TY - JOUR
T1 - Development of inhibitory synaptic transmission to the superior salivatory nucleus in rats
AU - Mitoh, Yoshihiro
AU - Funahashi, Makoto
AU - Fujii, Akihito
AU - Fujita, Masako
AU - Kobashi, Motoi
AU - Matsuo, Ryuji
N1 - Funding Information:
This work was supported by Grants-in Aid for Scientific Research (17591935) from the Ministry of Education, Culture, Science, Sports and Technology, and Ryobi Teien Memorial Foundation of Japan.
PY - 2008/1/29
Y1 - 2008/1/29
N2 - The primary parasympathetic center of the submandibular and sublingual salivary glands is the superior salivatory (SS) nucleus, neurons of which receive excitatory (glutamatergic) and inhibitory (GABAergic and glycinergic) synaptic transmissions in rats. In the present study, to examine postnatal neural development, we focused on inhibitory transmission to the SS neurons in neonatal rats from postnatal day 2 (P2) to P14. Conventional and gramicidin-perforated whole-cell patch-clamp techniques were applied to the neurons in brainstem slices. The decay time constants of GABAergic and glycinergic postsynaptic currents (PSCs) consisted of fast (τfast) and slow (τslow) components. Both τfast and τslow of PSC components tended to become faster with development. The equilibrium potential of Cl- (ECl-) was estimated from the reversal potentials of total PSCs (GABAergic plus glycinergic). The ECl- in the P8-P14 group was significantly more negative than ECl- in the P2-P7 group. Exogenous GABA application at the resting potentials produced depolarization in 83% of SS neurons at P2-P7 and accompanied the action potential in some neurons. In contrast, at P8-P14, GABA evoked hyperpolarization in 78% of SS neurons; therefore, SS neurons did not acquire mature inhibitory systems until P14. The development of SS neurons is discussed as compared with the development of peripheral salivary gland tissue and brainstem neurons that participate in oral motor and sensory functions.
AB - The primary parasympathetic center of the submandibular and sublingual salivary glands is the superior salivatory (SS) nucleus, neurons of which receive excitatory (glutamatergic) and inhibitory (GABAergic and glycinergic) synaptic transmissions in rats. In the present study, to examine postnatal neural development, we focused on inhibitory transmission to the SS neurons in neonatal rats from postnatal day 2 (P2) to P14. Conventional and gramicidin-perforated whole-cell patch-clamp techniques were applied to the neurons in brainstem slices. The decay time constants of GABAergic and glycinergic postsynaptic currents (PSCs) consisted of fast (τfast) and slow (τslow) components. Both τfast and τslow of PSC components tended to become faster with development. The equilibrium potential of Cl- (ECl-) was estimated from the reversal potentials of total PSCs (GABAergic plus glycinergic). The ECl- in the P8-P14 group was significantly more negative than ECl- in the P2-P7 group. Exogenous GABA application at the resting potentials produced depolarization in 83% of SS neurons at P2-P7 and accompanied the action potential in some neurons. In contrast, at P8-P14, GABA evoked hyperpolarization in 78% of SS neurons; therefore, SS neurons did not acquire mature inhibitory systems until P14. The development of SS neurons is discussed as compared with the development of peripheral salivary gland tissue and brainstem neurons that participate in oral motor and sensory functions.
KW - Development
KW - GABA
KW - Gamicidin
KW - Glycine
KW - Inhibitory synaptic transmission
KW - Patch-clamp
KW - Superior salivatory nucleus
UR - http://www.scopus.com/inward/record.url?scp=38349051973&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=38349051973&partnerID=8YFLogxK
U2 - 10.1016/j.brainres.2007.11.020
DO - 10.1016/j.brainres.2007.11.020
M3 - Article
C2 - 18155184
AN - SCOPUS:38349051973
SN - 0006-8993
VL - 1191
SP - 47
EP - 54
JO - Molecular Brain Research
JF - Molecular Brain Research
ER -