Biology subjects

Hillman, C. S.

Publications and source records attributed to Hillman, C. S..

5 recordsLinked to original sources

bioRxiv2025

Fentanyl and Alcohol Co-Exposure Induce Robust, Sustained Hyperlocomotion and Neural Circuit Disruption in Larval Zebrafish

The constantly evolving trends in substance abuse are a major concern for health authorities worldwide, and these trends include an increasing prevalence of poly-substance misuse. For instance, opioid overdoses are frequently accompanied by alcohol co-use, yet the combined effects of these substances remain poorly understood. Using zebrafish as a highly relevant vertebrate model of neuropharmacology, we investigated the interactions between fentanyl and alcohol, uncovering a unique and robust hyperlocomotor response characterized by initial locomotor suppression followed by persistent, erratic hyperlocomotion. Alcohol was found to be critical to this phenomenon, as substitution with other GABAA modulators failed to replicate the effect. However, the response was replicable with heroin and remifentanil, suggesting an opioid-class wide effect. In vivo whole brain imaging further demonstrated dysregulated neuronal activity, with co-administration with alcohol causing potentiated neuronal activity compared to individual drug exposures and controls. Collectively, these findings suggested an integral role of ethanol and fentanyl co-administration in dysregulated neuronal responses and reveals a complex neurobehavioral mechanism. These observations suggest further investigation is warranted into the use of the larval zebrafish model for studying the neuropharmacological interactions of multiple substances of abuse.

animal behavior and cognition↗

bioRxiv2025

Genetic disruption of leucine rich repeat transmembrane protein 4 like 1 induces a pro-social behavioural phenotype in zebrafish

BackgroundSocial behaviour encompasses the wide range of interactions that occur between members of the same species. In humans, disruptions in social behaviour are characteristic of many neuropsychiatric disorders, where both genetic risk factors and synaptic dysfunctions can contribute to the phenotype. Among the genes implicated in synaptic regulation, the synaptic adhesion protein leucine-rich repeat transmembrane protein 4 (LRRTM4) has been identified as a key player in maintaining synaptic function and neuronal circuit integrity. Despite its established role in the nervous system, the potential involvement of LRRTM4 in modulating social behaviour and its contribution to social deficits has yet to be explored. MethodsIn the current study, we used zebrafish to study how genetic deletion of lrrtm4l1, a zebrafish orthologue of LRRTM4, affects sociality. For this, the social behaviour of homozygous lrrtm4l1 knockout (KO) zebrafish was analysed in multiple behavioural assays and the brain transcriptome of mutant animals was investigated by RNAseq. ResultsKO zebrafish displayed a pro-social phenotype in multiple behavioural assays. Groups of lrrtm4l1 KO zebrafish formed more cohesive shoals and KO individuals spent more time in the vicinity of conspecifics during a social interaction test. They were also less aggressive and in contrast to wild-type zebrafish did not differentiate in their interactions with known and unknown groups of fish. Neurotranscriptomic analysis revealed 560 differentially expressed genes including changes in glutamatergic neurotransmitter signalling, tryptophan- kynurenine metabolism and synaptic plasticity. ConclusionThese findings suggest that lrrtm4l1 is an important regulator of social behaviour in zebrafish. In a translational perspective, LRRTM4 is a promising potential therapeutic target that warrants further investigation in the framework of neuropsychiatric conditions characterized by major social impairments.

neuroscience↗

bioRxiv2025

Neural and Behavioral Dynamics of Acute Fentanyl Administration and Implications for Hazard Assessment of Novel Synthetic Opioids in Larval Zebrafish

Rationale Synthetic opioids pose a significant public health risk due to their rapid synthesis and potentially lethal potency. New compounds are emerging continuously, meaning current testing platforms struggle to keep pace. Objectives Consequently, there is a critical need for simple, rapid, translatable models to provide a scalable screening platform to identify and hazard-assess emerging synthetic opioids, and test potential intervention strategies. Methods Here, we exposed 4 days post-fertilization (dpf) larval zebrafish to a range of concentrations of the prototypical class representative, fentanyl, to investigate behavioral and neural responses. Results Fentanyl caused low concentration hyperactivity, and high concentration hypolocomotion (sedation) which was reversed by the opioid antagonist naloxone. We confirmed predictive validity by replicating the behavioral responses with other class representatives (diacetylmorphine [heroin] and remifentanil). We also confirmed, pharmacologically, that low concentration hyperlocomotion was mediated by dopamine D2 receptors, replicating effects observed in mammals. Further mechanistic investigation using whole-brain in vivo imaging revealed disrupted connectivity in opioid-related circuits, such as the habenulae and dorsal thalamus, alongside novel pathways, including circuits associated with the pineal gland, torus semicircularis and eminentia granularis, potentially highlighting previously uncharacterized sensory and cerebellar neuronal networks. Conclusions These findings support the use of the larval zebrafish as a scalable model for assessment of synthetic opioids to provide novel insights into opioid-induced behaviors and mechanisms of action that may aid strategies in the growing challenge of interventive treatments for synthetic opioid intoxication. Impact StatementLarval zebrafish reveal neurobehavioral pathways affected by synthetic opioids, offering a valuable tool for rapid hazard assessment.

animal behavior and cognition↗

bioRxiv2024

The effect of laboratory diet and feeding on growth parameters in zebrafish

Despite being one of the most used laboratory species in biomedical, behavioural and physiological research, the nutritional requirements of zebrafish (Danio rerio) are poorly understood, and no standardised laboratory diet exists. Diet and feeding regimen can significantly impact the welfare of the fish and in turn experimental reproducibility. Consequently, the establishment of a standardised diet and feeding protocol for laboratory zebrafish is imperative to enhance animal welfare, guarantee research reproducibility and advance the economic and environmental sustainability of laboratory dietary practices. The aim of this systematic review was to determine the optimal feed for juvenile zebrafish growth and development. A comprehensive search was conducted in PubMed, Scopus and Google Scholar to identify relevant studies published up to August 2023 and the studies were selected based on the predefined inclusion/exclusion criteria. A total of 1065 articles were identified in the databases, of which 14 were included in this review. We conducted data extraction and risk-of-bias analysis in the included studies. Statistical comparisons for specific growth rate, weight gain (%) and length gain (%) parameters were performed to determine the optimal feed for enhanced juvenile growth. We identify an insect-based diet as optimal for juvenile growth for all three growth parameters. We also identify areas of potential heterogeneity and conclude by encouraging a standardised laboratory diet to ensure reproducible data and encourage zebrafish welfare.

developmental biology↗

bioRxiv2023

A Unified Approach to Investigating 4 dpf Zebrafish Larval Behaviour through a Standardised Light/Dark Assay

Zebrafish have emerged as a dynamic research model in the domains of neuropsychopharmacology, biological psychiatry and behaviour. Working with larvae [≤] 4 days post-fertilisation (dpf) offers an avenue for high-throughput investigation whilst aligning with the 3Rs principles of animal research. The light/dark assay, which is the most used behavioural assay for larval neuropharmacology research, lacks experimental reliability and standardisation. This study aimed to formulate a robust, reproducible and standardised light/dark behavioural assay using 4 dpf zebrafish larvae. Considerable between-batch and inter-individual variability was found, which we rectified with a normalisation approach to ensure a reliable foundation for analysis. We then identified that 5-minute light/dark transition periods are optimal for locomotor activity. We also found that a 30-minute acclimation in the light was found to produce significantly increased dark phase larval locomotion. Next, we confirmed the pharmacological predictivity of the standardised assay using ethanol which, as predicted, caused hyperlocomotion at low concentrations and hypolocomotion at high concentrations. Finally, the assay was validated by assessing the behavioural phenotype of hyperactive transgenic (adgrl3.1-/-) larvae, which was rescued with psychostimulant medications. Our standardised assay not only provides a clear experimental and analytical framework to work with 4 dpf larvae, but also facilitates between-laboratory collaboration using our normalisation approach.

animal behavior and cognition↗