Glutamate-Pyruvate Transaminase (GPT), also known as Alanine Aminotransferase (ALT), is a pivotal enzyme in the metabolism of amino acids, specifically in the transamination process where an amino group from alanine is transferred to α-ketoglutarate, forming pyruvate and glutamate. This enzyme is predominantly found in the liver, where it plays a critical role in gluconeogenesis and the urea cycle, processes that are essential for maintaining the body's nitrogen balance and glucose levels. The expression of GPT is subject to regulation by various biochemical pathways and can be indicative of alterations in metabolic function. As such, understanding the substances that can induce the expression of GPT is vital for a comprehensive grasp of liver metabolism and amino acid biochemistry.
Several chemicals have been identified that can potentially increase the expression of GPT. For instance, compounds like retinoic acid are known to upregulate GPT by binding to nuclear receptors, thereby influencing the transcription of genes associated with cellular differentiation and metabolism. Similarly, ethanol exposure can lead to an adaptive increase in GPT expression, possibly as a compensatory mechanism mitigating ethanol-induced hepatocellular damage. On the other hand, oleanolic acid might bolster GPT synthesis through hepatoprotective signaling pathways, fostering liver cell repair and regeneration. Moreover, peroxisome proliferator-activated receptor alpha (PPAR-alpha) activators such as fenofibrate have been shown to enhance GPT transcription, aligning with their role in upregulating genes involved in fatty acid oxidation. Substances like valproic acid also appear to raise GPT levels by inhibiting histone deacetylase, which consequently results in a more transcriptionally active chromatin state around liver enzyme genes. It's notable that while these chemicals can induce GPT expression, the specific mechanisms and pathways involved are complex and subject to ongoing research to fully elucidate their biological significance.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | $65.00 $319.00 $575.00 $998.00 | 28 | |
Retinoic acid may upregulate GPT by activating nuclear receptors that bind to DNA responsive elements of genes involved in cellular differentiation and liver metabolism, thereby promoting synthesis of this enzyme. | ||||||
Oleanolic Acid | 508-02-1 | sc-205775 sc-205775A | 100 mg 500 mg | $84.00 $296.00 | 8 | |
Oleanolic acid might stimulate GPT synthesis as part of its hepatoprotective response by initiating signaling pathways that promote liver cell repair and regeneration, leading to heightened enzyme activity for amino acid processing. | ||||||
Fenofibrate | 49562-28-9 | sc-204751 | 5 g | $40.00 | 9 | |
Fenofibrate can upregulate GPT expression via activation of PPAR-alpha, which in turn increases transcription of genes involved in fatty acid oxidation in the liver, including those coding for transaminases like GPT. | ||||||
Ursodeoxycholic acid | 128-13-2 | sc-204935 sc-204935A | 1 g 5 g | $51.00 $128.00 | 4 | |
Ursodeoxycholic acid may prompt an increase in GPT activity to cope with altered bile composition and maintain metabolic homeostasis in hepatocytes, reflecting an adaptive response to changes in the biliary environment. | ||||||
Valproic Acid | 99-66-1 | sc-213144 | 10 g | $85.00 | 9 | |
Valproic acid can stimulate an upsurge in GPT expression by inhibiting histone deacetylase, leading to a more open chromatin structure around genes encoding liver enzymes, thereby enhancing their transcription. | ||||||
Lead(II) Acetate | 301-04-2 | sc-507473 | 5 g | $83.00 | ||
Lead acetate exposure can trigger a rise in GPT levels as part of the liver's defensive response against oxidative stress and to mitigate the toxic effects of lead by enhancing amino acid metabolism for detoxification processes. | ||||||
Thioacetamide | 62-55-5 | sc-213031 | 25 g | $53.00 | ||
Thioacetamide exposure can prompt the liver to elevate GPT expression, which is a response mechanism to counteract the hepatocellular damage and fibrosis caused by this compound through increased amino acid metabolism and detoxification. | ||||||
Iron-Dextran | 9004-66-4 | sc-215191 sc-215191A | 25 ml 100 ml | $200.00 $520.00 | 2 | |
Iron-Dextran can cause an upturn in GPT expression as a means to manage the oxidative stress associated with iron overload in the liver, ensuring efficient amino acid transamination during periods of increased metabolic demand. | ||||||
Cadmium chloride, anhydrous | 10108-64-2 | sc-252533 sc-252533A sc-252533B | 10 g 50 g 500 g | $55.00 $179.00 $345.00 | 1 | |
Cadmium chloride can induce GPT expression as a defense mechanism to hepatic injury by stimulating pathways that enhance the liver’s capacity to metabolize amino acids and regenerate damaged tissue. | ||||||