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Chapter 11 Medicinal and aromatic plants with antioxidant properties 403
pounds, particularly ferulic acid and caffeic acid, as evidenced by the significant positive correlations found between total phenolic content and antioxidant potential [79]. Accord­ing to in vitro antioxidant tests, at a concentration of 0.5 mg/mL of Angelica essential oil (EO), the scavenging ability of 2,2-azino-bis-3-ethyl-benzothiazoline-6-sulfonic acid (ABTS) and 1,1-diphenyl-2picrylhydrazyl (DPPH) for free radicals approached 100%. Further­more, there was a concentration-dependent link between EO and the iron-reducing ca­pacity. These findings show that Angelica EO has a strong antioxidant activity [80].
Anise: Pimpinella anisum is an annual herb belonging to the Apiaceae family of parsleys that is grown primarily for its aniseed fruits, which have a flavor similar to licorice. Home lands are Egypt, the eastern Mediterranean, southern Europe, the Middle East, North Africa, and America. Anise seed is a popular flavoring for many kinds of alcoholic beverages and is used extensively to flavor food in many parts of the world. According to reports, anise contains larvicidal, ovicidal, carminative, relaxing, antiviral, and antioxi­dant qualities. Flavonoids, terpenes, and essential oils are among the several substances that are known to be present in aniseed extracts. Several antioxidant tests, such as reduc­ing power, free radical scavenging, superoxide anion radical scavenging, hydrogen perox­ide scavenging, and metal chelating activities, were used to assess the antioxidant quali­ties of aniseed extracts. In the linoleic acid system, water and ethanol extracts at 20.00 μg/ mL showed 99.1 and 77.5% inhibition of peroxidation, respectively, which was higher than the same dose of α-tocopherol (36.1%) [81]. The extract showed high antioxidant ac­tivity in another investigation using three methods: DPPH, ABTS, and iron-reducing power tests. With an IC
value of 17.92 g/mL by the DPPH method, aniseed extracts dem-
50
onstrated greater antioxidant activity than vitamin C as standard compound, which is considered to be caused by polyphenolic acids and flavonoids. Aniseed extract has en­couraging antioxidant activity because of its high phenolic and flavonoid content [82].
Basil: Ocimum basilicum, also called great basil, is an aromatic herb of the family Lam- iaceae. Although there are other types, the general name “basil” refers to the type com­monly called Genovese basil or sweet basil. This sturdy, fragrant annual plant is grown extensively across Europe. Digestive, antifungal, antibacterial, antimelanoma, antimi­crobial, radioprotective, anthelmintic, and antioxidant properties have been docu­mented for basil. Numerous investigations looked into the various biological activities of basil essential oils and extracts. The study by Nadeem et al. (2022) [83] found that ethanol extracts had the highest concentration of plant secondary metabolites, such as total phenolic acid, flavonoids, and tannin content. In the DPPH, FRAP, and H
2O2
tests, ethanol extracts likewise showed the best antioxidant activity. When compared to ex­tracts from other locations, it was also found that the examined basil extracts had higher phenolic content (82.45 mg pyrocatechol equivalents (PE)/g) and antioxidant ac­tivity, as measured by the DPPH assay (IC
1.29 mg/mL). Using LC-ESI-MS/MS analysis,
50
basil extracts were shown to be a prospective source of well-known medicinal and health-promoting substances such as umbelliferone, ellagic acid, rosmarinic acid, cate-
404 Amra Alispahić et al.
chin, and liquiritigenin. According to the findings, basil is a powerful source of bioac­tive chemicals [83]. In another investigation, Minia basil extract demonstrated a high total phenolic content of 82.45 mg PE/g and radical scavenging activity with an IC
50
value of 1.29 mg/mL. Antioxidant activity and the total phenolic content of basil extracts were shown to be highly correlated. There was a wide range in the essential oils’ capac­ity to scavenge free radicals. Minia basil essential oil contained 41.3 mg PE/g of total phenolics and had strong DPPH radical scavenging activity, with an IC
of 11.23 mg/mL
50
[84]. Carbon dioxide was used to extract bioactive compounds from basil leaves in the study of Romano et al. [ with supercritical CO
85]. The most effective technique was found to be extraction
for two hours while utilizing 10% ethanol as a cosolvent. The ex-
2
tracts made using this method were tested for antioxidant activity, phenolic acid con­tent, and volatile organic compounds. The ABTS assay revealed high antiradical activity with bergamotene (11–14%), linalool (35–27%), and caffeic acid (1.69–1.92 mg/g) contents that were significantly higher than the control. Besides enabling the production of ex­tracts rich in bioactive compounds in an environmentally friendly way, supercritical CO2 also reduced the need for ethanol and other solvents [85].
Bay/bay leaf: Laurus nobilis, sweet bay tree, an evergreen plant belonging to the Laur- aceae family, is native to countries that border the Mediterranean. It can be used whole, dried, or fresh, in which case, it is taken out of the food before eating, or, less frequently, ground. Although the bay laurel (Laurus nobilis) is the most widely utilized source of bay leaves, they are used from a variety of species of this plant for their unique flavor and smell. The flavor and aroma of bay leaves are enhanced by the pres­ence of essential oils that contain methyl eugenol, terpenes, and eucalyptol. In addition to its unique function as an insect repellent, bay leaf has been shown to possess antifun­gal, antibacterial, hypolipidemic, gastroprotective, digestive, antimicrobial, and antioxi­dant qualities. Using various antioxidant assays, numerous studies have documented the chemical composition and antioxidant properties of Laurus nobilis leaves. Terpenes including a-terpinol, a-terpinyl acetate, thymol, caryophyllene, selinene, farnesene, and cadinene. Eugenol and methyl eugenol, vitamin E, and sterols, are also known to be abundant in laurel. Extracts from bay leaves demonstrated strong radical scavenging activity, with an IC oil is lower than that of extracts. With IC demonstrated a scavenging effect on the DPPH radical. With an IC
87], the leaf EO exhibited the highest antioxidant activity in the β-carotene/linoleic acid
[ system. The findings showed that
value of 1 mg/mL [86]. The antioxidant activity of bay leaf essential
50
values of 66.1 µg/mL, bay leaf essential oil
50
value of 35.6 µg/mL
50
L. nobilis EO has strong antioxidant activity, which
may be because of its high 1,8-cineole content [87].
Clove: Syzygium aromaticum is an evergreen tropical tree from family Myrtaceae. It is indigenous to Indonesia and is frequently used as a flavoring, spice, or aroma in commer­cial goods like soaps, toothpaste, and makeup. Its increased polyphenol content is re­ported to be closely associated with its very strong antioxidant action. Antifungal, anes­thetic, antiseptic, carminative, antispasmodic, antibacterial, antiviral, anti-inflammatory,
Chapter 11 Medicinal and aromatic plants with antioxidant properties 405
and antioxidant qualities have all been documented for cloves. Eugenol and eugenyl ace­tate, the main components of clove buds’ scent, exhibit antioxidant activity on par with that of natural antioxidants as α-tocopherol (vitamin E) [71]. The maximum antioxidant activity was demonstrated by TPC and TFC, which had contents of 247.61 and 141.70 mg/ 100 dry weight, respectively. Clove’s antioxidant capacity was assessed by its total phenol content, total flavonoid content, ferric reducing antioxidant power (FRAP), and 2,2­diphenyl-1-picrylhydrazyl (DPPH). The maximum antioxidant activity in this investigation was demonstrated by the FRAP and DPPH methods (437.29 mg TE/100 g dry weight and
87.50%, respectively) [88]. Total phenolic content, free radical DPPH scavenging activity, hydrogen peroxide scavenging, and reducing power test were used in other studies to measure antioxidant activity. With a higher absorbance value at the highest concentra­tion of methanolic extract (0.198 ± 0.001 A), ethanolic extract demonstrated the highest scavenging activity for free radicals (62.12%), followed by aqueous extract (48.32%). Addi­tionally, methanolic extract demonstrated the highest scavenging activity for hydrogen peroxide (76.99 ± 0.09) and less reducing power properties [89]. In a study by Alfikri et al. [90], clove EO’s antioxidant activity, which is highly significant economically, was exam­ined. At various flowering phases, the DPPH scavenging activity, expressed as IC
values,
50
varied from 15.80 to 108.85 µg/mL. The findings showed that the best essential oil constitu­ent and most effective source of natural antioxidants was clove during the flowering stage [90].
Hyssop: Hyssopus officinalis is a shrub from Lamiaceae family native to Southern Eu- rope, and the Middle East. It has been utilized in traditional herbal medicine because of its antibacterial, carminative, stimulant, stomachic, expectorant, cough-relieving, and antioxidant properties. In the study by Fathiazad et al. [91], according to a de­scription of the chemical composition of hyssop EO, the primary constituents were myrtenyl acetate, camphor, germacrene, and spathulenol. According to the same study, the total phenol content of the n-butanol and ethylacetate extracts of Hyssopus officinalis aerial parts were 246 mgGAE/g and 51 mgGAE/g, respectively. The DPPH rad­ical scavenging experiment was also used to assess the extracts’ antioxidant proper­ties, and the IC
values were 103 × 10
50
−3
and 25 × 10
−3
mg/mL, respectively. The largest concentration of phenolic components may have contributed to the best antioxidant activity of n-butanol extract [91]. The use of stirring, in conjunction with an ethanolic solvent, appears to be advantageous in optimizing the extraction of polyphenols from hyssop, leading to extracts with increased antioxidant activity, per the findings of Po­laki et al. [92]. The antioxidant activity was 582.23 ± 16.88 μmol ascorbic acid equiva­lents (AAE)/g using the FRAP method and 343.75 ± 15.61 μmol AAE/g dry weight using the DPPH method. The total polyphenol content was 70.65 ± 2.76 mgGAE/g dry weight. The therapeutic potential of hyssop extract was further highlighted by the discovery of a wide spectrum of polyphenolic chemicals, such as rutin, p-coumaric acid, and caf­feic acid, which are known for their medicinal and antioxidant properties [92]. Ac­cording to Moulodi et al. 2018., the main constituents of Hyssopus officinalis essential
406 Amra Alispahić et al.
oil were determined to be camphor (23.61%) and β-pinene (21.91%), with an IC
of
50
11.22 μg/mL and a total phenolic content of 23.16 mgGAE/g of essential oil. The findings showed that hyssop essential oil has good antioxidant activity and can be utilized as a natural antioxidant in the food and pharmaceutical industries [93].
Juniper/Juniperus: Juniperus communis is an evergreen perennial shrub belonging to the cypress family Cupressaceae. There are between 50 and 67 species of junipers in North America, Africa, parts of Asia, and Central America, depending on the taxonomy. Both alcoholic and nonalcoholic beverages contain juniper extracts and essential oils, which have been shown to have anti-inflammatory, carminative, diuretic, fungicide, anticholinesterase, antibacterial, and antioxidant properties. Using GC-MS analysis of juniper essential oils, the authors Ennajar et al. (2009) identified 30 compounds, the most prevalent of which were α-pinene, δ-3-carene, and γ-cadinene. The primary polyphenols found in methanol, ethanol, ethyl acetate, and dichloromethane juniper extract were tannins, flavonoids, and anthocyanins. As a result, the extract from methanol leaves had a high antioxidant activity (IC
value of 8.5 ± 0.3 mg/L), followed by the extract from
50
ethanolic leaves (49.1 ± 0.6 mg/L). The highest activity for the berries was found in the ethanol extract (54 ± 1 mg/L), which was followed by the methanolic (642 ± 7 and 664 ± 7 mg/L, respectively) and ethyl acetate extract. The DPPH assay of juniper essential oils of leaves and berries showed radical-scavenging activity, with IC
values of 5,364 ± 121
50
and 14,716 ± 411 mg/L, respectively. The high content of terpene hydrocarbons of essen­tial oils was responsible for this low reactivity [94]. In a study by Miceli et al. [95], the authors compared the biological potential and flavonoid composition of berry methanol extracts from two Turkish juniperus varieties. There were 59.17 mg GAE/g extract of total polyphenols. By the HPLC analysis, 16 flavonoids were separated, with hypolaetin­7-pentoside and quercetin-hexoside being the principal constituents. Using several tech­niques, the in vitro antioxidant activity was assessed; the DPPH method yielded an IC of 0.63 mg/mL, whereas the TBA test yielded an IC
of 4.44 μg/mL [95].
50
50
Mint: Mentha piperita, also called peppermint, is a hybrid species of mint, native to Eu- rope and the Middle East. Peppermint is the most widely used of the more than 25 species in the genus Mentha. It belongs to the Lamiaceae family of perennial herbaceous plants, Mentha. It was discovered that the two components of peppermint essential oil, methone and isomenthone, were the most powerful radical scavenging compounds. According to reports, mint has cytoprotective, hepatoprotective, antibacterial, antiviral, anti-inflamma tory, antiulcer, slightly anesthetic, antispasmodic, carminative, anthelmintic, and antioxi­dant properties. Polyphenols, flavonoids (such as luteolin and its derivative apigenin), fla­vanols (such as epicatechin and catechin), and coumarins (such as esculetin and scopoletin) are abundant in Mentha species. Mint essential oils are a primary emphasis in terms of formulations. Their primary constituents include alcohols, ketones, esters, ethers, and oxides, and they are either light yellow or greenish yellow in color. The primary com­ponents of essential oils made from various mint species are found to be menthol, men­thone, isomenthone, menthyl acetate, linalool, linalyl acetate, pulegone, carvone, piperite-
-
Chapter 11 Medicinal and aromatic plants with antioxidant properties 407
none oxide, and cis-piperitone epoxide. The researchers have effectively used a variety of in vitro antioxidant tests, including reducing power assays, ABTS suppression of linoleic acid peroxidation, and DPPH radical scavenging, to examine the antioxidant activity of mint. High concentrations of antioxidants, such as phenolic compounds, and vitamins that can postpone or prevent the oxidation of various molecules are found in many me dicinal plants, including those in the genus Mentha. According to the numerous investiga­tions on the antioxidant potential of Mentha species, M. longifolia was the most efficient of the nine species, exhibiting 88.6% antioxidant activity at a concentration of 100 µL/mL [96], which was higher than the 93.0% activity of ascorbic acid. Six Mentha species were found to have high antioxidant activity in an Algerian study, with the following findings for mint: Flavonoid content: 15.70 ± 0.10 mg RE/g DW, tannin content: 6.50 ± 0.41 mg CE/g DW, total phenolic content: 31.40 ± 0.80 mg GAE/g DW. The IC scavenging activity was 17.00 ± 0.88 μg/mL, while the IC
value for the b-carotene bleach-
50
value for DPPH radical
50
ing assay was 516.00 ± 0.25 μg/mL. The correlation coefficients between phenolic contents and antioxidant activity of the six Algerian mints suggested that mint antioxidant activity is mostly correlated to tannins and polyphenols and less to flavonoids [97].
Nigella: Nigella sativa, also known as black caraway black or cumin, is an annual flow- ering plant from the family Ranunculaceae. The plant is native to the Eastern Europe and Western Asia (Cyprus, Turkey, Iran, and Iraq). High antioxidant activity and a high correlation with the total phenolic content characterize this herbaceous, erect annual herb. Antipyretic, antidiabetic, analgesic, carminative, diuretic, antineoplastic, antibac terial, anti-inflammatory, stimulant, expectorant, and anthelmintic qualities have all been recorded for nigella. Results of an analysis of the phenolic content and antioxidant activity of extracts made from Nigella seeds using Soxhlet and ultrasonic extraction pro cedures were reported in the work of Goga et al. [98]. According to the Folin-Ciocalteu tmethod, the total phenolic content ranged from 11.867 ± 0.338 to 31.148 ± 0.293 mgGAE/g. This ranged from 2.70 ± 0.22 × 10
−5
to 32.7 ± 1.31 × 10
−5
mgQE/g (quercetin equivalent) for total flavone and flavanol content. The DPPH and ABTS tests were used to assess the samples’ radical scavenging activity. Samples varied from 3.01 ± 0.03 mg/mL to 12.04 ±
0.60 mg/mL in their capacity to reduce stable DPPH radicals, and in their ability to re­duce stable ABTS radicals from 14.02 ± 0.62 mg/mL to 18.67 ± 1.54 mg/mL [98]. A wide range of bioactive components, such as flavonoids, phenols, steroids, triterpenoids, pro­teins, alkaloids, tannin, sesquiterpenoid hydrocarbons, monoterpenoid alcohol, and monoterpenoid ketone, were discovered during the analysis of the nigella essential oil, which was isolated as a pale-yellow liquid. Nigella EO’s total flavonoid and phenolic content were measured at 442.25 μg QE/g and 641.23 μg GAE/g, respectively. At 1,000 µg/ mL, nigella EO exhibited the highest percentage of inhibition (65.80%) when compared to the standard ascorbic acid (73.57%) [99]. In a different study, the antioxidant activity of nigella EO was examined using TLC screening techniques, which revealed that thy­moquinone and its constituents carvacrol, t-anethole, and 4-terpineol demonstrated re­spectable radical scavenging properties. When examined for nonspecific hydrogen
-
-
-
408 Amra Alispahić et al.
atom or electron donating activity using the DPPH assay, these four components and the essential oil showed varied antioxidant activity. Additionally, they were efficient OH radical scavengers in the deoxyribose degradation assay and the nonenzymatic lipid peroxidation in liposomes experiment [100].
Oregano: Origanum vulgare is a species of flowering plant from the Lamiaceae family. It is native to the Mediterranean region. The woody perennial oregano plant has white, pink, or light purple flowers. While its close relative Origanum majorana is known as sweet majoran, it is sometimes referred to as wild marjoram. A variety of biological prop­erties, including carminative, antibacterial, antifungal, antiviral, anticancer, anti-inflam­matory, hepatoprotective, and antioxidant, have been reported for oregano. The extracts’ levels of sixteen bioactive phenolic compounds, total phenolic and total flavonoid content, and antioxidant activities (DPPH and FRAP tests) were all examined. With concentrations varying by subspecies, HPLC analyses revealed that rosmarinic acid (659.6–1646.9 mg/ 100 g dry weight (DW)) was by far the most prevalent constituent. It was followed by luteolin (46.5–345.4 mg/100 g DW), chicoric acid (36.3–212.5 mg/100 g DW), coumarin (65.7–
193.9 mg/100 g DW), and quercetin (10.6–106.1 mg/100 g DW). Rosmarinic acid and antioxi­dant activity were shown to be significantly and favorably correlated (r = 0.46) [101]. Ac­cording to Teixeira et al. [102], GC/MS research revealed that oregano essential oil in­cludes phenolic chemicals and monoterpene hydrocarbons. Carvacrol, fenchyl alcohol, p­cymene, thymol, and terpinene were the main constituents. According to the reducing power analysis, the hot water extract had the highest antioxidant activity, followed by the ethanolic, cold water, and essential oil extracts. The same pattern of declining power analysis was observed in the DPPH free radical scavenging activity. While ethanolic ex­tract (antioxidant activity index, AAI = 1.23), hot water extract (AAI = 3.16), and cold water extract (AAI = 0.55) were categorized as moderate, strong, and very strong antioxidants, respectively, oregano essential oil (AAI = 0.05) showed weak antioxidant activity. The au­thors came to the conclusion that Portuguese-origin oregano extracts and essential oils are excellent options to substitute industrially used synthetic compounds [102].
Rosemary: Salvia rosmarinus is a shrub with fragrant, evergreen, needle-like leaves and white, pink, purple, or bluish flowers. It is an aromatic plant from the Lamiaceae family, native to the Mediterranean region, but cultivated worldwide. Antimicrobial, antifungal, antiviral, antimicrobial, antiparasitic, antiproliferative, spasmolytic, anti­inflammatory, mildly analgesic, and antioxidant properties have all been docu mented. Among the most potent antioxidant components of rosemary are the cyclic diterpene diphenols, carnosolic acid, and carnosol, which are typically found in ex­tracts. The polyphenolic profile of this plant is characterized by the presence of carno­sic acid, carnosol, rosmarinic acid, and hesperidin as major components. According to reports, the primary constituents of rosemary essential oils are camphor, 1,8-cineole, α-pinene, p-cymene, and borneol [56]. The antioxidant properties of various solvent extracts and rosemary essential oil were assessed in the study of Al-Jaafreh 2024. The ethanol extract had the highest TPC 72.34 GAE mg/g and TFC 26.81 RE mg/g. Methanol
-
Figure 11.6: Flowering sage from Mostar, Bosnia and Herzegovina.
Chapter 11 Medicinal and aromatic plants with antioxidant properties 409
extract demonstrated the strongest antioxidant activity in the NO radical scavenging assay (86.68 RE mg/g) and DPPH (138.3 GAE mg/g) assays, while the aqueous extract demonstrated the maximum activity in ABTS (125.33 TE mg/g). The authors observed a strong correlation between antioxidant activity and TPC, TFC, and TTC. They came to the conclusion that this is because most bioactive compounds, including flavonoids, polyphenols, and tannins, are found in more polar solvents, making these phytochem icals the primary source of the antioxidant properties [103].
-
Sage: Salvia officinalis
(Figure 11.6), or common sage, is small evergreen subshrub used as an aromatic and culinary herb. Sage is a member of the Lamiaceae family and native to the Mediterranean region. Sage has been reported to have antiseptic, antimicrobial, anti cancer, antiproliferative, antidiabetic, anti-inflammatory, hypolipidemic, memory­enhancing effects, and antioxidant properties. Studies on
Salvia officinalis have demon­strated that certain phenolic antioxidants stop oxidative stress-induced cell death. Re­search has indicated that Salvia taxa have a large number of phenolic and flavonoid com­pounds. Extracts from the aerial parts of sage were shown to include a variety of phenolics, such as caffeic acid and chlorogenic acid, as well as flavonoids, such as apige nin and luteolin [7]. Three species of Salvia were compared by Pereira et al. [104]. The health benefits of their decoctions, specifically their antioxidant activity, were studied. The abundance of caffeic acid and its derivatives was closely associated with the sage decoctions’ greater activity [104]. Yu et al. [105] reported on sage methanolic extracts’ total phenols content of 50.89 ± 0.37 mgGAE/g DW, flavonoids of 43.92 ± 0.05 mgCATE/g
-
-
410 Amra Alispahić et al.
DW, tannins of 28.02 ± 1.40 mg ECE/g DW, ABTS 0.27 ± 0.01 mM Trolox/g DW, and DPPH
0.25 ± 0.00 mM Trolox/g DW [105].
Thyme: Thymus vulgaris, common or garden thyme is a species of flowering plant in the Lamiaceae family, native to southern Europe from the western Mediterranean to southern Italy. It is a perennial herbaceous shrub that bears clusters of purple or pink flowers in early summer along with tiny, very fragrant leaves. The plant’s phenolic and flavonoid levels are linked to its potent antioxidant properties. Antibacterial, anti­microbial, antifungal, anti-inflammatory, expectorant, and spasmolytic qualities have all been documented for thyme. Several volatile chemicals were detected by GC-MS analysis, with thymol, carvacrol, geraniol, and p-cymene being the main constituents. Caffeic acid, quinic acid, p-coumaric acid, quercetin-7-o-glucoside, ferulic acid, carno­sic acid, cinnamic acid, rosmarenic acid, apigenin, and naringenin were all detected in the methanolic extract by HPLC analysis. T. vulgaris had the highest levels of flavo­noids and phenols (62.40 ± 0.03 mg TAE/g DW and 8.55 mg QE/g DW, respectively). Using the 1,1-diphenyl-2-picrylhydrazyl (DPPH) and reducing power test, the antioxi­dant activities of the samples were assessed, and the IC
value was 289.3 μg/mL. The
50
authors suggest that thyme is a good source of essential oil and flavonoids, which have a high level of antioxidant activity [
106]. The total phenolic and flavonoid con­tent of thyme extracts was ascertained in the Mokhtari et al. 2023 [107] study. The findings revealed a total flavonoid content of 3.87 mg QE/g DW and a total phenolic content of 8.89 mg GAE/g DW. When plant extracts were compared for their ability to scavenge DPPH radicals, thyme had an IC
value of 69.39 μg/mL [107].
50

11.8 Conclusion

The era of herbal medicine is evident in both contemporary society and the scientific community. Numerous studies have demonstrated the biological benefits of MAPs, in­cluding their anti-inflammatory, antioxidant, immune-boosting, and antiaging proper­ties, which guarantee longer and healthier life for humans. Presenting MAPs’ scien­tific side requires analyzing their composition, medical uses, toxicity, physiological impacts, and converting their active ingredients into a useful product. Because they tend to enhance health and natural disease prevention, MAPs with high antioxidant content are highly sought after by consumers due to their greater safety and depend­ability. In addition to being well-known for their flavor and taste, these plants have paved the way for a new area of study where their antioxidant qualities help preserve food and improve health for customers, who are awaiting hard scientific evidence to support their interest in herbal therapy. Their natural antioxidants may provide an alternative to traditional treatments for oxidative stress, and these plant compounds have significant therapeutic effects with few side effects. They may also be good can­didates for preventing free radical-induced diseases like diabetes, cancer, aging, and
Chapter 11 Medicinal and aromatic plants with antioxidant properties 411
cardiovascular diseases. To further valorize MAPs, it would be crucial to increase the variety of parameters in research as well as the isolation, characterization, and identi­fication of active chemical compounds.

References

[1] Bakkali, F., Averbeck, S., Averbeck, D. and Idaomar, M. (2008). Biological effects of essential oils – A
review. Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research Association, 46, 446–475.
[2] Buchbauer, G. (2010). Biological activities of essential oils. In: Khc, B. & Buchbauer, G. (eds)
Handbook of Essential Oils: Science, Technology, and Applications, CRC Press, Taylor & Francis Group, Boca Raton, 1128.
[3] Karamaya, K. and Coşge Şenkal, B. (2022). The antioxidant capacities of leaf extracts from Salvia
viridis L. Current Perspectives on Medicinal and Aromatic Plants, 5(2), 127–135.
[4] Mammadov, R. (2014). Tohumlu Bitkilerde Sekonder Metabolitler, Nobel Akademik Yayıncılık,
Ankara, 15–129.
[5] Halliwell, B. and Gutteridge, J. M. C. (1990). A Role of free radicals and catalytic metal ions in human
disease: An overview. Methods Enzymology, 186, 1–85.
[6] Kahkönen, M. P., Hopia, A. I., Vuorela, H. J., Rauha, J. P., Pihlaja, K., Kujala, T. S. and Heinonen,
M. (1999). Antioxidant activity of plant extracts containing phenolic compounds. Journal of Agricultural and Food Chemistry, 47, 3954–3962.
[7] Rungsimakan, S. and Rowan, M. G. (2014). Terpenoids, flavonoids and caffeic acid derivatives from
Salvia viridis L. var. blue jeans. Phytochemistry, 108, 177–188.
[8] Bendini, A., Cerretani, L., Pizzolante, L., Gallina-Toschi, T., Guzzo, F., Cedolo, F., Andereetta, F. and
Levi, M. (2006). Phenol content related to antioxidant and antimicrobial activity of Passiflora spp. extracts. European Food Research & Technology, 223, 102–109.
[9] Baydar, H. (2013). Tıbbi Ve Aromatik Bitkiler Bilimi Ve Teknolojisi, Süleyman Demirel University
Faculty of Agriculture Publication, Isparta, 23–141.
[10] Aqil, F., Ahmad, I. and Mehmood, Z. (2006). Antioxidant and free radical scavenging properties of
twelve traditionally used Indian medicinal plants. Turkish Journal of Biology, 30, 77–183.
[11] Oraon, L., Jana, A., Prajapati, P. S. and Suvera, P. (2017). Application of medicinal and aromatic
plants in functional dairy products – A review. Journal of Dairy, Veterinary & Animal Research, 5(3), 109–115.
[12] Viuda-Martos, M., Ruiz-Navajas, Y., Fernández-López, J. and Pérez-Álvarez, J. A. (2010). Spices as
functional foods. Critical Reviews in Food Science and Nutrition, 51(1), 13–28. [13] Sies, H. (2020). Oxidative stress: Concept and some practical aspects. Antioxidants, 9(9), 852. [14] Rodrigo, R. (2009). Oxidative Stress and Antioxidants: Their Role in Human Disease. Nova
biomedical books, New York. [15] Čvorišćec, D. and Štrausova, Č. I. (2009). Medicinska Biokemija, Medicinska naklada, Zagreb,
Croatia. [16] Sun, W. and Shahrajabian, M. H. (2023). Therapeutic potential of phenolic compounds in medicinal
plants-natural health products for human health. Molecules, 28(4), 1845. [17] Kumpulainen, J. T. and Solonen, J. T. (1999). Natural Antioxidants and Anticarcinogens in Nutrition,
Health and Disease, The Royal Society of Chemistry, Thomas Graham House, Science Park, Milton
Road, Cambridge CB4 OW, UK. [18] Cook, N.C. and Samman, S. (1996). Flavonoids-Chemistry, Metabolism, Cardioprotective Effects, and
Dietary Sources. The Journal of Nutritional Biochemistry, 7, 66–76.
412 Amra Alispahić et al.
[19] Zampelas, A. and Micha, R. (2015). Antioxidants in Health and Disease, CRC Press Taylor & Francis
Group, Boca Raton, USA. [20] Charles, D. J. (2013). Antioxidant Properties of Spices, Herbs and Other Sources. Springer, New York. [21] Fujii, J., Soma, Y. and Matsuda, Y. (2023). Biological action of singlet molecular oxygen from the
standpoint of cell signaling, injury and death. Molecules, 28(10), 4085. [22] Kahkeshani, N., Farzaei, F., Fotouhi, M., Alavi, S. S., Bahramsoltani, R., Naseri, R., Momtaz, S.,
Abbasabadi, Z., Rahimi, R., Farzaei, M. H. and Bishayee, A. (2019). Pharmacological effects of gallic
acid in health and diseases: A mechanistic review. Iranian Journal of Basic Medical Sciences, 22(3),
225–237. [23] Dvoršak, K. (2013). Magistrska Naloga: Superoksid Dismutazna Aktivnost Stabilnih Nitroksidnih
Radikalov. Univerza v Ljubljani. Fakulteta za farmacijo, Ljubljana. [24] Ayala, A., Muñoz, M. F. and Argüelles, S. (2014). Lipid peroxidation: Production, metabolism, and
signaling mechanisms of malondialdehyde and 4-hydroxy-2-nonenal. Oxidative Medicine and
Cellular Longevity, 2014, 360438. [25] Salekeen, R., Haider, A. N., Akhter, F., Billah, M. M., Islam, M. E. and Didarul Islam, K. M. (2022).
Lipid oxidation in pathophysiology of atherosclerosis: Current understanding and therapeutic
strategies. Nternational Journal of Cardiology. Cardiovascular Risk and Prevention, 14, 200143. [26] Cai, Z. and Yan, L. J. (2013). Protein oxidative modifications: beneficial roles in disease and health.
Journal of Biochemical and Pharmacological Research, 1(1), 15–26. [27] Xu, Z., Huang, J., Gao, M., Guo, G., Zeng, S., Chen, X., Wang, X., Gong, Z. and Yan, Y. (2021). Current
perspectives on the clinical implications of oxidative RNA damage in aging research: Challenges
and opportunities. Gero Science, 43(2), 487–505. [28] Langseth, L. (1995). Oxidants, Antioxidants, and Disease Prevention. ILSI Europe, Brussels. [29] Zakaria, N. A., Ibrahim, D., Sulaiman, S. F. and Supardy, N. A. (2011). Assessment of antioxidant
activity, total phenolic content and in vitro toxicity of Malaysian red seaweed, Acanthophora
spicifera. Journal of Chemical and Pharmaceutical Research, 3, 182–191. [30] Halliwell, B. (1994). Free radicals and antioxidants free radicals, antioxidants, and human disease:
Curiosity, cause, or consequence. Lancet, 344, 721–724. [31] Wong, C. K., Ooi, V. E. and Ang, P. O. (2000). Protective effect of seaweeds against liver injury
caused by carbon tetra chloride in rats. Chemosphere, 41, 173–176. [32] Chen, K., Plumb, G. W., Bennett, R. N. and Bao, Y. (2005). Antioxidant activities of extracts from five
anti-viral medicinal plants. Journal of Ethnopharmacology, 96, 201–205. [33] Bjelakovic, G., Nikolova, D., Gluud, L. L., Simonetti, R. G. and Gluud, C. (2007). Mortality in
randomized trials of antioxidant supplements for primary and secondary prevention: Systematic
review and meta-analysis. Jama, 297, 842–857. [34] Niwa, T., Doi, U., Kato, Y. and Osawa, T. (2001). Antioxidant properties of phenolic antioxidants
isolated from corn steep liquor. Journal of Agricultural and Food Chemistry, 49, 177–182. [35] Kahl, R. and Kappus, H. (1993). Toxicology of the synthetic antioxidants BHA and BHT in comparison
with the natural antioxidants capacity and total vitamin E. Zeitschrift Für Lebensmittel-
Untersuchung und–Forschung, 196, 329–338. [36] Rietjens, I. M., Boersma, M. G., Haan, L., Spenkelink, B., Awad, H. M., Cnubben, N. H., Jj, V. Z.,
Woude, H., Alink, G. M. and Koeman, J. H. (2002). The pro-oxidant chemistry of the natural
antioxidants vitamin C, vitamin E, carotenoids and flavonoids. Environmental Toxicology
Pharmacology, 11, 321–333. [37] Kim, D. O. and Lee, C. Y. (2004). Comprehensive study on vitamin C equivalent antioxidant capacity
(VCEAC) of various polyphenolics in scavenging a free radical and its structural relationship. Critical
Reviews in Food Science and Nutrition, 44, 253–273. [38] Escarpa, A. and Gonzalez, M. C. (2001). An overview of analytical chemistry of phenolic compounds
in foods. Critical Reviews in Analytical Chemistry, 31, 57–139.