The Isolation and Identification of Galactitol from the Brains of Galactosemia Patients.
نویسندگان
چکیده
The presence of acyclic polyols in mammalian tissue was formerly considered a rare finding confined to specialized tissue (I). Van Heyningen reported the occurrence of significant quantities of galactitol in the lens of galactose-fed rats, although only minor amount,s of the hexitol were located in the heart and leg muscle (2). Other tissues which were examined, blood, liver, spleen, lung, and kidney, contained no detectable amounts of galactitol. Recently, however, galactitol was isolated from the urine of two’ male, galactosemia patients (3). By utilizing the convenient and sensitive technique of gas-liquid chromatography (4, 5) for the analysis of the urine and lens of rats fed a 35% galactose-containing diet, we have confirmed the ability of normal rats to convert significant amounts of galactose to galactitol.2 In addition, however, these studies led to the detection of large amounts of free galactitol in brain and kidney tissue. It therefore became of interest to examine organs of galactosemia subjects for possible deposition of galactitol. This report describes the analysis and isolation of galactitol from the brains of two galactosemia patients.
منابع مشابه
Isolation of Ornithobacterium rhinotracheale from the brains of commercial broiler breeder chickens with meningitis and encephalitis
Ornithobacterium rhinotracheale (ORT) has been identified as one of the respiratory bacterial pathogens in turkey and chicken flocks. Four live birds displaying severe torticollis were submitted from a 13-week-old commercial broiler breeder chicken flock located in Mazandaran province. These birds were suspected to pasteurellosis by the farm veterinarian. No other marked gross lesion except ema...
متن کاملMonitoring of biochemical status in children with Duarte galactosemia: utility of galactose, galactitol, galactonate, and galactose 1-phosphate.
BACKGROUND Duarte galactosemia (DG) is frequently detected in newborn-screening programs. DG patients do not manifest the symptoms of classic galactosemia, but whether they require dietary galactose restriction is controversial. We sought to assess the relationships of selected galactose metabolites (plasma galactose, plasma galactitol, erythrocyte (RBC) galactitol, RBC galactonate, and urine g...
متن کاملTopic Page: Galactosemia
Galactosemia is a rare autosomal recessive disorder due to a deficiency of galactose-1-P:uridyl transferase (GALT) (classical galactosemia), galactokinase (GALK), or UDP-galactose-4 epimerase (GALE). Of the three, GALT deficiency is the most severe and results in the accumulation of galactose-1-P in tissues, which damages the liver, eye, brain, ovary, and kidney. In GALK deficiency, ingested ga...
متن کاملTopic Page: Galactosemia
Galactosemia is a rare autosomal recessive disorder due to a deficiency of galactose-1-P:uridyl transferase (GALT) (classical galactosemia), galactokinase (GALK), or UDP-galactose-4 epimerase (GALE). Of the three, GALT deficiency is the most severe and results in the accumulation of galactose-1-P in tissues, which damages the liver, eye, brain, ovary, and kidney. In GALK deficiency, ingested ga...
متن کاملEVALU ATI ON OF THE CAUSES OF CHOLESTASIS IN INFANTS
During a period of three years from 1996 to 1998, 124 infants (64 male and 60 female) with an age range of 1-6 months (mean age 1.5 months) with cholestasis were studied. Idiopathic neonatal hepatitis was the most common cause of cholestasis, accounting for 48 cases with a rate of 3'8.70% in a total of 124 patients, followed by galactosemia in 29 patients (23.38%) and extrahepatic biliary ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- The Journal of biological chemistry
دوره 240 شماره
صفحات -
تاریخ انتشار 1965