**ABSTRACT NOT FOR
CITATION WITHOUT AUTHOR PERMISSION. The title, authors, and abstract for
this completion report are provided below. For a copy
of the full completion report, please contact the author via e-mail at zielin1@uwindsor.ca. Questions? Contact the GLFC
via email at slrp@glfc.org or via telephone
at 734-662-3018.**
Barbara Zielinski2, Réjean Dubuc3,
Weiming Li4
2Dept. of Integrative Biology and Great Lakes Institute for Environmental
Research,
University of Windsor,
Windsor, ON, N9B 3P4
3Dept. of Neuroscience, Université de Montréal,
Montréal, QC, H3P 3P8
4Dept of Fisheries and Wildlife, Michigan State University. East Lansing,
MI 48824
September 2019
ABSTRACT:
The goal of this project
was to provide new biological tools for sea lamprey population management, by
establishing which molecules are most effective at activating the different
solitary chemosensory cell (SCC) populations and inducing motor behaviour. Neural activity was recorded from cutaneous
papillae containing SCCs located around the mouth, nasal pore, gill and on the dorsal tail fin (1, 2, 3).
Chemo-stimulatory substances included sialic acid, glycine, proline,
serine, glutamate, histidine, taurocholic acid, as
well as water in which dead trout had been thawed (“dead trout water”). The
neural stimulation of brain regions that regulate movement was
investigated by recording neural activity from reticulospinal
cells of the middle rhobencephalic reticular nucleus
(1). Activity in this brain region was observed
following the electrical stimulation of cutaneous papillae containing SCCs or papillar nerves – the glossopharyngeal nerve and the vagus nerve (2). The application of the dead trout
water onto these papillae also stimulated reticulospinal
cell responses. Neuronal tract tracing of the pathway from the neural inputs in
the papillae to brain locomotor command neurons confirmed that there is a
prominent neural link between these chemosensory cutaneous papillae and
locomotor control centers in the brain. This is a di-synaptic neural connection
that utilizes the neurotransmitter glutamate (3). The chemostimulatory molecules within the “dead trout water” were identified through activity-guided fractionation. The
bile acid, taurocholic acid and 498 g/mol bile acid derivatives (taurodeoxycholic
acid, taurohyodeoxycholic acid, taurochenodeoxycholic
acid or tauroursodeoxycholic acid) as well as
possibly the fatty acid 2-hydroxyocatdecanoic acid were
identified in fractions prepared from this dead trout water (3).
Synthetic analogues of each compound elicited robust neural responses from the
dermal papillae (3). Components of the lamprey alarm substance (creatine, hypoxanthine and inosine) also evoked
chemosensory neural responses from the dermal papillae. These neural
chemosensory responses suggest that lampreys utilize chemosensory input from
dermal papillae for regulating movement during feeding, spawning migration and
reproduction. This project describes a non-olfactory chemosensory modality that
sea lamprey abatement strategies can utilize as a method of attracting or
repelling sea lampreys either independently or in conjunction with previously
developed th olfactory-based
strategies.