The Source of Glycolytic Intermediates in Mammalian Tissues. 2021

Tara TeSlaa, and Caroline R Bartman, and Connor S R Jankowski, and Zhaoyue Zhang, and Xincheng Xu, and Xi Xing, and Lin Wang, and Wenyun Lu, and Sheng Hui, and Joshua D Rabinowitz
Lewis Sigler Institute for Integrative Genomics and Department of Chemistry, Princeton University, Washington Road, Princeton, NJ 08544, USA.

Glycolysis plays a central role in organismal metabolism, but its quantitative inputs across mammalian tissues remain unclear. Here we use 13C-tracing in mice to quantify glycolytic intermediate sources: circulating glucose, intra-tissue glycogen, and circulating gluconeogenic precursors. Circulating glucose is the main source of circulating lactate, the primary end product of tissue glycolysis. Yet circulating glucose highly labels glycolytic intermediates in only a few tissues: blood, spleen, diaphragm, and soleus muscle. Most glycolytic intermediates in the bulk of body tissue, including liver and quadriceps muscle, come instead from glycogen. Gluconeogenesis contributes less but also broadly to glycolytic intermediates, and its flux persists with physiologic feeding (but not hyperinsulinemic clamp). Instead of suppressing gluconeogenesis, feeding activates oxidation of circulating glucose and lactate to maintain glucose homeostasis. Thus, the bulk of the body slowly breaks down internally stored glycogen while select tissues rapidly catabolize circulating glucose to lactate for oxidation throughout the body.

UI MeSH Term Description Entries
D008297 Male Males
D008810 Mice, Inbred C57BL One of the first INBRED MOUSE STRAINS to be sequenced. This strain is commonly used as genetic background for transgenic mouse models. Refractory to many tumors, this strain is also preferred model for studying role of genetic variations in development of diseases. Mice, C57BL,Mouse, C57BL,Mouse, Inbred C57BL,C57BL Mice,C57BL Mice, Inbred,C57BL Mouse,C57BL Mouse, Inbred,Inbred C57BL Mice,Inbred C57BL Mouse
D001786 Blood Glucose Glucose in blood. Blood Sugar,Glucose, Blood,Sugar, Blood
D002247 Carbon Isotopes Stable carbon atoms that have the same atomic number as the element carbon but differ in atomic weight. C-13 is a stable carbon isotope. Carbon Isotope,Isotope, Carbon,Isotopes, Carbon
D003964 Diaphragm The musculofibrous partition that separates the THORACIC CAVITY from the ABDOMINAL CAVITY. Contraction of the diaphragm increases the volume of the thoracic cavity aiding INHALATION. Respiratory Diaphragm,Diaphragm, Respiratory,Diaphragms,Diaphragms, Respiratory,Respiratory Diaphragms
D005943 Gluconeogenesis Biosynthesis of GLUCOSE from nonhexose or non-carbohydrate precursors, such as LACTATE; PYRUVATE; ALANINE; and GLYCEROL.
D006003 Glycogen
D006019 Glycolysis A metabolic process that converts GLUCOSE into two molecules of PYRUVIC ACID through a series of enzymatic reactions. Energy generated by this process is conserved in two molecules of ATP. Glycolysis is the universal catabolic pathway for glucose, free glucose, or glucose derived from complex CARBOHYDRATES, such as GLYCOGEN and STARCH. Embden-Meyerhof Pathway,Embden-Meyerhof-Parnas Pathway,Embden Meyerhof Parnas Pathway,Embden Meyerhof Pathway,Embden-Meyerhof Pathways,Pathway, Embden-Meyerhof,Pathway, Embden-Meyerhof-Parnas,Pathways, Embden-Meyerhof
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D013154 Spleen An encapsulated lymphatic organ through which venous blood filters.

Related Publications

Tara TeSlaa, and Caroline R Bartman, and Connor S R Jankowski, and Zhaoyue Zhang, and Xincheng Xu, and Xi Xing, and Lin Wang, and Wenyun Lu, and Sheng Hui, and Joshua D Rabinowitz
March 1995, Nihon rinsho. Japanese journal of clinical medicine,
Tara TeSlaa, and Caroline R Bartman, and Connor S R Jankowski, and Zhaoyue Zhang, and Xincheng Xu, and Xi Xing, and Lin Wang, and Wenyun Lu, and Sheng Hui, and Joshua D Rabinowitz
September 1999, Nihon rinsho. Japanese journal of clinical medicine,
Tara TeSlaa, and Caroline R Bartman, and Connor S R Jankowski, and Zhaoyue Zhang, and Xincheng Xu, and Xi Xing, and Lin Wang, and Wenyun Lu, and Sheng Hui, and Joshua D Rabinowitz
March 1959, The Journal of biological chemistry,
Tara TeSlaa, and Caroline R Bartman, and Connor S R Jankowski, and Zhaoyue Zhang, and Xincheng Xu, and Xi Xing, and Lin Wang, and Wenyun Lu, and Sheng Hui, and Joshua D Rabinowitz
January 1970, Enzymologia,
Tara TeSlaa, and Caroline R Bartman, and Connor S R Jankowski, and Zhaoyue Zhang, and Xincheng Xu, and Xi Xing, and Lin Wang, and Wenyun Lu, and Sheng Hui, and Joshua D Rabinowitz
June 1964, Biochemical and biophysical research communications,
Tara TeSlaa, and Caroline R Bartman, and Connor S R Jankowski, and Zhaoyue Zhang, and Xincheng Xu, and Xi Xing, and Lin Wang, and Wenyun Lu, and Sheng Hui, and Joshua D Rabinowitz
January 1974, Enzyme,
Tara TeSlaa, and Caroline R Bartman, and Connor S R Jankowski, and Zhaoyue Zhang, and Xincheng Xu, and Xi Xing, and Lin Wang, and Wenyun Lu, and Sheng Hui, and Joshua D Rabinowitz
January 1962, Acta biologica et medica Germanica,
Tara TeSlaa, and Caroline R Bartman, and Connor S R Jankowski, and Zhaoyue Zhang, and Xincheng Xu, and Xi Xing, and Lin Wang, and Wenyun Lu, and Sheng Hui, and Joshua D Rabinowitz
July 1969, Pediatrics,
Tara TeSlaa, and Caroline R Bartman, and Connor S R Jankowski, and Zhaoyue Zhang, and Xincheng Xu, and Xi Xing, and Lin Wang, and Wenyun Lu, and Sheng Hui, and Joshua D Rabinowitz
October 1975, Archives of oral biology,
Tara TeSlaa, and Caroline R Bartman, and Connor S R Jankowski, and Zhaoyue Zhang, and Xincheng Xu, and Xi Xing, and Lin Wang, and Wenyun Lu, and Sheng Hui, and Joshua D Rabinowitz
July 1980, The Journal of laboratory and clinical medicine,
Copied contents to your clipboard!