International Journal of Nutrition

International Journal of Nutrition

International Journal of Nutrition

Current Issue Volume No: 6 Issue No: 4

Research Article Open Access Available online freely Peer Reviewed Citation

Rosemary (Salvia rosmarinus): Health-Promoting Benefits and Food Preservative Properties

Jacob P. Veenstra 1,   Jeremy J. Johnson 1  

1University of Illinois at Chicago, College of Pharmacy, Department of Pharmacy Practice.

Abstract

Natural food preservatives in the form of herb extracts and spices are increasing in popularity due to their potential to replace synthetic compounds traditionally used as food preservatives. Rosemary (Salvia rosmarinus) is an herb that has been traditionally used as an anti-inflammatory and analgesic agent, and currently is being studied for anti-cancer and hepatoprotective properties. Rosemary also has been reported to be an effective food preservative due to its high anti-oxidant and anti-microbial activities. These properties allow rosemary prevent microbial growth while decreasing food spoilage through oxidation. Rosemary contains several classes of compounds, including diterpenes, polyphenols, and flavonoids, which can differ between extracts depending on the extraction method. In particular, the diterpenes carnosol and carnosic acid are two of the most abundant phytochemicals found in rosemary, and these compounds contribute up to 90% of the anti-oxidant potential of the herb. Additionally, several in vivo studies have shown that rosemary administration has a positive impact on gastrointestinal (GI) health through decreased oxidative stress and inflammation in the GI tract. The objective of this review is to highlight the food preservative potential of rosemary and detail several studies that investigate rosemary to improve in vivo GI health.

Author Contributions
Received 17 Jun 2021; Accepted 21 Jun 2021; Published 24 Jun 2021;

Academic Editor: Godwin Ajayi, Prof. Dr. med. G. O. Ajayi Prenatal Diagnosis and Therapy Centre College of Medicine, University of Lagos, Nigeria.

Checked for plagiarism: Yes

Review by: Single-blind

Copyright ©  2021 Jacob P. Veenstra, et al.

License
Creative Commons License     This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Competing interests

The authors have declared that no competing interests exist.

Citation:

Jacob P. Veenstra, Jeremy J. Johnson (2021) Rosemary (Salvia rosmarinus): Health-Promoting Benefits and Food Preservative Properties. International Journal of Nutrition - 6(4):1-10. https://doi.org/10.14302/issn.2379-7835.ijn-21-3874

Download as RIS, BibTeX, Text (Include abstract )

DOI 10.14302/issn.2379-7835.ijn-21-3874

Introduction

Rosemary (Salvia rosmarinus; formerly referred as Rosmarinus officinalis Linn) is an aromatic plant native to the Mediterranean region known to be rich in a variety of phytochemicals with anti-oxidant and anti-inflammatory properties. This perennial plant possesses a shrub shape reaching up to two meters high with a characteristic fragrance with uses including a spice for cooking, a medicinal plant, and a food preservative. 1 The health promoting properties of rosemary include hepatoprotective properties, therapeutic potential for Alzheimer’s, and anti-cancer properties. 2, 3, 4, 5 Spain, and more specifically, the province of Murcia (Southeast Spain), is a major processor and importer of rosemary, and the development of the commercial market has allowed for the use of rosemary to expand to the rest of Europe and the United States.6

The development of rosemary extract (RE) can generate a variety of unique formulations rich in compounds including rosmarinic acid (RA), carnosol (CL), and carnosic acid (CA). As with any other extract, the solvent and extraction method that is used will determine the resulting phytochemical composition, thereby impacting the physical and chemical properties of the extract. In the case of rosemary, a water soluble extract, which is typically rich in RA, will be effective in a water or polar matrix, while an oil soluble extract rich in diterpenes will be of value in an non-polar matrix such as a lipid formulation.7 Due to the variability in phytochemical composition that occurs from each extraction, the characterization of the phytochemical content of different extracts and essential oils is critical to report.

A more recent application of RE has been food preservation due to the ability to prevent oxidation and microbial contamination. 8, 9, 10 This rationale has provided a consumer and industry interest in replacing or decreasing synthetic antioxidants in foods. The European Food Safety Authority (EFSA) has reviewed the safety of RE for use as food additives, and the panel found that the No Observable Adverse Effects Level (NOAEL) of rosemary extracts in 90-day rat studies was 180-400 mg RE/kg/day, which equates to 20-60 mg/kg/day of CL plus CA.11 These values translate to mean intake estimates of 500-1500 mg/kg/day of CL and CA in human adults. The panel concluded through several toxicology studies that these margins do not pose any safety risks in humans. As a result, RE can be added to food and beverages at levels of up to 400 mg/kg (as the sum of CA and CL) in the European Union.

Due to the growing interest on the medicinal properties of Salvia rosmarinus, our objective is to present the role of RE as a food preservative with beneficial properties for gastrointestinal health. Therefore, this manuscript builds a literature gathering on rosemary to identify main bioactive compounds, extracts and essential oils and to characterize their application. The anti-oxidant and anti-microbial properties of various REs are described along with specific food preservation studies. Finally, in vivo studies that show the impact of REs on GI health are outlined with significant findings. The goal of this review is to highlight the potential of REs to be used as natural food preservatives and to provide the benefit of improved GI health.

Phytochemicals

The phytochemical content of RE can differ based on the method of extraction. Among the classes of compounds that RE contains include flavonoids, polyphenols, terpenoids, and volatile oils 12, 13, 14. Table III details the phytochemical content in rosemary and reports the most abundant phytochemicals found therein, and Figure 1 shows the structures of phytochemicals commonly associated with rosemary. Table 1, Table 2.

Figure 1.Phytochemicals from RE and REO reported in the literature.
Phytochemicals from RE and REO reported in the literature.

Table 1. List of publications detailing rosemary extracts and most abundant phytochemicals detected
Extraction method Major phytochemicals Citation
Essential oil 1,8-cineole (43.77% mass/total oil content) 29
Camphor (12.53%)
α-pinene (11.51%)
β-pinene (8.16%)
β-caryophyllene (3.93%)
Essential oil α-pinene (39.8% total oil composition) 30
1,8-cineole (18.3%)
Para-cymene-9-ol (7.7%)
Camphor (7.4%)
Camphene (6.6%)
Methanol Rosmarinic acid (8% mass/dry weight) 31
Carnosic acid (6%)
Acetonitrile + 2% formic acid Carnosic acid (121.08 mg/mL) 32
Carnosol (28.89 mg/mL)
Verbenone (77.59 μg/g)
α-thujene (76.26 μg/g)
Bornyl acetate (54.02 μg/g)
Supercritical fluid Carnosic acid (8.30% dry weight) 33
Micromeric acid (4.70%)
Betulinic acid (3.80%)
Ursolic acid (2.15%)
Carnosol (1.00%)
Ethanol (70%) Diacetone alcohol (72.80 mg/g dry weight) 34
Rosmarinic acid (50.43 mg/g)
Butyraldehyde semicarbazone (4.63 mg/g)
6-Iodo-2-methylquinazolin-4(3H)-one (3.60 mg/g)
Borneol (2.31 mg/g)
Methanol (70%) Rosmarinic acid (60.89 mg/g dry weight) 34
Diacetone alcohol (54.58 mg/g)
Propyl-propanedioic acid (14.45 mg/g)
2,1,3-benzothiadiazole (5.48 mg/g)
6-Iodo-2-methylquinazolin-4(3H)-one (4.93 mg/g)
Hydroalcoholic (65% ethanol) Rosmarinic acid (398.1 μg/mL) 28
Luteolin (199.5 μg/mL)
Caffeic acid (114.4 μg/mL)
Carnosol (80.1 μg/mL)
Apigenin (39.6 μg/mL)

Table 2. In vivo colitis models with rosemary extracts and essential oil
Model Experimental conditions Significant findings Citation
TNBS-induced colitis rats Animal strain: Wistar rats All treatments except 100 mg/kg RE and REO significantly reduced colonic damage scores, ulcer area, ulcer index, and width/length ratio 30
Study agent(s): Hydroalcoholic RE (100-400 mg/kg); REO (100-400 mg/kg)Groups (6 rats each): Intraperitoneal administration was superior in reducing crypt damage and total colitic index compared to oral gavage
Method: Colitis was induced by administration of 80 mg/kg TNBS. Treatments were given 6 hours after TNBS administration and daily for 5 consecutive days  
TNBS-induced colitis rats Animal strain: Wistar rats No significant colitis development was detected in any group 35
Study agent(s): REO (2 mmol/kg); thyme essential oil (2 mmol/kg); turmeric essential oil (2 mmol/kg); broccoli extract (2 mmol/kg) REO significantly increased expression of phase II-associated enzymes GSTK1, P1, T2, and the ARE-associated anti-oxidant enzyme GPx2
Method: Treatments were given for 14 consecutive days with DSS exposure beginning on day 7. Colitis was induced by 4% DSS exposure in drinking water REO decreased the mRNA level of IL-10
DSS-induced colitis mice Animal strain: Balb/C mice Both RE treatment groups reduced histological damage compared to DSS 36
Study agent(s): RE (50 and 100 mg/kg) Treatment of RE decreased the MPO activity and levels of TNF-α and IL-6
Method: Mice were fed RE in a 2% gum acacia matrix for 5 days before DSS exposure. Then, mice were fed RE for 5 additional days with DSS exposure (4%) RE reduced the nuclear translocation of Nf-κB protein, colonic levels of COX-2 and iNOS, and Nf-κB-DNA binding activity
DSS-induced colitis mice Animal strain: C57BL/6 Rosemary exract increased Sestrin-2 expression 37
Study agent(s): RE standardized to >40% carnosic acid (10 and 100 mg/kg) Rosemary extract prevented loss of intestinal barrier integrity
Method: Mice received RE by oral gavage for 3 days before DSS exposure. Then, mice were fed RE for 7 additional days with DSS exposure (3.5%) ZO-1 was significantly increased in mice receiving rosemary extract

The most studied and characterized phytochemicals in RE are CL, CA, and RA 15, 16, 17. The diterpenes CL and CA have been extensively studied for their anti-oxidant, anti-microbial, and anti-proliferative activities 11. In extracts, CL and CA are primarily found in oil-soluble (e.g. ethanol, methanol) RE fractions, and RA is the predominant phytochemical in the water-soluble (aqueous) RE fraction 1. Other phytochemicals that have been identified in RE are caffeic acid, luteolin, apigenin, camphor, and borneol. The total number of individual components in RE depends on the type of extraction and the source of the plant 1. For example, Cattaneo et al. identified 12 different compounds in a hydroalcoholic extract of Salvia rosmarinus by liquid chromatography-tandem mass spectrometry (LC-MS/MS), and Mena et al. identified 57 separate components by ultra-high performance liquid chromatography-electrospray ionization (UHPLES-MSn1. Hydro distillation of the rosemary leaves results in the REO, which contains primarily monoterpenes and sesquiterpenes and possesses anti-microbial and analgesic properties 11. The major individual components found in REO are 1,8-cineol, α-pinene, and camphor 11.

Applications of Rosemary as a Food Preservative

Anti-Oxidant Activity

The anti-oxidant properties of RE has been well established with a high degree of the anti-oxidant activity attributed to the phenolic compounds that rosemary possesses. Alizadeh et al. evaluated the anti-oxidant capacity of RE (24-26% total phenolic diterpenes, >16% CA) at 0.1%, 1.0%, and 10% (w/v) in methanol 18. The study found that RE scavenged free radicals in a concentration dependent manner, with 10% RE reducing 99% of free radical by the 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical-scavenging assay. The authors attributed the high anti-oxidant activity to the phenolic diterpenes contained in the extract. Nie et al. evaluated an ethanolic RE for anti-oxidant activity 18. The study identified 12 compounds from the extract, and each were tested against DPPH and OH free radicals. The main source of anti-oxidant activity in the RE was RA, achieving free radical scavenging rates of >80% for both assays. The extract was also tested by 2ʹ,7ʹ-dichlorofluorescin diacetate (DCFH-DA) assay in vitro using HeLa cells and was shown to greatly reduce the production of reactive oxygen species (ROS) generated by H2O2.

The REO, which contains more volatile phytochemicals than an extract, also possesses anti-oxidant activity. Rašković et al. determined the anti-oxidant capability of REO through the DPPH radical-scavenging assay and measured the total phenolic content (TPC) of the oil 11. Determining the TPC can be an indicator of the degree of anti-oxidant capacity of a sample because phenols are typically highly anti-oxidant. Sample analysis by GC-MS showed that REO contained mostly oxygenated monoterpenes (63.88%) and monoterpene hydrocarbons (31.22%), with the most abundant individual phytochemicals being 1,8-cineole (43.77%), camphor (12.53%), and α-pinene (11.51%). Analysis with DPPH assay revealed the IC50 (50% DPPH radical scavenged) to 77.6 µL/mL compared to 23.5 µg/mL by α-tocopherol. The TPC of REO was 153.35 mg GAE/L, suggesting that the abundance other compounds such as oxygenated monoterpenes also contributed to the high anti-oxidant activity. Bozin et al. also measured the anti-oxidant activity of REO (46.9% oxygenated monoterpenes, 46.7% monoterpene hydrocarbons) using DPPH and thiobarbituric acid reactive substance (TBARS) assays 11. The TBARS assay measures the formation of lipid peroxidation, which can be inhibited by anti-oxidant compounds. The IC50 of REO in the DPPH assay was 3.82 μL/mL, which was lower than the positive control butylated hydroxytoluene (BHT) (5.67 μL/mL). Two peroxide-generating systems were used for the TBARS assay, Fe2+/ascorbate and Fe2+/H2O2. In the Fe2+/ascorbate system, REO at 10% inhibited 75.79% of peroxide formation, compared to 37.04% with BHT. In the Fe2+/ H2O2 system, REO at 10% only inhibited 58.33% of peroxide formation, while BHT inhibited 66.67% of peroxide formation. The discrepancy between the two systems may result from REO possessing a mode of action that favors inhibition of peroxides generated by the Fe2+/ascorbate system over the Fe2+/H2O2.

Anti-Microbial Activity

Rosemary has been extensively studied for its anti-microbial activity against both Gram-negative and Gram-positive bacteria. Oliveira et al. investigated the anti-microbial activity of RE (200 mg/mL in propylene glycol) against C. albicans, S. aureus, E. faecalis, S. mutans, and P. aeruginosa in planktonic cultures and against biofilm formation 18. RE showed the strongest activity against C. albicans with a MIC and a minimum microbicidal concentration (MMC) of 0.78 mg/mL and 3.13 mg/mL, respectively. Additionally, RE showed strong activity against P. aeruginosa with both an MIC and MMC of 6.25 mg/mL. S. aureus, S. mutans, and E. faecalis growths were inhibited at >25 mg/mL, but a microbicidal concentration was not reached. The study also revealed that RE was effective against biofilm formation of C. albicans, P. aeruginosa, S. aureus, and S. mutans. In poly-microbial films, C. albicans was cultured with the other four bacteria for 48 hours in this study and treated with 200 mg/mL RE for 5 minutes. The most significant reduction in microbial growth with RE occurred in C. albicans plus E. faecalis and C. albicans plus P. aeruginosa (P ≤ 0.0001).

Methanol and ethanol RE were also evaluated against eight different bacterial strains grown on agar, including E. coli, S. aureus, P. aeruginosa, B. cereus, E. faecalis, C. albicans, V. fluvialis, and V. damsel1. The methanol extract showed a higher degree of inhibition against bacterial growth compared to the ethanol extract. The authors noted that the presence of CA in the methanol extract was likely the reason for the increased anti-microbial activity. In fact, several studies have associated the concentration of CA in RE with its effectiveness against microbial growth 19, 20, 21.

In a separate study, REO was evaluated against 60 clinical samples of multi-drug resistant E. coli 22. The chemical composition of REO was determined by GC-MS, and the major phytochemicals were 1,8-cineole (46.4%), camphor (11.4%), and α-pinene (11.0%). The MIC of REO against the clinical samples ranged from 18.0 to 20.0 µL/mL, although these values were less effective than basil essential oil tested in the same study (8.0 to 11.5 µL/mL). Jardak et al. also evaluated the anti-microbial effects of REO against S. aureus and S. epidermidis by microdilution method 7. The REO had a greater effect against S. epidermidis with an MIC of 0.312-0.625 µL/mL and MMC of 2.5 µL/mL versus an MIC and MMC of 1.25-2.5 µL/mL and 5 µL/mL, respectively, for S. aureus.

Food Preservation

Rosemary has been studied extensively for a variety of biological properties including anti-oxidant and anti-microbial activities 23. These properties make rosemary of particular interest as a natural food preservative2 24. The EU approved RE as a food preservative after extensive toxicity studies and determining that the o observed adverse effect level (NOAEL) range was wide enough to not pose any safety concerns 1. Published reports have suggested that up to 90% of the anti-oxidant capacity of RE can be attributed to the CL and CA content 18, 22. Therefore, RE used in food preservation is most often defined by the CL and CA content to ensure consistent potency and safety. Additionally, the significant anti-microbial activity of RE and REO further enables food preservation through inhibition of bacterial or mold growth on food products 11.

Several food matrix models have also been used to evaluate the ability of RE and REO as a food preservative. In fattening lambs with diets supplemented with RE through the animal feed, packaged meat showed a greater degree of protection from oxidation and microbial growth with RE supplementation 7. Additionally, shelf life and sensory qualities such as odor and color were improved in lamb given RE, and these factors were improved with higher CL intake 18. Addition of RE to pork patties packaged in modified-atmosphere packaging (MAP) protected against protein and lipid oxidation greater than BHT, a common synthetic preservative 18. Addition of REO at 0.2% in combination with MAP had a positive effect in sensory qualities and decreased lipid oxidation in poultry fillets, although no significant effects on microbial growth were detected 11. Addition of RE at 2.0% (v/v) to edible gelatin coating significantly inhibited growth of Listeria monocytogenes inoculated on raw beef for 48 hours 1. Altogether, these studies show the potential for RE as a natural alternative to synthetic food preservatives, although optimization of the extract needs to be done to achieve the maximum benefits of RE.

In vivo GI Health Benefits

In addition to being a natural food preservative, evidence suggests that rosemary extract may improve gastrointestinal health. Inflammatory bowel disease (IBD) is one area in particular that RE administration has been evaluated 7. Due to its anti-oxidant and anti-inflammatory properties, RE has been hypothesized to prevent or treat IBD. To test this hypothesis, several in vivo models of acute colitis have been developed to study the underlying mechanisms of IBD and to test the efficacy of various compounds against the disease (Table IV). These models evaluate parameters such as pro-inflammatory cytokine expression, myeloperoxidase activity, colonic weight and length, and histological assessment of colonic sections and crypt formation to determine the effectiveness of treatment 25, 26, 27.

Rosemary has been evaluated in these in vivo models with positive results for preventing and treating colitis. In a study in rats given TNBS to induce colitis, RE and REO at doses above 100 mg/kg given 6 consecutive days were shown to reduce the weight per length ratio of the colon, which is increased in moderate to severe colitis 11. Treatments with RE and REO were also shown by histological analysis to significantly reduce inflammation, crypt damage, and total colonic index. This study attributed the majority of the effects of RE to RA due to its anti-oxidant properties and high lipid solubility. Analysis of REO by GC-MS revealed the most abundant component was α-pinene, which has significant anti-inflammatory activity through inhibition of nuclear factor kappa-light-chain-enhancer of activated B cells (Nf-κB) nuclear translocation 28.

In vitro, RE possesses anti-inflammatory properties that translate to being effective at treating in vivo colitis models. In RAW 264.7 macrophages stimulated with lipopolysaccharide (LPS) to induce inflammatory conditions, RE lowered expression levels of TNF-α, IL-6, and nitrite levels compared to LPS stimulation alone 4. The redox sensitive transcription factor Nf-κB nuclear translocation was also decreased, along with iNOS and COX-2 expression, when treated with 5 and 10 µg/mL RE. In mice induced with colitis by dextran sodium sulfate (DSS) administration, disease activity index, scored by stool consistency, body weight loss, and presence of blood in feces, improved with treatment of 50 and 100 mg/kg RE compared to DSS only. Mice given RE also had less apparent colonic damage and leukocyte infiltration. Analysis of intestinal proteins also revealed that mice treated with RE had lower expression of the inflammatory markers NF-kB, COX-2, and iNOS, similar to the in vitro results. The study also found that DSS treatment increased the expression of the mitogen-activated protein kinase (MAPK) proteins p38, ERK, and JNK. However, RE treatment was able to restore the expression of these proteins to control values. These results suggest the in vivo efficacy for RE to treat colitis through its anti-oxidant and anti-inflammatory function at doses that do not present toxicity risk.

Conclusion

This review summarizes food preservation properties and the health promoting properties to the gastrointestinal tract with rosemary extracts. Rosemary extracts and essential oils present promising methods of natural food preservation due to their bioactivities that prevent many types of food spoilage and microbial growth. Beyond food preservation, however, these herbs have also been shown to promote GI health. Studies performed in mice have shown positive effects of lowering GI inflammation and lessening the symptoms of DSS exposure. These studies suggest that health promoting properties specific to gastrointestinal health are an additional benefit to using rosemary extract as a natural food preservative.

Acknowledgements

Johnson JJ is supported by the National Institutes of Health (R37 CA227101)

References

  1. 1.A-Sereiti M R, Abu-Amer K M, Sen P. (1999) Pharmacology of rosemary (Rosmarinus officinalis Linn.) and its therapeutic potentials. , Indian J Exp Biol 37(2), 124-30.
  1. 2.Hegazy A M. (2018) Hypolipidemic and hepatoprotective activities of rosemary and thyme in gentamicin-treated rats. Hum Exp Toxicol. 37(4), 420-430.
  1. 3.Lipton S A.Therapeutic advantage of pro-electrophilic drugs to activate the Nrf2/ARE pathway in Alzheimer's disease models. , Cell Death Dis 7(12), 2499.
  1. 4.Borras-Linares I. (2015) A bioguided identification of the active compounds that contribute to the antiproliferative/cytotoxic effects of rosemary extract on colon cancer cells. , Food Chem Toxicol 80, 215-222.
  1. 5.Berrington D, Lall N. (2012) Anticancer Activity of Certain Herbs and Spices on the Cervical Epithelial Carcinoma (HeLa) Cell Line. Evid Based Complement Alternat Med. 564927.
  1. 6.Cuvelier M E, Richard H, Berset C. (1996) Antioxidative activity and phenolic composition of pilot-plant and commercial extracts of sage and rosemary. , J Amer Oil Chem Soc 73, 645.
  1. 7.Amar Y. (2017) . Antioxidant and Antiproliferative Properties of Rosmarinus officinalis L on U937 and CaCo-2 Cells. Iran J Pharm Res 16(1), 315-327.
  1. 8.Nieto G, Banon S, Garrido. (2012) Administration of distillate thyme leaves into the diet of Segurena ewes: effect on lamb meat quality. Animal. 6(12), 2048-56.
  1. 9.Nieto G. (2010) Dietary administration of ewe diets with a distillate from rosemary leaves (Rosmarinus officinalis L.): influence on lamb meat quality. Meat Sci. 84(1), 23-9.
  1. 10.Nieto G, Bañón S, Garrido. (2012) Incorporation of thyme leaves in the diet of pregnant and lactating ewes: Effect on the fatty acid profile of lamb. Small Ruminant Research.105(1-3):. 140-147.
  1. 11.Aguilar F. (2008) Use of Rosemary Extracts as a food additive - Scientific opinion of the panel on food additives, flavourings, processing aids and materials in contact with food. , The EFSA Journal 8(7), 1-29.
  1. 12.Hassani F V, Shirani K, Hosseinzadeh H. (2016) Rosemary (Rosmarinus officinalis) as a potential therapeutic plant in metabolic syndrome: a review. Naunyn Schmiedebergs Arch Pharmacol. 389(9), 931-49.
  1. 13.Moore J, Yousef M, Tsiani E. (2016) Anticancer Effects of Rosemary (Rosmarinus officinalis L.) Extract and Rosemary Extract Polyphenols. Nutrients. 8-11.
  1. 14.Raskovic A. (2015) Analgesic effects of rosemary essential oil and its interactions with codeine and paracetamol in mice. Eur Rev Med Pharmacol Sci. 19(1), 165-72.
  1. 15.Choi S H. (2019) Development and Validation of an Analytical Method for Carnosol, Carnosic Acid and Rosmarinic Acid in Food Matrices and Evaluation of the Antioxidant Activity of Rosemary Extract as a Food Additive. Antioxidants (Basel). 8-3.
  1. 16.Nakagawa S, Hillebrand G G, Nunez G. (2020) Rosmarinus officinalis L. (Rosemary) Extracts Containing Carnosic Acid and Carnosol are Potent Quorum Sensing Inhibitors of Staphylococcus aureus Virulence. Antibiotics (Basel). 9-4.
  1. 17.Rahbardar Ghasemzadeh, H. (2020) Therapeutic effects of rosemary (Rosmarinus officinalis L.) and its active constituents on nervous system disorders. Iran J Basic Med Sci. 23(9), 1100-1112.
  1. 18.Albalawi A. (2017) Protective effect of carnosic acid against acrylamide-induced toxicity in RPE cells. Food Chem Toxicol. 108(Pt B): 543-553.
  1. 19.Vázquez N M. (2016) Carnosic acid acts synergistically with gentamicin in killing methicillin-resistant Staphylococcus aureus clinical isolates. Phytomedicine. 23(12), 1337-1343.
  1. 20.Bernardes W A. (2010) Antimicrobial activity of rosmarinus officinalis against oral pathogens: relevance of carnosic acid and carnosol. Chem Biodivers. 7(7), 1835-40.
  1. 21.Klancnik A. (2009) In vitro antimicrobial and antioxidant activity of commercial rosemary extract formulations. J Food Prot. 72(8), 1744-52.
  1. 22.Aruoma O I. (1992) Antioxidant and pro-oxidant properties of active rosemary constituents: carnosol and carnosic acid. Xenobiotica. 22(2), 257-68.
  1. 23.Park J, Rho S J, Kim Y R. (2019) Enhancing antioxidant and antimicrobial activity of carnosic acid in rosemary (Rosmarinus officinalis L.) extract by complexation with cyclic glucans. Food Chem. 299-125119.
  1. 24.Ortuño J, Serrano R, Bañón S. (2017) Incorporating rosemary diterpenes in lamb diet to improve microbial quality of meat packed in different environments. Anim Sci J. 88(9), 1436-1445.
  1. 25.Sann H. (2013) Efficacy of drugs used in the treatment of IBD and combinations thereof in acute DSS-induced colitis in mice. Life Sci. 92(12), 708-18.
  1. 26.Singh V. (2019) Microbiota fermentation-NLRP3 axis shapes the impact of dietary fibres on intestinal inflammation. Gut. 68(10), 1801-1812.
  1. 27.Walldorf J. (2015) In-vivo monitoring of acute DSS-Colitis using Colonoscopy, high resolution Ultrasound and bench-top Magnetic Resonance Imaging in Mice. Eur Radiol. 25(10), 2984-91.
  1. 28.Cattaneo L. (2015) Anti-Proliferative Effect of Rosmarinus officinalis L. Extract on Human Melanoma A375 Cells. PLoS One. 10(7), 0132439.
  1. 29.Rašković A. (2014) Antioxidant activity of rosemary (Rosmarinus officinalis L.) essential oil and its hepatoprotective potential. , BMC Complement Altern Med 14, 225.
  1. 30.Minaiyan M. (2011) Effects of extract and essential oil of Rosmarinus officinalis L. on TNBS-induced colitis in rats. Res Pharm Sci. 6(1), 13-21.
  1. 31.Erkan N, Ayranci G, Ayranci E. (2008) Antioxidant activities of rosemary (Rosmarinus Officinalis L.) extract, blackseed (Nigella sativa L.) essential oil, carnosic acid, rosmarinic acid and sesamol. Food Chem. 110(1), 76-82.
  1. 32.Mena P. (2016) Phytochemical Profiling of Flavonoids, Phenolic Acids, Terpenoids, and Volatile Fraction of a Rosemary (Rosmarinus officinalis L.) Extract. Molecules. 21-11.
  1. 33.Borrás-Linares I. (2015) A bioguided identification of the active compounds that contribute to the antiproliferative/cytotoxic effects of rosemary extract on colon cancer cells. Food Chem Toxicol. 80, 215-222.
  1. 34.Kozłowska M. (2015) . , CHEMICAL COMPOSITION AND ANTIBACTERIAL ACTIVITY OF SOME MEDICINAL PLANTS FROM LAMIACEAE FAMILY. Acta Pol Pharm 72(4), 757-67.
  1. 35.Mueller K, Blum N M, Mueller A S. (2013) Examination of the Anti-Inflammatory, Antioxidant, and Xenobiotic-Inducing Potential of Broccoli Extract and Various Essential Oils during a Mild DSS-Induced Colitis in Rats. ISRN Gastroenterol 710856.
  1. 36.Medicherla K. (2016) Rosmarinus officinalis L. extract ameliorates intestinal inflammation through MAPKs/NF-κB signaling in a murine model of acute experimental colitis. Food Funct. 7(7), 3233-43.
  1. 37.Veenstra J. (2021) Pharmacokinetic Analysis of Carnosic Acid and Carnosol in Standardized Rosemary Extract and the Effect on the Disease Activity Index of DSS-Induced Colitis. Nutrients. 13-3.

Cited by (17)

  1. 1.Xue Yang, bin Ismail Abdul Jabbar, Lansing Meryl Grace, bin Mohd Hayati Mohd Firdaus, 2023, Novel green synthesis of zinc oxide nanoparticles using Salvia rosmarinus extract for treatment of human lung cancer, Open Chemistry, 21(1), 10.1515/chem-2023-0113
  1. 2.Letsiou Sophia, Pyrovolou Katerina, Konteles Spyros J., Trapali Maria, Krisilia Sophia, et al, 2024, Exploring the Antifungal Activity of Various Natural Extracts in a Sustainable Saccharomyces cerevisiae Model Using Cell Viability, Spot Assay, and Turbidometric Microbial Assays, Applied Sciences, 14(5), 1899, 10.3390/app14051899
  1. 3.Piecuch Małgorzata, Garbicz Jagoda, Waliczek Martyna, Malinowska-Borowska Jolanta, Rozentryt Piotr, 2022, I Am the 1 in 10—What Should I Eat? A Research Review of Nutrition in Endometriosis, Nutrients, 14(24), 5283, 10.3390/nu14245283
  1. 4.Kabubii Zelipha N., Mbaria James M., Mathiu Peter Mbaabu, Wanjohi John M., Nyaboga Evans N., 2024, Diet Supplementation with Rosemary (Rosmarinus officinalis L.) Leaf Powder Exhibits an Antidiabetic Property in Streptozotocin-Induced Diabetic Male Wistar Rats, Diabetology, 5(1), 12, 10.3390/diabetology5010002
  1. 5.Irakli Maria, Skendi Adriana, Bouloumpasi Elisavet, Christaki Stamatia, Biliaderis Costas G., et al, 2023, Sustainable Recovery of Phenolic Compounds from Distilled Rosemary By-Product Using Green Extraction Methods: Optimization, Comparison, and Antioxidant Activity, Molecules, 28(18), 6669, 10.3390/molecules28186669
  1. 6.Meziane Hanae, Zraibi Linda, Albusayr Reem, Bitari Abdelhamid, Oussaid Abdelouhad, et al, 2024, Rosmarinus officinalis Linn.: unveiling its multifaceted nature in nutrition, diverse applications, and advanced extraction methods, Journal of Umm Al-Qura University for Applied Sciences, (), 10.1007/s43994-024-00144-y
  1. 7.Bakri Marwah M., Alghonaim Mohammed Ibrahim, Alsalamah Sulaiman A., Yahya Reham Omar, Ismail Khatib Sayeed, et al, 2024, Impact of Moist Heat on Phytochemical Constituents, Anti-Helicobacter Pylori, Antioxidant, Anti-Diabetic, Hemolytic and Healing Properties of Rosemary Plant Extract in Vitro, Waste and Biomass Valorization, (), 10.1007/s12649-024-02490-8
  1. 8.Yang Jun, Goksen Gulden, Zhang Wanli, 2023, Rosemary essential oil: Chemical and biological properties, with emphasis on its delivery systems for food preservation, Food Control, 154(), 110003, 10.1016/j.foodcont.2023.110003
  1. 9.MOUFAKKIR Chaimae, KHARBACH Yassine, TANGHORT Mariam, DASSOULI Abdelilah, REMMAL Adnane, 2022, Antioxidant effect of natural rosemary on the oxidation of mid-oleic sunflower frying oil on chicken wings, Food Science and Technology, 42(), 10.1590/fst.70122
  1. 10.Cancemi Gabriella, Cicero Nicola, Allegra Alessandro, Gangemi Sebastiano, 2023, Effect of Diet and Oxidative Stress in the Pathogenesis of Lymphoproliferative Disorders, Antioxidants, 12(9), 1674, 10.3390/antiox12091674
  1. 11.Park Jae-Hyung, Leem Jaechan, Lee Sun-Jae, 2022, Protective Effects of Carnosol on Renal Interstitial Fibrosis in a Murine Model of Unilateral Ureteral Obstruction, Antioxidants, 11(12), 2341, 10.3390/antiox11122341
  1. 12.Khalil Maha A., El-Zaher Eman H.F. Abd, El-Salam Olaa Abd, Ali Sameh S., 2022, Exploring the therapeutic potential of acetonic plant extracts in the healing of skin wounds infected with multidrug resistant pathogens, Journal of Applied Biomedicine, 20(2), 45, 10.32725/jab.2022.006
  1. 13.Sahoo Maitreya Mohan, Perach Omer, Shachter Alona, Gonda Itay, Porwal Alok, et al, 2022, Spectral estimation of carnosic acid content in in vivo rosemary plants, Industrial Crops and Products, 187(), 115292, 10.1016/j.indcrop.2022.115292
  1. 14.Wei Kun, Louis Hitler, Emori Wilfred, Idante Precious S., Agwamba Ernest C., et al, 2022, Antispasmodic activity of carnosic acid extracted from rosmarinus officinalis: Isolation, spectroscopic characterization, DFT studies, and in silico molecular docking investigations, Journal of Molecular Structure, 1260(), 132795, 10.1016/j.molstruc.2022.132795
  1. 15.Kuć Aleksandra Joanna, Szymanek Wojciech Piotr, 2023, Nutrition in the prevention and management of endometriosis symptoms - a current literature review, Emergency Medical Service, 10(2), 113, 10.36740/EmeMS202302106
  1. 16.Khnissi Samia, Bomboi Giovanni, Khémiri Ikram, Salem Imen Ben, Dattena Maria, et al, 2023, Incorporation of fresh leaves of wormwood (Artemisia herba alba) and/or rosemary (Rosmarinus officinalis) in the diet of rams: Effect on testicular function, sexual behavior, and blood parameters, Food Science & Nutrition, 11(6), 3121, 10.1002/fsn3.3293
  1. 17.Guimarães Natalia S. S., Ramos Vyctória S., Prado-Souza Laura F. L., Lopes Rayssa M., Arini Gabriel S., et al, 2023, Rosemary (Rosmarinus officinalis L.) Glycolic Extract Protects Liver Mitochondria from Oxidative Damage and Prevents Acetaminophen-Induced Hepatotoxicity, Antioxidants, 12(3), 628, 10.3390/antiox12030628