retinol-palmitate and 1-5-bis(p-aminophenoxy)pentane

retinol-palmitate has been researched along with 1-5-bis(p-aminophenoxy)pentane* in 2 studies

Other Studies

2 other study(ies) available for retinol-palmitate and 1-5-bis(p-aminophenoxy)pentane

ArticleYear
Mechanism of action of aromatic amines that short-circuit the visual cycle.
    Biochemistry, 1986, Jun-03, Volume: 25, Issue:11

    DAPP [1,5-bis(p-aminophenoxy)pentane] is an antischistosomal drug that can inhibit dark adaptation in vertebrates by impairing formation of 11-cis-retinoids in the eye and by depleting preformed stores of them [Bernstein, P. S., & Rando, R. R. (1985) Vis. Res. 25, 741-748]. It has recently been shown that p-phenetidine and other monofunctional analogues of DAPP (a symmetric bifunctional molecule) can duplicate DAPP's effects, and it was proposed that these retinotoxic compounds exert their effects in vivo by "short-circuiting" the visual cycle, catalyzing the thermodynamically downhill isomerization of 11-cis-retinal to all-trans-retinal [Bernstein, P. S., Lichtman, J. R., & Rando, R. R. (1986) Proc. Natl. Acad. Sci. U.S.A. 83, 1632-1635]. In this paper, the "short-circuit" hypothesis is investigated more fully. Numerous phenetidine-like molecules are assayed for their ability to inhibit rhodopsin formation and 11-cis-retinyl palmitate formation in the living frog eye. It is found that virtually any aromatic amine with a moderately hydrophobic alkyl chain "tail" is an active inhibitor in vivo. The tail can be in either the para or the meta position and can be attached to the aromatic ring either by direct linkage or by an ether linkage. Compounds that can be metabolized in vivo to such active compounds are also inhibitory. Amino group modification studies demonstrate an absolute requirement for structures that can form a Schiff base with retinal.(ABSTRACT TRUNCATED AT 250 WORDS)

    Topics: Adaptation, Ocular; Amines; Aniline Compounds; Animals; Diterpenes; Magnetic Resonance Spectroscopy; Rana pipiens; Retinal Pigments; Retinyl Esters; Rhodopsin; Schiff Bases; Structure-Activity Relationship; Vision, Ocular; Vitamin A

1986
The specific inhibition of 11-cis-retinyl palmitate formation in the frog eye by diaminophenoxypentane, an inhibitor of rhodopsin regeneration.
    Vision research, 1985, Volume: 25, Issue:6

    The antischistosomal drug 1,5-di-(p-aminophenoxy) pentane (DAPP), an inhibitor of rhodopsin regeneration in the vertebrate retina, is shown to completely block the production of 11-cis-retinyl palmitate in the frog eye. An untreated frog generates a large amount of 11-cis-retinyl palmitate during 1-2 days in the dark after a strong bleach. Also, it is demonstrated that DAPP can deplete the stores of 11-cis-retinyl palmitate in the dark-adapted frog eye. The specificity of DAPP's inhibition of dark-adaptation is explored, and the usefulness of employing retinotoxic drugs to investigate the physiology and biochemistry of rhodopsin regeneration is discussed.

    Topics: Aniline Compounds; Animals; Chromatography, High Pressure Liquid; Dark Adaptation; Diterpenes; Dose-Response Relationship, Drug; Pigment Epithelium of Eye; Rana pipiens; Retina; Retinyl Esters; Rhodopsin; Vitamin A

1985