48 research outputs found
Excitatory neurotransmitters in the tentacle flexor muscles responsible for space positioning of the snail olfactory organ
Recently, three novel flexor muscles (M1, M2 and M3) in the posterior tentacles of the snail have been described, which are responsible for the patterned movements of the tentacles of the snail, Helix pomatia. In this study, we have demonstrated that the muscles received a complex innervation pattern via the peritentacular and olfactory nerves originating from different clusters of motoneurons of the cerebral ganglia. The innervating axons displayed a number of varicosities and established neuromuscular contacts of different ultrastructural forms. Contractions evoked by nerve stimulation could be mimicked by external acetylcholine (ACh) and glutamate (Glu), suggesting that ACh and Glu are excitatory transmitters at the neuromuscular contacts. Choline acetyltransferase and vesicular glutamate transporter immunolabeled axons innervating flexor muscles were demonstrated by immunohistochemistry and in Western blot experiments. Nerve- and transmitter-evoked contractions were similarly attenuated by cholinergic and glutamatergic antagonists supporting the dual excitatory innervation. Dopamine (DA, 10â5 M) oppositely modulated thin (M1/M2) and thick (M3) muscle responses evoked by stimulation of the olfactory nerve, decreasing the contractions of the M1/M2 and increasing those of M3. In both cases, the modulation site was presynaptic. Serotonin (5-HT) at high concentration (10â5 M) increased the amplitude of both the nerve- and the ACh-evoked contractions in all muscles. The relaxation rate was facilitated suggesting pre- and postsynaptic site of action. Our data provided evidence for a DAergic and 5-HTergic modulation of cholinergic nerves innervating flexor muscles of the tentacles as well as the muscles itself. These effects of DA and 5-HT may contribute to the regulation of sophisticated movements of tentacle muscles lacking inhibitory innervation
Oxytocin receptor gene polymorphisms are associated with human directed social behavior in dogs (Canis familiaris)
The oxytocin system has a crucial role in human sociality;
several results prove that polymorphisms of the oxytocin
receptor gene are related to complex social behaviors in humans.
Dogs' parallel evolution with humans and their adaptation to the
human environment has made them a useful species to model human
social interactions. Previous research indicates that dogs are
eligible models for behavioral genetic research, as well. Based
on these previous findings, our research investigated
associations between human directed social behaviors and two
newly described (â212AG, 19131AG) and one known (rs8679684)
single nucleotide polymorphisms (SNPs) in the regulatory regions
(5Ⲡand 3ⲠUTR) of the oxytocin receptor gene in German Shepherd
(N = 104) and Border Collie (N = 103) dogs. Dogs' behavior
traits have been estimated in a newly developed test series
consisting of five episodes: Greeting by a stranger, Separation
from the owner, Problem solving, Threatening approach, Hiding of
the owner. Buccal samples were collected and DNA was isolated
using standard protocols. SNPs in the 3Ⲡand 5ⲠUTR regions were
analyzed by polymerase chain reaction based techniques followed
by subsequent electrophoresis analysis. The geneâbehavior
association analysis suggests that oxytocin receptor gene
polymorphisms have an impact in both breeds on (i) proximity
seeking towards an unfamiliar person, as well as their owner,
and on (ii) how friendly dogs behave towards strangers, although
the mediating molecular regulatory mechanisms are yet unknown.
Based on these results, we conclude that similarly to humans,
the social behavior of dogs towards humans is influenced by the
oxytocin system
Structural and Functional Hierarchy in Photosynthetic Energy Conversionâfrom Molecules to Nanostructures
Basic principles of structural and functional requirements of photosynthetic energy conversion in hierarchically organized machineries are reviewed. Blueprints of photosynthesis, the energetic basis of virtually all life on Earth, can serve the basis for constructing artificial light energy-converting molecular devices. In photosynthetic organisms, the conversion of light energy into chemical energy takes places in highly organized fine-tunable systems with structural and functional hierarchy. The incident photons are absorbed by light-harvesting complexes, which funnel the excitation energy into reaction centre (RC) protein complexes containing redox-active chlorophyll molecules; the primary charge separations in the RCs are followed by vectorial transport of charges (electrons and protons) in the photosynthetic membrane. RCs possess properties that make their use in solar energy-converting and integrated optoelectronic systems feasible. Therefore, there is a large interest in many laboratories and in the industry toward their use in molecular devices. RCs have been bound to different carrier matrices, with their photophysical and photochemical activities largely retained in the nano-systems and with electronic connection to conducting surfaces. We show examples of RCs bound to carbon-based materials (functionalized and non-functionalized single- and multiwalled carbon nanotubes), transitional metal oxides (ITO) and conducting polymers and porous silicon and characterize their photochemical activities. Recently, we adapted several physical and chemical methods for binding RCs to different nanomaterials. It is generally found that the P(+)(Q(A)Q(B))(â) charge pair, which is formed after single saturating light excitation is stabilized after the attachment of the RCs to the nanostructures, which is followed by slow reorganization of the protein structure. Measuring the electric conductivity in a direct contact mode or in electrochemical cell indicates that there is an electronic interaction between the protein and the inorganic carrier matrices. This can be a basis of sensing element of bio-hybrid device for biosensor and/or optoelectronic applications