HUMAN SKIN AND PLATELET MINOXIDIL SULFOTRANSFERASE ACTIVITIES - BIOCHEMICAL-PROPERTIES, CORRELATIONS AND CONTRIBUTION OF THERMOLABILE PHENOL SULFOTRANSFERASE
Pe. Kudlacek et al., HUMAN SKIN AND PLATELET MINOXIDIL SULFOTRANSFERASE ACTIVITIES - BIOCHEMICAL-PROPERTIES, CORRELATIONS AND CONTRIBUTION OF THERMOLABILE PHENOL SULFOTRANSFERASE, The Journal of pharmacology and experimental therapeutics, 273(2), 1995, pp. 582-590
Human scalp skin high speed supernatants were used to test whether min
oxidil sulfotransferase (MNX-ST) and phenol sulfotransferase (PST) act
ivities were present. Platelet homogenates from the same skin donors w
ere used to test whether levels of sulfotransferase activities in the
blood platelet would reflect levels of the enzyme activities in skin.
Dopamine, p-nitrophenol and minoxidil were used as substrates for skin
and platelet thermolabile (TL PST), thermostable (TS PST) and MNX-ST
activities, respectively. Biochemical properties of each skin enzyme w
ere the same as the platelet enzymes with respect to apparent K-m valu
es for substrates, pH optima, thermal stabilities and responses to inh
ibition by 2,6-dichloro-4-nitrophenol (DCNP). An unexpected finding wa
s that skin and platelet MNX-ST thermal stabilities and responses to D
CNP were more similar to TL PST than to TS PST, the enzyme reported to
be responsible for MNX-ST activity. There were significant positive c
orrelations of platelet sulfotransferases with the relative levels of
activities of the same skin sulfotransferases. Unexpected findings wer
e significant positive correlations of MNX-ST and TL PST activities. P
artially purified platelet TS PST assayed with minoxidil as the substr
ate showed a response to DCNP and thermal stability that were the same
as TS PST. Platelet TL PST assayed with minoxidil showed thermal stab
ility and a response to DCNP that were essentially the same as TL PST.
The results indicated that not only TS PST, but also TL PST activitie
s in human skin and platelet contributed to MNX-ST activity. It will b
e feasible to test whether measures of platelet PST activities will pr
edict physiologic responses to minoxidil.