# Antioxidant Potential of Myrciaria tenella Fruit Extracts: In Vitro and In Vivo Protection Against Oxidative Stress

**Authors:** Verônica Giuliani de Queiroz Aquino-Martins, Maria Lúcia da Silva Cordeiro, Ariana Pereira da Silva, Georggia Fátima Silva Naliato, Elielson Rodrigo Silveira, Raquel Cordeiro Theodoro, Deborah Yara Alves Cursino dos Santos, Hugo Alexandre Oliveira Rocha, Katia Castanho Scortecci

PMC · DOI: 10.3390/molecules31040602 · Molecules · 2026-02-09

## TL;DR

This study shows that extracts from Myrciaria tenella fruits have strong antioxidant properties, protecting cells and larvae from oxidative stress.

## Contribution

The study introduces new evidence on the antioxidant potential of Myrciaria tenella fruit extracts using both in vitro and in vivo models.

## Key findings

- Hydroethanolic unripe extract (VE) showed the highest metal-chelating activity and phenolic content.
- All extracts were non-cytotoxic and provided protection against oxidative stress in cell models.
- VE extract resulted in 80% larval survival in in vivo oxidative stress tests.

## Abstract

Myrciaria tenella (cambuí) is a native Brazilian fruit traditionally recognized for its sensory attributes and medicinal properties, including antidiabetic, anti-inflammatory, antimicrobial, and gastroprotective activities. This study evaluated the antioxidant activity of unripe and ripe M. tenella fruits using in vitro and in vivo experimental models. Four extracts were prepared: aqueous unripe (VA), aqueous ripe (MA), hydroethanolic unripe (VE), and hydroethanolic ripe (ME). Antioxidant activity was assessed through biochemical assays and cellular models using NIH/3T3 fibroblasts and RAW 264.7 macrophages. In RAW 264.7 cells, oxidative stress modulation was investigated using hydrogen peroxide-induced stress and lipopolysaccharide (LPS)-stimulated nitric oxide (NO) production. In NHI/3T3 cells, wound healing, copper sulphate (CuSO4)-induced oxidative stress, intracellular reactive oxygen species (ROS) generation, and nuclear morphology following DAPI staining were evaluated. Total phenolic content was quantified using the Folin–Ciocalteu method and analyzed by HPLC-DAD. In vivo toxicity and antioxidant protection were assessed using Tenebrio molitor larvae exposed to CuSO4-induced oxidative stress. Among the extracts, VE exhibited the highest metal-chelating activity (Cu: 78.6%; Fe: 37.7%) and total phenolic content (50.64 mg GAE/mg). HPLC-DAD analysis identified gallic acid in all extracts, kaempferol derivatives in hydroethanolic extracts (VE and ME), and catechin derivatives in aqueous extracts (VA and MA). All extracts were non-cytotoxic and demonstrated protective effects against oxidative stress in vitro. In vivo assays confirmed the absence of toxicity and significant antioxidant protection, with VE resulting in 80% larval survival.

## Linked entities

- **Chemicals:** gallic acid (PubChem CID 370), kaempferol (PubChem CID 5280863), catechin (PubChem CID 1203), copper sulphate (PubChem CID 24462), hydrogen peroxide (PubChem CID 784), nitric oxide (PubChem CID 145068)
- **Species:** Myrciaria tenella (taxon 3110331), Tenebrio molitor (taxon 7067)

## Full-text entities

- **Genes:** Glb1 (galactosidase, beta 1) [NCBI Gene 316033], Pcx (pyruvate carboxylase) [NCBI Gene 18563] {aka Pc, Pcb}
- **Diseases:** kidney diseases (MESH:D007674), breast cancer (MESH:D001943), liver damage (MESH:D056486), cardiovascular diseases (MESH:D002318), cytotoxic (MESH:D064420), anemia (MESH:D000740), Death (MESH:D003643), neurological disorders (MESH:D009461), metabolic disorders (MESH:D008659), Wilson's disease (MESH:D006527), gastric adenocarcinoma (MESH:D013274), organ failure (MESH:D009102), microbial infections (MESH:D015163), diabetes (MESH:D003920), cancer (MESH:D009369), cervical adenocarcinoma (MESH:D000230), liver cirrhosis (MESH:D008103), asthma (MESH:D001249), injury to (MESH:D014947), neurodegenerative and cardiovascular diseases (MESH:D019636), chronic inflammation (MESH:D007249)
- **Chemicals:** KCl (MESH:D011189), acetate (MESH:D000085), potassium ferrocyanide (MESH:C031835), ellagic acid (MESH:D004610), hydrogen (MESH:D006859), anthocyanins (MESH:D000872), molybdenum (MESH:D008982), glucose (MESH:D005947), chloramphenicol (MESH:D002701), 4',6-diamidino-2-phenylindole (MESH:C007293), DMSO (MESH:D004121), Flavonoids (MESH:D005419), saponins (MESH:D012503), ROS (MESH:D017382), sulfuric acid (MESH:C033158), fructose (MESH:D005632), CO2 (MESH:D002245), GSH (MESH:D005978), L-glutamine (MESH:D005973), LPS (MESH:D008070), sucrose (MESH:D013395), lipid (MESH:D008055), paraformaldehyde (MESH:C003043), p-coumaric acid (MESH:C495469), NBT (MESH:D009580), peroxide (MESH:D010545), phosphoric acid (MESH:C030242), RNS (MESH:D026361), MTT (MESH:C070243), Nitrite (MESH:D009573), TCA (MESH:D014238), tannins (MESH:D013634), riboflavin (MESH:D012256), ferrozine (MESH:D005297), malondialdehyde (MESH:D008315), H2O2 (MESH:D006861), sodium bicarbonate (MESH:D017693), superoxide (MESH:D013481), AcOH (-), Potassium ferricyanide (MESH:C028033), curcumin (MESH:D003474), ammonium molybdate (MESH:C022175), sodium citrate (MESH:D000077559), sulfanilamide (MESH:D000077145), Copper sulfate (MESH:D019327), Penicillin (MESH:D010406), sodium phosphate (MESH:C018279), FeCl2 (MESH:C029451), acetic acid (MESH:D019342), Ascorbate (MESH:D001205), alkaloids (MESH:D000470), Copper (MESH:D003300), N-(1-naphthyl)ethylenediamine dihydrochloride (MESH:C008588), ethanol (MESH:D000431), flavonol (MESH:C041477), NO (MESH:D009569), hydroxyl radicals (MESH:D017665), water (MESH:D014867), free radical (MESH:D005609), carotenoids (MESH:D002338)
- **Species:** M. ferruginea [taxon 438351], Bolanthus spergulifolius (species) [taxon 1930806], Tenebrio molitor (yellow mealworm, species) [taxon 7067], Camellia sinensis (black tea, species) [taxon 4442], Nephelium lappaceum (rambutan, species) [taxon 151071], Myrciaria dubia (camu-camu, species) [taxon 468946], Rattus norvegicus (brown rat, species) [taxon 10116], Mutela dubia (species) [taxon 152234], Homo sapiens (human, species) [taxon 9606], Psidium guajava (guava, species) [taxon 120290], Eugenia stipitata (species) [taxon 1453397], Myrciaria floribunda (species) [taxon 375265], Myrciaria glazioviana (species) [taxon 2083144], Mus musculus (house mouse, species) [taxon 10090], Houttuynia cordata (chameleon-plant, species) [taxon 16752], Caenorhabditis elegans (species) [taxon 6239], Syzygium cumini (jaman, species) [taxon 260142], Eugenia uniflora (Brazil-cherry, species) [taxon 119951], Plinia cauliflora (species) [taxon 375264], Glycine max (soybean, species) [taxon 3847]
- **Cell lines:** HeLa — Homo sapiens (Human), Human papillomavirus-related endocervical adenocarcinoma, Cancer cell line (CVCL_JX14), AGS — Homo sapiens (Human), Gastric adenocarcinoma, Cancer cell line (CVCL_X019), 116 — Mus musculus (Mouse), Hybridoma (CVCL_G220), 3T3 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0594), TIB-71 — Homo sapiens (Human), Cri du chat syndrome, Finite cell line (CVCL_4150), NC — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_4536), ATCC  CRL-1658TM — Homo sapiens (Human), Nevoid basal cell carcinoma syndrome, Finite cell line (CVCL_2Z69), RAW 264.7 — Mus musculus (Mouse), Mouse leukemia, Cancer cell line (CVCL_0493), 3T3-L1 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0123), ATCC — Homo sapiens (Human), Lung adenocarcinoma, Cancer cell line (CVCL_0023), HepG2 — Homo sapiens (Human), Hepatoblastoma, Cancer cell line (CVCL_0027), NIH/3T3 fibroblasts — Mus musculus (Mouse), Transformed cell line (CVCL_L992), NHI/3T3 — Rattus norvegicus (Rat), Rat insulinoma, Cancer cell line (CVCL_M461)

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## Figures

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## References

83 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942716/full.md

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Source: https://tomesphere.com/paper/PMC12942716