# The chemistry of the nitrate–nitrite–nitric oxide pathway: regulating muscle oxygenation and exercise performance

**Authors:** Jing Liang, Taibin Huang, Jinping Li, Zhiyu Yang, Jin Ni, Yanchao Wang

PMC · DOI: 10.1039/d6ra00317f · 2026-03-20

## TL;DR

This review explains how the nitrate-nitrite-nitric oxide pathway helps regulate muscle oxygen and exercise performance, beyond the traditional nitric oxide production method.

## Contribution

The paper provides a detailed chemistry-focused analysis of the nitrate–nitrite–NO pathway and its role in muscle physiology.

## Key findings

- Nitrate from diet is reduced to nitrite and then to NO, especially under hypoxic conditions in muscles.
- Key proteins like xanthine oxidoreductase and deoxyhemoglobin help convert nitrite to NO in muscles.
- Dietary nitrate may improve exercise performance, but results vary due to genetic and microbiome factors.

## Abstract

Nitric oxide (NO) is a pleiotropic signaling molecule fundamentally involved in regulating skeletal muscle physiology, including blood flow, contractility, and metabolism. For decades, the synthesis of NO was attributed solely to the l-arginine-dependent nitric oxide synthase (NOS) enzymes. However, the discovery and characterization of the nitrate–nitrite–NO pathway have revealed an alternative, NOS-independent mechanism for NO generation. This pathway is particularly significant under hypoxic and acidic conditions, which are characteristic of exercising skeletal muscle. Dietary inorganic nitrate, abundant in green leafy vegetables and beetroot, is sequentially reduced to nitrite and then to bioactive NO. This review critically examines the intricate chemistry underpinning this pathway, from the initial enzymatic reduction of nitrate by both mammalian and microbial reductases to the diverse chemical routes of nitrite reduction to NO within the muscle milieu. We delve into the specific roles of key proteins such as xanthine oxidoreductase, deoxyhemoglobin/deoxymyoglobin, and mitochondrial complexes in catalyzing these transformations. Furthermore, we explore how NO generated via this pathway modulates muscle oxygenation through vasodilation and regulation of mitochondrial respiration. The ergogenic potential of dietary nitrate supplementation is discussed in the context of human exercise performance, highlighting the significant controversies, methodological challenges, and sources of inter-individual variability, including genetics and the microbiome. This review aims to provide a comprehensive, chemistry-focused perspective on the nitrate–nitrite–NO pathway, bridging fundamental biochemical mechanisms with their physiological consequences in exercise.

This review comprehensively elucidates the redox chemistry and physiological integration of the nitrate–nitrite–nitric oxide pathway in regulating skeletal muscle oxygenation and exercise performance.

## Linked entities

- **Chemicals:** nitrate (PubChem CID 943), nitrite (PubChem CID 946), nitric oxide (PubChem CID 145068), l-arginine (PubChem CID 232)

## Full-text entities

- **Genes:** NOS2 (nitric oxide synthase 2) [NCBI Gene 4843] {aka HEP-NOS, INOS, NOS, NOS2A}, XDH (xanthine dehydrogenase) [NCBI Gene 7498] {aka XAN1, XDH/XO, XO, XOR}
- **Diseases:** hypoxic (MESH:D002534)
- **Chemicals:** NO (MESH:D009569), nitrate (MESH:D009566), inorganic nitrate (-), l-arginine (MESH:D001120), nitrite (MESH:D009573)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13003460/full.md

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Source: https://tomesphere.com/paper/PMC13003460