242 research outputs found
Catecholaminergic connectivity to the inner ear, central auditory, and vocal motor circuitry in the plainfin midshipman fish porichthys notatus
Author Posting. © John Wiley & Sons, 2014. This is the author's version of the work. It is posted here by permission of John Wiley & Sons for personal use, not for redistribution. The definitive version was published in Journal of Comparative Neurology 522 (2014): 2887-2927, doi:10.1002/cne.23596.Although the neuroanatomical distribution of catecholaminergic
(CA) neurons has been well documented across all
vertebrate classes, few studies have examined CA connectivity
to physiologically and anatomically identified neural
circuitry that controls behavior. The goal of this study was
to characterize CA distribution in the brain and inner ear
of the plainfin midshipman fish (Porichthys notatus) with
particular emphasis on their relationship with anatomically
labeled circuitry that both produces and encodes social
acoustic signals in this species. Neurobiotin labeling of the
main auditory end organ, the saccule, combined with tyrosine
hydroxylase immunofluorescence (TH-ir) revealed a
strong CA innervation of both the peripheral and central
auditory system. Diencephalic TH-ir neurons in the periventricular
posterior tuberculum, known to be dopaminergic,
send ascending projections to the ventral telencephalon and prominent descending projections to
vocal–acoustic integration sites, notably the hindbrain
octavolateralis efferent nucleus, as well as onto the base
of hair cells in the saccule via nerve VIII. Neurobiotin backfills
of the vocal nerve in combination with TH-ir revealed
CA terminals on all components of the vocal pattern generator,
which appears to largely originate from local TH-ir
neurons but may include input from diencephalic projections
as well. This study provides strong neuroanatomical
evidence that catecholamines are important modulators of
both auditory and vocal circuitry and acoustic-driven social
behavior in midshipman fish. This demonstration of TH-ir
terminals in the main end organ of hearing in a nonmammalian
vertebrate suggests a conserved and important
anatomical and functional role for dopamine in normal
audition.National Institutes of Health; Grant number:
SC2DA034996 (to P.M.F.); Grant sponsor: The Professional Staff Congress/
The City University of New York (PSC-CUNY); Grant number:
65650-00 43 (to P.M.F.); Grant sponsor: Leonard and Claire Tow Travel
Award (to P.M.F.); Grant sponsor: Whitman Investigator Faculty Research
Fellowships from the Marine Biological Laboratory, Woods, Hole, MA
(where the study was partly conducted) (to P.M.F. and J.A.S.).2015-05-0
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Effects of Trichoderma harzianum Strain T22 on the Arthropod Community Associated with Tomato Plants and on the Crop Performance in an Experimental Field
Fungi belonging to the genus Trichoderma have received much attention in recent years due to their beneficial effects on crop health and their use as pest control agents. Trichoderma activates direct plant defenses against phytophagous arthropods and reinforces indirect plant defense through the attraction of predators. Although the plant defenses against insect herbivores were demonstrated in laboratory experiments, little attention has been paid to the use of Trichoderma spp. in open field conditions. In the present study, we investigated the effects of the inoculation of the commercial Trichoderma harzianum strain T22 on the arthropod community associated with tomato plants and on the crop performance in an experimental field located in South Italy. Our results showed that inoculation with T. harzianum could alter the arthropod community and reduce the abundance of specific pests under field conditions with respect to the sampling period. The present study also confirmed the beneficial effect of T. harzianum against plant pathogens and on tomato fruit. The complex tomato–arthropod–microorganism interactions that occurred in the field are discussed to enrich our current information on the possibilities of using Trichoderma as a green alternative agent in agricultur
Catecholaminergic Innervation of Central and Peripheral Auditory Circuitry Varies with Reproductive State in Female Midshipman Fish, Porichthys notatus
In seasonal breeding vertebrates, hormone regulation of catecholamines, which include dopamine and noradrenaline, may function, in part, to modulate behavioral responses to conspecific vocalizations. However, natural seasonal changes in catecholamine innervation of auditory nuclei is largely unexplored, especially in the peripheral auditory system, where encoding of social acoustic stimuli is initiated. The plainfin midshipman fish, Porichthys notatus, has proven to be an excellent model to explore mechanisms underlying seasonal peripheral auditory plasticity related to reproductive social behavior. Recently, we demonstrated robust catecholaminergic (CA) innervation throughout the auditory system in midshipman. Most notably, dopaminergic neurons in the diencephalon have widespread projections to auditory circuitry including direct innervation of the saccule, the main endorgan of hearing, and the cholinergic octavolateralis efferent nucleus (OE) which also projects to the inner ear. Here, we tested the hypothesis that gravid, reproductive summer females show differential CA innervation of the auditory system compared to non-reproductive winter females. We utilized quantitative immunofluorescence to measure tyrosine hydroxylase immunoreactive (TH-ir) fiber density throughout central auditory nuclei and the sensory epithelium of the saccule. Reproductive females exhibited greater density of TH-ir innervation in two forebrain areas including the auditory thalamus and greater density of TH-ir on somata and dendrites of the OE. In contrast, non-reproductive females had greater numbers of TH-ir terminals in the saccule and greater TH-ir fiber density in a region of the auditory hindbrain as well as greater numbers of TH-ir neurons in the preoptic area. These data provide evidence that catecholamines may function, in part, to seasonally modulate the sensitivity of the inner ear and, in turn, the appropriate behavioral response to reproductive acoustic signals
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Metabolic profile reflects stages of fibrosis in patients with non-alcoholic fatty liver disease
Nonalcoholic fatty liver disease (NAFLD) is a leading cause of chronic liver disease worldwide, with fibrosis stage being the main predictor for clinical outcomes. Here, we present the metabolic profile of NAFLD patients with regards to fibrosis progression. We included all consecutive new referrals for NAFLD services between 2011 and 2019. Demographic, anthropometric and clinical features and noninvasive markers of fibrosis were recorded at baseline and at follow-up. Significant and advanced fibrosis were defined using liver stiffness measurement (LSM) as LSM ≥ 8.1 kPa and LSM ≥ 12.1 kPa, respectively. Cirrhosis was diagnosed either histologically or clinically. Fast progressors of fibrosis were defined as those with delta stiffness ≥ 1.03 kPa/year (25% upper quartile of delta stiffness distribution). Targeted and untargeted metabolic profiles were analysed on fasting serum samples using Proton nuclear magnetic resonance (1H NMR). A total of 189 patients were included in the study; 111 (58.7%) underwent liver biopsy. Overall, 11.1% patients were diagnosed with cirrhosis, while 23.8% were classified as fast progressors. A combination of metabolites and lipoproteins could identify the fast fibrosis progressors (AUROC 0.788, 95% CI: 0.703–0.874, p < 0.001) and performed better than noninvasive markers. Specific metabolic profiles predict fibrosis progression in patients with nonalcoholic fatty liver disease. Algorithms combining metabolites and lipids could be integrated in the risk-stratification of these patients
Gap junction-mediated glycinergic inhibition ensures precise temporal patterning in vocal behavior
Precise neuronal firing is especially important for behaviors highly dependent on the correct sequencing and timing of muscle activity patterns, such as acoustic signaling. Acoustic signaling is an important communication modality for vertebrates, including many teleost fishes. Toadfishes are well known to exhibit high temporal fidelity in synchronous motoneuron firing within a hindbrain network directly determining the temporal structure of natural calls. Here, we investigated how these motoneurons maintain synchronous activation. We show that pronounced temporal precision in population-level motoneuronal firing depends on gap junction-mediated, glycinergic inhibition that generates a period of reduced probability of motoneuron activation. Super-resolution microscopy confirms glycinergic release sites formed by a subset of adjacent premotoneurons contacting motoneuron somata and dendrites. In aggregate, the evidence supports the hypothesis that gap junction-mediated, glycinergic inhibition provides a timing mechanism for achieving synchrony and temporal precision in the millisecond range for rapid modulation of acoustic waveforms
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