TY - JOUR
T1 - 5-HT(1B) receptor-mediated presynaptic inhibition of retinal input to the suprachiasmatic nucleus
AU - Pickard, Gary E.
AU - Smith, Bret N.
AU - Belenky, Michael
AU - Rea, Michael A.
AU - Dudek, F. Edward
AU - Sollars, Patricia J.
PY - 1999/5/15
Y1 - 1999/5/15
N2 - The suprachiasmatic nucleus (SCN) receives glutamatergic afferents from the retina and serotonergic afferents from the midbrain, and serotonin (5- HT) can modify the response of the SCN circadian oscillator to light. 5- HT(1B) receptor-mediated presynaptic inhibition has been proposed as one mechanism by which 5-HT modifies retinal input to the SCN (Pickard et al., 1996). This hypothesis was tested by examining the subcellular localization of 5-HT(1B) receptors in the mouse SCN using electron microscopic immunocytochemical analysis with 5-HT(1B) receptor antibodies and whole-cell patch-clamp recordings from SCN neurons in hamster hypothalamic slices. 5- HT(1B) receptor immunostaining was observed associated with the plasma membrane of retinal terminals in the SCN. 1-[3(Trifluoromethyl)phenyl]- piperazine HCl (TFMPP), a 5-HT(1B) receptor agonist, reduced in a dose- related manner the amplitude of glutamatergic EPSCs evoked by stimulating selectively the optic nerve. Selective 5-HT(1A) or 5-HT7 receptor antagonists did not block this effect. Moreover, in cells demonstrating an evoked EPSC in response to optic nerve stimulation, TFMPP had no effect on the amplitude of inward currents generated by local application of glutamate. The effect of TFMPP on light-induced phase shifts was also examined using 5- HT(1B) receptor knock-out mice. TFMPP inhibited behavioral responses to light in wild-type mice but was ineffective in inhibiting light-induced phase shifts in 5-HT(1B) receptor knock-out mice. The results indicate that 5-HT can reduce retinal input to the circadian system by acting at presynaptic 5- HT(1B) receptors located on retinal axons in the SCN.
AB - The suprachiasmatic nucleus (SCN) receives glutamatergic afferents from the retina and serotonergic afferents from the midbrain, and serotonin (5- HT) can modify the response of the SCN circadian oscillator to light. 5- HT(1B) receptor-mediated presynaptic inhibition has been proposed as one mechanism by which 5-HT modifies retinal input to the SCN (Pickard et al., 1996). This hypothesis was tested by examining the subcellular localization of 5-HT(1B) receptors in the mouse SCN using electron microscopic immunocytochemical analysis with 5-HT(1B) receptor antibodies and whole-cell patch-clamp recordings from SCN neurons in hamster hypothalamic slices. 5- HT(1B) receptor immunostaining was observed associated with the plasma membrane of retinal terminals in the SCN. 1-[3(Trifluoromethyl)phenyl]- piperazine HCl (TFMPP), a 5-HT(1B) receptor agonist, reduced in a dose- related manner the amplitude of glutamatergic EPSCs evoked by stimulating selectively the optic nerve. Selective 5-HT(1A) or 5-HT7 receptor antagonists did not block this effect. Moreover, in cells demonstrating an evoked EPSC in response to optic nerve stimulation, TFMPP had no effect on the amplitude of inward currents generated by local application of glutamate. The effect of TFMPP on light-induced phase shifts was also examined using 5- HT(1B) receptor knock-out mice. TFMPP inhibited behavioral responses to light in wild-type mice but was ineffective in inhibiting light-induced phase shifts in 5-HT(1B) receptor knock-out mice. The results indicate that 5-HT can reduce retinal input to the circadian system by acting at presynaptic 5- HT(1B) receptors located on retinal axons in the SCN.
KW - 5-HT(1b) receptor knock-out mice
KW - Circadian rhythms
KW - Hypothalamic slice
KW - Presynaptic
KW - Retinal ganglion cells
KW - Serotonin
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U2 - 10.1523/jneurosci.19-10-04034.1999
DO - 10.1523/jneurosci.19-10-04034.1999
M3 - Article
C2 - 10234032
AN - SCOPUS:0033561801
SN - 0270-6474
VL - 19
SP - 4034
EP - 4045
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 10
ER -