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In Vitro Effect of D-004, a Lipid Extract of the Fruit of the Cuban Royal Palm (Roystonea regia),on Prostate Steroid 5alpha-Reductase Activity

机译:古巴皇家棕榈(Roystonea regia)的脂质提取物D-004对前列腺甾体5α-还原酶活性的体外作用

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Background: D-004, a lipid extract of the fruit of the Cuban royal palm (Roystonea regia), has been found to reduce prostatic hyperplasia (PH) induced with testosterone (T), but not PH induced with dihydrotestosterone (DHT), in rodents, suggesting the inhibition of prostate 5a-reductase activity.Objectives: The aims of this study were to assess whether D-004 inhibits prostate 5oc-reductase activity in vitro and to examine the effects of D-004 on enzyme kinetics.Methods: This experimental study was conducted at the Pharmacology Department, Center of Natural Products, National Center for Scientific Research, Havana, Cuba. Soluble rat prostate preparations were used as the source of 5alpha~reductase, and (~3H)-DHT production was measured to determine prostate 5a-reductase activity. Cell-free rat prostate homogenates were pre-incubated with carboxymethyl cellulose 2% alone (control tubes) or D-004 (0.24-125 pg/mL) suspended in the vehicle (treated tubes) for 10 minutes prior to adding the labeled substrate (~3H)-T. Once the reaction was stopped, sterols were extracted with chloroform and aliquots were applied on silica gel plates developed in benzene-acetone (4:1, v/v). Areas containing DHT were scraped and radioactivity was counted. The median inhibitory concentration (IC_(50)) was determined by measuring the conversion of T to DHT. The apparent Michaelis-Menten constant (K) and V_(max) values before and after adding D-004 were determined in kinetic studies using labeled T (0.5-25 umol/L).Results: Compared with controls, D-004 significantly and dose-dependently inhibited the enzymatic reaction at doses of 1.95 to 125.0 ug/mL (all, P< 0.05). The IC50 of D-004 required to inhibit 5oc-reductase activity was 2.25 ug/mL. Enzyme inhibition was noncompetitive, since D-004 lowered the V_(max) from 15.3 to 10.0 nmol DHT/min mg~(-1) protein, while the K_m (4.54 umol/L) was almost unaffected.Conclusions: D-004 dose-dependently and noncompetitively inhibited in vitro 5a-reductase activity in soluble fractions of rat prostate. Although the extent of the maximal inhibition was high and the value of IC_(50) was low, the relevance of such inhibition requires further study in vivo
机译:背景:D-004是古巴皇家棕榈(Roystonea regia)果实的脂质提取物,已被发现能减少睾丸激素(T)诱导的前列腺增生(PH),但不能减少二氢睾丸激素(DHT)诱导的前列腺增生。目的:本研究的目的是评估D-004是否在体外抑制前列腺5α-还原酶的活性,并研究D-004对酶动力学的影响。实验研究是在古巴哈瓦那国家科学研究中心天然产物中心的药理学系进行的。将可溶性大鼠前列腺制剂用作5α-还原酶的来源,并测量(〜3H)-DHT的含量以确定前列腺5a-还原酶的活性。将无细胞的大鼠前列腺匀浆与单独2%的羧甲基纤维素(对照管)或D-004(0.24-125 pg / mL)悬浮在溶媒(处理过的管)中预先孵育10分钟,然后添加标记的底物( 〜3H)-T。一旦反应停止,就用氯仿萃取固醇,并将等分试样施加到在苯-丙酮(4∶1,v / v)中展开的硅胶板上。刮擦含有DHT的区域并计算放射性。通过测量T到DHT的转化率来确定中值抑制浓度(IC_(50))。在动力学研究中,使用标记的T(0.5-25 umol / L)确定添加D-004前后的表观Michaelis-Menten常数(K)和V_(max)值。剂量依赖性地在1.95至125.0 ug / mL的剂量下抑制酶促反应(全部,P <0.05)。抑制5α-还原酶活性所需的D-004的IC50为2.25 ug / mL。由于D-004将D_004的V_(max)从15.3 nmol DHT / min mg〜(-1)降低至10.0 nmol DHT / min mg〜(-1)蛋白,而K_m(4.54 umol / L)几乎不受影响,因此酶抑制作用是非竞争性的。结论:D-004剂量依赖性和非竞争性抑制大鼠前列腺可溶部分中的体外5a-还原酶活性。尽管最大抑制的程度很高,而IC_(50)的值却很低,但这种抑制作用的相关性还需要在体内进行进一步研究

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