# Salvia coccinea and Apigenin: A Natural Treasure of Lamiaceae in Pharmacological Innovation

**Authors:** Muhammad Usman Khalid, Muhammad Tauseef Sultan, Muhammad Maaz, Shehnshah Zafar, Anum Shoukat, Nudrat Khursheed, Matteo Bordiga, Amna Junaid

PMC · DOI: 10.1002/fsn3.71354 · Food Science & Nutrition · 2026-02-03

## TL;DR

Salvia coccinea and its compound apigenin show promise in treating chronic diseases due to their antioxidant, anti-inflammatory, and antimicrobial properties.

## Contribution

This review highlights the pharmacological potential of Salvia coccinea and apigenin for developing new pharmaceutical and nutraceutical applications.

## Key findings

- Salvia coccinea and apigenin reduce oxidative stress and tumor cell metastasis through multiple molecular pathways.
- They exhibit antimicrobial activity against various bacterial, viral, and fungal strains.
- Apigenin promotes hypoglycemic effects by improving insulin resistance and regulating key metabolic pathways.

## Abstract

Human health and ever‐increasing disease burden demand the inclusion of traditional medicines in modern healthcare sectors. Phytochemicals extracted from medicinal plants can be utilized to prepare nutritious and quality food products that could offer nutritional and curative benefits. This review highlights the nutritional, phytochemical, and therapeutic profile of 
Salvia coccinea
 and its bioactive compound i.e., apigenin. 
Salvia coccinea
, the urban green, scarlet, lance‐shaped flower, is cultivated in warm climatic conditions from summer to autumn. The micronutrient‐dense (sodium, calcium, potassium, zinc, nitrogen, and copper) leaves can prevent micronutrient‐deficiency disorders among consumers. Furthermore, apigenin along with other bioactive constituents e.g., luteolin, flavonoids, and phenolic acids offer strong antioxidants, anticancer, anti‐inflammatory, antidiabetic, antimicrobial, and anti‐cardiovascular properties. The free radical scavenging potential of 
Salvia coccinea
 and apigenin is responsible for reduced oxidative stress and tumor cell metastasis modulated through PARP‐cleavage, caspase‐3, ERK, CDK‐1, JAK2/STAT3, Bax/Bcl‐2, AMPK, and Wnt/β‐catenin pathways. They attenuate inflammation‐induced disorders such as cardiovascular and neurological disorders via down‐regulating pro‐inflammatory cytokines (IL‐6, CRP, COX‐2, LPO, TGF‐β1, NF‐κB, and TNF‐α), and pathways (IRAK4, MAPK, JAK/STAT3, TLR4, and ERK). The antimicrobial properties against multiple bacterial, viral, and fungal strains make them effective candidates for alleviating microbial disorders. Furthermore, apigenin and 
Salvia coccinea
 promote hypoglycemic effect by attenuating α‐amylase activity, cholesterol levels, insulin resistance, DRP1 expression by improving GLUT4, GSK‐3β, AMPK/PI3K/Nrf2, and Akt pathways. Moreover, 
Salvia coccinea
 regulates wound healing after infection, injury, or surgery, in addition to improving agricultural productivity by reducing rodent attacks.

Salvia coccinea
 is rich in bioactive phytochemicals, notably the flavonoid apigenin, offering strong antioxidant, anti‐inflammatory, and antimicrobial effects. By modulating inflammatory and oxidative pathways, it shows potential for managing chronic diseases. This supports its use in developing novel pharmaceutical and nutraceutical applications.

## Linked entities

- **Genes:** PARP1 (poly(ADP-ribose) polymerase 1) [NCBI Gene 142], Casp3 (caspase 3) [NCBI Gene 12367], EPHB2 (EPH receptor B2) [NCBI Gene 2048], CDK1 (cyclin dependent kinase 1) [NCBI Gene 983], JAK2 (Janus kinase 2) [NCBI Gene 3717], STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774], BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581], BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596], PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1) [NCBI Gene 5562], IL6 (interleukin 6) [NCBI Gene 3569], CRP (C-reactive protein) [NCBI Gene 1401], COX2 (cytochrome c oxidase subunit II) [NCBI Gene 4513], LPO (lactoperoxidase) [NCBI Gene 4025], TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040], NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790], TNF (tumor necrosis factor) [NCBI Gene 7124], IRAK4 (interleukin 1 receptor associated kinase 4) [NCBI Gene 51135], MAPK (mitogen activated kinase-like protein) [NCBI Gene 7446652], TLR4 (toll like receptor 4) [NCBI Gene 7099], CRMP1 (collapsin response mediator protein 1) [NCBI Gene 1400], SLC2A4 (solute carrier family 2 member 4) [NCBI Gene 6517], GSK3B (glycogen synthase kinase 3 beta) [NCBI Gene 2932], PIK3CA (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) [NCBI Gene 5290], GABPA (GA binding protein transcription factor subunit alpha) [NCBI Gene 2551], AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207]
- **Chemicals:** apigenin (PubChem CID 5280443), luteolin (PubChem CID 5280445)
- **Species:** Salvia coccinea (taxon 260612)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, SLC2A4 (solute carrier family 2 member 4) [NCBI Gene 6517] {aka GLUT4}, GSK3B (glycogen synthase kinase 3 beta) [NCBI Gene 2932], JAK2 (Janus kinase 2) [NCBI Gene 3717] {aka JTK10}, CDK1 (cyclin dependent kinase 1) [NCBI Gene 983] {aka CDC2, CDC28A, P34CDC2}, COX2 (cytochrome c oxidase subunit II) [NCBI Gene 4513] {aka COII, MTCO2}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}, BAX (BCL2 associated X, apoptosis regulator) [NCBI Gene 581] {aka BCL2L4}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, COL11A2 (collagen type XI alpha 2 chain) [NCBI Gene 1302] {aka DFNA13, DFNB53, FBCG2, HKE5, OSMEDA, OSMEDB}, CRMP1 (collapsin response mediator protein 1) [NCBI Gene 1400] {aka CRMP-1, DPYSL1, DRP-1, DRP1, ULIP-3}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, PRKAA1 (protein kinase AMP-activated catalytic subunit alpha 1) [NCBI Gene 5562] {aka AMPK, AMPK alpha 1, AMPKa1}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}, IRAK4 (interleukin 1 receptor associated kinase 4) [NCBI Gene 51135] {aka IMD67, IPD1, IRAK-4, NY-REN-64, REN64}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, CTNNB1 (catenin beta 1) [NCBI Gene 1499] {aka CTNNB, EVR7, MRD19, NEDSDV, armadillo}, CASP3 (caspase 3) [NCBI Gene 836] {aka CPP32, CPP32B, SCA-1}
- **Diseases:** fungal (MESH:D009181), inflammation (MESH:D007249), metastasis (MESH:D009362), insulin resistance (MESH:D007333), cardiovascular and neurological disorders (MESH:D002318), tumor (MESH:D009369), microbial disorders (MESH:D015163), micronutrient-deficiency disorders (MESH:D030342), infection (MESH:D007239)
- **Chemicals:** flavonoids (MESH:D005419), cholesterol (MESH:D002784), LPO (MESH:D008054), potassium (MESH:D011188), copper (MESH:D003300), phenolic acids (MESH:C017616), sodium (MESH:D012964), luteolin (MESH:D047311), zinc (MESH:D015032), calcium (MESH:D002118), nitrogen (MESH:D009584), Apigenin (MESH:D047310)
- **Species:** Homo sapiens (human, species) [taxon 9606], Salvia coccinea (blood sage, species) [taxon 260612], Rodentia (rodent, order) [taxon 9989]

## Full text

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## Figures

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## References

194 references — full list in the complete paper: https://tomesphere.com/paper/PMC12865503/full.md

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Source: https://tomesphere.com/paper/PMC12865503