Determination of Volatile Compounds of Mentha piperita and Lavandula multifida and Investigation of Their Antibacterial, Antioxidant, and Antidiabetic Properties

Mentha piperita and Lavandula multifida are widely used in Moroccan traditional medicine for the treatment of diabetes and infectious diseases. The aims of this work were the determination of the chemical composition of Mentha piperita (MPEO) and Lavandula multifida (LMEO) essential oils and the evaluation of their antibacterial, antioxidant, and antidiabetic activities. The chemical composition was determined by GC-MS analysis. The antibacterial effects were evaluated against several bacterial strains using disc diffusion, MIC, and MBC methods. The antioxidant activity was evaluated in vitro using DPPH, H2O2, and xanthine oxidase, and the antidiabetic activity was estimated by the inhibitory effects of α-amylase, α-glucosidase, and lipase activities. GC-MS results showed that the main compounds of MPEO were menthone (29.24%), levomenthol (38.73%), and eucalyptol (6.75%). However, eucalyptol (28.11%), 2-bornanone (11.57%), endo-borneol (7.82%), and linalyl acetate (5.22%) are the major compounds of LMEO. The results exhibited important inhibitory effects against some bacterial strains with MIC = MBC = 0.39 mg/mL for MPEO against Staphylococcus aureus ATCC. However, LMEO exhibited remarkable antioxidant and antidiabetic activities compared to MPEO. Indeed, LMEO inhibited DPPH, H2O2, and xanthine oxidase with concentrations of 15.23, 21.52, and 8.89 µg/mL, respectively. Moreover, LMEO exhibited α-amylase and α-glucosidase at IC50 = 85.34 and IC50 = 59.36 µg/mL, respectively. The findings showed that both MPEO and LMEO exhibit promising biological properties. However, the application of these species or their main bioactive compounds requires further investigation.


Introduction
Despite the significant advancements in modern medicine, traditional medicine continues to attract the interest of people all over the globe. Up to 80% of the world's population relies on traditional medicine as their main health care supplier [1,2]. Unfortunately, modern medicine has been unable to stop the rapid spread of infectious illnesses. According to the World Health Organization, infectious illnesses are still the second biggest cause of mortality worldwide [3]. e demand for novel antimicrobial agents and antibiotics, on the other hand, is higher than ever [4][5][6]. Pathogenic infections are continually evolving in terms of genetic characteristics, complicating the development of antibiotics and vaccines against infectious diseases. is genetic adaptability allows a wide range of pathogenic organisms to change or mutate into more lethal forms that humans cannot fight off [7,8]; besides, antibiotic development is declining [9]. e United States Food and Drug Administration's (FDA) approval of novel antimicrobial drugs has been reduced by more than 50% [10].
On the other hand, complex intrinsic diseases and oxidative stress-related diseases are emerging currently and are inducing major problems in human health. Indeed, oxidative stress produces free radicals at cellular and molecular levels, which promotes several diseases, including diabetes and cancer. erefore, the screening of antioxidant natural products is a very promising strategy to prevent and treat these complex diseases [11][12][13].
Medicinal plants contain a variety of phytochemical compounds that exert distinct physiological effects on the human body and may serve as a source for novel antimicrobial agents. ese bioactive compounds include phenolic compounds, flavonoids, alkaloids, diterpenes, triterpenes, naphthoquinones, and sesquiterpene lactones [14,15].
Lavandula latifolia Medicus (spike lavender), a member of the Lamiaceae family, is a fragrant shrub native to the Mediterranean area and cultivated worldwide for its oil, which is known as lavender oil [16]. e essential oil of lavender is widely utilized in massage, aromatherapy, fragrance, and cosmetics. Many animal and human studies support its use as a sedative, anxiolytic, and mood modulator. Lavender oil has antibacterial properties and may be used to treat germs, fungus, and insects. e essential oil of lavender has spasmolytic properties in smooth muscle, which supports its traditional usage as a natural digestive aid [17,18].
Mentha piperita L. (peppermint) is a popular plant whose oils are extensively utilized for a variety of applications. It is used in cosmeceuticals, personal hygiene products, meals, and pharmaceutical items for both flavoring and aroma qualities. It is also used to treat irritation and inflammation. It is also used in aromatherapy, mouthwashes, bath preparations, toothpaste, chewing gum, and topical preparations [19,20]. Rosmarinic acid and various flavonoids, including eriocitrin, hesperidin, and luteolin, are phenolic elements of the leaves. Menthol and menthone are the two major volatile components of the essential oil of Mentha piperita [21]. e purpose of this study was to examine some biological properties (antibacterial, antioxidant, and antidiabetic activities) of two commonly used Moroccan medicinal herbs, Mentha piperita and Lavandula multifida.

Plant Material and Essential Oil Extraction.
Aerial parts of two plants, belonging to the Lamiaceae family, were collected from the El Gharb region (Morocco). Mentha piperita and Lavandula multifida were collected in April (2021) and dried in the dark. EOs were extracted using the hydrodistillation method and then stored at 4°C until experimental use.

Determination of Chemical Compounds by GC-MS.
e chemical components of Mentha piperita (MPEO) and Lavandula multifida (LMEO) essential oils were determined by using gas-chromatography/mass-spectrometry (GC/MS) analysis conditions as described in our latterly published study [22].

Disc-Diffusion Test.
e disc diffusion test was used to assess the antibacterial potential of essential oils, with minor modifications to the procedure published previously [22]. To enhance diffusion in the culture medium, the examined essential oils were combined with dimethyl sulfoxide (DMSO) at a concentration of 5%. Simultaneously, a 0.5 McFarland (10 8 CFU/mL) bacterial solution representing each examined species was produced in sterile saline water (0.9% NaCl) and inoculated on Mueller-Hinton Agar (Biokar, Beauvais, France) plates by swabbing. en, 10 µL of each essential oil was put onto sterile paper discs with a diameter of 6 mm, with a disc containing 10 µL of DMSO at a concentration of 5% serving as a negative control and 30 µg of chloramphenicol serving as a reference test. After that, all of the plates were incubated for 24 hours at 37°C. e inhibition diameter was measured in millimeters (disk included) after incubation and given as the mean ± standard deviation of three repetitions.

Determination of MIC and MBC.
Microbroth dilution on 96-well microplates was used to determine the minimum inhibitory concentration (MIC) of each essential oil following the procedure published by Eloff [23] with minor 2 Evidence-Based Complementary and Alternative Medicine modifications. In brief, in each microplate row, decreasing amounts of each essential oil were prepared in DMSO using the serial twofold dilution procedure. e microplates were then incubated at 37°C for 24 hours with 20 μL of bacterial suspensions adjusted to 0.5 McFarland and 160 μL of Mueller-Hinton broth (MHB, Biokar, Beauvais, France). After that, the bacterial growth was examined by incubating for 30 minutes at 37°C with 40 μL of 2, 3, 5-triphenyltetrazolium chloride (TTC) (Sigma-Aldrich, Switzerland) at a concentration of 0.2 µg/mL. e TTC uses a red dye to stain the bacteria, indicating which wells have bacterial growth. e MIC was determined using microplate wells with the lowest concentration of essential oils and no evident bacterial growth. e minimal bactericide concentration (MBC) test [24] was determined by subculturing 10 μL from a microplate well that did not show bacterial growth on Mueller-Hinton Agar (Biokar, Beauvais, France), and then incubating the plates at 37°C for 24 hours. e MBC was defined as the lowest concentration that did not cause any growth in the medium. e reference test in this investigation was chloramphenicol (Sigma-Aldrich).

In Vitro Antioxidant Activity.
e antioxidant activity of the two tested EOs was evaluated using the following three commonly used in vitro complementary assays: DPPH, H 2 O 2 , and xanthine oxidase (XO) methods, and following the same procedures as described previously by the research group [25][26][27]. Each assay was carried out in triplicate, and allopurinol and ascorbic acid were used as positive controls. In each assay, the concentrations of the essential oils (EOs) that provided 50% inhibition (IC 50 ) were determined, and their values were presented in µg/mL.

Chemical Composition. As shown in
e EO of L. Multifida is characterized by the presence of eucalyptol (28.11%), trans-β-ocimene (4.93%), 3-carene  latifolia and Mentha piperita essential oils are potential sources of antibacterial agents against Gram-positive and Gram-negative bacteria, respectively. e disc diffusion technique was used to determine the antibacterial potential of the essential oils of Lavandula latifolia and Mentha piperita. e results are presented in Figure 3. e findings indicated that essential oils from the two plants had substantial antibacterial activity against all bacteria tested when compared to the conventional antibiotic (chloramphenicol). M. piperita was shown to have stronger antibacterial properties than L. latifolia. Gram-positive bacteria were more sensitive than Gram-negative bacteria. In terms of Gram-positive bacteria, Staphylococcus aureus had the largest mean zone of inhibition (31.1 ± 0.2 and 27.9 ± 0.2 mm), followed by Bacillus subtilis (29.8 ± 0.  Table 2).
Previous research validates our results. Mentha piperita was reported to possess significant broad-spectrum antibacterial properties [36][37][38][39]. On the other hand, data on Lavandula latifolia's antibacterial activity is scarce. However, it was reported that Lavandula latifolia essential oil had strong antibacterial activity against a variety of bacterial pathogens and that this activity was significantly enhanced when coupled with camphor oil [40]. Notably, the Lavandula genus has over 39 species and approximately 400 recognized cultivars, several of which have antimicrobial activity against bacteria and fungi [41]. For example, the essential oils of Lavandula heterophylla demonstrated significant antibacterial action against a variety of bacteria, including Staphylococcus aureus, MRSA, Streptococcus pyogenes, Proteus vulgaris, Citrobacter freundii, Escherichia coli, and Pseudomonas aeruginosa [42]. e Lavandula stoechas cultivars that came from ailand have remarkable antibacterial activity against Klebsiella pneumoniae and Salmonella typhimurium [43]. Moreover, numerous in vitro and in vivo investigations indicate that EOs from different medicinal plants have remarkable antimicrobial effects against a broad spectrum of pathogens [44]. Essential oils with antibacterial activity may have benefits over antibiotics in that their antibacterial properties may have beneficial effects on the digestive organs, such as preventing the spread of potentially harmful microbes without influencing the normal flora or regulating dysbiosis [45].
Our study also showed that the MIC values of Lavandula latifolia and Mentha piperita essential oils were less than the referenced antibiotic (chloramphenicol), meaning a great inhibitory effect. is breakthrough finding has the potential to be exploited in the food or pharmaceutical industries, as well as in synergistic formulations with other natural products, to develop novel antibacterial agents to combat antibiotic-resistant organisms. As a conclusion, more future pharmacological investigations into these two plants are recommended.

Antioxidant Activity.
e antioxidant activity of essential oils (EOs) of MP and LM was evaluated by DPPH, H 2 O 2 , and xanthine oxidase. e percentages of inhibition of DPPH, H 2 O 2 , and xanthine oxidase were mathematically modelled to calculate IC 50 s ( tests are considered promising compared to those recorded by ascorbic acid, used as a control. Furthermore, the inhibition of xanthine oxidase induced by allopurinol, used as a standard, was important (IC 50 � 1.24 µg/mL).
Previous investigations have shown that both plants exert varying antioxidant activities [46][47][48][49][50]. e results of these studies do not completely corroborate those obtained in our investigation.
is is attributed, of course, to the origin of the plant material, the plant part used, the harvest period, the phenological stage, and the extraction and storage conditions. Indeed, as indicated in the phytochemical section, a remarkable variation of the bioactive compounds is observed in the different studies carried out on both plants, which justifies the fluctuations of the results. Additionally, some studies have highlighted correlations between major compounds and antioxidant activity. In our study, the antioxidant effects recorded are certainly attributed to the presence of certain majority compounds in the aerial parts of MP such as levomenthol (38.73%) and menthone (29.24%), and of LM such as eucalyptol (28.11%) and 2-bornanone (11.57%). Indeed, pharmacological studies have already reported the antioxidant activities of these compounds [51][52][53].
e antioxidant mechanisms of volatile compounds are not fully elucidated compared to polyphenols and flavonoids, which exert, according to several recent investigations, an antioxidant activity through their ability to share single electrons, which justifies the activity of essential oils not having this property against DPPH and H 2 O 2 .
On the other hand, the remarkable inhibitory activity against xanthine oxidase reinforces this suggestion and Evidence-Based Complementary and Alternative Medicine shows that volatile compounds inhibit this enzyme via a competitive or noncompetitive interaction. Indeed, terpenoids are considered as inhibitors of enzymatic biomarkers involved in human pathologies, including xanthine oxidase [54,55], which has, in addition to its oxidizing activity, considerable inflammatory activity. In addition, its inhibition will constitute a preventive pathway against stress and chronic inflammation.

Antidiabetic
Activity. α-Amylase and α-glucosidase are two carbohydrate-hydrolyzing enzymes, and the inhibition of their activity will be a promising therapeutic approach in reducing blood glucose levels and, consequently, in the management of type 2 diabetes mellitus (T2DM). Indeed, LMEO showed a higher antidiabetic effect than MPEO with IC 50 values of 85.34 and 59.36 µg/mL against α-amylase and α-glucosidase, respectively. Table 4 shows that the activity of   these two plants was very different from that of acarbose, which we used as a standard, indicating remarkable antidiabetic activity.
In contrast, the inhibition of lipid degradation limits their absorption. In fact, lipid concentrations indirectly regulate glucose concentrations; a decrease in lipids implies a significant breakdown of sugars, which lowers blood glucose. Dietary lipids in the intestine are broken down by lipases before being absorbed. Indeed, the specific inhibition of this enzyme prevents the degradation and, therefore, the decrease in lipid concentration. In this sense, lipases constitute a major therapeutic target for the pharmaceutical industry to fight against the majority of metabolic disorders, including T2DM.
In our study, MP and LM essential oils were tested against lipase and the results showed inhibition with IC 50 values of 71.36 and 30.94 µg/mL, respectively. ese results remain promising when compared with orlistat (IC 50 � 11.25 µg/mL), the standard reference. Other peppermint species have also shown significant anti-hyperglycemic effects [56][57][58].
In terms of Lavandula species, a recent study evaluated the inhibitory potential of Lavandula angustifolia leaf EO against the enzyme α-glucosidase, finding an inhibition of the activity of this digestive enzyme with an IC 50 of 609.44 μg/mL compared to acarbose (IC 50 of 526.5 μg/mL [59]. Concerning the in vivo tests, the administration of increasing doses of Lavandula stoechas hydroalcoholic extracts (50, 100, and 150 mg/kg·b.w.) to alloxan-induced diabetic mice significantly reduced blood glucose concentration in these animals in a dose-dependent manner [60]. In another more recent study, the antihyperglycemic activity of Lavandula pedunculata aqueous extract was investigated in vivo using an oral glucose tolerance test (OGTT) and an in vitro test targeting the two enzymes, pancreatic α-amylase and intestinal α-glucosidase. As a result, this extract improved rat oral glucose tolerance while inhibiting pancreatic α-amylase (IC 50 � 0.44 ± 0.05 μg/mL) and intestinal α-glucosidase (IC 50 � 131 ± 20 μg/mL) [61]. e promising results of these two species are likely due to their major bioactive molecules, which have been scientifically shown to have the antidiabetic potential [62]. ese molecules were found and determined in the phytochemical section.

Conclusion and Perspectives
Here, we report the chemical composition and biological activities of MPEO and LMEO. Both species showed a variability in volatile compounds with a predominance of phenolic bioactive compounds. e findings showed that MPEO exhibits remarkable antibacterial effects compared to LMEO, which suggests the presence of antibacterial compounds in MPEO. LMEO and MPEO showed important in vitro antioxidant effects, with more efficiency for LMEO. Moreover, LMEO exhibited remarkable in vitro antidiabetic effects compared to MPEO. Results suggest the use of MPEO and LMEO to develop bioactive molecules with antibacterial, antidiabetic, and antioxidant properties. Future perspectives should be addressed to confirm and validate the biological and pharmacological properties of LMEO and MPEO main compounds. Indeed, studies concerning the mechanisms of action against pathogenic bacteria and others related to antidiabetic effects and oxidative stress-related diseases should be investigated importantly to determine the pharmacodynamic action of each compound. Moreover, toxicological investigations using different doses at different times should also be tested to confirm the safety of both EOs and their main bioactive compounds.

Data Availability
e data used to support the findings of this study are included within the article.

Conflicts of Interest
e authors declare that they have no conflicts of interest for this study.