and salmon showed almost no digging below pH 5.0 and 6.0 (Kitamura and Ikuta, 2000), respectively. When the ambient water was returned to nearly neutral (pH6.6) conditions, digging in hime salmon reappeared in 4 of the 6 fish tested (Kitamura and Ikuta, 2000), whereas digging in brown trout reappeared in all 6 fish tested. The above-mentioned differences in behavioral response between the two species appear to reflect the species difference in terms of vulnerability to acidification (Ikuta et al., 1992). Avoidance of slightly acidic water in selection of spawning site or cessation of spawning behavior in weakly acidic environments may be the most potent cause of the reduction of salmonid populations in the early stages of acidification.

Characterization and maturational differences of melatonin binding sites in the masu salmon brain

To obtain a better understanding of the roles of melatonin in the mediation of photoperiodic signaling, we have examined the pharmacological characteristics, guanine nucleotide modulation, and maturational differences of melatonin binding sites in the brain of masu salmon Oncorhynchus masou by radioreceptor assay using 2-[125I]iodomelatonin as the radioligand. The specific binding of 2-[125I]iodomelatonin was rapid, stable, saturable, and reversible. Saturation experiments demonstrated that 2-[125I]iodomelatonin binds to a single class of receptor sites with an affinity constant (K(d)) of 6.3+/-0.5 pM and a total binding capacity (B(max)) of 15.18+/-0.22 fmol/mg protein in underyearling precocious males in July. Competition experiments revealed that the binding sites are highly specific for melatonin and related analogues. Treatment with guanosine 5()-O-(3-thiotriphosphate) significantly reduced the specific binding, indicating that melatonin binding sites in the masu salmon brain are coupled to G protein. Significant differences were seen in B(max), but not K(d), among the fish groups differing in maturity. In the underyearling fish in July, the B(max) of precocious males and immature males was significantly higher than that of immature females. Then, the B(max) of precocious males decreased in October, when the fish spermiated. In the 2-year-old fish, B(max) was significantly higher in spermiating males than ovulated females. These results indicate that melatonin plays neuromodulatory roles in the central nervous system through specific receptors. Furthermore, gonadal maturation affects the density of melatonin binding sites in the masu salmon brain by an unknown mechanism.

Two differing salmon GnRH precursor mRNAs are co-expressed in the brain of sockeye salmon (Oncorhynchus nerka)

Abstractu2002The localization of two salmon-type gonadotropin-releasing hormone (sGnRH) precursors, pro-sGnRH-I (short type) and pro-sGnRH-II (long type), was investigated by using in situ hybridization techniques in the brain of the landlocked sockeye salmon, Oncorhynchus nerka. We used 30-mer oligonucleotide probes complementary to pro-sGnRH-I and pro-sGnRH-II cDNA. No significant differences were observed in the localization of sGnRH neurons expressing pro-sGnRH-I and pro-sGnRH-II mRNAs; both were expressed in the olfactory nerve, the olfactory bulbs, the regions between the olfactory bulb and telencephalon, the ventral telencephalon, the preoptic area, and the hypothalamus. Almost all sGnRH neurons examined co-expressed both precursors. The expression of two sGnRH precursors in the same neuron and the wide distribution of such neurons in the brain suggest that there are no functional differences between the two precursors.