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Comparative study between apocynin and protocatechuic acid regarding antioxidant capacity and vascular effects.

Publication ,  Journal Article
Graton, ME; Ferreira, BHSH; Troiano, JA; Potje, SR; Vale, GT; Nakamune, ACMS; Tirapelli, CR; Miller, FJ; Ximenes, VF; Antoniali, C
Published in: Front Physiol
2022

Reactive oxygen species (ROS) derived from NOX enzymes activity play an important role in the development of cardiovascular diseases. Compounds able to decrease oxidative stress damage are potential candidates as drugs and/or supplements for hypertension treatment. Here, we aimed to compare in vitro ROS scavenging potency, effective NOX inhibition and effects on vascular reactivity of apocynin to another phenolic compound, protocatechuic acid, in vascular cells from spontaneously hypertensive rat (SHR), where redox signaling is altered and contributes to the development and/or maintenance of hypertension. We evaluated the in vitro antioxidant capacity and free radical scavenging capacity of both phenolic compounds. Moreover, we investigated the effect of both compounds on lipid peroxidation, lucigenin chemiluminescence, nitric oxide (NO•) levels and ROS concentration in vascular cells of SHR or human umbilical vein endothelial cell (HUVEC). Apocynin and protocatechuic acid presented antioxidant capacity and ability as free radical scavengers, decreased thiobarbituric acid reactive substances (TBARS) in aortic cells from SHR, and increased NO• concentration in isolated HUVEC. Both compounds were able to reduce lucigenin chemiluminescence and increased the potency of acetylcholine in aorta of SHR. However, in SHR aortas, only apocynin diminished the contraction induced by phenylephrine. In conclusion, these results strongly reinforce the potential application of substances such as apocynin and protocatechuic acid that combine abilities as scavenging and/or prevention of ROS generation, establishment of NO bioactivity and modulation of vascular reactivity. Due to its phytochemical origin and low toxicity, its potential therapeutic use in vascular diseases should be considered.

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Published In

Front Physiol

DOI

ISSN

1664-042X

Publication Date

2022

Volume

13

Start / End Page

1047916

Location

Switzerland

Related Subject Headings

  • 3208 Medical physiology
  • 3101 Biochemistry and cell biology
  • 1701 Psychology
  • 1116 Medical Physiology
  • 0606 Physiology
 

Citation

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ICMJE
MLA
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Graton, M. E., Ferreira, B. H. S. H., Troiano, J. A., Potje, S. R., Vale, G. T., Nakamune, A. C. M. S., … Antoniali, C. (2022). Comparative study between apocynin and protocatechuic acid regarding antioxidant capacity and vascular effects. Front Physiol, 13, 1047916. https://doi.org/10.3389/fphys.2022.1047916
Graton, Murilo E., Bruno H. S. H. Ferreira, Jéssica A. Troiano, Simone R. Potje, Gabriel T. Vale, Ana Cláudia M. S. Nakamune, Carlos R. Tirapelli, Francis J. Miller, Valdecir F. Ximenes, and Cristina Antoniali. “Comparative study between apocynin and protocatechuic acid regarding antioxidant capacity and vascular effects.Front Physiol 13 (2022): 1047916. https://doi.org/10.3389/fphys.2022.1047916.
Graton ME, Ferreira BHSH, Troiano JA, Potje SR, Vale GT, Nakamune ACMS, et al. Comparative study between apocynin and protocatechuic acid regarding antioxidant capacity and vascular effects. Front Physiol. 2022;13:1047916.
Graton, Murilo E., et al. “Comparative study between apocynin and protocatechuic acid regarding antioxidant capacity and vascular effects.Front Physiol, vol. 13, 2022, p. 1047916. Pubmed, doi:10.3389/fphys.2022.1047916.
Graton ME, Ferreira BHSH, Troiano JA, Potje SR, Vale GT, Nakamune ACMS, Tirapelli CR, Miller FJ, Ximenes VF, Antoniali C. Comparative study between apocynin and protocatechuic acid regarding antioxidant capacity and vascular effects. Front Physiol. 2022;13:1047916.

Published In

Front Physiol

DOI

ISSN

1664-042X

Publication Date

2022

Volume

13

Start / End Page

1047916

Location

Switzerland

Related Subject Headings

  • 3208 Medical physiology
  • 3101 Biochemistry and cell biology
  • 1701 Psychology
  • 1116 Medical Physiology
  • 0606 Physiology