Irwin Richard D
National Toxicology Program, National Institute of Environmental Health Sciences, P.O. Box 12233, Research Triangle Park, NC 27709, USA.
J Appl Toxicol. 2006 Jan-Feb;26(1):72-80. doi: 10.1002/jat.1110.
1,4-Butanediol is an industrial chemical used primarily as an intermediate in the manufacture of other organic chemicals. It has recently been associated with deaths, addiction and withdrawal related to its promotion and use as a dietary supplement. The rapid absorption and conversion of 1,4-butanediol to gamma-hydroxybutyric acid (GHB, or date rape drug) in animals and humans is well documented and is the basis for its abuse potential. A disposition and metabolism study conducted in F344 rats by the National Toxicology Program (NTP) confirmed the rapid conversion of 1-(14)C-1,4-butanediol to (14)CO2. Because of this, the toxicological profile of 1,4-butanediol resembles that of gamma-hydroxybutyric acid. Gamma-hydroxybutyric acid occurs naturally in the brain and peripheral tissues and is converted to succinate and metabolized through the TCA cycle. Although the function of gamma-hydroxybutyric acid in peripheral tissues is not known, the presence of specific high affinity receptors for gamma-hydroxybutyric acid suggests that it functions as a neuromodulator in the brain and neuronal tissue. Gamma-hydroxybutyric acid readily crosses the blood-brain barrier and elicits characteristic neuropharmacologic responses after oral, i.p., or i.v. administration. The same responses are observed after administration of 1,4-butanediol. The cyclic lactone of gamma-hydroxybutyric acid, gamma-butyrolactone, is also rapidly converted to gamma-hydroxybutyric acid by enzymes in the blood and liver in animals and humans, and produces pharmacological effects identical to those produced by 1,4-butanediol and gamma-hydroxybutyric acid. Gamma-butyrolactone was previously evaluated by the NTP in 14-day and 13-week prechronic toxicology studies and in 2-year chronic toxicology and carcinogenesis studies in F344 rats and B6C3F1 mice. No organ specific toxicity occurred. In the carcinogenesis studies there was an equivocal response in male mice based on a marginal increase in the incidence of pheochromocytomas of the adrenal medulla. Because the absence of chronic toxicity and significant carcinogenicity of gamma-hydroxybutyric acid were established in NTP prechronic and chronic studies with gamma-butyrolactone, it is concluded that similar results would be obtained in a 2-year study with 1,4-butanediol, and that 1,4-butanediol is not a carcinogen.
1,4 - 丁二醇是一种工业化学品,主要用作制造其他有机化学品的中间体。最近,它与因作为膳食补充剂推广和使用而导致的死亡、成瘾及戒断反应有关。1,4 - 丁二醇在动物和人体内迅速吸收并转化为γ-羟基丁酸(GHB,即迷奸药),这一点有充分的文献记载,也是其具有滥用潜力的基础。美国国家毒理学计划(NTP)在F344大鼠身上进行的一项处置和代谢研究证实了1-(14)C - 1,4 - 丁二醇能迅速转化为(14)CO2。因此,1,4 - 丁二醇的毒理学特征与γ-羟基丁酸相似。γ-羟基丁酸天然存在于大脑和外周组织中,会转化为琥珀酸并通过三羧酸循环进行代谢。虽然γ-羟基丁酸在外周组织中的功能尚不清楚,但γ-羟基丁酸特异性高亲和力受体的存在表明它在大脑和神经组织中起神经调节剂的作用。γ-羟基丁酸很容易穿过血脑屏障,口服、腹腔注射或静脉注射后会引发特征性的神经药理学反应。给予1,4 - 丁二醇后也会观察到相同的反应。γ-羟基丁酸的环状内酯γ-丁内酯在动物和人体内也会被血液和肝脏中的酶迅速转化为γ-羟基丁酸,并产生与1,4 - 丁二醇和γ-羟基丁酸相同的药理作用。γ-丁内酯先前已由NTP在F344大鼠和B6C3F1小鼠身上进行了为期14天和13周的慢性毒理学预试验以及为期2年的慢性毒理学和致癌性研究。未出现器官特异性毒性。在致癌性研究中,雄性小鼠肾上腺髓质嗜铬细胞瘤发病率略有增加,反应不明确。由于在NTP对γ-丁内酯进行的慢性毒理学预试验和慢性研究中确定了γ-羟基丁酸不存在慢性毒性和显著致癌性,因此得出结论,在对1,4 - 丁二醇进行的为期2年的研究中也会得到类似结果,且1,4 - 丁二醇不是致癌物。