Wound-Healing Efficacy of Daucus carota Bioactive Compounds: Targeting Oxidative Stress, Inflammation, and Apoptosis

<b>Background/Objectives</b>: Carrot seed essential oil (CSEO) from <i>Daucus carota</i> is rich in sesquiterpenoids and oxygenated sesquiterpenoids known for anti-inflammatory and antioxidant activities. This study evaluated the wound-healing potential of chemically validated CSEO in albino rats and examined its effects on oxidative stress, inflammation, and apoptosis. <b>Methods</b>: CSEO was chemically characterized using GC-MS with retention-index validation. Eighteen constituents (>1% peak area) were identified. An excision wound model in albino rats was used to assess wound closure, physiological parameters, inflammatory cytokines (IL-1β, TNF-α), antioxidant status (SOD, GSH, ROS, MDA), and histological markers of tissue repair. Apoptosis was evaluated through caspase-3 immunohistochemistry to determine its role in tissue remodeling. <b>Results</b>: CSEO exhibited an oxygenated sesquiterpene-rich chemotype with oxygenated sesquiterpenes (~36%) and sesquiterpene hydrocarbons (~29%) as major groups. In vivo, CSEO significantly accelerated wound closure, achieving closure on Day 16 (<i>p</i> < 0.01) and complete closure by Day 21 (<i>p</i> < 0.001), compared with the Reference and Control groups. CSEO significantly improved body weight from Day 4 to Day 21 (<i>p</i> < 0.001) and showed consistently higher feed intake (<i>p</i> < 0.001) relative to other groups. Inflammatory markers were markedly reduced, with TNF-α and IL-1β significantly lower than in the Control group (<i>p</i> < 0.001). CD68 levels were also significantly decreased (<i>p</i> < 0.001). CSEO significantly lowered ROS and MDA (<i>p</i> < 0.001) while enhancing GSH and SOD levels (<i>p</i> < 0.001). Caspase-3 IHC revealed restored physiological apoptotic activity, supporting regulated tissue remodeling. <b>Conclusions</b>: CSEO modulates inflammation, oxidative stress, and apoptosis to promote efficient wound healing, supporting its relevance as a promising therapeutic candidate for wound management.

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Journal
Pharmaceuticals
Published
2025-12-17
DOI
https://doi.org/10.3390/ph18121905
Citations
1
Primary Topic
Wound Healing and Treatments
Type
article
Field-Weighted Citation Impact
1.03
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article

Wound-Healing Efficacy of Daucus carota Bioactive Compounds: Targeting Oxidative Stress, Inflammation, and Apoptosis

Malarkodi Velraj, Kousalya Prabahar, Khalid A. Asseri, Nizar Sirag et al.
1 citations
Pharmaceuticals
Wound Healing and Treatments
1.03
article

Wound-Healing Efficacy of Daucus carota Bioactive Compounds: Targeting Oxidative Stress, Inflammation, and Apoptosis

Malarkodi Velraj, Kousalya Prabahar, Khalid A. Asseri, Nizar Sirag, Rehab Ahmed, Premalatha Paulsamy, Shaimaa Elsayed Ramadan Genena, Krishnaraju Venkatesan, Durgaramani Sivadasan, Mahmoud Elodemi, Vadivel Velmurugan, Kalpana Krishnaraju, Pooja Muralidharan, Hassabelrasoul Elfadil
article en
1 citations

Abstract

<b>Background/Objectives</b>: Carrot seed essential oil (CSEO) from <i>Daucus carota</i> is rich in sesquiterpenoids and oxygenated sesquiterpenoids known for anti-inflammatory and antioxidant activities. This study evaluated the wound-healing potential of chemically validated CSEO in albino rats and examined its effects on oxidative stress, inflammation, and apoptosis. <b>Methods</b>: CSEO was chemically characterized using GC-MS with retention-index validation. Eighteen constituents (>1% peak area) were identified. An excision wound model in albino rats was used to assess wound closure, physiological parameters, inflammatory cytokines (IL-1β, TNF-α), antioxidant status (SOD, GSH, ROS, MDA), and histological markers of tissue repair. Apoptosis was evaluated through caspase-3 immunohistochemistry to determine its role in tissue remodeling. <b>Results</b>: CSEO exhibited an oxygenated sesquiterpene-rich chemotype with oxygenated sesquiterpenes (~36%) and sesquiterpene hydrocarbons (~29%) as major groups. In vivo, CSEO significantly accelerated wound closure, achieving closure on Day 16 (<i>p</i> < 0.01) and complete closure by Day 21 (<i>p</i> < 0.001), compared with the Reference and Control groups. CSEO significantly improved body weight from Day 4 to Day 21 (<i>p</i> < 0.001) and showed consistently higher feed intake (<i>p</i> < 0.001) relative to other groups. Inflammatory markers were markedly reduced, with TNF-α and IL-1β significantly lower than in the Control group (<i>p</i> < 0.001). CD68 levels were also significantly decreased (<i>p</i> < 0.001). CSEO significantly lowered ROS and MDA (<i>p</i> < 0.001) while enhancing GSH and SOD levels (<i>p</i> < 0.001). Caspase-3 IHC revealed restored physiological apoptotic activity, supporting regulated tissue remodeling. <b>Conclusions</b>: CSEO modulates inflammation, oxidative stress, and apoptosis to promote efficient wound healing, supporting its relevance as a promising therapeutic candidate for wound management.

PharmaceuticalsVol. 18(12)
Vels University (IN), SRM Institute of Science and Technology (IN), Lifeline Hospital (IN), University of Tabuk (SA), King Khalid University (SA), Jazan University (SA)
Openalex Percentile: Top 16%
Wound Healing and Treatments
1.03
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