THE expression of metabotropic glutamate receptors (mGluRs) in primary
cultures of cerebellar granule neurones can be: (i) modulated by the
degree of depolarization during the culture period, rendering neurones
differently sensitive to agonist-stimulated inositol phosphate (IP) h
ydrolysis; (ii) down-regulated by specific mGluR agonists. In this cul
ture the new rigid glutamate analogue, (+/-)-trans-azetidine-2,4-dicar
boxylic acid (t-ADA) and the known mGluR agonist 1S,3R-aminocyclopenta
ne-1,3-dicarboxylic acid (1S,3R-ACPD) stimulated IP formation in line
with the depolarization-modified expression of mGluR1. However, the tw
o compounds caused different patterns of mGluR down-regulation. The ef
fects of t-ADA and 1S,3R-ACPD were also tested on transformed human em
bryonic kidney 293 cells transfected with mGluR1. Only IS,3R-ACPD, but
not t-ADA, stimulated IP hydrolysis, suggesting that t-ADA acts on a
subtype of metabotropic receptors different from mGluR1. Hence, t-ADA
might prove useful in differentiating the function of various mGluR su
btypes.