Добавил:
kiopkiopkiop18@yandex.ru t.me/Prokururor I Вовсе не секретарь, но почту проверяю Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз: Предмет: Файл:
Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_5409_Библиотеки_им_академика_М_И_Перельмана.pdf
Скачиваний:
0
Добавлен:
15.09.2026
Размер:
13 Мб
Скачать
☆
Plant Extracts With Antibiotic Eect
antibacterial compounds isolated from S. officinalis leaves, potentiate the effects of aminoglycosides on methicillin-resistant S. aureus (Horiuchi et al., 2007, Pavić et al., 2019).
Thymus vulgaris L.
Plant Description
T. vulgaris L. or thyme, also known as “garden thyme,” is an aromatic, perennial plant belonging to the Lamiaceae family. Thymus vulgaris, presents several chemovarieties: T. vulgaris geranoliferum, T. vulgaris linaloliferum, T. vulgaris mircenoliferum and T. vulgaris terpenoliferum, chemovarieties rich in monoterpenic alcohols; T. vulgaris cineoliferum, rich in monoterpenic oxides; T. vulgaris thujanoliferum, rich in monoterpenic hydrocarbons; T. vulgaris carvacroliferum and T. vulgaris thymoliferum rich in monoterpenic phenols (carvacrol and thymol). The aerial parts of the plant are traditionally used for bronchitis, whooping cough, flu, fermentative colitis, biliary colic, intestinal parasitosis, buccopharyngeal infections, myalgia, for various skin problems such as acne, dermatitis, insect bites.
Biological Activities
The various extracts of T. vulgaris L. (ethanol and water) and essential oils obtained from the plant were evaluated and reported as having broad-spectrum antibacterial action (chemotypes thymoliferum, geranioliferum and linanoliferum) and of choice on Chlamydia (T. vulgaris thujanoliferum). In a study, Hammad et al., (2007) investigated the effect of aqueous extracts of T. vulgaris on the growth and adhesion of Streptococcus mutans to human oral epithelial cells. The 20% aqueous extract resulted in a signifi­cant inhibition of bacterial cell growth (96%), and a greater reduction in bacterial cell adhesion to oral epithelial cells compared to the effect of chlorhexidine digluconate. The ethanolic extract obtained from the aerial parts of Thymus vulgaris showed MIC between 3.12-6.25 mg/μL on the bacteria Escherichia
coli, Klebsiella pneumoniae, Staphylococcus aureus, Listeria monocytogenes, Yersinia enterocolitica, Enterococcus faecalis (Gnat et al.). Another in vivo study in an animal model showed that methanolic
extract of T. vulgaris L. is effective against methicillin-resistant S. aureus (MRSA); MIC was 2.53 and
3.83 CFU / mL, for bacteria isolated from the throat and lungs, respectively (Arshad et al., 2017). Thyme essential oil develops antimicrobial activity on both Gram-positive and Gram-negative bacteria.
In vitro studies have shown strong antibacterial action of Thymus vulgaris oil on S. pyogenes, S. mutans, A. actinomycetemcomitans and P. gingivalis. In the case of Salmonella typhirium, the essential oil of T. vulgaris L. showed a MIC of 25.5 mm (Fadil et al., 2018), and the biofilm of Salmonella enteritidis was
inhibited at MIC/MBC of 0.156/0.315 μL/mL (Čabarkapa et al., 2019). Thyme essential oil has also been shown to act against methicillin resistant S. aureus (MIC 18.50 μg/mL) (Tohidpour et al., 2010). The most intense antibacterial activity of this essential oil was observed against blaCTX-M-1-producing E. coli S22 / 12 and ESBL-producing Klebsiella pneumoniae S34 / 15 with a MIC of 2.87 μg / mL. In addition, E. coli producing blaCTX-M-1 was more sensitive than E. coli producing blaSHV-12 (Benameur et al.,
2019). Even thyme essential oil vapors are highly effective against respiratory tract pathogens (Inouye
et al., 2006). The antimicrobial properties are mainly attributed to monoterpenic phenols, thymol and carvacrol, strong anti-infective agents, but also to geraniol, linalool alcohols. Experimental studies have suggested that a higher content of phenolic terpene compounds results in a higher inhibitory activity (Fani et al., 2017). In addition to thymol and carvacrol, phenolic acids, polyphenolic carboxylic acids
58
EBSCOhost - printed on 2/13/2023 11:18 AM via . All use subject to https://www.ebsco.com/terms-of-use
Plant Extracts With Antibiotic Eect
(chlorogenic acid, rosmarinic acid) and tannins are also compounds responsible for the antibacterial potential of thyme. Regarding the antibacterial activity, thyme essential oil develops a higher inhibitory activity compared to that of aqueous extracts, ethanol and even some antibiotics (Fadil et al., 2018).
Rosmarinus officinalis L.
Plant Description
Rosemary belongs to the Lamiaceae family. It is an aromatic shrub, evergreen, native to the Mediterranean region, naturalized worldwide. It is traditionally used to relieve muscle pain, to support the immune and circulatory system, to maintain the health of the digestive system due to its choleretic, stomachic, anti­spasmodic, antioxidant, antibacterial properties. The species has several chemovars, of which the most used are: R. officinalis camphoriferum, R. officinalis L. cineoliferum, R. officinalis L. verbenoniferum. R. officinalis camphoriferum has a stronger antibacterial action than the other two.
Biological Activities
Numerous studies have shown the effectiveness of the essential oil obtained from the aerial parts of the species and its components on pathogens. Recently, Stojiljkovic et al. (2018) investigated the antibacte- rial action of rosemary volatile oil on Gram-positive and Gram-negative bacteria such as Staphylococcus aureus, Bacillus cereus, B. subtilis, B. pumilis, Pseudomonas aeruginosa, Salmonella poona, E. coli. The test results showed a higher antibacterial activity of the essential oil against Gram-positive bacteria
-1
(MIC 0.20-0.48 mg/mL
) than against Gram-negative bacteria (MIC 1.16-1.72 mg / mL-1). In vitro studies done by the micro-dilution method against S. aureus and S. epidermidis strains showed inhibi­tory and bactericidal effects of this oil, the minimum inhibitory concentration (MIC) varying between
-1
1.25 and 2.5 μl ml
for S. aureus and between 0.312 and 0.625 μl ml-1 for S. epidermidis. The minimum bactericidal concentration (MBC) against the two bacteria reached higher values and was of the order of 5.0 and 2.5 μl/mL, respectively. In addition, the tested oil resulted in an inhibition of S. epidermidis biofilm of over 57% at a concentration of 25 μL/ mL (Jardak et al., 2017). Experimentally, it has been shown that R. officinalis essential oil shows improved antibacterial effects in combination with other oils, such as clove essential oil (Syzygium aromaticum), results observed in testing on pathogens such as S. epidermidis, S. aureus, B. subtilis, E. coli, P. vulgaris, and P. aeruginosa (Fu et al., 2007). The antibacterial activity of rosemary volatile oil is mainly imprinted with 1.8 cineole, camphor, limonene, α-pinene, Z-linalool oxide and borneol, terpene compounds known for their anti-infective profile (Bozin et al., 2007). According to Manilal et al., (2021), the hydroalcoholic extract of R. officinalis leaves reduced the growth in different degrees of some clinical isolates of MDR. The best inhibitory values (MIC) were recorded against S. aureus, Enterococcus sp. and Salmonella sp. and ranged from
4.103 to 32.103 µg/mL. Inhibitory activity on S. pyogenes, Proteus sp. and Campylobacter sp., proved to be small. In a comparative analysis, Moreno et al. (2006) evaluated the antibacterial efficacy of a methanolic extract with a content of 30% carnosic acid, 16% carnosol and 5% rosmarinic acid and an aqueous extract containing only 15% rosmarinic acid. They concluded that the antimicrobial activity of rosemary extracts is associated with the content of phenolic compounds; rosmarinic acid and carnosic acid being the main bioactive compounds with antimicrobial action. Furthermore, the study suggested that the methanolic extract was effective against both Gram-positive bacteria (MIC between 2 and 15
EBSCOhost - printed on 2/13/2023 11:18 AM via . All use subject to https://www.ebsco.com/terms-of-use
59
Plant Extracts With Antibiotic Eect
μg/mL) and Gram-negative bacteria (MIC between 2 and 60 μg / mL) as opposed to the aqueous extract which showed low activity, the study indicating a synergistic action of the compounds in the methanolic extract. The antibacterial potential of rosemary was also observed in a clinical study, which evaluated the efficacy of a mouthwash containing hydroalcoholic extracts of Zingiber officinale, R. officinalis and Calendula officinalis, concluding that the preparation was effective in patients with gingivitis, and the effectiveness was comparable to chlorhexidine mouthwash. (Mahyari et al., 2016).
Melaleuca alternifolia (Maiden & Betche) Cheel
Plant Description
Tea tree is a shrub or tree from Myrtaceae family, native to Australia. It has been used by Australians in traditional medicine as antiseptic and anti-inflammatory to treat various infections for almost 100 years. Tea tree essential oil contains terpinene-4-ol, α-terpinene, γ-terpinene, α-terpineol, 1,8-cineole, ρ-cymene, terpinolene, and limonene, as major constituents and exerts a strong antioxidant and antibac­terial activity, as confirmed by many in vitro tests.
Biological Activities
Zhang et al. (2018) noticed that the essential oil of M. alternifolia displayed significant antimicrobial activity on Gram-positive and Gram-negative bacteria as Staphylococcus aureus, Pseudomonas aerugi- nosa, P. italicum, P. digitatum and Escherichia coli strains, with a MIC raging between 2 and 24 mg/mL. According to these authors, ” the hydrophobic terpenes from the essential oil interact with the membrane lipids of the pathogenic microorganisms, which affect the permeability of the membrane, leading to a deficit in the production of cellular energy caused by the decrease in ATP generation, and cellular lyses due to leakage or coagulation of the cytoplasm” (Zhang et al., 2018). Ferrini et al. (2006) found that from terpien-4-ol, from the tea tree essential oil has an efficient antibacterial activity on Staphylococ- cus aureus, even for the antibiotic resistant strains. Another in vitro study performed by Kokina et al. (2019) showed the inhibition of tea tree essential oil on the bacterial growth of Staphylococcus aureus and Salmonella Typhimurium with a MIC of 10, respectively > 10 μg/mL.
Allium sativum L.
Plant Description
Garlic is an alimentary plant belonging to Amaryllidaceae family. Garlic has been used in traditional medicine since ancient times. It contains phenolic, polysaccharides and thiosulfinates as major com­ponents. Garlic also contains flavonoids, saponins, aminoacids, enzymes, vitamins A, B and C, and minerals (Parham et al., 2020). The alliinase enzyme transforms alliin to allicin which is one of the main components of garlic (Figure 17.4). Allicin is the thiosulfinate responsible for the antimicrobial activity of this medicinal plant, having both bacteriostatic and bactericidal effects.
60
EBSCOhost - printed on 2/13/2023 11:18 AM via . All use subject to https://www.ebsco.com/terms-of-use
Plant Extracts With Antibiotic Eect
Figure 4. The conversion of Alliin to Allicin in Garlic
Biological Activities
Many in vitro studies demonstrated the antibacterial effect of garlic extracts against Gram positive and Gram-negative bacteria, including those resistant to antibiotics, such as Staphylococcus aureus, Pseu- domonas, Klebsiella, Salmonella typhi, Enterococcus faecalis, Proteus, and Escherichia coli (Bakri & Douglas, 2005; Yadav et al., 2015; Rawat, 2015; Petropoulos et al., 2018; Ismail et al., 2020; Parham et al., 2020; Pancu et al., 2021). The antibacterial effect of Allium sativum was proved using different extracts: crude extracts, powder, various solvents extracts, and also the biocompounds isolated from this plant. The aqueous and alcoholic extract of garlic contain organosulfur compounds as S-allyl cysteine, S-methyl cysteine, and S-allylmercapto- that garlic distilled oil with diallyl disulfide and diallyl trisulfide is effective on different Gram-positive and negative bacteria cultures (S. aureus, B. subtilis, P. aeruginosa and E. coli). The mechanism of action consists in binding to the thiol groups of enzymes in bacteria, which leads to the microbial inactivation.
l-cysteine (Bhatwalkar et al., 2021). Avato et al. (2000) revealed
Arctostaphylos uva-ursi L.
Plant Description
Arctostaphylos uva-ursi L., from the Ericaceae family, is an evergreen shrub that grows in the northern hemisphere, abounds in the Arctic regions, and only at high altitudes in the temperate and Mediterranean area. For a long time, the leaves of this plant have been used in traditional medicine to combat and treat urinary tract diseases, like infections such as cystitis or urethritis, as a diuretic and anti-inflammatory agent for various diseases of the urogenital tract.
Biological Activities
Many studies have shown the effectiveness of bearberry leaf extracts in urinary tract infections through antibacterial activity and the ability to reduce recurrences in people at risk of contracting these infec­tions. Moskalenko (1986) showed that the ethanolic extract of Uvae ursi folium has strong bacteriostatic activity on Bacillus subtilis, Escherichia coli, Shigella sonnei and Shigella flexneri. In another study,
EBSCOhost - printed on 2/13/2023 11:18 AM via . All use subject to https://www.ebsco.com/terms-of-use
61
Plant Extracts With Antibiotic Eect
Anukk et al., (1999) reported that aqueous bearberry leaf extracts show remarkable bacteriostatic activ- ity on H. pylori strains. This activity could be related to the ability of the aqueous extract to modulate the hydrophobicity of the cell surface and to increase the aggregation of cells, an effect determined by the high content of tannins. Various extracts (aqueous, ethanolic and ethyl acetate) from A. uva - ursi leaves were tested on strains of Enterococcus faecalis and strains of Escherichia coli, etiological agents of urinary tract infections. In vitro results concluded that the aqueous extract has a stronger antibacte­rial effect on E. coli (MIC 0.625-5 mg/mL) compared to ethanolic and ethyl acetate extracts (MIC 10 mg/mL), while the effect on Enterococcus faecalis was similar for the three types of extracts. It should be noted that the extracts showed stronger antibacterial activity against Gram-positive strains (Vučić et al., 2013). Arbutin metabolites (hydroquinone, hydroquinone glucuronide, hydroquinone sulfate) are considered to be the compounds responsible for the urinary antiseptic activity of the plant. They exert antimicrobial action on a wide range of pathogens involved in the infectious pathology of the urinary tract, E. coli, Proteus vulgaris, Acinetobacter baumanii, Ataphylococcus aures, Bacillus subtilis, Entero- coccus faecalis, Neisseria gonorrhoeae (Ștefănescu et al., 2019). Although it was initially thought that hydroquinone could be released from arbutin only by alkalizing urine, more recent research challenges this hypothesis. Hydroquinone deconjugation is now thought to be catalyzed by intracellular enzymes present in the bacterial cytoplasm. Alkalization of urine does not appear to be a prerequisite for the release of hydroquinone from arbutin (Quintus et al., 2005). The pharmacology of the whole plant has also been shown to be different from that of arbutin alone. Crude plant extracts are more medically effective than isolated arbutin (Asensio et al., 2020). In addition, A. uva - ursi extracts have been shown to be helpful in increasing the susceptibility of antibiotic-resistant bacteria such as beta-lactams. A group of Japanese researchers studied the effect of corilagin, a polyphenolic compound isolated from A. uva - ursi, against methicillin-resistant Staphylococcus aureus. Corilagin reduced the minimum inhibitory concentration of oxacillin and other beta-lactam antibiotics by 100 to 2000 times, the effect of corilagin and oxacillin being synergistic (Shimizu et al., 2001).
Glycyrrhiza glabra L.
Plant Description
Liquorice is an herbaceous perennial plant from Fabaceae family, native to Southern Europe, Western Asia, and North Africa. This specie has an important therapeutical value, being used since centuries for a wide range of pharmacological properties, including anti‐inflammatory, antibacterial, antiviral, anti­ulcer, and antidiabetic activities. Many biological compounds have been found in this medicinal plant: simple glucides, polysaccharides, pectins, gums, resins, coumarins, tannins, oestrogens, phytosterols, amino acids, proteins, minerals, vitamins (B
, B2, B3, B5, C and E), Triterpenoid saponins (glycyrrhizin,
1
responsible for the sweet taste), and flavonoids (liquiritigenin and isoliquiritigenin) are the most impor­tant constituents (Pastorino et al., 2018).
Biological Activities
Gupta et al., 2008 and Wang et al., 2015 showed the antimicrobial action of G. glabra extract on Gram‐ positive and Gram‐negative bacteria cultures, as Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli, and Bacillus subtilis (Gupta et al., 2008; Wang et al., 2015). Responsible for the
62
EBSCOhost - printed on 2/13/2023 11:18 AM via . All use subject to https://www.ebsco.com/terms-of-use
Plant Extracts With Antibiotic Eect
antibacterial effect are the secondary metabolites from plant: flavonoids, saponins, and alkaloids, (his­paglabridin A, hispaglabridin B, glabridin, glabrol glabrene, 40‐methylglabridin, and 3‐hydroxyglabrol). Authors noticed that “the mechanism behind this could be the decrease of bacterial gene expression, the inhibition of bacterial growth, and the reduction of bacterial toxin production” (Gupta et al., 2008; Wang et al., 2015). Liquorice may inactivate methicillin resistant Staphylococcus aureus (MRSA) through a mechanism that involves lowering the expression of the key virulence genes of MRSA and can also have an inhibitory action on Streptococcus pyogenes, as Fukai et al. (2002) has shown. Gupta et al. (2008) also demonstrated the antibacterial action of G. glabra against Mycobacterium tuberculosis, glabridin beeing the responsible compound for this activity. Asha et al. (2013) noticed that the flavonoid glabridin from liquorice exherts activity against H. pylori, by inhibition of the protein synthesis, DNA gyrase, and dihydrofolate reductase. Another in vitro study showed that the liquorice polysaccharides also present activity against Porphyromonas gingivalis adhesion (Chinsembu, 2016).
Hypericum perforatum L.
Plant Description
Hypericum perforatum L. (Hypericaceae) is a perennial plant native to Asia and Europe, known as St. John’s wort. In traditional medicine it is used as a remedy against skin lesions, sunburn, for diseases of the gallbladder, depression, dysentery, and diarrhea. More recent studies have focused on the antidepres­sant effects and antimicrobial activity of St. John’s wort extracts and their components.
Biological Activities
Avato et al., 2004 tested the microbiological activity of various extracts against Gram-positive bacteria (Bacillus subtilis, B. cereus, Staphylococcus aureus, Enterococcus) as well as Gram-negative (Pseudo-
monas aeruginosa, Acinetobacter calcoaceticus, A. baumanii). It turned out that the pharmacological activity depends on the type of extract and the solvent used to obtain it. The most active were chloroform and ethanolic extracts against B. subtilis and B. cereus with a MIC value of 12.5 μg / mL. In addition, the ethanolic extract significantly inhibited all other Gram-positive bacteria tested, showing a MIC of 12.5 μg/mL, except for E. faecalis (MIC = 50 μg/ mL). The active compounds responsible for the antibacte- rial activity have been shown to be hypericin, hyperforin and its stable ammonium dicyclohexyl salt. In a study on the antibacterial activity of an extract in petroleum ether from aerial parts of H. perforatum, Reichling et al. (2001) reported that hyperforin is the major active compound against Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus strains, with a MIC of 1 μg / mL. Vari­ous extracts and isolated fractions of aerial parts of Hypericum perforatum have been tested for anti­Helicobacter activity. In such a study, the butanolic fraction showed anti-Helicobacter pylori activity at MIC values between 15.6 and 31.2 μg/mL (Saddiqe et al., 2010).
CONCLUSION
As most of the studies that proved the antibacterial effect of plant extracts have been performed on in vitro cultures of bacteria, in vivo studies and clinical trials are required to be realized in future. The
EBSCOhost - printed on 2/13/2023 11:18 AM via . All use subject to https://www.ebsco.com/terms-of-use
63
Table 1. Antibacterial Activity of Some Plant Extracts
Plant Extracts With Antibiotic Eect
Plant Extract Tested bacteria /MIC
• Staphylococcus aureus, Streptococcus pneumoniae, E. coli, P. aeruginosa, Salmonella typhi and Klebsiella pneumoniae /
0.5–8 μg/mL
• Salmonella enterica/4.12μg/mL
• S. aureus, P. aeruginosa, E. coli, and K. pneumoniae
• Salmonella typhius, B. subtilis, S. aureus,, Staphylococcus epidermititis, P.aeruginosa, and Klebsiella pneumonia
• Helicobacter pylori /25–100 μg/mL
• Asaia bogorensis, and A. lannensis
• Aeromonashydrophila, Aero monassobria, E. coli, Klebsiella
oxytoca, Pseudomonas morgani, Salmonella anatum, Klebsiella pneumonia, Salmonella enteritidis, Salmonella typhi
and Shigella sonaan/
12.5-225 μg / mL
• Strptococcus puogenes and Staphylococcus aures/ 62.5 and 300 μg / mL
• S pyogenes, S mutans, P. gingivalis and A actinomycetemcomitans
• Salmonella enteritidis/ 0.156 μl / ml
• S. aureus (MRSA)/ 2.53 and 3.83 CFU (log10) / ml
• Escherichia coli, Klebsiella pneumoniae, Yersinia enterocolitica, Staphylococcus aureus, Listeria monocytogenes, Enterococcus faecalis / 3.12-6.25 mg / μL
• Staphylococcus aureus, Bacillus cereus, Bacillus pumilis Bacillus subtilis, Escherichia coli, Pseudomonas aeruginosa, Salmonella poona,
• Staphylococcus aureus (ATCC 9144)/ 1.25 to 2.5 μl ml
• Staphylococcus epidermidis/ 0.312 to 0.625 μl ml
• S. aureus, Salmonella sp and Enterococcus sp / 4.103 to
32.103 µg / mL.
• Staphylococcus saprophyticus, S. epidermidis, P. aeruginosa, and Enterococcus faecalis /70–350 μg / mL
• E. coli, S. aureus,, P. italicum Wehmer, P. aeruginosa and P. digitatum Sacc. / 2 - 24 mg/mL
• Staphylococcus aureus and Salmonella Typhimurium/ 10, and > 10 μg/mL
• Neisseria gonorrhoeae, S. aureus, and Enterococcus faecalis
• M. tuberculosis, S. aureus, S. mutans, and P. aeruginosa
• S. aureus, Bacillus subtilis, E. col,i and P. aeruginosa
• Bacillus subtilis, Escherichia coli, Helicobacter pylori, Shigella sonnei and Shigella flexner
• E.coli /MIC 0.625-5 mg / mL)
• Staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa, and Bacillus subtilis
• S. aureus (MRSA)
• Helicobacter pylori
• Mycobacterium tuberculosis
• B. subtilis and B. cereus / 12.5 μg / ml
• Bacillus subtilis, B. cereus, Staphylococcus aureus, 25923, Enterococcus faecalis / 12.5 - 50 μg / ml μg / ml
•Helicobacter pylori / 15.6 - 31.2 μg / ml
Mentha x piperita
Salvia officinalis
Thymus vulgaris
Rosmarinus officinalis
Melaleuca alternifolia
Allium sativum
Arctostaphylos uva-ursi
Glycyrrhiza glabra
Hypericum perforatum
• essential oil
• methanolic extract
• ethanolic extract
• essential oil
• ethanolic extracts
• essential oil
• methanolic extract
• ethanolic extract
• essential oil
•hydroalcoholic extract
• ethanol extracts
• essential oil
• aqueous extract
• ethanolic extract
• distilled oil
• ethanolic extract
• aqueous extract
• ethanolic extract
• chloroform extract •ethanolic extracts
• butanol extract in
Responsible antibacterial
compounds
• mentol, menthone
• carvone, menthol, and menthone
• menthol, menthone, camphane, menthofuran
• carvone, carveol, menthone, menthol
• phenolic compounds
• gallic, chlorogenic, neochlorogenic, p-coumaric, ferulic, rosmarinic acids, epicatechin, quercetin-3­rutinoside and quercetin
• thujone, 1,8-cineole and camphor
• rosmarinic acid, quercetin, ellagic acid, chlorogenic acid
• thymol, carvacrol, p-cymene
• thymol, carvacrol, p-cymene
• phenolic and
polyphenolcarboxylic acids
• phenolic and polyphenolcarboxylic acids
• Limonene, camphor, eucalyptol, α-pinene, Z-linalool
-1
-1
oxide and borneol
• carnosic acid, carnosol, rosmarinic acid
• carnosic acid, carnosol, rosmarinic acid
• terpinene-4-ol, γ-terpinene, and α-terpinene
• valencene, trans-cadina-1(6),4­diene, aromadendrene
• S-allyl cysteine,
S-allylmercapto- S-methyl cysteine
• allicin
• diallyl and allyl methyl sulfides
• arbutin metabolites (hydroquinone, hydroquinone glucuronide, hydroquinone sulfate)
• glycyrrhizin, 18β-glycyrrhetinic acid, liquiritigenin, licochalcone A, licochalcone E, and glabridin
• flavonoids
• vestitol, licoricone, 1-methoxyphaseollidin and gancaonol glycyrrhizin, 18β-glycyrrhetinic acid, liquiritigenin, licochalcone A, licochalcone E, and glabridin
• glabardin
• hypericin, hyperforin, ammonium dicyclohexyl salt
l-cysteine, and
Authors
• Abolfazl et al., 2014
• Valková et al., 2021
• Osanloo et al., 2020
• Saba & Anwar, 2018
• Mahady et al., 2005
• Antolak et al., 2018
• Ghorbani et al., 2017; Santos et al.; 2017; Sonboli, et al., 2006
• Wijesundara and Rupasinghe, 2019
• Fani et al., 2017
• Čabarkapa et al., 2019
• Arshad et al., 2017
• Gnat et al., 2017
• Stojiljkovic et al.,2018; Bozin et al.
2007
• Jardak et al., 2017
• Manilal et al., 2021
• Petrolini et al., 2013
• Zhang et al., 2018
• Kokina et al., 2019
• Bhatwalkar et al., 2021
• Bhatwalkar et al., 2021
• Avato et al., 2011
• Moskalenko, 1986
• Vučić et al., 2013
• Wang et al., 2015
• Fukai et al., 2002
• Fukai et al., 2002
• Gupta et al., 2008
• Avato et al., 2004
• Reichling et al., 2001
64
EBSCOhost - printed on 2/13/2023 11:18 AM via . All use subject to https://www.ebsco.com/terms-of-use
Plant Extracts With Antibiotic Eect
mechanisms of antimicrobial action of biological compounds from plants must be completely elucidated, and additionally, their toxicity on humans should be evaluated.
This chapter summarizes the significance of the antibacterial activity of some plant extracts due to their constituents, as demonstrated by the scientific studies. Biological compounds from plants can be used as an alternative to chemical, synthetic antibiotics, or used complementary, synergistic for better therapeutically results.
REFERENCES
Abad Martínez, M. J., & Bermejo Benito, P. (2005). Biological activity of quinones. In Studies in Natural Products Chemistry; Atta-ur-Rahmen (Vol. 30, pp. 303–366). Elsevier.
Abolfazl, M. (2014). In vitro antibacterial activity and phytochemical analysis of some medicinal plants. Journal of Medicinal Plants Research, 8(3), 186–194. doi:10.5897/JMPR12.1298
Akhtar, M. Q., Qamar, N., Yadav, P., Kulkarni, P., Kumar, A., & Shasany, A. K. (2017). Comparative glandular trichome transcriptome-based gene characterization reveals reasons for differential (-)-men­thol biosynthesis in Mentha species. Physiologia Plantarum, 160(2), 128–141. doi:10.1111/ppl.12550 PMID:28188954
Al Sheikh, H., Sultan, I., Kumar, V., Rather, I. A., Al-Sheikh, H., Tasleem Jan, A., & Haq, Q. (2020). Plant-Based Phytochemicals as Possible Alternative to Antibiotics in Combating Bacterial Drug Re­sistance. Antibiotics (Basel, Switzerland), 9(8), 480. doi:10.3390/antibiotics9080480 PMID:32759771
Álvarez-Martínez, F. J., Barrajón-Catalán, E., Herranz-López, M., & Micol, V. (2021). Antibacterial plant compounds, extracts and essential oils: An updated review on their effects and putative mechanisms of action. Phytomedicine: International Journal of Phytotherapy and Phytopharmacology, 90, 153626. doi:10.1016/j.phymed.2021.153626 PMID:34301463
Annuk, H., Hirmo, S., Türi, E., Mikelsaar, M., Arak, E., & Wadström, T. (1999). Effect on cell surface hydrophobicity and susceptibility of Helicobacter pylori to medicinal plant extracts. FEMS Microbiology Letters, 172(1), 41–45. doi:10.1111/j.1574-6968.1999.tb13447.x PMID:10079525
Antolak, H., Czyżowska, A., & Kręgiel, D. (2018). Activity of Mentha piperita L. Ethanol Extract against Acetic Acid Bacteria Asaia spp. Foods (Basel, Switzerland), 7(10), 171. doi:10.3390/foods7100171
PMID:30340348
Arshad, N., Mehreen, A., Liaqat, I., Arshad, M., & Afrasiab, H. (2017). In vivo screening and evaluation of four herbs against MRSA infections. BMC Complementary and Alternative Medicine, 17(1), 498. doi:10.118612906-017-2001-z PMID:29169369
Asensio, E., Vitales, D., Pérez, I., Peralba, L., Viruel, J., Montaner, C., Vallès, J., Garnatje, T., & Sales, E. (2020). Phenolic Compounds Content and Genetic Diversity at Population Level across the Natural Distribution Range of Bearberry (Arctostaphylos uva-ursi, Ericaceae) in the Iberian Peninsula. Plants (Basel, Switzerland), 9(9), 1250. doi:10.3390/plants9091250 PMID:32971908
EBSCOhost - printed on 2/13/2023 11:18 AM via . All use subject to https://www.ebsco.com/terms-of-use
65
Plant Extracts With Antibiotic Eect
Asha, M. K., Debraj, D., Prashanth, D., Edwin, J. R., Srikanth, H. S., Muruganantham, N., Dethe, S. M., Anirban, B., Jaya, B., Deepak, M., & Agarwal, A. (2013). In vitro anti-Helicobacter pylori activ­ity of a flavonoid rich extract of Glycyrrhiza glabra and its probable mechanisms of action. Journal of Ethnopharmacology, 145(2), 581–586. doi:10.1016/j.jep.2012.11.033 PMID:23220194
Avato, P., Raffo, F., Guglielmi, G., Vitali, C., & Rosato, A. (2004). Extracts from St John’s Wort and their antimicrobial activity. Phytotherapy Research: PTR, 18(3), 230–232. doi:10.1002/ptr.1430 PMID:15103670
Avato, P., Tursi, F., Vitali, C., Miccolis, V., & Candido, V. (2000). Allylsulfide constituents of garlic volatile oil as antimicrobial agents. Phytomedicine, 7(3), 239–243. doi:10.1016/S0944-7113(00)80010-0 PMID:11185736
Bakri, I. M., & Douglas, C. W. (2005). Inhibitory effect of garlic extract on oral bacteria. Archives of Oral Biology, 50(7), 645–651. doi:10.1016/j.archoralbio.2004.12.002 PMID:15892950
Benameur, Q., Gervasi, T., Pellizzeri, V., Pľuchtová, M., Tali-Maama, H., Assaous, F., Guettou, B., Rahal, K., Gruľová, D., Dugo, G., Marino, A., & Ben-Mahdi, M. H. (2019). Antibacterial activity of Thymus vulgaris essential oil alone and in combination with cefotaxime against bla
producing multidrug
ESBL
resistant Enterobacteriaceae isolates. Natural Product Research, 33(18), 2647–2654. doi:10.1080/147
86419.2018.1466124 PMID:29726697
Bhatwalkar, S. B., Mondal, R., Krishna, S., Adam, J. K., Govender, P., & Anupam, R. (2021). Antibacte­rial Properties of Organosulfur Compounds of Garlic (Allium sativum). Frontiers in Microbiology, 12,
613077. doi:10.3389/fmicb.2021.613077 PMID:34394014
Bozin, B., Mimica-Dukic, N., Samojlik, I., & Jovin, E. (2007). Antimicrobial and antioxidant properties of rosemary and sage (Rosmarinus officinalis L. and Salvia officinalis L., Lamiaceae) essential oils. Journal of Agricultural and Food Chemistry, 55(19), 7879–7885. doi:10.1021/jf0715323 PMID:17708648
Čabarkapa, I., Čolović, R., Đuragić, O., Popović, S., Kokić, B., Milanov, D., & Pezo, L. (2019). Anti­biofilm activities of essential oils rich in carvacrol and thymol against Salmonella Enteritidis. Biofouling, 35(3), 361–375. doi:10.1080/08927014.2019.1610169 PMID:31088182
Castro, M. Á., Gamito, A. M., Tangarife-Castaño, V., Zapata, B., Miguel del Corral, J. M., Mesa-Arango, A. C., Betancur-Galvis, L., & San Feliciano, A. (2013). Synthesis and antifungal activity of terpenyl­1,4-naphthoquinone and 1,4-anthracenedione derivatives. European Journal of Medicinal Chemistry, 67, 19–27. doi:10.1016/j.ejmech.2013.06.018 PMID:23831506
Céspedes, C. L., Avila, J. G., García, A. M., Becerra, J., Flores, C., Aqueveque, P., Bittner, M., Hoeneisen, M., Martinez, M., & Silva, M. (2006). Antifungal and antibacterial activities of Araucaria araucana (Mol.) K. Koch heartwood lignans. Zeitschrift fur Naturforschung. C. Journal of Biosciences, 61(1-2), 35–43. PMID:16610214
Chassagne, F., Samarakoon, T., Porras, G., Lyles, J. T., Dettweiler, M., Marquez, L., Salam, A. M., Shabih, S., Farrokhi, D. R., & Quave, C. L. (2021). A Systematic Review of Plants With Antibacterial Activi­ties: A Taxonomic and Phylogenetic Perspective. Frontiers in Pharmacology, 11, 586548. doi:10.3389/ fphar.2020.586548 PMID:33488385
66
EBSCOhost - printed on 2/13/2023 11:18 AM via . All use subject to https://www.ebsco.com/terms-of-use
Plant Extracts With Antibiotic Eect
Chinsembu, K. C. (2016). Plants and other natural products used in the management of oral infec­tions and improvement of oral health. Acta Tropica, 154, 6–18. doi:10.1016/j.actatropica.2015.10.019 PMID:26522671
Cowan, M. M. (1999). Plant products as antimicrobial agents. Clinical Microbiology Reviews, 12(4), 564–582. doi:10.1128/CMR.12.4.564 PMID:10515903
de Oliveira, J. R., Vilela, P., Almeida, R., de Oliveira, F. E., Carvalho, C., Camargo, S., Jorge, A., & de Oliveira, L. D. (2019). Antimicrobial activity of noncytotoxic concentrations of Salvia officinalis extract against bacterial and fungal species from the oral cavity. General Dentistry, 67(1), 22–26. PMID:30644826
Drusano, G. L. (2004). Antimicrobial pharmacodynamics: Critical interactions of ‘bug and drug’. Nature Reviews. Microbiology, 2(4), 289–300. doi:10.1038/nrmicro862 PMID:15031728
Ekalu, A., Ayo, R. G. O., Habila, J. D., & Hamisu, I. (2019). In vitro antimicrobial activity of lignan from the stem bark of Strombosia grandifolia Hook.f. ex Benth. Bulletin of the National Research Center, 43(1), 115. doi:10.118642269-019-0159-x
Fadil, M., Fikri-Benbrahim, K., Rachiq, S., Ihssane, B., Lebrazi, S., Chraibi, M., Haloui, T., & Farah, A. (2018). Combined treatment of Thymus vulgaris L., Rosmarinus officinalis L. and Myrtus communis L. essential oils against Salmonella typhimurium: Optimization of antibacterial activity by mixture design methodology. European Journal of Pharmaceutics and Biopharmaceutics, 126, 211–220. doi:10.1016/j. ejpb.2017.06.002 PMID:28583590
Fani, M., & Kohanteb, J. (2017). In Vitro Antimicrobial Activity of Thymus vulgaris Essential Oil Against Major Oral Pathogens. Journal of Evidence-Based Complementary & Alternative Medicine, 22(4), 660–666. doi:10.1177/2156587217700772 PMID:28397552
Ferrini, A. M., Mannoni, V., Aureli, P., Salvatore, G., Piccirilli, E., Ceddia, T., Pontieri, E., Sessa, R., & Oliva, B. (2006). Melaleuca alternifolia essential oil possesses potent anti-staphylococcal activity extended to strains resistant to antibiotics. International Journal of Immunopathology and Pharmacol- ogy, 19(3), 539–544. doi:10.1177/039463200601900309 PMID:17026838
Fournomiti, M., Kimbaris, A., Mantzourani, I., Plessas, S., Theodoridou, I., Papaemmanouil, V., Kapsiotis, I., Panopoulou, M., Stavropoulou, E., Bezirtzoglou, E. E., & Alexopoulos, A. (2015). Antimicrobial activity of essential oils of cultivated oregano (Origanum vulgare), sage (Salvia officinalis), and thyme (Thymus vulgaris) against clinical isolates of Escherichia coli, Klebsiella oxytoca, and Klebsiella pneumoniae. Microbial Ecology in Health and Disease, 26(0), 23289. doi:10.3402/mehd.v26.23289 PMID:25881620
Fu, Y., Zu, Y., Chen, L., Shi, X., Wang, Z., Sun, S., & Efferth, T. (2007). Antimicrobial activity of clove and rosemary essential oils alone and in combination. Phytotherapy Research: PTR, 21(10), 989–994. doi:10.1002/ptr.2179 PMID:17562569
Fukai, T., Marumo, A., Kaitou, K., Kanda, T., Terada, S., & Nomura, T. (2002). Antimicrobial activity of licorice flavonoids against methicillin-resistant Staphylococcus aureus. Fitoterapia, 73(6), 536–539. doi:10.1016/S0367-326X(02)00168-5 PMID:12385884
EBSCOhost - printed on 2/13/2023 11:18 AM via . All use subject to https://www.ebsco.com/terms-of-use
67