Concentrations of phenylalanine and tyrosine in plasma and brain of rats treated with phenylalanine loads.
نویسندگان
چکیده
one or more adenosine triphosphatase units in discrete assemblies (Ernster et al., 1973). If proved, this finding would present a very serious challenge to the classical chemiosmotic view, which is necessarily based on a generalized rather than a specific association of the oxidation and phosphorylation processes. In contrast, the presence of assemblies is in no way damaging to the p-zone interpretation. The zones of electrostatic potential could exist as a series of discontinuous ‘patches’ on the membrane surface, as shown in Fig. 2. The mosaic structure of membranes would suggest that this is more likely than the continuous ‘strip’ p-zone shown earlier (Archbold et ul., 1975c, Fig. 1). These ‘patches’ would reflect, topographically, the fixed-charge pattern of the membrane which, in turn, would be related to the sites of proton release from individual transport chains. If this view is correct we shall be dealing with electron-transport-chain-Apkadenosine triphosphatase assemblies of greater complexity than the assemblies already proposed.
منابع مشابه
Comparison of phenylalanine and tyrosine in urine of patients with vitiligo and normal subjects
Amino acids are one of the most necessary substances in intracellular metabolic processes.aromatic aminoacids such as phenylalanine and tyrosine are precursor of melanin so are important materials for the skin pigmentation.metabolic disorders in the melanin synthesis causes milky macules on the skin of patients,known as vitiligo.these patients are hypersensitive to sunlight and consequently at ...
متن کاملPresumptive brain influx of large neutral amino acids and the effect of phenylalanine supplementation in patients with Tyrosinemia type 1
INTRODUCTION Hereditary Tyrosinemia type 1 (HT1) is a rare metabolic disease caused by a defect in the tyrosine degradation pathway. Current treatment consists of 2-(2-nitro-4-trifluoromethylbenoyl)-1,3-cyclohexanedione (NTBC) and a tyrosine and phenylalanine restricted diet. Recently, neuropsychological deficits have been seen in HT1 patients. These deficits are possibly associated with low bl...
متن کاملآشنایی با فنیل کتونوری
Background: Phenylketonuria is an inherited metabolic disease. It is genetic disorder autosomal recessive type. It is caused by absent or deficiency Phenylalanine hydroxylase enzyme activity that converts Phenylalanine to Tyrosine. It leads to increasing Phenylalanine in the blood. Tyrosine is important for production of some neurotransmitters. So it caused deficiencies of dopamine and serotoni...
متن کاملMolecular Diagnosis of Plasma Phenylalanine in Neonates with Phenylketonuria Disease Using Biological Sensors Based on Surface-Enhanced Raman Spectroscopy (SERS)
In this study, silver nanoparticles were chemically synthesized and deposited on glass substrates using a reducing agent of sucrose, at 50°C. Different characterizations including atomic force microscopy (AFM), field emission scanning electron microscopy (FESEM), and Raman spectroscopy were obtained to study silvery substrates. Then, the silvery substrates were used as the SERS substrates to de...
متن کاملP 124: Decrease Signs Parkinson`s Disease with DOPAMINE in Apple
After Alzheimer's disease, Parkinson's disease is the most common nerve-damaging disease. Parkinson's is a progressive and chronic disease where cells secrete dopamine-cut black flesh and in the absence of dopamine in the brain destroyed the irregular body movements. Man eats the food that causes the formation of the neurotransmitters. Tthree neurotransmitters: dopamine, serotonin, norepinephri...
متن کاملSimulation of Phenylketonuria in Rats by Extended p-Chlorophenylalanine Treatment
The brain damage which occurs in untreated phenylketonuria probably results from the high plasma phenylalanine concentration prevailing in this condition, as treatment with a low-phenylalanine diet mitigates the situation. The actual cause of the brain damage is not known, but investigations have been carried out with high phenylalanine loads to simulate phenylketonuria and so elucidate the nat...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Biochemical Society transactions
دوره 4 1 شماره
صفحات -
تاریخ انتشار 1976