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Plants & Agriculture Research

Review Article Volume 2 Issue 3

Antioxidant, antibacterial and therapeutic properties of some endemic medicinal plants of Iran: a review

Sara Haghju,1 Hadi Almasi2

1Department of Food Science and Technology, University of Tabriz, Iran
2Department of Food Science and Technology, University of Urmia, Iran

Correspondence: Hadi Almasi, Department of Food Science and Technology, Faculty of Agriculture, University of Urmia, Urmia, Tel +989144002691

Received: April 28, 2014 | Published: May 21, 2015

Citation: Haghju S, Almasi H. Antioxidant, antibacterial and therapeutic properties of some endemic medicinal plants of Iran: a review. Adv Plants Agric Res. 2015;2(3):146-153. DOI: 10.15406/apar.2015.02.00053

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Abstract

Bioactive compounds of medicinal herbs have possible health benefits with antioxidative, anticarcinogenic, antihypertensive, antimutagenic and antimicrobial activities. Iranian folk medicine is rich of various herbs which have been employed as drug for treatment of various diseases and disorders since ancient times. The present paper provides a brief overview of the medicinal benefits of some important endemic herbal plants of Iran. Studies on these herbs have revealed that they contain powerful active components that might be effective for increasing human health. The main results of the most important recently researches on the medicinal properties of these plants also mentioned in this review paper.

Keywords: herbal plants, iranian flora, antioxidant activity, antimicrobial properties, medicinal benefits

Abbreviations

ROS, reactive oxygen species; BHA, butylated hydroxy anisole; BHT, butylated hydroxy toluene; TBHQ, tertiary butylated hydroquinon; LDL-C, low density lipoprotein cholesterol; HDL-C, high density lipoprotein cholesterol; DPPH, 2, 2-diphenyl-1-picrylhydrazyl; GC-MS, gas chromatography-mass spectrometry; OHH, obese hyperglycemic hyperlipidemic

Introduction

Lipid oxidation is one of the major causes of quality deterioration and decreasing the shelf life of food products because it leads to color alteration, off-flavor, off-odor and loss of nutrients. It is also related with some diseases such as carcinogenesis, mutagenesis, ageing and arteriosclerosis.1 Reactive oxygen species (ROS) including superoxide anion radicals (O2•−), hydroxyl radicals (OH•) and non-free radical species such as hydrogen peroxide (H2O2) and singlet oxygen (1O2) are continuously produced during body’s normal metabolism.2,3 ROS are major causes of oxidation in foods and are also involved in occurrence of diseases such as ageing, cancer, etc.4 Antioxidant compounds protect the human body from free radicals and ROS effects. They can also provide food protection against oxidative degradation; hence antioxidants increase food quality and acceptability.5 Various synthetic antioxidants such as butylated hydroxy anisole (BHA) butylated hydroxy toluene (BHT), tertiary butylated hydroquinon (TBHQ) and gallic acid esters are used in the food industry to delay lipid oxidation. However, concerns have been raised about using synthetic antioxidants because of their possible side-effects such as liver damage and carcinogenesis that reported in laboratory animals. For this reason, there is a growing tendency to replace synthetic antioxidants with natural ones.6

Recently researchers and food manufacturers have become increasingly interested in plant extracts as natural sources of antioxidants. The antioxidant and antimicrobial properties of various extracts from medicinal plants have been of great interest because of their potential use as natural additives for the prevention of oxidation, controlling pathogens and/or toxin-producing microorganisms in foods.7 Medicinal plants have been used as traditional medicines all over the world for thousands of years. A report by Gen8 showed that out of the 104 compounds that are used globally as drugs over 37 years, 60 of them originated from Chinese traditional medicinal plants.

Bioactive compounds of medicinal herbs especially polyphenolics have possible health benefits with antioxidative, anticarcinogenic, antihypertensive, antimutagenic and antimicrobial activities.9 Polyphenols are secondary metabolites of all vascular plants which are distinguished by the presence of several phenol groups (i.e., aromatic rings with hydroxyls) in their structure.10 They are divided into soluble compounds such as phenolic acids, phenylpropanoids, flavonoids, quinones and non-soluble compounds including condensed tannins and cell wall bound hydroxycinnamic acids. Phenolics possess different biological activities, but most important are antioxidant and antimicrobial activities.11 Antioxidant activities of polyphenolic compounds is generally due to their redox potential which allow them to have various functions such as hydrogen donors, reducing agents, nascent oxygen quenchers and chelating metal ions in numerous food applications. There are also many other compounds that have functional and nutritional value in edible plants, such as ascorbic acid, nitrogen compounds (amino acids, amines, alkaloids and chlorophyll derivatives) and carotenoids.12 These compounds play a role as nutrients, bioactive substances, as well as antioxidants. Most natural antioxidants are obtained from plant resources including culinary herbs, spices, fruits, vegetables and oilseed products.13

Many previous studies have focused on herbs and spices obtained from and consumed in Europe, Southern Asia and Southeast Asia.14 This review introduces 8 endemic medicinal plants of Iran that have antioxidant, antimicrobial and therapeutic activities. Functional chemical compounds and also traditional medicinal usage of these herbs among Iranian people were investigated.

Some medicinal plants of Iran

Apiaceae family

Anethum graveolens “Shevid”: Anethum graveolens L. (Dill), a member of the Apiaceae family, is a herbal plant characterized with a single stem and a terminal or primary umbellate flower.15,16 Dill has been used in various foods such as cans, soups, sauces and also flavoring salads.17 It is traditionally used in Iran as a treatment for some gastrointestinal ailments such as flatulence, indigestion, stomachache and colic and has also antispasmodic effect on the smooth muscles of the gastrointestinal tract.18 Hajhashemi et al.,19 determined hypolipidemic activity of dill powder and its essential oil in male Wistar rats fed a high cholesterol diet. Results showed that A. graveolens powder (10% w/w) reduced the total cholesterol, low density lipoprotein cholesterol (LDL-C), triglyceride and increased the high density lipoproteincholesterol (HDL-C) concentration. Yazdanparast et al.,20 also reported decreasing of LDL/HDL ratio in rats which were fed high fat diet after treatment with A. graveolens extract for 30days.20 Shyu et al.,21 evaluated antioxidant activities of ethanolic extract from dill flower and its various fractions using different methods including 2, 2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging, Trolox equivalent antioxidant capacity, reducing power, chelating power and β-carotene bleaching assays. Flower extract had higher antioxidant activity than the leaf and seed extracts in all assays. According to this study, antioxidant activity of flower extract of dill was due to phenols including flavonoids and proanthocyanidins.21 Singh et al.,22 studied antioxidant, antifungal and antibacterial activities of essential oil and acetone extract of A. graveolens.

According to Gas chromatography-Mass spectrometery (GC-MS) investigation, carvone (55.2%), limonene (16.6%), dill apiole (14.4%), linalool (3.7%), trans-dihydrocarvone (2.8%), cis-dihydrocarvone (2.6%), trans-isocroweacin (0.8%) was the major components, respectively (Table 1). The extract had excellent antioxidant activity against primary and secondary oxidation products in rapeseed oil and also showed a good antioxidant activity measured by different methods such as thiocyanate method in linoleic acid system, reducing power and scavenging effect on DPPH radical in comparison with BHA and BHT. Antimicrobial analyzes indicated that using inverted Petri plate method, the oil had 100% antifungal activity against Fusarium graminearum at 6μL dose.22 Orhan et al.,23 determined inhibitory effect of the n-hexane, dichloromethane, ethyl acetate and ethanol extracts from Dill cultivated under organic (AG-O) and conventional (AG-C) conditions against acetylcholinesterase (AChE), butyrylcholinesterase (BChE) and tyrosinase at 200µg/mL. The extracts of AG-O and AG-C screened herein exhibited modest level of BChE-inhibiting properties, while the ethanol extracts had relatively higher antioxidant activity than rest of the extracts.23 Tian et al.24 determined in vitro and in vivo antifungal activity of the essential oil extracted from the seeds of dill as a potential food preservative.

This activity was evaluated against Aspergillus flavus, Aspergillus oryzae, Aspergillus Niger and Alternaria alternate. The results showed that mycelia growth was noticeably reduced with increasing concentration of dill essential oil while their growth increased with incubation time. The percentages of perished cherry tomatoes were significantly reduced in all treatment groups compared with the control groups and also significantly reduced with increasing concentration of dill oil.24 Kaur et al.,25 determined antibacterial activity of aqueous and organic seed extracts of dill. In addition antibacterial effect of these extracts was compared with some standard antibiotics. Hot water and acetone seed extracts were noticeably effective against E. faecalis, S. aureus, E. coli, P. aeroginosa, S. typhimurium and S. flexneri but Klebsiella pneumoniae and one strain of Pseudomonas aeruginosa were not sensitive to those extracts. Furthermore aqueous and acetone seed extracts were better or similarly active against some of the bacteria in comparison to standard antibiotics.25 Reports on the side effects of dill are limited. The most common side effect is dermatitis but it is considered very rare and usually only when dealing with large quantities of the live plant outdoors in the presence of ultra-violet light.26

In another study Monsefi et al.,27 determined the effects of dill extracts on the female reproductive system of 54 wistar rats. Results showed a significant increase in the duration of the estrous cycle and in the diestrus phase and the progesterone concentration in high dose extract treatment. These authors suggested that dill can be used either as a regulatory agent of the menstrual cycle for women with irregular cycles or as an antifertility agent.27

Coriandrum sativum “Geshniz”: Coriandrum sativum L. (Coriander) is a culinary and medicinal plant from the Umbelliferae family which is used as flavoring agent in food products, perfumes and cosmetics.28 It is generally cultivated for its seeds. The seeds contain an essential oil and the linalool (monoterpenoid compound), as the main components.29 Coriander traditionally used in Iran to treat some ailments including dyspeptic complaints, loss of appetite, convulsion, insomnia and anxiety.30 Aissaoui et al.,31 determined hypoglycemic and hypolipidemic activities of aqueous extract of C. sativum. These activities were evaluated after a single oral dose and after daily dosing for 30 days in normal and obese–hyperglycemic–hyperlipidemic (OHH) Meriones shawi rats. A single dose of Coriander extract inhibited hyperglycemia in OHH rats and normo-glycemia was achieved after 6hours of treatment. The extract was not effective on amount of lipids, triglycerides or insulin, but insulin resistance decreased significantly.31 De Almeida Melo et al.,32 isolated phenolic compounds of aqueous Coriander extract using gas chromatography and mass spectrometry (GC-MS). Four fractions were recognized from the crude extract and all had caffeic acid in common. Determination of antioxidant activity with β-carotene/linoleic acid model showed that all fractions had similar activity; however, it was less than BHT and the crude aqueous extract.32 Sreelatha et al.,33 assessed antioxidant activity of ethanolic-water extract of C. sativum on carbon tetrachloried (CCl4) treated oxidative stress in Wistar albino rats. They also evaluated the activities of enzymes like alkaline phosphatase, acid phosphatase and protein and bilirubin in serum.

The levels of mentioned enzymes were significantly reduced with increasing concentration of C. sativum in a dose-dependent manner. The results indicated that oral administration of the leaf extract at a dose of 200mg/kg body weight significantly reduced the toxic effects of CCl4.33 In another study Wangensteen et al.,34 studied antioxidant activity of different solvent extracts from leaves and seeds and oil of C. sativum using different assays such as DPPH scavenging activity, inhibition of 15-lipoxygenase (15-LO) and inhibition of Fe2+ induced porcine brain phospholipid peroxidation. Ethyl acetate extracts of both seeds and leaves had highest amounts of phenolic compounds and strongest radical-scavenging activity. In addition leaves extracts were more effective antioxidants than the seeds one. The results of the study indicated that the compounds with medium polarity were the most potential antioxidants.34 Wong et al.,35 evaluated antioxidant and antibacterial activities of methanolic and water extracts of freeze-dried and irradiated Parsley (Petroselinum crispum) and Cilantro (C. sativum) leaves and stems. Methanolic extract of parsley had higher total phenolic content and DPPH radical-scavenging activity than cilantro extract. Additionally, methanolic extracts of leaves showed significantly superior radical-scavenging activity, which was related to the total phenolic content. Methanolic stem extracts had greatest bacterial cell damage which led to greater growth inhibition towards Bacillus subtilis and Escherichia coli.35 Matasyoh et al.,36 analyzed the essential oil of leaves of C. sativum by GC-Mass and evaluated its antimicrobial activity.

The major constituents were 2E-decenal, decanal, 2E-decen-1-ol and n-decanol. Results showed that the oil has great antimicrobial activity against K. pneumonia and Proteus mirabilis but the best activity was observed for the Gram positive bacteria.36 Duarte et al.,37 determined synergistic antibacterial effect between corianders (C. sativum) essential oil and six different antibacterial drugs (Cefoperazone, Chloramphenicol, Ciprofloxacin, Gentamicin, Tetracycline and Piperacillin). According to their results there was a synergistic action between Chloramphenicol, Ciprofloxacin, Tetracycline or Gentamicin and the commercial coriander essential oil.37 Zoubiri et al.,29 considered the effect of coriander seed essential oil as a fumigant against Sitophilus granarius in chickpea grains. They reported that coriander is potentially useful grain protectant with fumigant activity. They concluded that the major compounds from coriander fruit essential oil, mainly linalool, can be developed as a potential fumigant for stored-products protection.29 Michalczyk et al.,38 evaluated the effect of adding essential oils of hyssop and coriander at the highest concentration (0.02% v/w) sensorially acceptable to a panel of assessors on the microbiological and biochemical characteristics of stored ground beef. According to GC analysis cis-pinocamphone in essential oil of hyssop and linalool in essential oil of coriander was the main components respectively. Sensory evaluation showed that the addition of coriander in ground beef improved sensory attributes as compared with control sample. The considerable inhibitory effect of both oils addition was observed on Enterobacteriaceae family bacteria but they were having minor effects on lactic acid bacteria, total viable bacterial count and other groups of microorganisms.38 Pat et al.,39 studied the acute toxicity profile of hydro-methanolic extract of Coriander seeds (CS). In this research, mice were once orally administered 1000, 3000 and 5000mg/kg body weight of CS extract. Results showed that CS extract is non-toxic up to 3000mg/kg body weight and LD50 value was more than 5000mg/kg body weight.39

Özbek et al.,40 determined lethal doses of volatile and fixed oils of several plants including Coriandrum sativum. According to their study LD50 value of essential and free oil extract of coriander were 2.257 and 13.300ml/mg, respectively.40

Cuminum cyminum “Zireye sabz: Cuminum cyminum is an annual herbaceous plant, belongs to the Apiaceae family. Each fruit of this plant contains a green seed with aromatic characteristics. It is used in Iranian folk medicine since more than 200 years ago.41 The fruits have been extensively used as an Iranian traditional medicine for treatment of toothache, diarrhea and epilepsy.42 Dhandapani et al.,43 evaluated the effect of C. cyminum seed powder supplementation on the plasma and tissue lipids in alloxan diabetic rats. Results showed that oral administration of cumin extract to diabetic rats significantly reduced the blood glucose levels and increased levels of plasma cholesterol, phospholipids, free fatty acids and triglycerides.,43 Jagtap e al.,44 studied the effect of methanolic extract of C. cyminum seeds on diabetes, oxidative stress and compared it with Glibenclamide. They reported that treatment with C. cyminum seeds extract and Glibenclamide reduced the elevated blood glucose and increased serum insulin and glycogen content. The extract exhibited DPPH and superoxide scavenging activity in a dose dependent manner and the best activity of extract has been shown at concentration of 10–1600lg/ml. In addition half maximal inhibitory concentration (IC50) value of C. cyminum seeds extract for inhibition of DPPH and superoxide was found to be 230 and 1120l g/ml respectively.44

El-Ghorab et al.,45 investigated chemical composition and antioxidant activity of ginger (Zingiber officinale) and cumin (C. cyminum). Cuminal (27.7%), γ-terpinene (23.7%), pinocarveol (11.4%), 1-methyl-2-(1-methylethyl) benzene (7.7%), copaene (6.0%), (5R)-5-methyl-2-(1-methylethylidene) cyclohexanone (5.5%), carotol (4.4%), 2-ethylidene-6-methyl-3,5-heptadienal (2.8%) and sabinene (1.2%) were the major components of cumin essential oil which identified with GC. Cumin had the highest amount of volatiles; also highest total phenolic contents were observed in the methanol extract of fresh ginger. According to DPPH assay, maximum antioxidant activity has been shown for cumin essential oil followed by dried ginger essential oil and fresh ginger essential oil.45 Oroojalian et al.,46 analyzed essential oils of three Apiaceae species, including Bunium persicum, C. cyminum and Carum copticum, extracted by hydrodistillation, using GC and GC-MS. The main components of C. cyminum were cuminaldehyde (30.2%), q-cymene (14.1%), c-terpinene (12.8%), safranal (9.4%) and β-pinene. The in vitro antibacterial activities of B. persicum, C. cyminum and C. copticum essential oils were evaluated against major bacterial food-borne pathogens by using the microdilution method. Results showed that there is a synergistic activity between B. persicum and C. cyminum against Gram-positive bacteria, including Staphilococcus aureus, Bacillus cereus and Listeria monocytogenes, compared to use of each essential oil alone.46 Derakhshan et al.,47 investigated antibacterial activity of cumin seed essential oil and alcoholic extract against K. pneumonia ATCC 13883 and clinical K. pneumonia isolates. The essential oil had inhibition zone of 12–16mm/20µL, but the alcoholic extract showed no inhibition zone against any of the K. pneumonia strains. Furthermore cumin aldehyde was the major component of the oil determined by GC-MS spectrometry.47 Table 1 summarizes the bioactive compounds and health effects of some herbs of Apiaceae family grown in Iran.

Herbal plant

Phytochemicals

Potential benefits

References

Anethum graveolens (Dill, shevid)

Carvone, limonene, dill apiole, linalool, trans-dihydrocarvone, cis-dihydrocarvone, trans-isocroweacin

Used as a treatment for some gastrointestinal ailments such as flatulence, indigestion, stomachache and colic and has also antispasmodic effect on the smooth muscles of the gastrointestinal tract.

Hosseinzadeh et al.,18 Singh et al.22

Coriandrum sativum (Geshniz)

2E-decenal, decanal, 2E-decen-1-ol and n-decanol

To treat some ailments including dyspeptic complaints, loss of appetite, convulsion, insomnia and anxiety.

Matasyoh et al.,36 Emamghoreishi et al.30

Cuminum cyminum (Zireye sabz)

γ-terpinene, pinocarveol,

Extensively used as an Iranian traditional medicine for treatment of toothache, diarrhea and epilepsy.

Janahmadi et al.m42 El-Ghorab et al.45

1-methyl-2-(1-methylethyl) benzene, copaene,

(5R)-5-methyl-2-(1-methylethylidene) cyclohexanone, carotol, 2-ethylidene-6-methyl-3,5-heptadienal and sabinene

Table 1 Bioactive compounds and health effects of herbal plants of Apiaceae family

Asteraceae (Compositae)

Cichorium intybus “Kasni”: Cichorium intybus (Chicory) belongs to the Compositae family is called as “Kasni” in Iran. It is used for treatment of acne, inflammation of throat, enlargement of the spleen, diarrhea and vomiting.48 Chicory has also used as an herbal medicine due to its tonic effects upon the liver and digestive tract.49 Fresh chicory consists of 68% inulin, 14% sucrose, 5% cellulose, 6% protein, 4% ash and 3% other compounds, whereas dried chicory contains about 98% inulin and 2% other compounds.50 Ahmed51 investigated protective effects of C. intybus in short and long-term diabetes in albino rat models. Feeding with dried powder of Chicory leaves lowered the blood glucose level to near normal level (85-100mg/dl).51 Heimler et al.,52 compared conventionally and biodynamically-grown chicory for its polyphenol content and antiradical activity. Results indicated that total polyphenol content was higher in plants exposed to water stress. Also individual polyphenols including five hydroxycinnamic acids and eight flavonoids (quercetin, kaempferol, luteolin and apigenin glycosides) were identified using HPLC/DAD/MS analysis.52 Nørbæk et al.,53 determined anthocyanins of blue perianth segments of C. intybus by HPLC. The identified pigments included delphinidin 3,5-di-O-(6-O-malonyl-b-d-glucoside) and delphinidin 3-O-(6-O-malonyl-b-d-glucoside)-5-O-b-d-glucoside and the known compounds were delphinidin 3-O-b-d-glucoside-5-O-(6-O-malonyl-b-d-glucoside) and delphinidin 3,5-di-O-b-d-glucoside.53 Shaikh et al.,54 evaluated antimicrobial screening of ethanol, ethyl acetate and aqueous seed extracts of C. intybus by agar well diffusion assay against S. aureus, P. aeruginosa, C. albicans and E.coli. All the extracts exhibited antimicrobial activity against mentioned microorganisms while S. aureus was the most sensitive pathogen against aqueous extract and had the widest zone of inhibition.54

Lamiaceae

Melissa officinalis “Badranjbooye”: Melissa officinalis L. is an Iranian medicinal plant locally named Badranjbooye, Varangboo and Faranjmoshk and grows in the north, north-west and western parts of the country.55 It is traditionally used as a treatment for headaches, flatulence, indigestion, colic, nausea, nervousness, anaemia, vertigo, syncope, malaise, asthma, bronchitis, amenorrhea, cardiac failure, arrhythmias, insomnia, epilepsy, depression, psychosis, hysteria, ulcers and wounds. The leaves of M. officinalis L. are also utilized in Iranian traditional medicine as digestive, carminative, antispasmodic, sedative, analgesic, tonic and diuretic as well as for functional gastrointestinal disorders. The analysis of chemical composition of the essential oil of the leaf identified citronellal, citral and β-caryophyllene as major components.56 Saeb & Gholamrezaee57 analyzed the essential oil of M .officinalis obtained by hydro distillation using GC/MS in three different stages: before flowering stage, flowering stage and after flowering stage. Results showed that the major components before flowering stage were decadienal (29.38%), geraniol (25.3%), caryophyllene oxide (8.75%), geranyl acetate, (5.41%) decadienal (28.04%), geraniol (24.97%), caryophyllene oxide (7.55%) and caryophyllene E (4.65%). Also carvacrol (37.62%), methyl citronellate (32.34%), geranyl acetate (5.82%) and caryophyllene (5.50%) were identified as major components in the flowering stage and after flowering stage of plant.57

Lara et al.,58 investigated antioxidant activity of two natural extracts (R. officinalis and M. officinalis) in cooked pork patties packed in modified atmosphere packaging (MAP) using TBARS (thiobarbituric acid reactive substances) method and results compared with BHT. It has been shown that lipid oxidation was considerably reduced in samples with added antioxidants compared to control one. According to this study Rosemary extract (Nutrox) was the most potent antioxidant (90.7%) followed by BHT (76.3%) and lemon balm extract (Meliox) (74.8%).58 Hussain et al.,59 evaluated the antibacterial activity of six Lamiaceae essential oils, against pathogenic and food spoilage bacteria (S.aureus, B.cereus, B.subtilis, Bacillus pumilis, P. aeruginosa, Salmonella Poona (S. Poona) and E. coli) using modified resazurin microtitre-plate assay. According to the results, inhibition zone of M. officinalis varied from 13.7 to 28.2mm and also MIC value ranged from 72.0-1000.3mm. GC/MS experiments showed that citronellal (20.5%), β- geraniol (17.0%), β-citronellol (11.5%) were the major components of M. officinalis.59

Mentha piperita (Na’na): Mentha piperita (Peppermint) belongs to the Lamiaceae family and is probably originated in Eastern Asia. This medicinal plant is particularly beneficial in building the immune system and fighting secondary infections. M. piperita is rich in polyphenolic compounds and therefore has strong antioxidant activity. Menthol is the most abundant constituent of the essential oil which has antibacterial effects.60 Fadaei et al.,61 investigated antibacterial activity of essential oil of M. piperita against E.coil, B.subtilis and S.typhimurium using MIC method. Results showed that MIC value of essential oil for these three microorganisms was lower in comparison to this value in Sodium Benzoate. It can be concluded that antimicrobial activity of the essential oil was stronger than Sodium Benzoate.61 Yadegarinia et al.,62 investigated antibacterial effect of M. piperita oil against C. albicans and E. coli. Results showed that M. piperita oil was active at higher dilutions against mentioned microbial strains. C.albicans was the most sensitive microorganism and E. coli was the second susceptible microorganism to the essential oil of M. piperita. According to GC/MS results, α-terpinene (19.7%), isomenthone (10.3%), trans-carveol (14.5%), pipertitinone oxide (19.3%) and β-caryophyllene (7.6%) were the major compounds.62 Tyagi et al.,63 evaluated antimicrobial activity and chemical composition of M. piperita oil against food spoilage microorganisms including (E.coli, P. aeruginosa, Pseudomonas fluorescens, B. subtilis and S. aureus), fungal strains (Penicillium digitatum, A. flavus, A. niger, Mucor spp and F. oxysporum) and yeasts (C. albicans and Sacchromyces cerevisiae) by agar dilution method. Results showed that MIC and Minimum bactericidal and fungicidal concentration (MBC/MFC) of M. piperita oil ranged from 1.13 to 2.25mg/ml and 2.25 to 9mg/ml for bacterial strains, 1.13 to 2.25mg/ml and 2.25 to 4.5 mg/ml for fungal strains and 1.13mg/ml and 2.25mg/ml for yeasts, respectively. Analysis of chemical composition by GC/MS showed the presence of menthol (19.1%), isomenthone (14.8%), limonene (10.6%), iso-menthanol (8.8%), menthyl acetate (6.6%), β-pinene (5.6%), α-pinene (4.8%), 1,8-cineole (3.5%), isopulegol (3%), pulegone (2.3%), piperitone (2.1%) and β-phellandrene (2.8%) as major components of the oil.63

Mentha pulegium “Pooneh”: Mentha pulegium L. commonly known as pennyroyal is a medicinal plant of Labiatae (Lamiaceae) family. The flowering aerial parts of the plant has been conventionally used for its antiseptic properties to treat cold, sinusitis, cholera, food poisoning, bronchitis and tuberculosis and also used as antiflatulent, carminative, expectorant, diuretic, antitussive and menstruate.64 Kamkar et al.,65 investigated antioxidative activities of the essential oil, methanol and water extracts of Iranian pennyroyal in vegetable oil during storage. Antioxidant activity of the essential oil and extracts were evaluated using DPPH and β-carotene–linoleic acid methods. According to GC/MS results, pulegone (40.5%), menthone (35.4%) and piperitone (5.2%) were identified as major components and the other compounds were Gamma-sitosterol (2.3%), Benzene, 1-methoxy-4-(2-propenyl) (1.9%), 3-octanol (1.9%), α-amyrin (1.2%), α-pinene (0.9%), α-terpineol (0.9%), β– pinene (0.8%), Germacerene-D (0.6%) and Mint furanone (0.5%).65 Ait-Ouazzou et al.,66 evaluated the chemical composition and antimicrobial activity of M. pulegium, Juniperus phoenicea and Cyperus longus against four gram-positive bacteria including S. aureus, Enterococcus faecium, L. monocytogenes and three Gram negative bacteria including Salmonella enteritidis, E. coli and P. aeruginosa. In determining zone of growth inhibition (mm), M. pulegium oil showed the widest antibacterial spectra ranged from 12.6±0.5 mm (E. coli) to 35.6±0.6 mm (L. monocytogenes EGD-e) depending on the susceptibility of the tested organism. It has been shown that M. pulegium had the best bacteriostatic and bactericidal effect between the tested herbal plants as it displayed bacteriostatic activity against all strains tested (with the exception of P. aeruginosa) with MIC values of <0.5 (E. faecium) and 1μL/mL (S. aureus, L. monocytogenes, E. coli and S. Enteritidis). Investigation of MBC showed that M. pulegium had antibacterial activity against five of the seven bacteria at concentrations ranged from 0.5μL/mL to10μL/mL. According to GC/MS results, Pulegone (69.8%) was the most abundant compound in M. pulegium oil followed by piperitenone (3.1%), Isopulegone (1.8%) and piperitone epoxide cis (1.7%).66

Urticaceae

Urtica dioica “Gazaneh”: Urtica dioica L. (nettle) is an herbaceous perennial flowering plant, belongs to the Urticaceae family. Herbal infusion of leaves is used to treat diarrhea, vaginal discharge, internal/external bleeding.67 In addition leaves have been shown to have hypotensive and anti-inflammatory effects, diuretic and immunomodulatory activity and to alleviate rheumatic pain.68 Steroids, terpenoids, phenylpropanoids, coumarins, polysaccharides, lectins; and seven flavonol glycosides (kaempherol-3-O-glucoside and -3-O-rutinoside; quercetin-3-Oglucoside and -3-O-rutinoside, isorhamnetin-3-O-glucoside, -3-O-rutinoside and -3-Oneohesperidoside) have been identified as major components of root and flowers of U .dioica respectively.69 Gülçin et al.70 evaluated antioxidant activity of aqueous extract of nettle. The percentage of inhibition of peroxidation in linoleic acid emulsion and reductive capability of the nettle extract were more than α-tocopherol. In addition, nettle extract in the same concentrations, exhibited more inhibition percentage of superoxide generation than of BHA, BHT and α-tocopherol. DPPH-scavenging activities of the extract and BHA were equal but lower than that of quercetin. The metal chelating ability of the extract was higher than that of BHT, α-tocopherol, or BHA.70

Antioxidant activity of hydroalcoholic solution extracts of U. dioica and M. neglecta Wallr plants and their mixture were investigated. Hydroalcoholic extracts of both plants had strong antioxidant activity, reducing power, superoxide anion radical scavenging, hydrogen peroxide scavenging, free radical scavenging and metal chelating activities in comparison to natural and synthetic standard antioxidants such as BHA, BHT and α-tocopherol. The total antioxidant activity of these two plants was nearly the least while that of the mixture extract was higher than estimated. As a consequence, the antioxidant activity of herbal plants synergistically improves by using their mixture.71 Antioxidant activity and total phenol content of fifteen different extracts from the leaves of U. dioica, Pilea microphylla and Elatostema umbellatum were determined. According to the results, butanol and ethyl acetate extracts of U. dioica had the highest DPPH radical scavenging activity.72 Erdogrul73 evaluated antibacterial activities of ethyl acetate, ethanol, chloroform and acetone extracts of U. dioica against some bacterial species including Bacillus brevis, M. luteus, Mycobacterium smegmatus, E.coli, L. monocytogenes and S. aureus, using the agar diffusion method. The results indicated that the all plant extracts of stinging nettle displayed no antibacterial activity against any of the test microorganisms.73

Future trends

When consumed consciously and systematically, many herbal plants are very important for human health because of their phenolic compounds. Most medicines are produced synthetically today and many microorganisms can develop resistance very quickly against them, which is not possible in the case of phytochemicals. In recent years, especially in the developed countries, there is a tendency towards increased use of phytochemicals. Medicinal herbs as a source of phytochemicals can help people to stay fit. Healing and nourishing processes may go together. However, endemicity and seasonal or periodical growth of the most of these plants has limited their availability. Accordingly, cultivation, processing and preservation of herbal plants could be a good idea for increasing the availability of endemic plants for all people around the world. The herbs of these plants can also be provided in the form of capsules and powders, as dietary supplements and thus differ from conventional foods or food ingredients. On the other hand, more research into the medicinal effects and health benefits of all the endemic herbal plants in different organs is needed, both from the epidemiological perspective and in animal and cell models. Medicinal benefits and possible harmful effects of the herbal plants should be completely introduced to the consumers.

Conclusion

Results reported here contribute to the knowledge of antibacterial and therapeutic activities of 8 Iranian medicinal plants. The literature reviews presented in this paper strongly approved the medicinal properties of the all mentioned herbal plants. The finding that these medicinal plants possess antioxidant and therapeutic activity implies that making these plants as an integral part of daily consumption may prevent more diseases. So this review paper could be a useful reference for researchers in this area for increasing their knowledge about Iranian medicinal herbs. Also we hope that our paper will provide a starting point for discovering new plants with better activity than those mentioned here.

Acknowledgements

None

Conflicts of interest

The author declares no conflict of interest.

References

  1. Yagi K. Lipid peroxides and human diseases. Chem Phys Lipids. 1987;45(2–4):337–351.
  2. Ak T, Gülçin İ. Antioxidant and radical scavenging properties of curcumin. Chem Biol Interact. 2008;174(1):27–37.
  3. Gülçin İ. Antioxidant properties of resveratrol: a structure–activity insight. Innovative Food Science & Emerging Technologies. 2010;11(1):210–218.
  4. Oktay M, Gülçin IL, Küfrevioğlu Öİ. Determination of in vitro antioxidant activity of fennel (Foeniculum vulgare) seed extracts. LWT–Food Sci Technol. 2003;36(2):263–271.
  5. Gülçın I, Beydemır Ş, Alici HA, et al. In vitro antioxidant properties of morphine. Pharmacol Res. 2014;49(1):59–66.
  6. Bandyopadhyay M, Chakraborty R, Raychaudhuri U. Antioxidant activity of natural plant sources in dairy dessert (Sandesh) under thermal treatment. LWT–Food Sci Technol. 2008;41(5):816–825.
  7. Kratchanova M, Denev P, Ciz M, et al. Evaluation of antioxidant activity of medicinal plants containing polyphenol compounds. Comparison of two extraction systems. Acta Biochim Pol. 2010;57(2):229–234.
  8. Gen P, Xiao. Medicinal plants: the Chinese approach. World Health Forum. 1986;7(1):84–85.
  9. Belščak–Cvitanović A, Stojanović R, et al. Encapsulation of polyphenolic antioxidants from medicinal plant extracts in alginate–chitosan system enhanced with ascorbic acid by electrostatic extrusion. Food Res Int. 2011;44(4):1094–1101.
  10. Petti S, Scully C. Polyphenols, oral health and disease: A review. J Dent. 2009;37(6):413–423.
  11. Rispail N, Morris P, Webb KJ. Phenolic compounds: extraction and analysis. Lotus japonicus Handbook: Springer; 2005. p. 349–354.
  12. Hall C, Cuppett S. Structure–activities of natural antioxidants. Antioxidant Methodology: In vivo and in vitro Concepts. AOCS Press Champaign, IL. 1997;76:141–172.
  13. Shahidi F, Zhong Y. Novel antioxidants in food quality preservation and health promotion. Eur J Lipid Sci Technol. 2010;112(9):930–940.
  14. Kim SJ, Shin HJ, Lee YJ, et al. Evaluation of the antioxidant activities and nutritional properties of ten edible plant extracts and their application to fresh ground beef. Meat Sci. 2012;93(3):715–722.
  15. Callan NW, Johnson DL, Westcott MP, et al. Herb and oil composition of dill (Anethum graveolens L.): Effects of crop maturity and plant density. Ind Crop Prod. 2007;25(3):282–287.
  16. Stavri M, Gibbons S. The antimycobacterial constituents of dill (Anethum graveolens). Phytother Res. 2005;19(11):938–941.
  17. Cankur O, Yathavakilla SK, Caruso JA. Selenium speciation in dill (Anethum graveolens L.) by ion pairing reversed phase and cation exchange HPLC with ICP–MS detection. Talanta. 2006;70(4):784–790.
  18. Hosseinzadeh H, Karimi GR, Ameri M. Effects of Anethum graveolens L. seed extracts on experimental gastric irritation models in mice. BMC Pharmacol. 2002;2(1):21–28.
  19. Hajhashemi V, Abbasi N. Hypolipidemic activity of Anethum graveolens in rats. Phytother Res. 2008;22(3):372–375.
  20. Yazdanparast R, Bahramikia S, Ardestani A. Nasturtium officinale reduces oxidative stress and enhances antioxidant capacity in hypercholesterolaemic rats. Chem Biol Interact. 2008;172(3):176–184.
  21. Shyu YS, Lin JT, Chang YT, et al. Evaluation of antioxidant ability of ethanolic extract from dill (Anethum graveolens L.) flower. Food Chem. 2009;115(2):515–521.
  22. Singh G, Maurya S, Lampasona M, et al. Chemical constituents, antimicrobial investigations, and antioxidative potentials of Anethum graveolens L. essential oil and acetone extract:Part 52. J Food Sci. 2005;70(4):M208–M215.
  23. Orhan IE, Sezer Senol F, Ozturk N, et al. Phytochemical contents and enzyme inhibitory and antioxidant properties of Anethum graveolens L. (dill) samples cultivated under organic and conventional agricultural conditions. Food Chem Toxicol. 2013;81:678–684.
  24. Tian J, Ban X, Zeng H, et al. In vitro and in vivo activity of essential oil from dill (Anethum graveolens L.) against fungal spoilage of cherry tomatoes. Food Control. 2011;22(12):1992–1999.
  25. Kaur GJ, Arora DS. Antibacterial and phytochemical screening of Anethum graveolens, Foeniculum vulgare and Trachyspermum ammi. BMC Complement Altern Med. 2009;9(1):30–39.
  26. Pathak MA. Phytophotodermatitis. Clin Dermatol. 1986;4(2):102–121.
  27. Monsefi M, Ghasemi M, Bahaoddini A. The effects of Anethum graveolens L. on female reproductive system. Phytother Res. 2006;20(10):865–868.
  28. Msaada K, Hosni K, Taarit MB, et al. Changes on essential oil composition of coriander (Coriandrum sativum L.) fruits during three stages of maturity. Food Chem. 2007;102(4):1131–1134.
  29. Zoubiri S, Baaliouamer A. Essential oil composition of Coriandrumsativum seed cultivated in Algeria as food grains protectant. Food Chem. 2010;122(4):1226–1228.
  30. Emamghoreishi M, Khasaki M, Aazam MF. Coriandrumsativum: evaluation of its anxiolytic effect in the elevated plus–maze. J Ethnopharmacol. 2005;96(3):365–370.
  31. Aissaoui A, Zizi S, Israili ZH, et al. Hypoglycemic and hypolipidemic effects of Coriandrum sativum L. in Meriones shawi rats. J Ethnopharmacol. 2011;137(1):652–661.
  32. De Almeida Melo E, Mancini Filho J, Barbosa Guerra N. Characterization of antioxidant compounds in aqueous coriander extract (Coriandrum sativum L.). LWT–Food Sci Technol. 2005;38(1):15–19.
  33. Sreelatha S, Padma P, Umadevi M. Protective effects of Coriandrum sativum extracts on carbon tetrachloride–induced hepatotoxicity in rats. Food Chem Toxicol. 2009;47(4):702–708.
  34. Wangensteen H, Samuelsen AB, Malterud KE. Antioxidant activity in extracts from coriander. Food Chem. 2004;88(2):293–297.
  35. Wong PY, Kitts DD. Studies on the dual antioxidant and antibacterial properties of parsley (Petroselinum crispum) and cilantro (Coriandrum sativum) extracts. Food Chem. 2006;97(3):505–515.
  36. Matasyoh J, Maiyo Z, Ngure R, et al. Chemical composition and antimicrobial activity of the essential oil of Coriandrum sativum. Food Chem. 2009;113(2):526–529.
  37. Duarte A, Ferreira S, Silva F, et al. Synergistic activity of coriander oil and conventional antibiotics against Acinetobacter baumannii. Phytomedicine. 2012;19(3–4):236–238.
  38. Michalczyk M, Macura R, Tesarowicz I, et al. Effect of adding essential oils of coriander (Coriandrum sativum L.) and hyssop (Hyssopus officinalis L.) on the shelf life of ground beef. Meat sci. 2012;90(3):842–850.
  39. Patel D, Desai S, Devkar R, et al. Acute and sub–chronic toxicological evaluation of hydro–methanolic extract of coriandrum sativum l. seeds. Excli J. 2012;11:566–575.
  40. Hanefi Ö, Mustafa Ö, Abdurrahman Ö, et al. Determination of lethal doses of volatile and fixed oils of several plants. East J Med. 2013;9(1):4–6.
  41. Saiedirad M, Tabatabaeefar A, Borghei A, et al. Effects of moisture content, seed size, loading rate and seed orientation on force and energy required for fracturing cumin seed (Cuminum cyminum Linn.) under quasi–static loading. J Food Eng. 2008;86(4):565–572.
  42. Janahmadi M, Niazi F, Danyali S, et al. Effects of the fruit essential oil of Cuminum cyminum Linn. (Apiaceae) on pentylenetetrazol–induced epileptiform activity in F1 neurones of Helix aspersa. J Ethnopharmacol. 2006;104(1–2):278–282.
  43. Dhandapani S, Subramanian VR, Rajagopal S, et al. Hypolipidemic Effect of cuminum cyminum L. on alloxan–induced diabetic rats. Pharmacol Res. 2002;46(3):251–255.
  44. Jagtap A, Patil P. Antihyperglycemic activity and inhibition of advanced glycation end product formation by Cuminum cyminum in streptozotocin induced diabetic rats. Food Chem Toxicol. 2010;48(8):2030–2036.
  45. El–Ghorab AH, Nauman M, Anjum FM, et al. A comparative study on chemical composition and antioxidant activity of ginger (Zingiber officinale) and cumin (Cuminum cyminum). J Agric Food Chem. 2010;58(14):8231–8237.
  46. Oroojalian F, Kasra–Kermanshahi R, Azizi M, Bassami M. Phytochemical composition of the essential oils from three Apiaceae species and their antibacterial effects on food–borne pathogens. Food Chem. 2010;120(3):765–770.
  47. Derakhshan S, Sattari M, Bigdeli M. Effect of subinhibitory concentrations of cumin (Cuminum cyminum L.) seed essential oil and alcoholic extract on the morphology, capsule expression and urease activity of Klebsiella pneumoniae. Int J Antimicrob Agents. 2008;32(5):432–436.
  48. Heibatollah S, Reza NM, Izadpanah G, et al. Hepatoprotective effect of Cichorium Intybus on CCl4–induced liver damage in rats. African J Biochem Res. 2008;2(6):141–144.
  49. Pushparaj P, Low H, Manikandan J, et al. Anti–diabetic effects of Cichorium intybus in streptozotocin–induced diabetic rats. J Ethnopharmacol. 2007;111(2):430–434.
  50. Hassan HA, Yousef MI. Ameliorating effect of chicory (Cichorium intybus L.)–supplemented diet against nitrosamine precursors–induced liver injury and oxidative stress in male rats. Food Chem Toxicol. 2010;48(8–9):2163–2169.
  51. Ahmed N. Alloxan diabetes–induced oxidative stress and impairment of oxidative defense system in rat brain: neuroprotective effects of Cichorium intybus. Int J Diabetes & Metabolism. 2009;17:105–109.
  52. Heimler D, Isolani L, Vignolini P, et al. Polyphenol content and antiradical activity of Cichorium intybus L. from biodynamic and conventional farming. Food Chem. 2009;114(3):765–770.
  53. Nørbæk R, Nielsen K, Kondo T. Anthocyanins from flowers of Cichorium intybus. Phytochemistry. 2002;60(4):357–369.
  54. Shaikh T, Rub RA, Sasikumar S. Antimicrobial screening of Cichorium intybus seed extracts. Arabian J Chem. 2012;34:111–119.
  55. Dastmalchi K, Damien Dorman H, Oinonen PP, et al. Chemical composition and in vitro antioxidative activity of a lemon balm (Melissa officinalis L.) extract. LWT–Food Sci Technol. 2008;41(3):391–400.
  56. Sadraei H, Ghannadi A, Malekshahi K. Relaxant effect of essential oil of Melissa officinalis and citral on rat ileum contractions. Fitoterapia. 2003;74(5):445–452.
  57. Saeb K, Gholamrezaee S. Variation of essential oil composition of Melissa officinalis L. leaves during different stages of plant growth. Asian Pac J Trop Biomed. 2012;2(2):s547–s559.
  58. Lara M, Gutierrez J, Timón M, et al. Evaluation of two natural extracts (Rosmarinus officinalis L. and Melissa officinalis L.) as antioxidants in cooked pork patties packed in MAP. Meat Sci. 2011;88(3):481–488.
  59. Hussain AI, Anwar F, Nigam PS, et al. Antibacterial activity of some Lamiaceae essential oils using resazurin as an indicator of cell growth. LWT– Food Sci Technol. 2011;44(4):1199–1206.
  60. Toghyani M, Toghyani M, Gheisari A, et al. Growth performance, serum biochemistry and blood hematology of broiler chicks fed different levels of black seed (Nigella sativa) and peppermint (Mentha piperita).Livestock Sci. 2010;129(1–3):173–178.
  61. Fadaei S, Abroumand AP, Sharifan A, et al. Evaluation of Antimicrobial Activity of Mentha piperita L. Essential Oil and Its Comparison with Sodium Benzoate. J Food Technol Nutr. 2011;8(1):34–41.
  62. Yadegarinia D, Gachkar L, Rezaei MB, et al. Biochemical activities of Iranian Mentha piperita L. and Myrtus communis L. essential oils. Phytochemistry. 2006;67(12):1249–1255.
  63. Tyagi AK, Malik A. Antimicrobial potential and chemical composition of Mentha piperita oil in liquid and vapour phase against food spoiling microorganisms. Food Control. 2011;22(2011):1707–1714.
  64. Mahboubi M, Ghazian Bidgoli F. In vitro synergistic efficacy of combination of amphotericin B with Myrtus communis essential oil against clinical isolates of Candida albicans. Phytomedicine. 2010;17(10):771–774.
  65. Kamkar A, Javan AJ, Asadi F, et al. The antioxidative effect of Iranian Mentha pulegium extracts and essential oil in sunflower oil. Food Chem Toxicol. 2010;48(7):1796–1800.
  66. Ait–Ouazzou A, Lorán S, Arakrak A, et al. Evaluation of the chemical composition and antimicrobial activity of Mentha pulegium, Juniperus phoenicea, and Cyperus longus essential oils from Morocco. Food Res Int. 2012;45(1):313–319.
  67. Kukric Z, Topalic–Trivunovic L, Kukavica B, et al. Characterization of antioxidant and antimicrobial activities of nettle leaves (Urtica dioica L.). Acta per tech. 2012;43(43):257–272.
  68. Özen T, Korkmaz H. Modulatory effect of Urtica dioica L. (Urticaceae) leaf extract on biotransformation enzyme systems, antioxidant enzymes, lactate dehydrogenase and lipid peroxidation in mice. Phytomedicine. 2003;10(5):405–415.
  69. Yener Z, Celik I, Ilhan F, et al. Effects of Urtica dioica L. seed on lipid peroxidation, antioxidants and liver pathology in aflatoxin–induced tissue injury in rats. Food Chem Toxicol. 2009;47(2):418–424.
  70. Gülçin I, Küfrevioǧlu Öİ, Oktay M, et al. Antioxidant, antimicrobial, antiulcer and analgesic activities of nettle (Urtica dioica L.). J Ethnopharmacol. 2004;90(2–3):205–215.
  71. Güder A, Korkmaz H. Evaluation of in–vitro Antioxidant Properties of hydroalcoholic Solution Extracts Urtica dioica L., Malva neglecta Wallr. and their Mixture. Iran J Pharm Res. 2012;11(3):913–923.
  72. Chahardehi AM, Ibrahim D, Sulaiman SF. Antioxidant activity and total phenolic content of some medicinal plants in Urticaceae family. J Applied Biol Sci. 2009;3(2):27–31.
  73. Erdogrul ÖT. Antibacterial activities of some plant extracts used in folk medicine. Pharm Biol. 2002;40(4):269–273.
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