Hyperammonemia in the brain leads to poorly understood alterations of nitric oxide (NO) synthesis. Arginine, the substrate of nitric oxide synthases, might be recycled from the citrulline produced with NO by argininosuccinate synthetase (AS) and argininosuccinate lyase (AL). The regulation of AS and AL genes during hyperammonemia is unknown in the brain. We used brain cell aggregates cultured from dissociated telencephalic cortex of rat embryos to analyze the regulation of AS and AL genes in hyperammonemia. Using RNase protection assay and non-radioactive in situ hybridization on aggregate cryosections, we show that both AS and AL genes are induced in astrocytes but not in neurons of aggregates exposed to 5 mM NH4Cl. Our work suggests that ...
The urea cycle disorder (UCD) argininosuccinate lyase (ASL) deficiency, caused by a defective ASL en...
Impaired liver function may lead to hyperammonemia and risk for hepatic encephalopathy. In brain, de...
Argininosuccinate lyase (ASL) is central to two metabolic pathways: i) the liver-based urea cycle, w...
Hyperammonemia in the brain leads to poorly understood alterations of nitric oxide (NO) synthesis. A...
Hyperammonemia in the brain leads to poorly understood alterations of nitric oxide (NO) synthesis. A...
Chronic hyperammonemia impairs the glutamate-nitric oxide- cGMP pathway in rat brain in vivo. The ai...
Nitric oxide (NO) is synthesized from a unique precursor, arginine, by nitric oxide synthase (NOS). ...
Argininosuccinate lyase (ASL) belongs to the hepatic urea cycle detoxifying ammonia, and the citrull...
Argininosuccinate lyase (ASL) belongs to the hepatic urea cycle detoxifying ammonia, and the citrull...
Nitric oxide (NO) is synthesized from a unique precursor, arginine, by nitric oxide synthase (NOS). ...
Hyperammonemia is mainly found in hepatic encephalopathy and in genetic defects of the urea cycle or...
Previously we had shown that ammonia stimulates nitric oxide (NO) synthesis in astrocytes by increas...
Previously we had shown that ammonia stimulates nitric oxide (NO) synthesis in astrocytes by increas...
Hyperammonemia is defined as an elevated ammonia concentration, which is caused by an impairment of ...
The urea cycle disorder (UCD) argininosuccinate lyase (ASL) deficiency, caused by a defective ASL en...
The urea cycle disorder (UCD) argininosuccinate lyase (ASL) deficiency, caused by a defective ASL en...
Impaired liver function may lead to hyperammonemia and risk for hepatic encephalopathy. In brain, de...
Argininosuccinate lyase (ASL) is central to two metabolic pathways: i) the liver-based urea cycle, w...
Hyperammonemia in the brain leads to poorly understood alterations of nitric oxide (NO) synthesis. A...
Hyperammonemia in the brain leads to poorly understood alterations of nitric oxide (NO) synthesis. A...
Chronic hyperammonemia impairs the glutamate-nitric oxide- cGMP pathway in rat brain in vivo. The ai...
Nitric oxide (NO) is synthesized from a unique precursor, arginine, by nitric oxide synthase (NOS). ...
Argininosuccinate lyase (ASL) belongs to the hepatic urea cycle detoxifying ammonia, and the citrull...
Argininosuccinate lyase (ASL) belongs to the hepatic urea cycle detoxifying ammonia, and the citrull...
Nitric oxide (NO) is synthesized from a unique precursor, arginine, by nitric oxide synthase (NOS). ...
Hyperammonemia is mainly found in hepatic encephalopathy and in genetic defects of the urea cycle or...
Previously we had shown that ammonia stimulates nitric oxide (NO) synthesis in astrocytes by increas...
Previously we had shown that ammonia stimulates nitric oxide (NO) synthesis in astrocytes by increas...
Hyperammonemia is defined as an elevated ammonia concentration, which is caused by an impairment of ...
The urea cycle disorder (UCD) argininosuccinate lyase (ASL) deficiency, caused by a defective ASL en...
The urea cycle disorder (UCD) argininosuccinate lyase (ASL) deficiency, caused by a defective ASL en...
Impaired liver function may lead to hyperammonemia and risk for hepatic encephalopathy. In brain, de...
Argininosuccinate lyase (ASL) is central to two metabolic pathways: i) the liver-based urea cycle, w...