Nicotinamide nucleotide synthesis in regenerating rat liver
- PMID: 4398891
- PMCID: PMC1176642
- DOI: 10.1042/bj1210655
Nicotinamide nucleotide synthesis in regenerating rat liver
Abstract
1. The concentrations and total content of the nicotinamide nucleotides were measured in the livers of rats at various times after partial hepatectomy and laparotomy (sham hepatectomy) and correlated with other events in the regeneration process. 2. The NAD content and concentration in rat liver were relatively unaffected by laparotomy, but fell to a minimum, 25 and 33% below control values respectively, 24h after partial hepatectomy. NADP content and concentration were affected similarly by both laparotomy and partial hepatectomy, falling rapidly and remaining depressed for up to 48h. 3. The effect of injecting various doses of nicotinamide on the liver DNA and NAD 18h after partial hepatectomy was studied and revealed an inverse correlation between NAD content and DNA content. 4. Injections of nicotinamide at various times after partial hepatectomy revealed that the ability to synthesize NAD from nicotinamide was impaired during the first 12h, rose to a peak at 26h and fell again by 48h after partial hepatectomy. 5. The total liver activity of NAD pyrophosphorylase (EC 2.7.7.1) remained at or slightly above the initial value for 12h after partial hepatectomy and then rose continuously until 48h after operation. The activity of NMN pyrophosphorylase (EC 2.4.2.12) showed a similar pattern of change after partial hepatectomy, but was at no time greater than 5% of the activity of NAD pyrophosphorylase. 6. The results are discussed with reference to the control of NAD synthesis in rapidly dividing tissue. It is suggested that the availability of cofactors and substrates for NAD synthesis is more important as a controlling factor than the maximum enzyme activities. It is concluded that the low concentrations of nicotinamide nucleotides in rapidly dividing tissues are the result of competition between NAD synthesis and nucleic acid synthesis for common precursor and cofactors.
Similar articles
-
The control of nucleic acid and nicotinamide nucleotide synthesis in regenerating rat liver.Biochem J. 1972 Jul;128(4):869-77. doi: 10.1042/bj1280869. Biochem J. 1972. PMID: 4404767 Free PMC article.
-
The concentration and biosynthesis of nicotinamide nucleotides in the livers of rats treated with carcinogens.Biochem J. 1966 Feb;98(2):546-56. doi: 10.1042/bj0980546. Biochem J. 1966. PMID: 4380162 Free PMC article.
-
[Nicotinamide coenzyme content in the normal and regenerating liver of rats].Biull Eksp Biol Med. 1985 Apr;99(4):432-4. Biull Eksp Biol Med. 1985. PMID: 3986366 Russian.
-
Physiology aspects of pyridine nucleotide regulation in mammals.Mol Cell Biochem. 1980 Dec 16;33(3):135-43. doi: 10.1007/BF00225285. Mol Cell Biochem. 1980. PMID: 6450878 Review.
-
Regeneration of nicotinamide cofactors for use in organic synthesis.Appl Biochem Biotechnol. 1987 Mar;14(2):147-97. doi: 10.1007/BF02798431. Appl Biochem Biotechnol. 1987. PMID: 3304160 Review.
Cited by
-
NAD metabolism and the SLC34 family: evidence for a liver-kidney axis regulating inorganic phosphate.Pflugers Arch. 2019 Jan;471(1):109-122. doi: 10.1007/s00424-018-2204-2. Epub 2018 Sep 14. Pflugers Arch. 2019. PMID: 30218374 Review.
-
The control of nucleic acid and nicotinamide nucleotide synthesis in regenerating rat liver.Biochem J. 1972 Jul;128(4):869-77. doi: 10.1042/bj1280869. Biochem J. 1972. PMID: 4404767 Free PMC article.
-
Nicotinamide adenine dinucleotide biosynthesis promotes liver regeneration.Hepatology. 2017 Feb;65(2):616-630. doi: 10.1002/hep.28912. Epub 2016 Dec 24. Hepatology. 2017. PMID: 27809334 Free PMC article.
-
SIRT3 is required for liver regeneration but not for the beneficial effect of nicotinamide riboside.JCI Insight. 2021 Apr 8;6(7):e147193. doi: 10.1172/jci.insight.147193. JCI Insight. 2021. PMID: 33690226 Free PMC article.
-
Hepatectomy-related hypophosphatemia: a novel phosphaturic factor in the liver-kidney axis.J Am Soc Nephrol. 2014 Apr;25(4):761-72. doi: 10.1681/ASN.2013060569. Epub 2013 Nov 21. J Am Soc Nephrol. 2014. PMID: 24262791 Free PMC article.
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources