Search

Salinity stress is one of the main limiting factors of medicinal plant growth and may affect their characteristics and chemical composition. In order to evaluate the response of different species of Iranian mint to salinity stress, an experiment was designed in greenhouse conditions. In this experiment, six Iranian mint species were cultivated in pots under different salinity stress including 0, 2.5, 5, and 7.5 dS/m. The chlorophyll indices (a, b, total, and a/b ratio), carotenoids, total anthocyanin, total phenolic and flavonoid content, antioxidant activity, dry matter yield, and essential oil content were measured in two different harvest stages. Salinity stress affected various measured traits. The results showed that despite the negative effect of salinity stress on photosynthetic pigments, in some ecotypes and species, photosynthetic pigments were not affected by salinity stress. The amount of total phenolic content, total flavonoid content, and total anthocyanin increased in response to salinity stress. The dry matter decreased under salinity stress, but the content of essential oil increased as a result of salinity stress increment. The results of PCA biplot showed that the E16 and E18 ecotypes were separated by a large distance. Among the various ecotypes, E18 had the most desirable traits which can be recognized as a salt‐tolerant ecotype. Also, piperita species was the best among the species in all salinity stress levels., Among the various ecotypes, E18 accounted for the most desirable traits in most of the studied traits and was recognized as a salt‐tolerant ecotype.

The genus Stachys is a member of the Lamiaceae family. These are important medicinal plants which grow all over the world and are known for their flavoring and therapeutic effects and Stachys lavandulifolia is an endemic species of Iran. To acquire high‐quality essential oil (EO), drying technique was implemented which is an essential part of this process. The present study designed to evaluate the influences of different drying techniques (fresh sample, shade, sunlight, freeze‐drying, microwave, and oven‐drying (40, 60, and 80°C) on EO yield and composition of S. lavandulifolia. The results indicated that the maximum EO yield was obtained by the shade‐drying method. The main compounds found in the fresh samples were spathulenol, myrcene, β‐pinene, δ‐cadinene, and α‐muurolol, while spathulenol, cyrene, δ‐cadinene, p‐cymene, decane, α‐terpinene, β‐pinene, and intermedeol were found to be the dominant compounds in the dry samples. Drying techniques were found to have a significant impact on the values of the main compositions, for example, monoterpene hydrocarbons such as α‐pinene, β‐pinene, myrcene, and β‐phellandrene were significantly reduced by microwave drying, oven‐drying (40, 60, and 80°C), and sunlight‐drying methods. Drying techniques increased the antioxidant activity of S. lavandulifolia EOs especially those acquired by freeze‐drying with the half‐maximal inhibitory concentration (IC50) values 101.8 ± 0.8 mg/ml in DPPH assay and 315.2 ± 2.1 mg/ml in decreasing power assay. As a result, shade‐, sun‐, and oven‐drying (40°C) were found to be the most important techniques for attaining maximum yields of EO., The present study designed to evaluate the influences of different drying techniques (fresh sample, shade‐drying, sunlight‐drying, freeze‐drying, and oven‐drying (40, 60, and 80°C), and microwave‐drying) on EO yield and composition of Stachys lavandulifolia.

Heracleum persicum, commonly named Persian hogweed, is a principal native medicinal plant in Iran. Collecting H. persicum at the most appropriate growing stage is the key factor to achieve the high phytochemical quality to meet consumer's needs. In the present experiment, the aerial parts of this plant were harvested at up to six different developmental stages during the growing season to determine the phytochemical profiles. Our results indicated that the highest essential oil content was obtained in the mid‐mature seed stage (3.5%). The most elevated extract content was recorded in the floral budding stage (10.4%). In the vegetative stage, limonene (18.1%), in floral budding stage, caryophyllene (14.1%), anethole (14.6%), and β‐bisabolene (12.7%), in the full flowering stage, myristicin (15.0%), and hexyl butyrate (9.1%), in the early development of seeds stage, hexyl butyrate (32.1%), and octyl acetate (11.7%), in the mid‐mature seeds stage hexyl butyrate (38.8%), octyl acetate (14.5%), in the late‐mature/ripe seeds stage, hexyl butyrate (23.6%), and octyl acetate (10.5%) are recorded as the main components. The highest phenolic acids content was obtained in the floral budding stage (287.40 mg/g dried extract). The analysis of phenolic acids demonstrated cinnamic acid (8.0–225.3 mg/g extract), p‐coumaric acid (1.7–39.2 mg/g extract), p‐hydroxybenzoic acid (0.8–16.8 mg/g extract), and ferulic acid (2.4–15.8 mg/g extract) as the main phenolic acids. Cinnamic acid was found as the major phenolic compound in the vegetative stage following by floral budding, the full flowering stage, the early development of seeds, and late‐mature/ripe seeds stages. P‐coumaric acid was the most abundant phenolic compounds in the mid‐mature seeds stage. In this regard, the harvest time of H. persicum aerial parts can be selected to achieve the highest secondary metabolites of interest. The results of this study can be used as a guideline for grower to obtain the highest possible amount of desirable metabolites, beneficial in both food and pharmaceutical industries as well as their undeniable economical benefits.

The high demands for the consumption of edible oils have caused scientists to struggle in assessing wild plants as a new source of seed oils. Therefore, in this study, the oil yield, fatty acid and tocopherol compositions, antioxidant and antibacterial activities of the oils obtained from Iran's two endemic plants (Pyrus glabra and Pyrus syriaca) were investigated. The obtained oil yields from the P. glabra and P. syriaca seeds were 33 ± 0.51 and 26 ± 0.28 w/w%, respectively. Oleic acid (C18:1) with the amount of 49.51 ± 1.05% was the major fatty acid in the P. glabra oil, while the main fatty acids in the P. syriaca seed oil belonged to linoleic acid (C18:2) and oleic acid (C18:1) with the amounts of 46.99 ± 0.37 and 41.43 ± 0.23%, respectively. The analysis of tocopherols was done by HPLC, and the results indicated that the P. glabra and P. syriaca seed oils were rich in α‐tocopherol (69.80 ± 1.91 and 45.50 ± 1.86 mg/100 g oil, respectively), constituting 86.24 and 89.01% of total detected tocopherols, respectively. The study on the reducing capacity of the oils indicated that the P. glabra oil had more reducing capacity than the P. syriaca oil. Moreover, the antioxidant activity of the P. glabra seed oil (43.4 ± 0.7 µg/ml) was higher than the P. syriaca seed oil (46.3 ± 1.2 µg/ml). Also, the investigation of the antibacterial activities indicated that the P. glabra and P. syriaca oils have an inhibitory effect on the studied bacteria. The results indicate that the oils of these plants can be appropriate sources of plant oils which can act as natural antibacterial agents., One of the most important findings of this study is the introduction of Pyrus glabra and Pyrus syriaca as a new source of plant oils. The significant amount of antioxidants, especially in P. glabra oil, may serve as a dietary source of natural antioxidants and increase the stability and quality of food products. The results showed that the P. glabra seed oil is rich in α‐tocopherol. Hence, the potential utilization of these seed oils as a raw material for food, chemical, cosmetic, and pharmaceutical industries could be favorable.