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1.
J Comp Neurol ; 522(8): 1929-40, 2014 Jun 01.
Article in English | MEDLINE | ID: mdl-24288162

ABSTRACT

Olfactory sensory neurons that express transient receptor potential channel M5 (TrpM5) or neurotrophin-3 (NT-3) project to defined clusters of glomeruli situated ventrally in the main olfactory bulb. Using genetically labeled mice, we investigated whether expression of NT-3-driven ßgal and TrpM5-driven GFP marked overlapping sets of glomeruli and whether expression of these markers was coordinated. Our results indicate that these markers largely characterize independent sets of olfactory sensory neuron axons and glomeruli. Further, in glomeruli in which both TrpM5-GFP and NT-3-ßgal labeled axons occur, they are expressed independently. The nature of staining for these two markers also differs within glomeruli. Within each labeled TrpM5-positive glomerulus, the level of TrpM5-GFP expression was similar throughout the glomerular neuropil. In contrast, NT-3-driven ßgal expression levels are heterogeneous even within heavily labeled glomeruli. In addition, a population of very small TrpM5-GFP positive glomeruli is apparent while no similar populations of NT-3-ßgal glomeruli are evident. Taken together, these data suggest that TrpM5 and NT-3 characterize two largely independent receptor populations both conveying odorant information to the ventral olfactory bulb.


Subject(s)
Nerve Growth Factors/analysis , Nerve Growth Factors/biosynthesis , Olfactory Bulb/chemistry , Olfactory Bulb/metabolism , TRPM Cation Channels/analysis , TRPM Cation Channels/biosynthesis , Animals , Female , Male , Mice , Mice, Transgenic
2.
J Exp Biol ; 211(Pt 17): 2786-91, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18723536

ABSTRACT

Bile salts are known olfactory stimuli for teleosts, but only a single report has indicated that the taste system of a fish was sensitive to this class of stimuli. Here, gustatory responses of the channel catfish, Ictalurus punctatus, to four bile salts that included taurine-, glycine- and non-conjugated compounds along with three stimulatory amino acids as a comparison were investigated using extracellular electrophysiological techniques. Integrated multiunit responses were obtained from the branch of the facial nerve innervating taste buds on the maxillary barbel. Bile salts were shown to be highly effective facial taste stimuli, with estimated electrophysiological thresholds for three of the four tested bile salts of approximately 10(-11) mol l(-1) to 10(-10) mol l(-1), slightly lower by 1-2 log units than those to amino acids in the same species. Although the sensitivity of the facial taste system of the channel catfish to bile salts is high, the relative magnitude of the response to suprathreshold concentrations of bile salts was significantly less than that to amino acids. Multiunit cross-adaptation experiments indicate that bile salts and amino acids bind to relatively independent receptor sites; however, nerve-twig data and single-fiber recordings suggest that both independent and shared neural pathways exist for the transmission of bile salt and amino acid information to the primary gustatory nucleus of the medulla.


Subject(s)
Bile Acids and Salts/metabolism , Facial Nerve/metabolism , Ictaluridae/physiology , Taste/physiology , Animals , Bile Acids and Salts/chemistry , Dose-Response Relationship, Drug , Electrophysiology , Ictaluridae/metabolism , Molecular Structure , Neural Pathways/metabolism , Stimulation, Chemical
3.
J Neurophysiol ; 97(6): 4058-68, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17442768

ABSTRACT

A chemotopic map of biologically relevant odorants (that include amino acids, bile salts, and nucleotides) exists in the olfactory bulb (OB) of channel catfish, Ictalurus punctatus. Neurons processing bile salt odorant information lie medially within this OB map; however, information as to how single neurons process bile salt odorant information is lacking. In the present report, recordings were obtained from 51 OB neurons from 30 channel catfish to determine the excitatory molecular receptive range (EMRR) of bile salt responsive neurons. All recordings were performed in vivo within the medial portions of the OB using extracellular electrophysiological techniques. Excitatory thresholds to bile salts typically ranged between 0.1 and 10 muM. The bile salt specificity of OB neurons were divided into three groups: neurons excited by taurine-conjugated bile salts only (group T), neurons excited by nonconjugated bile salts only (group N), and neurons excited by at least one member of each of the three classes of bile salts tested (group G). In addition to the conjugating group at C24 of the side-chain, OB neurons discriminated bile salts by the molecular features present at three other carbon positions (C3, C7, and C12) along the steroid backbone. These data suggest that OB neurons are selectively excited by combinations of molecular features found on the side-chain and along the steroid nucleus of bile salt molecules.


Subject(s)
Bile Acids and Salts , Ictaluridae/physiology , Odorants , Olfactory Bulb/cytology , Olfactory Pathways/physiology , Olfactory Receptor Neurons/physiology , Action Potentials/drug effects , Animals , Bile Acids and Salts/pharmacology , Brain Mapping , Dose-Response Relationship, Drug , Neural Inhibition/drug effects , Neural Inhibition/physiology
4.
J Exp Biol ; 206(Pt 10): 1683-96, 2003 May.
Article in English | MEDLINE | ID: mdl-12682100

ABSTRACT

Electrophysiological responses of goldfish olfactory receptor neurons (ORNs) and goldfish behavioral responses to polyamines were investigated in vivo. Electro-olfactogram (EOG) recordings indicated that polyamines (putrescine, cadaverine and spermine) are potent olfactory stimuli for goldfish with estimated electrophysiological thresholds of 10(-8)-10(-7) mol l(-1), similar to that for L-arginine, the most stimulatory amino acid. Although thresholds were similar, the magnitude of the EOG responses to intermediate (10(-5)-10(-4) mol l(-1)) and high (10(-3) mol l(-1)) concentrations of polyamines dwarfed the responses to amino acids and related single amine containing compounds (amylamine and butylamine). The EOG responses to 0.1 mmol l(-1) putrescine, cadaverine and spermine were, respectively, 4.2x, 4.3x and 10.3x the response of the standard, 0.1 mmol l(-1) L-arginine. Electrophysiological cross-adaptation experiments indicated that polyamine receptor sites are independent from those to L-amino acids (alanine, arginine, glutamate, lysine, methionine and ornithine), bile salts (sodium taurocholate and taurolithocholate), the single amine containing compounds (amylamine and butylamine) and ATP. Further, the cross-adaptation experiments revealed the existence of independent receptor sites for the different polyamines tested. Pharmacological experiments suggested that polyamine odorant transduction does not primarily involve the cyclic AMP and IP(3) second messenger pathways. Behavioral assays indicated that polyamines are attractants that elicit feeding behavior similar to that elicited by L-amino acids.


Subject(s)
Biogenic Polyamines/pharmacology , Goldfish/physiology , Smell/drug effects , Amines/pharmacology , Animals , Arginine/pharmacology , Behavior, Animal/drug effects , Binding Sites , Biogenic Polyamines/metabolism , Butylamines/pharmacology , Cadaverine/metabolism , Cadaverine/pharmacology , Colforsin/pharmacology , Electrophysiology , Estrenes/pharmacology , Odorants , Olfactory Receptor Neurons/drug effects , Olfactory Receptor Neurons/physiology , Putrescine/metabolism , Putrescine/pharmacology , Pyrrolidinones/pharmacology , Second Messenger Systems , Smell/physiology , Spermine/metabolism , Spermine/pharmacology
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