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非极性维甲酸Ro 15 - 0778在啮齿动物中的皮脂抑制活性。

Sebum-suppressing activity of the nonpolar arotinoid Ro 15-0778 in rodents.

作者信息

Boris A, Hurley J, Wong C Q, Comai K, Shapiro S

机构信息

Department of Pharmacology and Chemotherapy, Hoffmann-La Roche, Nutley, NJ 07110.

出版信息

Arch Dermatol Res. 1988;280(4):246-51. doi: 10.1007/BF00513964.

Abstract

Retinoids are known to modulate sebaceous gland activity in humans and animals. The nonpolar arotinoid Ro 15-0778 [(E)-1,2,3,4-tetrahydro-1,1,4,4-tetramethyl-6-(1-methyl-2-phenylethen yl) naphthalene] does not contain a polar end group and is devoid of the classical retinoid side effects of hypervitaminosis A. The favorable toxicological profile stimulated the evaluation of this arotinoid in animal models of sebum production. In castrated, testosterone-stimulated male rats, Ro 15-0778 is 50 times more potent than 13-cis-retinoic acid in inhibiting the production and subsequent secretion of sebum. The oral ED50 value of Ro 15-0778 is 30 micrograms/kg, while an oral dose of 0.5 mg/kg inhibited sebum secretion nearly 100%. In testosterone-stimulated female rats, Ro 15-0778 inhibits sebum secretion significantly with an oral ED50 of 140 micrograms/kg and an s.c. ED50 of 75 micrograms/kg. Ro 15-0778 was also evaluated for its ability to prevent testosterone induction of the immature hamster flank organ. The topical ED50 is 0.53 mg/kg and the oral ED50 is 38 mg/kg. This arotinoid is similarly active in mature male hamsters without testosterone treatment. In addition, the retinoid is active topically and orally in reducing the size of the gerbil abdominal sebaceous gland. The compound exhibits no antiandrogenic activity when tested in ventral prostrate and seminal vesicle assays in rats. Additionally, the compound does not have estrogenic activity when tested in the rat uterine weight assay. High doses of Ro 15-0778 in humans did not demonstrate significant sebum-suppressing activity.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

已知类视黄醇可调节人和动物的皮脂腺活动。非极性芳维A酸Ro 15 - 0778 [(E)-1,2,3,4 - 四氢 - 1,1,4,4 - 四甲基 - 6 -(1 - 甲基 - 2 - 苯乙烯基)萘]不含极性端基,且没有维生素A过多症的典型类视黄醇副作用。良好的毒理学特性促使人们在皮脂生成的动物模型中对这种芳维A酸进行评估。在去势、睾酮刺激的雄性大鼠中,Ro 15 - 0778在抑制皮脂生成和随后的分泌方面比13 - 顺式维甲酸强50倍。Ro 15 - 0778的口服半数有效剂量(ED50)值为30微克/千克,而口服剂量0.5毫克/千克可使皮脂分泌抑制近100%。在睾酮刺激的雌性大鼠中,Ro 15 - 0778显著抑制皮脂分泌,口服ED50为140微克/千克,皮下注射ED50为75微克/千克。还评估了Ro 15 - 0778预防睾酮诱导未成熟仓鼠侧腹器官的能力。局部应用ED50为0.53毫克/千克,口服ED50为38毫克/千克。这种芳维A酸在未经睾酮处理的成熟雄性仓鼠中同样具有活性。此外,这种类视黄醇在局部和口服时均能减小沙鼠腹部皮脂腺的大小。在大鼠的前列腺腹侧和精囊试验中测试时,该化合物没有抗雄激素活性。此外,在大鼠子宫重量试验中测试时,该化合物没有雌激素活性。在人体中,高剂量的Ro 15 - 0778未表现出显著的皮脂抑制活性。(摘要截短至250字)

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