Schneck D W, Pritchard J F, Gibson T P, Vary J E, Hayes A H
Clin Pharmacol Ther. 1980 Jun;27(6):744-55. doi: 10.1038/clpt.1980.105.
The relationship between plasma levels of 4 propranolol metabolites--naphthoxylactic acid (NLA), 4-hydroxypropranolol (4-OH), naphthoxyacetic acid (NAA), and propranolol glycol (PG)--and propranolol plasma levels was determined in healthy, adult male subjects after increasing single oral doses of propranolol. NLA was present at plasma levels 6 to 25 times that of propranolol. More than 90% of circulating NLA was in the plasma fraction, where it was 95% protein bound. The ratio of plasma concentrations of the pharmacologically active metabolite 4-OH to propranolol approached unity 0.5 hr after propranolol, 160 mg or 320 mg orally, but fell rapidly. Plasma levels of NAA were in the same range as propranolol, especially as time progressed. PG circulated at plasma levels less than 12% of propranolol. As oral doses of propranolol were increased from 20 to 320 mg, there was a decrease in intrinsic plasma clearance (Cli) from 425 to 200 1/hr. Half-life rose from 3 to 5 hr. Urinary recovery of 4-OH fell as Cli rose. Urinary recovery of propranolol conjugates, NLA, and N-desisopropylpropranolol (NDIPP) rose as Cli fell. Our results suggest that naphthalene ring oxidation of propranolol represents a high-affinity low-capacity enzymatic pathway(s) that plays an important role in the extensive hepatic extraction of propranolol after small doses orally. Plasma NLA and plasma NAA were determined before and after hemodialysis in 14 uremic patients receiving long-term propranolol therapy. Mean plasma NLA was 4.372 ng/ml, and mean plasma NAA level was 238 ng/ml when mean plasma propranolol level was 15 ng/ml.
在健康成年男性受试者单次口服递增剂量的普萘洛尔后,测定了4种普萘洛尔代谢物——萘氧乳酸(NLA)、4-羟基普萘洛尔(4-OH)、萘氧乙酸(NAA)和普萘洛尔二醇(PG)的血浆水平与普萘洛尔血浆水平之间的关系。NLA的血浆水平是普萘洛尔的6至25倍。循环中的NLA超过90%存在于血浆部分,其中95%与蛋白质结合。口服160mg或320mg普萘洛尔后0.5小时,药理活性代谢物4-OH与普萘洛尔的血浆浓度比接近1,但迅速下降。NAA的血浆水平与普萘洛尔处于同一范围,尤其是随着时间的推移。PG的循环血浆水平低于普萘洛尔的12%。随着普萘洛尔口服剂量从20mg增加到320mg,内在血浆清除率(Cli)从425降至200 l/小时。半衰期从3小时升至5小时。随着Cli升高,4-OH的尿回收率下降。随着Cli下降,普萘洛尔结合物、NLA和N-去异丙基普萘洛尔(NDIPP)的尿回收率上升。我们的结果表明,普萘洛尔的萘环氧化代表了一种高亲和力低容量的酶促途径,在小剂量口服后普萘洛尔的广泛肝脏摄取中起重要作用。在14名接受长期普萘洛尔治疗的尿毒症患者进行血液透析前后,测定了血浆NLA和血浆NAA。当平均血浆普萘洛尔水平为15ng/ml时,平均血浆NLA为4.372ng/ml,平均血浆NAA水平为238ng/ml。