Ichihara K, Tanaka C
Department of Biochemistry, Kawasaki Medical School, Okayama, Japan.
Lipids. 1991 Jul;26(7):531-5. doi: 10.1007/BF02536599.
Progesterone 5 alpha-reductase partially purified from gastric mucosa microsomes was stimulated by short-chain synthetic phosphatidylcholines (PC), such as dilauroyl PC, but not by various PC from biological sources. Phosphatidylserine (PS) activated the gastric 5 alpha-reductase to a limited extent compared to the liver 5 alpha-reductase described previously [Ichihara, K., and Tanaka, C. (1987) Biochem. Biophys. Res. Commun. 149, 482-487]. In search of more effective phospholipid activators, we tested the effects of various lysophospholipids on 5 alpha-reductase activity. Strongly stimulatory effects were observed when lysophosphatidylcholine (lysoPC) and lysophosphatidylethanolamine (lysoPE) were used instead of PC and phosphatidylethanolamine. Examination of synthetic lysoPC and lysoPE differing in acyl chain lengths showed that fatty chains of 12 to 16 carbons were effective in stimulating the 5 alpha-reductase. By contrast, other lysophospholipids such as lysophosphatidic acid, lysophosphatidylglycerol or lysophosphatidylserine (lysoPS) greatly inhibited 5 alpha-reductase activity. These findings suggest that gastric 5 alpha-reductase may be under dual regulation; lysoPC and lysoPE may play important roles as positive effectors, whereas lysophosphatidic acid, lysophosphatidylglycerol and lysoPS act as negative effectors in progesterone 5 alpha-reductase regulation.
