# Unleashing the biological power and chemical profile of Paracaryum hedgei extracts based on chromatographic, in vitro, and bioinformatic tools

**Authors:** Enver Saka, Sakina Yagi, Bengusu H. Akgul, Eulogio J. Llorent-Martínez, Evren Yildiztugay, Ismail Koyuncu, Meltem Cayci, Ismail Yapıcı, Ilhami Gulcin, Yimao Wu, Meng-Yao Li, Gokhan Zengin

PMC · DOI: 10.1016/j.bbrep.2025.102408 · 2025-12-14

## TL;DR

This study explores the chemical makeup and health benefits of Paracaryum hedgei extracts, finding them to have strong antioxidant and cancer-fighting potential.

## Contribution

This is the first study to evaluate the chemical profile and biological activities of Paracaryum hedgei extracts.

## Key findings

- Root extracts of P. hedgei had the highest total phenolic content and antioxidant activity.
- Ethyl acetate extracts showed significant cytotoxic effects on cervical and colorectal cancer cells.
- Phenolic acids in P. hedgei may target cancer-related pathways like retinoic acid metabolism and inflammation.

## Abstract

Studies evaluating the chemical constituents and pharmacological potential of Paracaryum species (family Boraginaceae) were limited. The current study was designed to investigate, for the first time, the chemical profile, antioxidant, enzyme-inhibitory, and cytotoxic properties of P. hedgei Aytaç & R.R. Mill. Roots extracts recorded the highest total phenolic content (24.72–91.16 mg GAE/g). About 33 compounds were identified, and the aerial parts extracts were dominated by rosmarinic acid, rutin, and sagerinic acid. In general, the root extracts exhibited greater antioxidant activity than the extracts from the aerial parts. Among the solvents, The 70 % EtOH extract of roots showed the highest antiradical (DPPH: 207.90 mg TE/g; ABTS: 238.08 mg TE/g), ion-reducing (FRAP: 384.99 mg TE/g; CUPRAC: 615.27 mg TE/g), and total antioxidant activities (3.21 mmol TE/g), whereas the EtOAc and aqueous extracts from the aerial parts demonstrated the best chelating capacity. The enzyme inhibition varied according to the plant parts examined and the solvents employed for extraction. The EtOAc extract of the roots exerted the highest inhibitory effect towards the human carbonic anhydrase II (IC50: 2.32 μg/ml). The cytotoxicity of the extracts was tested against three cancer cell lines (HELA, A549, and HCT-116) and one healthy cell line (HEK-293). Specifically, the EtOAC extracts showed cytotoxic effects on HELA cells sourced from aerial parts (IC50: 106.30 μg/ml) and on HCT-116 cells sourced from roots (IC50: 96.82 μg/ml). Molecular docking results provided additional support for the enzyme inhibition capabilities of the extracts. Combined network pharmacology and molecular docking analyses revealed that phenolic acids from P. hedgei exert anti-cancer effects on cervical and colorectal adenocarcinoma by modulating key pathways, including retinoic acid metabolism, steroid biosynthesis, and inflammatory responses. These findings can provide a scientific starting point for the pharmaceutical potential of P. hedgei, and it can be considered a valuable source of natural bioactive compounds for functional nutraceutical and pharmaceutical applications.

Image 1

•Different extracts of Paracaryum hedgei were tested for the first time.•Thirty-three components were detected in the extracts.•The hydroalcoholic extract was the most active in the antioxidant assays.•Ethyl acetate extract exhibited remarkable cytotoxic effect on HELA cell line.•The plant can be an alternative raw material for therapeutic formulations.

Different extracts of Paracaryum hedgei were tested for the first time.

Thirty-three components were detected in the extracts.

The hydroalcoholic extract was the most active in the antioxidant assays.

Ethyl acetate extract exhibited remarkable cytotoxic effect on HELA cell line.

The plant can be an alternative raw material for therapeutic formulations.

## Linked entities

- **Chemicals:** rosmarinic acid (PubChem CID 639655), rutin (PubChem CID 5280805), sagerinic acid (PubChem CID 23760102)
- **Diseases:** cervical adenocarcinoma (MONDO:0005153), colorectal adenocarcinoma (MONDO:0005008)
- **Species:** Paracaryum hedgei (taxon 3143287)

## Full-text entities

- **Genes:** CA2 (carbonic anhydrase 2) [NCBI Gene 760] {aka CA-II, CAC, CAII, Car2, HEL-76, HEL-S-282}
- **Diseases:** inflammatory (MESH:D007249), cancer (MESH:D009369), cervical and colorectal adenocarcinoma (MESH:D003110), cytotoxic (MESH:D064420)
- **Chemicals:** steroid (MESH:D013256), CUPRAC (-), phenolic acids (MESH:C017616), DPPH (MESH:C004931), EtOH (MESH:D000431), ABTS (MESH:C002502), rosmarinic acid (MESH:C041376), rutin (MESH:D012431), retinoic acid (MESH:D014212)
- **Species:** Paracaryum (genus) [taxon 543579], Homo sapiens (human, species) [taxon 9606]

## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12765141/full.md

---
Source: https://tomesphere.com/paper/PMC12765141