59 research outputs found
Acute tryptophan depletion in accordance with body weight: influx of amino acids across the blood–brain barrier
Acute tryptophan depletion (ATD) is a method of reducing central nervous serotonin (5-HT) synthesis in humans by administering an amino acid (AA) beverage lacking in tryptophan (TRP), the physiological precursor of 5-HT. However, to date, the use of conventional ATD protocols in children and adolescents was limited due to frequently observed side effects (e.g., vomiting and nausea). This study investigated the effects of diminished central nervous system 5-HT synthesis on plasma concentrations of relevant AAs and TRP influx into the brain in 24 healthy young adults using the ATD procedure Moja-De, a test protocol that has been used in preliminary research in youths. Twenty-four healthy participants received ATD and a TRP-balanced amino acid load (BAL) using a randomized double-blind within-subject crossover design. Plasma concentrations of the relevant AAs that compete with TRP on the same transport system were assessed at baseline and 90, 180, and 240 min after ATD/BAL intake. TRP influx across the blood–brain barrier was calculated using Michaelis–Menten kinetics with a correction for multiple substrate competition, indicating a significant decrease in TRP influx into the central nervous system under Moja-De. ATD Moja-De decreased TRP influx into the brain and central nervous system 5-HT synthesis safely and effectively and was well tolerated, allowing it to be used in children and adolescents. Future research into other secondary, compensatory effects induced by ATD in patients with neuropsychiatric disorders and healthy populations is needed. ATD Moja-De allows this type of research with a focus on a developmental viewpoint. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00702-012-0793-z) contains supplementary material, which is available to authorized users
Effects of Acute Tryptophan Depletion on Brain Serotonin Function and Concentrations of Dopamine and Norepinephrine in C57BL/6J and BALB/cJ Mice
Acute tryptophan depletion (ATD) is a method of lowering brain serotonin (5-HT). Administration of large neutral amino acids (LNAA) limits the transport of endogenous tryptophan (TRP) across the blood brain barrier by competition with other LNAAs and subsequently decreases serotonergic neurotransmission. A recent discussion on the specificity and efficacy of the ATD paradigm for inhibition of central nervous 5-HT has arisen. Moreover, side effects such as vomiting and nausea after intake of amino acids (AA) still limit its use. ATD Moja-De is a revised mixture of AAs which is less nauseating than conventional protocols. It has been used in preliminary clinical studies but its effects on central 5-HT mechanisms and other neurotransmitter systems have not been validated in an animal model. We tested ATD Moja-De (TRP−) in two strains of mice: C57BL/6J, and BALB/cJ, which are reported to have impaired 5-HT synthesis and a more anxious phenotype relative to other strains of mice. ATD Moja-De lowered brain TRP, significantly decreased 5-HT synthesis as indexed by 5-HTP levels after decarboxlyase inhibition, and lowered 5-HT and 5-HIAA in both strains of mice, however more so in C57BL/6J than in BALB/cJ. Dopamine and its metabolites as well as norepinephrine were not affected. A balanced (TRP+) control mixture did not raise 5-HT or 5-HIAA. The present findings suggest that ATD Moja-De effectively and specifically suppresses central serotonergic function. These results also demonstrate a strain- specific effect of ATD Moja-De on anxiety-like behavior
Early development of Thyrsitops lepidopoides (Pisces: Gempylidae)
Thyrsitops lepidopoides larvae were caught with Bongo nets in the upper 200 m of the ocean from the coast of southern Brazil during 1975-1978. Based on a serie of 271 specimens ranging from 2.5 to 24.0 mm body lenght, morphological and osteological development of the larvae and juveniles is described. Small larvae (2.5-12.0 mm NL) can be distinguished from all known gempylid larvae by the presence of a distinct melanophore at the base of the dorsal and anal fins. The larvae have well developed dorsal and ventral spines. It is the only gempylid with six preopercular spines and non-serrated dorsal and ventral spines during the larval stage
A critical appraisal of appendage disparity and homology in fishes
Fishes are both extremely diverse and morphologically disparate. Part of this disparity can be observed in the numerous possible fin configurations that may differ in terms of the number of fins as well as fin shapes, sizes and relative positions on the body. Here, we thoroughly review the major patterns of disparity in fin configurations for each major group of fishes and discuss how median and paired fin homologies have been interpreted over time. When taking into account the entire span of fish diversity, including both extant and fossil taxa, the disparity in fin morphologies greatly complicates inferring homologies for individual fins. Given the phylogenetic scope of this review, structural and topological criteria appear to be the most useful indicators of fin identity. We further suggest that it may be advantageous to consider some of these fin homologies as nested within the larger framework of homologous fin‐forming morphogenetic fields. We also discuss scenarios of appendage evolution and suggest that modularity may have played a key role in appendage disparification. Fin modules re‐expressed within the boundaries of fin‐forming fields could explain how some fins may have evolved numerous times independently in separate lineages (e.g., adipose fin), or how new fins may have evolved over time (e.g., anterior and posterior dorsal fins, pectoral and pelvic fins). We favour an evolutionary scenario whereby median appendages appeared from a unique field of competence first positioned throughout the dorsal and ventral midlines, which was then redeployed laterally leading to paired appendages.Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/151971/1/faf12402_am.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/151971/2/faf12402.pd
Chromosome evolution in fishes: a new challenging proposal from Neotropical species
We present a database containing cytogenetic data of Neotropical actinopterygian fishes from Venezuela obtained in a single
laboratory for the first time. The results of this study include 103 species belonging to 74 genera assigned to 45 families and 17
out of the 40 teleost orders. In the group of marine fishes, the modal diploid number was 2n=48 represented in 60% of the
studied species, while in the freshwater fish group the modal diploid complement was 2n=54, represented in 21.21 % of the
studied species. The average number of chromosomes and the mean FN were statistically higher in freshwater fish than in
marine fish. The degree of diversification and karyotype variation was also higher in freshwater fish in contrast to a more
conserved cytogenetic pattern in marine fish. In contrast to the assumption according to which 48 acrocentric chromosomes
was basal chromosome number in fish, data here presented show that there is an obvious trend towards the reduction of the
diploid number of chromosomes from values near 2n=60 with high number of biarmed chromosomes in more basal species to
2n=48 acrocentric elements in more derived Actinopterygi
Evolutionary transitions among egg-laying, live-bearing and maternal inputs in sharks and rays
Sharks and rays are thought to have a large number of independent origins of live-bearing. We examined evolutionary transitions to live-bearing and maternal input to embryos in this subclass by optimizing reproductive characters onto a composite phylogeny. Egg-laying (40 per cent of all species) is the likely ancestral reproductive mode for this clade, and there is evidence that live-bearing has evolved independently 9–10 times and maternal input 4–5 times. Most transitions (12–15) have been toward live-bearing with provisioning limited to yolk. These have occurred from egg-laying ancestors or live-bearing taxa that provide maternal input to embryos. Only 2–3 transitions have occurred in the other direction, i.e. away from yolk-only bearing. Egg-laying has evolved from live-bearing ancestors in skates, Rajidae (25 per cent of all species) and possibly in the zebra shark, Stegostoma fasciata. Thus, although there has been an overall trend toward the evolution of live-bearing in elesmobranchs, the evolution of additional maternal input has been extremely labile
Acute tryptophan depletion in accordance with body weight: influx of amino acids across the blood–brain barrier
Acute tryptophan depletion (ATD) is a method of reducing central nervous serotonin (5-HT) synthesis in humans by administering an amino acid (AA) beverage lacking in tryptophan (TRP), the physiological precursor of 5-HT. However, to date, the use of conventional ATD protocols in children and adolescents was limited due to frequently observed side effects (e.g., vomiting and nausea). This study investigated the effects of diminished central nervous system 5-HT synthesis on plasma concentrations of relevant AAs and TRP influx into the brain in 24 healthy young adults using the ATD procedure Moja-De, a test protocol that has been used in preliminary research in youths. Twenty-four healthy participants received ATD and a TRP-balanced amino acid load (BAL) using a randomized double-blind within-subject crossover design. Plasma concentrations of the relevant AAs that compete with TRP on the same transport system were assessed at baseline and 90, 180, and 240 min after ATD/BAL intake. TRP influx across the blood–brain barrier was calculated using Michaelis–Menten kinetics with a correction for multiple substrate competition, indicating a significant decrease in TRP influx into the central nervous system under Moja-De. ATD Moja-De decreased TRP influx into the brain and central nervous system 5-HT synthesis safely and effectively and was well tolerated, allowing it to be used in children and adolescents. Future research into other secondary, compensatory effects induced by ATD in patients with neuropsychiatric disorders and healthy populations is needed. ATD Moja-De allows this type of research with a focus on a developmental viewpoint
- …