TY - JOUR
T1 - Effect of choline acetyltransferase inhibitors on mouse and guinea-pig brain choline and acetylcholine
AU - Krell, Robert D.
AU - Goldberg, Alan M.
N1 - Funding Information:
* Supported by United States Public Health Service Grants EHS 00034 and NS 08709. Presented in part in Tt~rls. Ant. Sot. N~,u,ocl~eri~. 4, I29 ( 1973) and Fe&l Proc. 32, 742 ( 1973). t Current address: Smith. Kline & French Labs., Dept of Pharmacology. I500 Spring Garden Street. Philadelphia. Pa. 19101.
PY - 1975/2/1
Y1 - 1975/2/1
N2 - These experiments measure the effect of two choline acetyltransferase (CAT) inhibitors, viz. 4-(1-naphthylvinyl) pyridine (NVP) and 4-(3-chlorophenylvinyl) pyridine (3'-chloro-4-stilbazole; CS), on mouse and guinea-pig brain acetylcholine (ACh) and choline. The intraperitoneal administration of NVP or CS appeared to inhibit CAT partially in both species, but both compounds were without effect on steadystate levels of ACh. In the mouse CS, but not NVP, increased brain choline. Both CS and NVP were shown to reduce, but not totally inhibit, the synthesis of mouse brain ACh. The inability of these compounds to decrease steady state levels, while apparently decreasing synthesis rates, suggests that CAT may not be the rate-limiting step in ACh synthesis.
AB - These experiments measure the effect of two choline acetyltransferase (CAT) inhibitors, viz. 4-(1-naphthylvinyl) pyridine (NVP) and 4-(3-chlorophenylvinyl) pyridine (3'-chloro-4-stilbazole; CS), on mouse and guinea-pig brain acetylcholine (ACh) and choline. The intraperitoneal administration of NVP or CS appeared to inhibit CAT partially in both species, but both compounds were without effect on steadystate levels of ACh. In the mouse CS, but not NVP, increased brain choline. Both CS and NVP were shown to reduce, but not totally inhibit, the synthesis of mouse brain ACh. The inability of these compounds to decrease steady state levels, while apparently decreasing synthesis rates, suggests that CAT may not be the rate-limiting step in ACh synthesis.
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U2 - 10.1016/0006-2952(75)90223-3
DO - 10.1016/0006-2952(75)90223-3
M3 - Article
C2 - 1125046
AN - SCOPUS:0016466847
SN - 0006-2952
VL - 24
SP - 391
EP - 396
JO - Biochemical Pharmacology
JF - Biochemical Pharmacology
IS - 3
ER -