Please use this identifier to cite or link to this item: http://scholarbank.nus.edu.sg/handle/10635/131058
Title: pH dependent inhibition of serum oxytocinase activity by prostaglandins and cyclic GMP
Authors: Roy, A.C. 
Yeang, M.
Karim, S.M.M.
Issue Date: 1982
Source: Roy, A.C., Yeang, M., Karim, S.M.M. (1982). pH dependent inhibition of serum oxytocinase activity by prostaglandins and cyclic GMP. Prostaglandins and Medicine 8 (2) : 173-179. ScholarBank@NUS Repository.
Abstract: The effect of pH in the range 6.2 to 7.7 on the inhibition of serum oxytocinase (EC 3.4.11.3) activity by various compounds was studied using S-benzyl-L-cysteine-p-nitroanilide (BCN) as substrate. Prostaglandins E1, E2, F(2α), 8-bromo-cGMP, cGMP, indomethacin and polyphloretin phosphate (PPP) produced a dose related pH dependent inhibition of serum oxytocinase. Their effect was maximum at pH 6.2 and minimum at pH 7.7. Hypertonic urea and saline also caused pH dependent inhibition; saline being most active at pH 6.2, and urea at pH 7.7. A similar pH dependent inhibition was found when these compounds were examined for their effect on the hydrolysis of L-leucine-p-nitroanilide (LN) by serum aminopeptidases at pH between 6.2 and 7.7. Although the inhibitors were more effective against the hydrolysis of LN than BCN substrate, cGMP and its 8-bromo derivative were more active against the BCN hydrolysis. cAMP, 8-bromo-cAMP, dibutyryl (db)-cAMP, db-cGMP, AMP, ADP, ATP, GDP, GTP, aspirin, sodium salicylate, paracetamol, theophylline and isobutylmethylxanthine (IBMX) at comparable concentrations and within the same pH range had no effect on the hydrolysis of either substrate. It is concluded that in serum obtained during pregnancy, the hydrolysis of LN may largely be attributed to oxytocinase activity. Thus, inhibition of LN hydrolysis by prostaglandins and other substances may be regarded as inhibition of oxytocinase activity.
Source Title: Prostaglandins and Medicine
URI: http://scholarbank.nus.edu.sg/handle/10635/131058
ISSN: 01614630
Appears in Collections:Staff Publications

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