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Chemical Senses 22: 93-103,
© 1997


research-article

Inositol-1,4,5-trisphosphate Induces Responses in Receptor Neurons in Rat Vomeronasal Sensory Slices

Kouhei Inamura, Makoto Kashiwayanagi and Kenzo Kurihara

Faculty of Pharmaceutical Sciences, Hokkaido University Sapporo 060, Japan

Correspondence to be sent to: Dr Makoto Kashiwayanagi, Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060, Japan

Using the whole-cell mode of the patch-clamp technique, we recorded action potentials, voltage-activated cationic currents and putative second messenger-activated currents in receptor neurons in the vomeronasal sensory epithelium of female rats. The resting membrane potential and input resistance were –45.5 ± 2.5 mV (mean ± SEM, n = 39) and 1.5 ± 0.2 G (mean ± SEM, n = 37). Current injection of 1–3 pA induced overshooting action potentials. The firing frequency increased with increasing current injections linearly from 1 to 10 pA and reached a plateau at 30 pA, suggesting that rat vomeronasal receptor neurons sensitively elicit action potentials in response to a small receptor potential. Under voltage clamp, voltage-dependent Na+ inward current, inward Ca22+ current, sustained outward K+ current and Ca2+-activated K+-current were identified. Dialysis of D-inositol-1,4,5-trisphosphate (D-IP3) induced inward currents with an increase in membrane conductance in ~54% of the cells and inward current fluctuations in 15% of the cells. L-IP3 also induced inward currents and current fluctuations in 53 and 13% of the cells respectively. The mean amplitude of inward currents induced by 100 µM D-IP3 and L-IP3 were 84.6 ± 14.0 pA (SEM, n = 82) and 66.1 ± 9.4 pA (SEM, n = 100) respectively. The IP3-induced responses were blocked by elimination of Na+ and Ca2+ in the external solution or application of 10 µM ruthenium red. The present study suggested that IP3-mediated transduction pathways exist in rat vomeronasal receptor neurons. Chem. Senses 22: 93–103, 1997.


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