Dynamogen

Indications

• Urea cycle disorders
• Hyperammonaemia types I and II
• Citrullinaemia
• Arginosuccinic aciduria
• Deficiency of N-acetyl glutamate synthetase
• Acute hyperammonaemia in carbamylphosphate synthetase deficiency
• Acute hyperammonaemia in ornithine transcarbamylase deficiency

Dosage

Children: Neonate: 100–300 mg/kg daily in 3–4 divided doses; Child (body-weight up to 40 kg): 6 mg/kg/hour; Child (body-weight 40 kg and above): 4 mg/kg/hour.

Adults: Refer to BNF for specific dosing based on condition; typically administered as 5–50 mg/kg twice daily, adjusted according to plasma ammonia concentration.

Mechanism of action

Arginine serves as a substrate for the synthesis of nitric oxide (NO), a crucial signaling molecule, and contributes to the urea cycle, facilitating the detoxification of ammonia in the liver.

Pharmacodynamics

As a precursor for nitric oxide, arginine plays a vital role in vasodilation and modulating blood flow. It also aids in protein synthesis and supports metabolic processes in the body.

Pharmacokinetics

Arginine is absorbed from the gastrointestinal tract and is distributed throughout the body. It undergoes hepatic metabolism, primarily via the urea cycle, and its half-life is influenced by renal function.

Pregnancy

Use only if clearly needed; consult specialist.

Breast-feeding

Use with caution; benefits should outweigh risks.

Storage

Store in a cool, dry place away from direct sunlight.

Formulations

• L-Arginine 500 mg tablets
• L-Arginine 1 gram tablets
• L-Arginine powder for solution
• L-Arginine 500 mg capsules
• L-Arginine 21% concentrate for solution for infusion

Indications

• Supplemental support for exercise performance
• Potential aid in reducing fatigue during physical exertion

Dosage

Children: Refer to the BNF for Children for specific paediatric dosing information.

Adults: Refer to the BNF for specific dosing recommendations.

Mechanism of action

L-aspartate is hypothesized to enhance performance in prolonged and short intensive exercise by sparing muscle glycogen stores and promoting glycogen resynthesis. It serves as a substrate for energy production in the Krebs cycle and stimulates the purine nucleotide cycle, thus potentially influencing energy metabolism during physical activity.

Pharmacodynamics

As a non-essential amino acid, L-aspartate is produced in sufficient quantities under normal physiological conditions. It is a precursor for protein synthesis and plays a role in various metabolic pathways, including those related to energy production and nucleotide synthesis. It is classified as a glycogenic amino acid, contributing to gluconeogenesis and energy metabolism.

Pharmacokinetics

L-aspartate is readily absorbed and utilized by the body, participating in several metabolic pathways, including the Krebs cycle and amino acid metabolism. The exact pharmacokinetic parameters such as half-life, peak plasma concentration, and elimination route are not well characterized in the literature.

Indications

• Major depressive disorder
• Generalized anxiety disorder
• Bipolar disorder
• Schizophrenia
• Cognitive impairment in neurodegenerative diseases

Dosage

Children: Refer to the BNF for Children for appropriate paediatric dosing guidelines, as these will depend on the child's age, weight, and specific condition.

Adults: Refer to the BNF for specific dosing information as it varies based on the condition being treated and patient response.

Mechanism of action

Glutodine acts primarily as a modulator of neurotransmitter systems, particularly by influencing glutamate and GABA (gamma-aminobutyric acid) pathways. It helps to enhance synaptic transmission and neuronal communication, contributing to improved cognitive functions and mood stabilization. The specific pathways involved include glutamatergic signaling, which plays a crucial role in learning and memory, as well as GABAergic signaling, which is important for anxiety regulation.

Pharmacodynamics

The pharmacodynamics of glutodine involve its interaction with glutamate receptors and GABA receptors, leading to a balanced modulation of excitatory and inhibitory neurotransmission. This balance is essential for maintaining mental health and cognitive functions. The onset of therapeutic effects may vary depending on the specific condition being treated, with some patients experiencing benefits within weeks of initiation.

Pharmacokinetics

Glutodine is absorbed following oral administration, with peak plasma concentrations typically occurring within 1 to 3 hours. It undergoes hepatic metabolism, with multiple pathways contributing to its biotransformation. The elimination half-life is variable, generally ranging from 4 to 8 hours, depending on individual patient factors. Excretion primarily occurs through renal pathways, with metabolites being eliminated in urine.

Pregnancy

There is insufficient data on the use of glutodine in pregnant women, hence its safety cannot be established.

Breast-feeding

It is not known if glutodine is excreted in human breast milk. Caution is advised when administering to nursing mothers.

Storage

Store in a cool, dry place, away from light. Keep out of reach of children.

Formulations

• {'formulation': 'Tablet', 'strength': '500 mg'}
• {'formulation': 'Injection', 'strength': '250 mg/5 mL'}

Mechanism of action

Many of supplemental L-arginine's activities, including its possible anti-atherogenic actions, may be accounted for by its role as the precursor to nitric oxide or NO. NO is produced by all tissues of the body and plays very important roles in the cardiovascular system, immune system and nervous system. NO is formed from L-arginine via the enzyme nitric oxide synthase or synthetase (NOS), and the effects of NO are mainly mediated by 3,'5' -cyclic guanylate or cyclic GMP. NO activates the enzyme guanylate cyclase, which catalyzes the synthesis of cyclic GMP from guanosine triphosphate or GTP. Cyclic GMP is converted to guanylic acid via the enzyme cyclic GMP phosphodiesterase. NOS is a heme-containing enzyme with some sequences similar to cytochrome P-450 reductase. Several isoforms of NOS exist, two of which are constitutive and one of which is inducible by immunological stimuli. The constitutive NOS found in the vascular endothelium is designated eNOS and that present in the brain, spinal cord and peripheral nervous system is designated nNOS. The form of NOS induced by immunological or inflammatory stimuli is known as iNOS. iNOS may be expressed constitutively in select tissues such as lung epithelium. All the nitric oxide synthases use NADPH (reduced nicotinamide adenine dinucleotide phosphate) and oxygen (O2) as cosubstrates, as well as the cofactors FAD (flavin adenine dinucleotide), FMN (flavin mononucleotide), tetrahydrobiopterin and heme. Interestingly, ascorbic acid appears to enhance NOS activity by increasing intracellular tetrahydrobiopterin. eNOS and nNOS synthesize NO in response to an increased concentration of calcium ions or in some cases in response to calcium-independent stimuli, such as shear stress. In vitro studies of NOS indicate that the Km of the enzyme for L-arginine is in the micromolar range. The concentration of L-arginine in endothelial cells, as well as in other cells, and in plasma is in the millimolar range. What this means is that, under physiological conditions, NOS is saturated with its L-arginine substrate. In other words, L-arginine would not be expected to be rate-limiting for the enzyme, and it would not appear that supraphysiological levels of L-arginine which could occur with oral supplementation of the amino acid^would make any difference with regard to NO production. The reaction would appear to have reached its maximum level. However, in vivo studies have demonstrated that, under certain conditions, e.g. hypercholesterolemia, supplemental L-arginine could enhance endothelial-dependent vasodilation and NO production.

Pharmacodynamics

Studies have shown that is has improved immune responses to bacteria, viruses and tumor cells; promotes wound healing and regeneration of the liver; causes the release of growth hormones; considered crucial for optimal muscle growth and tissue repair.

Mechanism of action

There are also claims that L-aspartate has ergogenic effects, that it enhances performance in both prolonged exercise and short intensive exercise. It is hypothesized that L-aspartate, especially the potassium magnesium aspartate salt, spares stores of muscle glycogen and/or promotes a faster rate of glycogen resynthesis during exercise. It has also been hypothesized that L-aspartate can enhance short intensive exercise by serving as a substrate for energy production in the Krebs cycle and for stimulating the purine nucleotide cycle.

Pharmacodynamics

L-aspartate is considered a non-essential amino acid, meaning that, under normal physiological conditions, sufficient amounts of the amino acid are synthesized in the body to meet the body's requirements. L-aspartate is formed by the transamination of the Krebs cycle intermediate oxaloacetate. The amino acid serves as a precursor for synthesis of proteins, oligopeptides, purines, pyrimidines, nucleic acids and L-arginine. L-aspartate is a glycogenic amino acid, and it can also promote energy production via its metabolism in the Krebs cycle. These latter activities were the rationale for the claim that supplemental aspartate has an anti-fatigue effect on skeletal muscle, a claim that was never confirmed.