Differences in renal ammonia metabolism in male and female kidney

Am J Physiol Renal Physiol. 2018 Aug 1;315(2):F211-F222. doi: 10.1152/ajprenal.00084.2018. Epub 2018 Mar 21.

Abstract

Renal ammonia metabolism has a major role in the maintenance of acid-base homeostasis. Sex differences are well recognized as an important biological variable in many aspects of renal function, including fluid and electrolyte metabolism. However, sex differences in renal ammonia metabolism have not been previously reported. Therefore, the purpose of the current study was to investigate sex differences in renal ammonia metabolism. We studied 4-mo-old wild-type C57BL/6 mice fed a normal diet. Despite similar levels of food intake, and, thus, protein intake, which is the primary determinant of endogenous acid production, female mice excreted greater amounts of ammonia, but not titratable acids, than did male mice. This difference in ammonia metabolism was associated with fundamental structural differences between the female and male kidney. In the female mouse kidney, proximal tubules account for a lower percentage of the renal cortical parenchyma compared with the male kidney, whereas collecting ducts account for a greater percentage of the renal parenchyma than in male kidneys. To further investigate the mechanism(s) behind the greater ammonia excretion in female mice, we examined differences in the expression of proteins involved in renal ammonia metabolism and transport. Greater basal ammonia excretion in females was associated with greater expression of PEPCK, glutamine synthetase, NKCC2, Rhbg, and Rhcg than was observed in male mice. We conclude that there are sex differences in basal ammonia metabolism that involve both renal structural differences and differences in expression of proteins involved in ammonia metabolism.

Keywords: acid-base; ammonia; collecting duct; proximal tubule; sex differences.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Ammonia / metabolism*
  • Animals
  • Cation Transport Proteins / genetics
  • Cation Transport Proteins / metabolism
  • Female
  • Gene Expression Regulation
  • Glutamate-Ammonia Ligase / genetics
  • Glutamate-Ammonia Ligase / metabolism
  • Glycoproteins / genetics
  • Glycoproteins / metabolism
  • Kidney / anatomy & histology
  • Kidney / metabolism*
  • Male
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism
  • Membrane Transport Proteins / genetics
  • Membrane Transport Proteins / metabolism
  • Mice, Inbred C57BL
  • Phosphoenolpyruvate Carboxykinase (ATP) / genetics
  • Phosphoenolpyruvate Carboxykinase (ATP) / metabolism
  • Renal Elimination*
  • Sex Factors
  • Solute Carrier Family 12, Member 1 / genetics
  • Solute Carrier Family 12, Member 1 / metabolism

Substances

  • Cation Transport Proteins
  • Glycoproteins
  • Membrane Glycoproteins
  • Membrane Transport Proteins
  • RhBG protein, mouse
  • Rhcg protein, mouse
  • Slc12a1 protein, mouse
  • Solute Carrier Family 12, Member 1
  • Ammonia
  • PEPCK-M protein, mouse
  • Phosphoenolpyruvate Carboxykinase (ATP)
  • Glutamate-Ammonia Ligase