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1,105 result(s) for "Pistacia"
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Revealing drought tolerance strategies in pistachio clonal hybrids: role of osmotic adjustment
Background Pistachio ( Pistacia vera L.) growth, yield and quality are affected by abiotic stress especially drought. Understanding the strategies that improve dehydration tolerance is essential for developing resistant pistachio rootstocks. In the experiment, nine-month-old saplings of seven clonal interspecies hybrids of Pistacia atlantica × P. integerrima (C1, C2, C16-1, C8-3, C4-2, C9-4 and UCB1) were assessed for growth and physiological responses to water withholding and recovery. Result Water deficit negatively impacted growth parameters, including shoot dry weight, root dry weight and leaf area, in all hybrids; however, the C1 demonstrated relatively minor reductions compared to the other hybrids. Glycine betaine content in leaves increased by 49.4% in C9-4 and 47% in C1, while only 7% and 11% increases were found in the most sensitive clones, C8-3 and C4-2. Notably, C9-4, identified as the most tolerant clone, displayed the highest proline levels, with increases of 29.5% in leaves and 41.5% in roots, in contrast to C8-3, which showed minimal increases of 6% and 11% in leaves and roots, respectively. Clones with higher compatible solutes maintained higher relative water content (RWC), lower osmotic potential and smaller reductions in leaf water potential. RWC declined by just 6% in C9-4, whereas it dropped by 88% in C8-3. Osmotic potentials in C9-4 were − 1.61 MPa in leaves and − 0.271 MPa in roots, while in C8-3, they were − 0.93 MPa and − 0.11 MPa in leaves and roots, respectively. Following recovery, evaluations of growth, physiological traits and visual observations indicated that C8-3 had poor recovery ability. Heatmap and PCA analyses categorized the clones into three groups: “tolerant” (C9-4, C1 and C2), “moderately tolerant” (UCB1) and “sensitive” (C8-3, C4-2 and C16-1). Conclusion The results of this study underscore the significance of osmotic adjustment as a more critical trait compared to growth and stomatal parameters in effectively differentiating tolerant clones from sensitive ones.
Morphological and pomological variations of Pistacia atlantica Desf. subsp. cabulica and subsp. mutica in Sistan-va-Baluchestan province, Iran
Background The genus Pistacia , belonging to the family Anacardiaceae, includes various species that hold ecological, nutritional, and medicinal significance. There is limited information on the morphological and pomological diversity of Pistacia atlantica Desf. subsp. cabulica and subsp. mutica . This study aims to examine this diversity and contribute to the improvement of sustainable use and agricultural practices. Results Morphological and pomological variation of 44 female accessions of P. atlantica (20 of subsp. cabulica and 24 of subsp. mutica ) grown naturally in Mount Taftan, Sistan-va-Baluchestan, Iran, was assessed. One-way ANOVA ( p  <  0.05 ) showed significant differences among the examined genotypes. The coefficient of variation (CV) ranged from 7.60% (kernel thickness) to 167.04% (kernel crispness), with 34 out of 48 traits (70.83%) showing CVs greater than 20%, indicating high variability. The range of leaf-related characters was as follows: leaf length: 87.52–157.80 mm, leaf width: 55.28–121.97 mm, leaflets per leaf: 5–7, petiole length: 25.87–66.91 mm, and petiole diameter: 1.15–2.2 mm. The range of fruit-related characters was as follows: bunchlets per bunch: 10–17, fruit pedicel length: 1.37–7.12 mm, fruit pedicel width: 0.9–1.23 mm, nut length: 5.49–8.23 mm, nut width: 6.19–8.42 mm, nut thickness: 4.39–6.42 mm, and 100-nut weight: 12.36–25.91 g. These variations indicate adaptability and agricultural potential. Most accessions showed moderate growth, intermediate vigor, and branching, optimizing photosynthesis. Leaf and petiole traits vary, reflecting adaptations to environmental conditions. Ripening times span from late September to mid-October, with yield potential mostly intermediate. According to correlation matrix analysis, high positive correlations were found between 100-nut weight and kernel thickness ( r  =  0.708** ), nut length ( r  =  0.764** ), and nut thickness ( r  =  0.603** ), and these correlations are also supported by multiple regression analysis ( β  = 0.47, β  = 0.69, β  = 0.31, P  < 0.00, respectively). According to principal components analysis, the first three principal components (PC1 = 13.39%, PC2 = 9.30%, and PC3 = 9.25%) represented 31.94% of the total variation. The datasets were evaluated together, and the first 14 accessions were detected, including four accessions of subsp. mutica (No. 23, 5, 11, and 16) and 11 accessions of subsp. cabulica (No. 5, 15, 18, 10, 20, 12, 1, 7, 17, and 13), respectively. The accessions 1 and 7 of subsp. cabulica , though among the first 14, fall outside the 95% confidence ellipse in the scatter plot, indicating that they differ significantly from the others in terms of their traits. This suggests they may possess unique characteristics. Conclusions This study highlights the significant morphological and pomological diversity between the P. atlantica subsp. cabulica and subsp. mutica , providing valuable insights for breeding and conservation. The key trait relationships identified through statistical analysis may guide trait selection for better yield and adaptability.
Pistacia atlantica can improve oxidative status in patients with metabolic dysfunction-associated fatty liver disease
Metabolic dysfunction-associated fatty liver disease (MAFLD) is a problem worldwide. Oxidative stress is important factor in beginning and progress of MAFLD. This study is the first clinical trial with the aim of determining the effect of Pistacia atlantica Sub. Kurdica gum on oxidative status in patients with metabolic dysfunction-associated fatty liver disease. In this double-blind randomized clinical trial 50 patients with metabolic dysfunction-associated fatty liver disease were randomized into two groups: those given syrup containing Pistacia atlantica sub. Kurdica gum (Group A), those on placebo (Group B). Over a two-month period, Group A given syrup containing 500 mg of P. atlantica sub. Kurdica gum per each tablespoon and Group B given syrup without P. atlantica sub. Kurdica gum. Anthropometric measures, serum oxidative markers and physical activity were evaluated at the beginning and end of the intervention. We observed a significant decrease in fatty liver grade in group A ( P  = 0.03). In the end of intervention had not been show significant change in serum total antioxidant capacity (TOS) in group A ( P  = 0.91) and group B (0.70). Serum total oxidant status (TAC) had been show increase in group A and decrease in group B but this changes not significant as within group ( P  = 0.36, P  = 0.53, respectively) and between group ( P  = 0.66). The mean of Malondialdehid (MDA) had significant decrease from baseline in group A ( P  = 0.002) and had non-significant increase in group B ( P  = 0.65). The between-group comparison of changes of MDA had been show a significant difference ( P  = 0.025). As well as, after adjusting for baseline characteristics (Age, Gender, Physical activity, BMI), there were not significant differences between A and B groups in the changes comparison of TOS and TAC except for MDA ( p  < 0.032). Weight had significant decrease in group A ( P  = 0 < 001). Pistacia atlantica sub. Kurdica gum can improve some oxidative status indices, particularly lipid peroxidation and subsequently MAFLD in patient with metabolic dysfunction-associated fatty liver disease, but further studies with larger samples, longer duration and dose-response assessment will be needed. Trial registration: IRCT20231219060466N1, 2024-01-05 (https//irct.behdasht.gov.ir/).
Influence of Pistachios on Performance and Exercise-Induced Inflammation, Oxidative Stress, Immune Dysfunction, and Metabolite Shifts in Cyclists: A Randomized, Crossover Trial
Pistachio nut ingestion (3 oz./d, two weeks) was tested for effects on exercise performance and 21-h post-exercise recovery from inflammation, oxidative stress, immune dysfunction, and metabolite shifts. Using a randomized, crossover approach, cyclists (N = 19) engaged in two 75-km time trials after 2-weeks pistachio or no pistachio supplementation, with a 2-week washout period. Subjects came to the lab in an overnight fasted state, and ingested water only or 3 oz. pistachios with water before and during exercise. Blood samples were collected 45 min pre-exercise, and immediately post-, 1.5-h post-, and 21-h post-exercise, and analyzed for plasma cytokines, C-reactive protein (CRP), F2-isoprostanes (F2-IsoP), granulocyte phagocytosis (GPHAG) and oxidative burst activity (GOBA), and shifts in metabolites. Performance time for the 75-km time trial was 4.8% slower under pistachio conditions (2.84 ± 0.11 and 2.71 ± 0.07 h, respectively, P = 0.034). Significant time effects were shown for plasma cytokines, CRP, F2-IsoP, GPHAG, and GOBA, with few group differences. Metabolomics analysis revealed 423 detectable compounds of known identity, with significant interaction effects for 19 metabolites, especially raffinose, (12Z)-9,10-Dihydroxyoctadec-12-enoate (9,10-DiHOME), and sucrose. Dietary intake of raffinose was 2.19 ± 0.15 and 0.35 ± 0.08 mg/d during the pistachio and no pistachio periods, and metabolomics revealed that colon raffinose and sucrose translocated to the circulation during exercise due to increased gut permeability. The post-exercise increase in plasma raffinose correlated significantly with 9,10-DiHOME and other oxidative stress metabolites. In summary, 2-weeks pistachio nut ingestion was associated with reduced 75-km cycling time trial performance and increased post-exercise plasma levels of raffinose, sucrose, and metabolites related to leukotoxic effects and oxidative stress. ClinicalTrials.gov NCT01821820.
The Molecular Cytogenetic Characterization of Pistachio (Pistacia vera L.) Suggests the Arrest of Recombination in the Largest Heteropycnotic Pair HC1: e0143861
This paper represents the first molecular cytogenetic characterization of the strictly dioecious pistachio tree (Pistacia vera L.). The karyotype was characterized by fluorescent in situ hybridization (FISH) with probes for 5S and 45S rDNAs, and the pistachio specific satellite DNAs PIVE-40, and PIVE-180, together with DAPI-staining. PIVE-180 has a monomeric unit of 176-178 bp and high sequence homology between family members; PIVE-40 has a 43 bp consensus monomeric unit, and is most likely arranged in higher order repeats (HORs) of two units. The P. vera genome is highly heterochromatic, and prominent DAPI positive blocks are detected in most chromosomes. Despite the difficulty in classifying chromosomes according to morphology, 10 out of 15 pairs (2n = 30) could be distinguished by their unique banding patterns using a combination of FISH probes. Significantly, the largest pair, designated HC1, is strongly heteropycnotic, shows differential condensation, and has massive enrichment in PIVE-40 repeats. There are two types of HC1 chromosomes (type-I and type-II) with differing PIVE-40 hybridization signal. Only type-I/II heterozygotes and type-I homozygotes individuals were found. We speculate that the differentiation between the two HC1 chromosomes is due to suppression of homologous recombination at meiosis, reinforced by the presence of PIVE-40 HORs and differences in PIVE-40 abundance. This would be compatible with a ZW sex-determination system in the pistachio tree.
Optimizing the extraction of essential oil yield from Pistacia lentiscus oleo-gum resin by superheated steam extraction using response surface methodology
Pistacia lentiscus L. is an aromatic plant containing a significant percentage of essential oil (EO) used in fragrance, pharmaceuticals, cosmetics, and the food industry. The purpose of this work is focused on the optimization of Pistacia lentiscus L. oleo gum resin EO yield extracted by superheated steam extraction (SHSE) by response surface methodology, including extraction parameters of particle size (0. 5 − 1 mm), temperature (140–180 °C) and time (90–150 min). The optimum conditions for Pistacia lentiscus L. EO extracted by SHSE were found to be (particle size: 0.75 mm, time: 120 min and temperature: 160 ℃) which produced the highest EO yield of 5.7%. A regression model was developed, demonstrating a robust quadratic correlation with an R 2 value of 0.9991, making it suitable for predictions. Furthermore, the yield of Pistacia lentiscus L. EO extracted by SHSE was compared with the conventional steam and hydro distillation techniques. The study revealed that SHSE yielded higher quantities of EO than other extraction methods. GC-MS analyzed the chemical composition of Pistacia lentiscus L. EO. The predominant compound of Pistacia lentiscus L. EO was determined to be α-pinene, while the other identified compounds include trans -verbenol, verbenol, cis -verbenone, camphene, β-myrcene, d-limonene, cymene, α-myrtenol, α-campholenal, α-copaene, and α-thujene, whose content differed according to different extraction techniques. Overall, superheated steam extraction is an efficient technique for extracting Pistacia lentiscus L. essential oil that enhances EO yield, requiring less time for extraction.
Antioxidative Efficacy of a Pistacia Lentiscus Supplement and Its Effect on the Plasma Amino Acid Profile in Inflammatory Bowel Disease: A Randomised, Double-Blind, Placebo-Controlled Trial
Oxidative stress is present in patients with Inflammatory Bowel Disease (IBD), and natural supplements with antioxidant properties have been investigated as a non-pharmacological approach. The objective of the present study was to assess the effects of a natural Pistacia lentiscus (PL) supplement on oxidative stress biomarkers and to characterise the plasma-free amino acid (AA) profiles of patients with active IBD (Crohn’s disease (CD) N = 40, ulcerative colitis (UC) N = 20). The activity was determined according to 5 ≤ Harvey Bradshaw Index ≤ 16 or 2 ≤ Partial Mayo Score ≤ 6. This is a randomised, double-blind, placebo-controlled clinical trial. IBD patients (N = 60) were randomly allocated to PL (2.8 g/day) or to placebo for 3 months being under no treatment (N = 21) or under stable medical treatment (mesalamine N = 24, azathioprine N = 14, and corticosteroids N = 23) that was either single medication (N = 22) or combined medication (N = 17). Plasma oxidised, low-density lipoprotein (oxLDL), total serum oxidisability, and serum uric acid were evaluated at baseline and follow-up. OxLDL/LDL and oxLDL/High-Density Lipoprotein (HDL) ratios were calculated. The plasma-free AA profile was determined by applying a gas chromatography/mass spectrometry analysis. oxLDL (p = 0.031), oxLDL/HDL (p = 0.020), and oxLDL/LDL (p = 0.005) decreased significantly in the intervention group. The mean change differed significantly in CD between groups for oxLDL/LDL (p = 0.01), and, in the total sample, both oxLDL/LDL (p = 0.015) and oxLDL/HDL (p = 0.044) differed significantly. Several changes were reported in AA levels. PL ameliorated a decrease in plasma-free AAs seen in patients with UC taking placebo. In conclusion, this intervention resulted in favourable changes in oxidative stress biomarkers in active IBD.
Determination of superior Pistacia chinensis accession with high-quality seed oil and biodiesel production and revelation of LEC1/WRI1-mediated high oil accumulative mechanism for better developing woody biodiesel
Background Based on our previous studied on different provenances of Pistacia chinensis , some accessions with high quality and quantity of seed oils has emerged as novel source of biodiesel. To better develop P. chinensis seed oils as woody biodiesel, a concurrent exploration of oil content, FA profile, biodiesel yield, and fuel properties was conducted on the seeds from 5 plus germplasms to determine superior genotype for ideal biodiesel production. Another vital challenge is to unravel mechanism that govern the differences in oil content and FA profile of P. chinensis seeds across different accessions. FA biosynthesis and oil accumulation of oil plants are known to be highly controlled by the transcription factors. An integrated analysis of our recent transcriptome data, qRT-PCR detection and functional identification was performed as an attempt to highlight LEC1/WRI1-mediated transcription regulatory mechanism for high-quality oil accumulation in P. chinensis seeds. Results To select ideal germplasm and unravel high oil accumulative mechanism for developing P. chinensis seed oils as biodiesel, five plus trees (accession PC-BJ/PC-AH/PC-SX/PC-HN/PC-HB) with high-yield seeds were selected to assess the variabilities in weight, oil content, FA profile, biodiesel yield and fuel property, revealing a variation in the levels of seed oil (50.76–60.88%), monounsaturated FA (42.80–70.72%) and polyunsaturated FA (18.78–43.35%), and biodiesel yield (84.98–98.15%) across different accessions. PC-HN had a maximum values of seed weight (26.23 mg), oil (60.88%) and biodiesel yield (98.15%), and ideal proportions of C18:1 (69.94%), C18:2 (17.65%) and C18:3 (1.13%), implying that seed oils of accession PC-HN was the most suitable for ideal biodiesel production. To highlight molecular mechanism that govern such differences in oil content and FA profile of different accessions, a combination of our recent transcriptome data, qRT-PCR detection and protein interaction analysis was performed to identify a pivotal role of LEC1/WRI1-mediated transcription regulatory network in high oil accumulation of P. chinensis seeds from different accessions. Notably, overexpression of PcWRI1 or PcLEC1 from P. chinensis seeds in Arabidopsis could facilitate seed development and upregulate several genes relevant for carbon flux allocation (plastidic glycolysis and acetyl-CoA generation), FA synthesis, TAG assembly and oil storage, causing an increase in seed oil content and monounsaturated FA level, destined for biodiesel fuel property improvement. Our findings may present strategies for better developing P. chinensis seed oils as biodiesel feedstock and bioengineering its high oil accumulation. Conclusions This is the first report on the cross-accessions assessments of P. chinensis seed oils to determine ideal accession for high-quality biodiesel production, and an effective combination of PcWRI1 or PcLEC1 overexpression, morphological assay, oil accumulation and qRT-PCR detection was applied to unravel a role of LEC1/WRI1-mediated regulatory network for oil accumulation in P. chinensis seeds, and to highlight the potential application of PcWRI1 or PcLEC1 for increasing oil production. Our finding may provide new strategies for developing biodiesel resource and molecular breeding.
Seasonal and Diurnal Variation in Leaf Phenolics of Three Medicinal Mediterranean Wild Species: What Is the Best Harvesting Moment to Obtain the Richest and the Most Antioxidant Extracts?
Mediterranean plants biosynthesize high amounts of polyphenols, which are important health-promoting compounds. Leaf polyphenolic composition changes according to environmental conditions. Therefore, it is crucial to know the temporal variation in their production. This study aimed to: i) evaluate the monthly and daily changes in polyphenols of Phyllirea latifolia, Cistus incanus, and Pistacia lentiscus to identify their best harvesting moment, ii) verify the possible correlations between phenolic production and temperature and irradiation, iii) evaluate their antioxidant capacity using 2,2-diphenyl-1-picrylhydrazyl (DPPH) and hydroxyl radical (OH)scavenging assays. The extracts of leaves harvested at 8:00, 13:00 and 18:00, in May, July, and October for two years were analysed by HPLC-DAD. Both “month” and “time of the day” affected the polyphenolic content in all species. July at 13:00 was the best harvesting moment for all polyphenolic classes of P. latifolia and only for some classes of C. incanus and P. lentiscus. Environmental parameters positively correlated with the polyphenols of C. incanus and P. latifolia, while the antioxidant capacity only varied in this last species, reaching the highest value in July. Results of the study allow to determine the balsamic time for each species. Moreover, the relationship between polyphenols and environmental data can be useful for the cultivation of these plants under controlled conditions.
Evaluation of Genetic Variability among Three Pistacia Species Using Internal Transcribed Spacer 1 (ITS1) Marker
Diversity in Pistacia has been evaluated at all molecular levels using the internal transcribed spacer 1 (ITS1) marker in three species (Pistacia atlantica subsp. atlantica; Pistacia vera and Pistacia terebinthus), and compared with other Pistacia species. Results showed that the ITS amplification and sequencing, followed by phylogenetic analyses, identify the species and confirm their classification, which revealed that it can be used as a marker. Our results suggest that ITS1 analyses might provide a simple and inexpensive approach to validate the species of samples collected from the natural population, where species identification can be difficult, especially if hybrids are present or if the season is not optimal for identifying differences in morphological traits.