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Microscopic study of the transverse section of the bark.  

Microscopic study of the transverse section of the bark.  

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Pistacia integerrima, is a well known plant among Pakistani indigenous medicinal plants and used very commonly in the management of various diseases. In this research work the pharmacognostic profile, phytochemical and physicochemical parameters of the P. integerrima bark was carried out for standardization, quality, purity and sample identificatio...

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... is also present in the bark. The transverse section is shown in Figure 2. ...

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... stem bark at a concentration of 100 mg kg −1 showed strong in vivo anti-GIT motility effect (p < .05) in BALB-c mice, compared with control group receiving atropine sulphate. As atropine exerts its antimotility effect on GIT through blockage of gastric muscarinic cholinergic receptors, P. integerrima extract is thought to act via same mechanism(Almubayedh et al., 2018;Ismail et al., 2011). Another in vivo study in mice animal model evaluated the antidiarrheal activity for P. integerrima plant, where a potent protective activity against castor oil-induced diarrhea was observed. ...
... In the group administrated with the extract mixture prior to CCl 4 administration, the serum levels of AST, ALT and ALP decreased to 310, 105.80 and 571 U L −1 , respectively, whereas the group treated with the mixture following CCl 4 administration revealed a considerable decrease in enzyme levels to 109.2, 79.4 and 225.8 U L −1 , respectively. These results demonstrate that the curative effect of P. integerrima is more potent than its protective effect against CCl 4 -induced injury(Khan et al., 2011). A parallel study conducted on P. integerrima extract alone showed similar results(Khan et al., 2004). ...
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Pistacia chinensis subsp. integerrima (J. L. Stewart ex Brandis) Rech. F. is a valuable medicinal plant used in south Asian communities for the treatment of asthma, diarrhea, diabetes, liver diseases, fever, pain and inflammation. This review critically evaluates the available information on P. integerrima’s ethnobotany, ethnopharmacology, phytochemistry, pharmacology and toxicology. Electronic databases such as Google Scholar, PubMed, Springer Link, and so forth, books and theses were used to find relevant information about P. integerrima using keywords such as “Pistacia integerrima ,” “P. integerrima ,” “Ethnopharmacology,” “Phytochemistry,” “Traditional uses”. A number of in vitro and in vivo pharmacological activities have been reported; however, the most promising and attractive activity observed was its role in Alzheimer, diabetes, convulsions, cancer, asthma, diabetes, diarrhea and as an immunomodulatory, analgesic and antiinflammatory. In addition, Pistagremic acid exerted anti‐Alzheimer’s activity based on a hitherto unknown mechanism through interference with the amyloidogenic pathway. Most of the pharmacological activities were linked with traditional uses. A range of compounds have been reported from P. integerrima extracts including triterpenes, volatile oils, flavonoids, fatty acids, phenolic, phytosterols, tannins and oligosaccharides as well as unknown triterpenes and flavonoids. Pistagremic acid, a novel triterpene, was attributed to most of the activities. in vivo toxicological studies in animal suggested a toxic dose of 1,500 mg kg⁻¹, for its methanolic extract. All reported pharmacological activities were carried out in vitro and a gap in research, that is, preclinical and clinical investigation exists. Its outstanding activity as an antiglycating agent is the most promising and a so far unique activity and needs further evaluation. In‐depth research and clinical trials on human subjects in order to investigate P. integerrima pharmacological activity, clinical efficacy and safety are crucial next steps.
... The depressant action of P. integerrima on the central nervous system has been reported. Different types of phenolic compounds with antioxidant potentials have been isolated from the galls of Pistacia integerrima [12,13]. A number of other bioactive compounds like monoterpenes, triterpenoids, sterol dihydromalvalic acid and flavonoids, have also been reported from the different parts of Pistacia species [14,15,16]. ...
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... Antimicrobial effects of the gall extracts on Bacillus, Pseudomonas, and filamentous fungi have been proven [41]. The galls of Pistacia integerrima J. L. Stewart (zebrawood), a variety of Pistacia chinensis, are well-investigated [42]. These gall extracts have anti-diarrheal [43], anti-asthmatic, anti-psoriatic, antipyretic, and hepatoprotective attributes [44][45][46]. ...
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... Pistacia integerrima belongs to family Anacardiacea, commonly known as kakar singhi which is found in Eastern Himalayan range from Indus to Kumaon (Ismail et al., 2011), at height of 12000 to 8000 feet. P. integerrima is a medium sized deciduous tree having medicinal value such as anti-inflammatory, blood purifier, and remedy for gastrointestinal disorders, expectorant, cough, asthma, fever, vomiting and diarrhea according to our former studies (Uddin et al., 2011) (Ahmad et al., 2010). ...
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Phytochemical investigation of Pistacia integerrima delighted the isolation of two known compounds naringenin (1) and dihydrokaempferol (2). The crude extract and its isolated compounds naringenin (1) and dihydrokaempferol (2) were evaluated for their effects on the reversion of multidrug resistant (MDR) mediated by P-glycoprotein ((P-gp). The multidrug resistant P-glycoprotein is target for chemotherapeutic drugs from cancer cells. In the present study rhodamine- 123 exclusion screening test on human mdr1 gene transfected mouse gene transfected L5178 and L5178Y mouse T-cell lymphoma which showed excellent MDR reversing effect in a dose dependent manner against mouse T-lymphoma cell line. In the present work, in-silico molecular docking investigation was also carried out to analyzed, a common binding site for Rhodamine123, compounds naringenin (1) and dihydrokaempferol (2). Our results showed that the relative docking energies estimated by docking softwares were in satisfactory correlation with the experimental activities. Preliminary interaction profile of P-gp docked complexes were also analysed in order to understand the nature of binding modes of these compounds. Our computational investigation suggested that the compounds interactions with the hydrophobic pocket of P-gp are mainly related to the inhibitory activity. Moreover this study will provide a platform for the discovery of novel natural compounds from herbal origin, as inhibitor molecules against the P-glycoprotein for the treatment of cancer.
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... The pharmacognostic profile of the plant was reported using our previous reported method (Muhammad et al., 2012;Ismail et al., 2011). Vein islet number, vein termination number, palisade ratio, stomatal number and stomatal indices were calculated from 1 mm 2 pieces of leaf of A. aspera boiled in concentrated chloral hydrate solution under high power compound microscope. ...
... There are several plants within the same genus with similar structure and with different microscopic characteristics, however the medicinal value of these morphological similar plants vary from each other. Pharmacognostic studies help in the identification of specific plants possessing organoleptic and microscopic characteristics (Ismail et al., 2011). Glibenclamide is a sulfonylurea derivative and commonly used in the management of diabetes mellitus type II; it causes hypoglycemia by stimulating beta cells of pancreas and increasing release of insulin and inhibiting glucagon secretion. ...
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In the present study, the ethanolic extract of Achyranthus aspera L. Leaves (EEA) were investigated for their pharmacognostic characteristics and hypoglycemic effects. The pharmacognosy of the plant was carried out using microscopic and macroscopic tools. Macroscopic studies revealed that the leaves were cauline, ramel, opposite, exstipulate, simple, sub-sessile, ovate, entire, acute, unicostate, reticulate, rough, coriaceous and hairy. The stem was erect, herbaceous, quadrangular, branched, solid, green and pubescent, while various internal parts were observed using powder drug for microscopic study. The hypoglycemic effect of the plant was studied in healthy normoglycemic rabbits. The EEA was tested in three doses (100, 150 and 200 mg/kg), and a dose dependent hypoglycemic effect was observed. The most significant hypoglycemic effect was observed against higher dose (200 mg/kg) which remained for 5 h while the hypoglycemic effect remained significant for 3 h against the lower dose. It was concluded that EEA has hypoglycemic properties and it is recommended for the treatment of diabetes mellitus II.
... The pharmacognostic study of crude drug is very essential for the identification of medicinal plants and prevention of adulteration ( Ismail et al., 2011). Medicinal plants have acquired increasing significance in development of cooperation among various organizations in the recent years. ...
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... actions is the part of our research work on Pakistani medicinal plants ( Barkatullah et al., 2011;Ismail M et al., 2011;Muhammad and Saeed, 2011;Rahman et al., 2011a;Rahman et al., 2011b;Raziq et al., 2011). ...
... actions is the part of our research work on Pakistani medicinal plants ( Barkatullah et al., 2011;Ismail M et al., 2011;Muhammad and Saeed, 2011;Rahman et al., 2011a;Rahman et al., 2011b;Raziq et al., 2011). ...
... Saponins were identified by formation of froth upon simple shaking (frothing test). Tannins and phenols were identified on addition of ferric chloride to the extract solution; the appearance of blue or green ppt indicated the presence of tannins [16]. Sterols and triterpenoids were identified on addition of few drops of acetic anhydride to the extract solution, boiled, cooled and then add concentrated sulphuric acid, producing brown ring at the junction of two layers, the turning of upper layer to green indicated sterols and deep red color indicated triterpenoids [17]. ...
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Pyrexia, algesia and inflammation are associated with several pathological conditions. Synthetic drugs available for the treatment of these conditions cause multiple unwanted effects. Several studies are ongoing worldwide to find natural healing agents with better safety profile. The current study was thus aimed at evaluating antipyretic, analgesic and anti-inflammatory activities of the methanolic extract of whole plant of V. betonicifolia (VBME). VBME was employed to assess antipyretic activity in yeast induced hyperthermia. Analgesic profile was ascertained in acetic acid induced writhing, hot plat and tail immersion test. Nevertheless, the anti-inflammatory activity was tested in carrageenan induced paw edema and histamine induced inflammatory tests. BALB/c mice were used at test doses of 100, 200 and 300 mg/kg body weight intra peritoneally (i.p). In yeast induced pyrexia, VBME demonstrated dose dependently (78.23%) protection at 300 mg/kg, similar to standard drug, paracetamol (90%) at 150 mg/kg i.p. VBME showed a dose dependent analgesia in various pain models i.e. acetic acid, hot plat and tail immersion having 78.90%, 69.96% and 68.58% protection respectively at 300 mg/kg. However, the analgesic action of VBME was completely antagonized by the injection of naloxone like opiate antagonists. Similarly carrageenan and histamine induces inflammation was significantly antagonized by VBME, 66.30% and 60.80% respectively at 300 mg/kg. It is concluded that VBME has marked antipyretic, analgesic and anti-inflammatory activities in various animal models and this strongly supports the ethnopharmacological uses of Viola betonicifolia as antipyretic, analgesic and anti-inflammatory plant.