Hon Yuen Yi, Jusko William J, Zhou Hong-Hao, Chen Guo-Lin, Guo Dong, Zhou Gan, Spratlin Vicky E, Jann Michael W
Department of Clinical and Administrative Sciences, Mercer University Southern School of Pharmacy, Atlanta, Georgia, USA.
Mol Diagn Ther. 2006;10(2):109-14. doi: 10.1007/BF03256450.
Histamine N-methyltransferase (HNMT) catalyzes the methylation of histamine and plays an important role in histamine biotransformation in bronchial epithelium. Enzymatic activity of HNMT has been shown to be regulated by genetic factors, including polymorphisms in the HNMT gene. In this pilot study we determined endogenous levels of histamine and cortisol in plasma and whole blood samples from subjects with different genotypes for the HNMT C314T polymorphism, and investigated whether these parameters differed between individuals with the HNMT CC genotype and those with the CT genotype.
Blood samples were collected from 48 unrelated volunteers (36 males, 12 females), aged 21-40 years, who participated in the study. PCR-restriction fragment length polymorphism analysis was used to determine HNMT C314T genotypes. Erythrocyte HNMT activity was determined as well as plasma and whole blood levels of histamine and cortisol. Two-group comparisons of the various parameters were analyzed by Blocked Wilcoxon test and Wilcoxon Rank Sum test as appropriate.
Thirty-seven subjects (24 Caucasians, three African Americans, one Middle Eastern, five Indians, three Chinese, and one Filipino) were found to have the homozygous CC genotype. Ten subjects (eight Caucasians, one Middle Eastern, and one Chinese) were heterozygous and one individual (Pakistani) was homozygous for the variant 314T allele. The frequency of HNMT CT heterozygotes in the small Caucasian cohort was 0.125. Median enzyme activity was significantly lower in subjects with the heterozygous CT genotype than in those with the homozygous CC genotype (485 vs 631 U/mL of red blood cells; p=0.023). A broad range of histamine levels in plasma and whole blood was observed for all subjects. Whereas the median plasma histamine level was found to be higher in heterozygotes for the wild-type 314C allele than homozygotes (3.32 vs 2.30 nmol/L; p=0.021), there was no difference between the two groups in histamine levels in whole blood. Cortisol levels were similar between individuals with the homozygous CC genotype and those with the heterozygous CT genotype.
Wide variability of plasma and whole-blood histamine levels was observed in subjects with different HNMT C314T genotypes. Endogenous levels of histamine are likely to be affected by various genes and polymorphisms.
组胺N - 甲基转移酶(HNMT)催化组胺的甲基化反应,在支气管上皮细胞的组胺生物转化过程中发挥重要作用。已有研究表明,HNMT的酶活性受遗传因素调控,包括HNMT基因的多态性。在这项初步研究中,我们测定了具有HNMT C314T多态性不同基因型受试者血浆和全血样本中组胺和皮质醇的内源性水平,并研究了HNMT CC基因型个体与CT基因型个体之间这些参数是否存在差异。
从48名年龄在21 - 40岁的无关志愿者(36名男性,12名女性)中采集血样,这些志愿者参与了本研究。采用聚合酶链反应 - 限制性片段长度多态性分析来确定HNMT C314T基因型。测定红细胞HNMT活性以及血浆和全血中组胺和皮质醇的水平。对各项参数进行两组比较时,根据情况采用成组Wilcoxon检验和Wilcoxon秩和检验进行分析。
发现37名受试者(24名白种人、3名非裔美国人、1名中东人、5名印度人、3名中国人和1名菲律宾人)具有纯合CC基因型。10名受试者(8名白种人、1名中东人和1名中国人)为杂合子,1名个体(巴基斯坦人)为314T变异等位基因的纯合子。在小型白种人队列中,HNMT CT杂合子的频率为0.125。杂合CT基因型受试者的酶活性中位数显著低于纯合CC基因型受试者(红细胞中为485 U/mL对631 U/mL;p = 0.023)。所有受试者的血浆和全血组胺水平范围较广。野生型314C等位基因杂合子的血浆组胺水平中位数高于纯合子(3.32对2.30 nmol/L;p = 0.021),但两组全血组胺水平无差异。纯合CC基因型个体与杂合CT基因型个体的皮质醇水平相似。
在具有不同HNMT C314T基因型的受试者中,观察到血浆和全血组胺水平存在广泛差异。组胺的内源性水平可能受多种基因和多态性的影响。