Effects of acid-base imbalance on vascular reactivity

A. C. Celotto, V. K. Capellini, C. F. Baldo, M. B. Dalio, A. J. Rodrigues, P. R B Evora

Research output: Contribution to journalReview articlepeer-review

31 Scopus citations

Abstract

Acid-base homeostasis maintains systemic arterial pH within a narrow range. Whereas the normal range of pH for clinical laboratories is 7.35-7.45, in vivo pH is maintained within a much narrower range. In clinical and experimental settings, blood pH can vary in response to respiratory or renal impairment. This altered pH promotes changes in vascular smooth muscle tone with impact on circulation and blood pressure control. Changes in pH can be divided into those occurring in the extracellular space (pHo) and those occurring within the intracellular space (pHi), although, extracellular and intracellular compartments influence each other. Consistent with the multiple events involved in the changes in tone produced by altered pHo, including type of vascular bed, several factors and mechanisms, in addition to hydrogen ion concentration, have been suggested to be involved. The scientific literature has many reports concerning acid-base balance and endothelium function, but these concepts are not clear about acid-base disorders and their relations with the three known mechanisms of endothelium-dependent vascular reactivity: nitric oxide (NO/cGMP-dependent), prostacyclin (PGI2/cAMP-dependent) and hyperpolarization. During the last decades, many studies have been published and have given rise to confronting data on acid-base disorder and endothelial function. Therefore, the main proposal of this review is to provide a critical analysis of the state of art and incentivate researchers to develop more studies about these issues.

Original languageEnglish (US)
Pages (from-to)439-445
Number of pages7
JournalBrazilian Journal of Medical and Biological Research
Volume41
Issue number6
DOIs
StatePublished - 2008

Keywords

  • Acid-base balance
  • Acidosis
  • Alkalosis
  • Endothelium
  • Nitric oxide
  • Vascular reactivity

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