期刊
EPILEPSIA
卷 41, 期 -, 页码 S35-S39出版社
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1111/j.1528-1157.2000.tb06047.x
关键词
topiramate; epilepsy; carbonic anhydrase inhibitors; carbonic anhydrase isoenzymes; acetazolamide
Purpose: This study investigated the effectiveness of topiramate (TPM) as an inhibitor of six isozymes of carbonic anhydrase (CA). Methods: The inhibition constants (K-i) of TPM and acetazolamide (AZM) for CA I, CA II, CA III, CA IV, CA V, and CA VI were determined for human (HCA), rat (RCA), or mouse (MCA). The activity of CA was studied by using purified isozymes, erythrocytes, subcellular fractions of kidney or brain, and saliva, and was assayed at 37 degrees C or 25 degrees C by O-18 mass spectrometry and/or by measuring the pH shift at 0 degrees C. Results: Topiramate K-i values for HCA I, HCA II, HCA IV, and HCA VI were similar to 100, 7, 10, and >100 mu M, respectively. TPM K-i values for RCA I, RCA II, RCA III, RCA IV, and RCA V were similar to 180, 0.1 to 1, >100, 0.2 to 10 and 18 mu M, respectively. For RCA II and RCA IV, the K-i values were temperature dependent. TPM K-i values for MCA II and MCA IV ranged between 1 and 20 mu M. Conclusions: These results indicate that TPM is more potent as an inhibitor of CA II and CA IV than of CA I, CA III, and CA VI. In all three species, AZM was usually 10 to 100 times more potent than TPM as an inhibitor of CA isozymes.
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