<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">AJPS</journal-id><journal-title-group><journal-title>American Journal of Plant Sciences</journal-title></journal-title-group><issn pub-type="epub">2158-2742</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ajps.2020.114042</article-id><article-id pub-id-type="publisher-id">AJPS-99763</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biomedical&amp;Life Sciences</subject></subj-group></article-categories><title-group><article-title>
 
 
  The Anatomical Structure of Leaves and Thorns Plants &lt;i&gt;Astragalus pterocephalus&lt;/i&gt; Bunge, Growing in Uzbekistan
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Manzura</surname><given-names>A. Agzamova</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Guljan</surname><given-names>M. Duschanova</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Hasan</surname><given-names>A. Rakhmatov</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Abdulaziz</surname><given-names>A. Janibekov</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Institute of Plant Chemistry Named after Acad. S. Yu. Yunusov Academy of Sciences of the Republic of Uzbekistan, Tashkent, Uzbekistan</addr-line></aff><aff id="aff2"><addr-line>Laboratory Anatomy and Cytoembryology of the Tashkent Botanical Garden Named after Academician F.N. Rusanov, Institute of Botany of the Academy of Sciences, Tashkent, Uzbekistan</addr-line></aff><pub-date pub-type="epub"><day>07</day><month>04</month><year>2020</year></pub-date><volume>11</volume><issue>04</issue><fpage>569</fpage><lpage>577</lpage><history><date date-type="received"><day>23,</day>	<month>September</month>	<year>2019</year></date><date date-type="rev-recd"><day>23,</day>	<month>April</month>	<year>2020</year>	</date><date date-type="accepted"><day>26,</day>	<month>April</month>	<year>2020</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  The results of a study conducted by light microscopy of the anatomical structure of the leaf and thorns of 
  Astragalus pterocephalus
   growing in the natural habitat of the Amankutan Mountains of the Samarkand region (Uz
  bekistan) are presented. The following diagnostic features were identified: lea
  f
  —isolateral-palisade type of mesophyll leaf; thick-walled outer walls of the epidermis; the outline of epidermal cells is rectilinear, the projection is polygonal; amphystomatic leaves; submerged numerous stomata of hemiparacitic and anomocytic type; chlorophyll-bearing palisade and spongy parenchyma; closed collateral type of vascular bundles and more sclerified, due to sclerenchymal cells.
   
  Thorn
  —parenchymal-beam type of structure; thin-walled outer walls of the epidermis; under the epidermis is a lamellar collenchyma; closed collateral type of vascular bundles and more sclerified, due to sclerenchymal cells.
   
  The complex of the above features reflects the species specificity of the structure of the leaf and spines. Identified and described features that can be used in the taxonomy of the studied tribes and can serve to identify plant materials.
 
</p></abstract><kwd-group><kwd>&lt;i&gt;Astragalus pterocephalus&lt;/i&gt;</kwd><kwd> Anatomy</kwd><kwd> Leaf</kwd><kwd> Thorn</kwd><kwd> Amankutan Mountains Samarkand</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>A number of representatives of plants of the genus Astragalus are used in traditional medicine of many peoples of the world. This genus is represented in the flora of Central Asia by 592 species, in Uzbekistan—239 [<xref ref-type="bibr" rid="scirp.99763-ref1">1</xref>]. According to the literature the genus Astragalus L. is very extensive and polymorphic, numbering from 1200 to 2200 species [<xref ref-type="bibr" rid="scirp.99763-ref2">2</xref>] - [<xref ref-type="bibr" rid="scirp.99763-ref7">7</xref>], the world’s flora.</p><p>In the early 80-ies in chemistry lab glycosides, Institute of Plant Chemistry of the Academy of Sciences of the Republic of Uzbekistan for the first time shown that plants of the genus Astragalus (Leguminosae) produces triterpene glycosides cycloartane series. Subsequently, our scientists and foreign colleagues discovered glycosides of this class with a wide spectrum of biological activity: cardiotonic, hypotensive, hypoglycemic, hypocholesterolemic and anti-blastoma.</p><p>Preparations based on biologically active substances from Astragalus sieversianus Pall. have hypocholesterolemic activity [<xref ref-type="bibr" rid="scirp.99763-ref8">8</xref>] [<xref ref-type="bibr" rid="scirp.99763-ref9">9</xref>], contributing to the normalization of lipid metabolism and improving cardiac activity. The activity of glycosides—Cyclosiversioside A and Cycloorbicoside G on metabolic processes in rat myocardium was revealed [<xref ref-type="bibr" rid="scirp.99763-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.99763-ref11">11</xref>]. Cycloartane glycosides isolated from Astragalus orbiculatus showed an interferon inducing effect [<xref ref-type="bibr" rid="scirp.99763-ref12">12</xref>], cytotoxic activity [<xref ref-type="bibr" rid="scirp.99763-ref13">13</xref>].</p><p>A wide pharmacological and chemical study of glycoside, Cyclosiversioside F—3-O-β-D-xylopyranoside, 6-O-β-D-glucopyranoside-20R, 24S-epoxycycloartan-3β, 6α, 16β, 25-tetraol, is currently underway which was obtained from a wild plant Astragalus pterocephalus, an astragalus of the winged-headed legume family, Leguminosae [<xref ref-type="bibr" rid="scirp.99763-ref14">14</xref>] [<xref ref-type="bibr" rid="scirp.99763-ref15">15</xref>].</p><p>The main goal of this scientific study is to study the anatomical structure and determine the diagnostic characteristics of the leaves and thorns of the medicinal plant Astragalus pterocephalus, the main component of which is the triterpene glycoside of the cycloartan series Cyclosiversiverside F.</p></sec><sec id="s2"><title>2. Materials and Methods</title><p>Astragalus pterocephalus Bunge (Tragacantha pterocephala Bunge.)—perennial branched shrub up to 1.5 m in height; the branches are covered with straight, 5 - 7 cm long, thick, slightly deviated, often blackening, spines (altered leaf petioles). Stipules about 1.5 cm long, lanceolate, sharp, membranous, almost transparent, multi-nerve, silky-hairy on the outside at the bottom. Leaflets are 4 - 5-paired, oblong-lanceolate, 15 - 17 mm long, about 3 - 4-(5) mm wide, green, sparsely pressed on both sides of the hairy. Flowers in the axils of the leaves of 10 - 12, collected in spherical inflorescences 3 - 5 cm wide. Bracts oblong-lanceolate, about 15 mm long, transparent, yellowish, one-nervous, glabrous, ciliate along the edge. Calyx 18 - 25 mm long, long and densely hairy, its teeth thin, purple, almost twice as long as the tube, covered with long protruding hairs. Flag about 17 mm long, shorter than calyx; its plate is narrowed upward, almost without ears, longer than a wide marigold. The wings are shorter than the flag; plate 1 - 1.5 mm wide, almost twice as short as a marigold. The boat is slightly shorter than or equal to the wings. The column is only fluffy at the base. Bob is oblong-elliptical, white-haired. The seeds are kidney-shaped, about 3 mm long, light brown. The plant flowering in May-June bears fruit in July-August [<xref ref-type="bibr" rid="scirp.99763-ref1">1</xref>]. Species identified by F. O. Khassanov (<xref ref-type="fig" rid="fig1">Figure 1</xref>).</p><p>Plant samples were collected in the natural habitat of the Amankutan Mountains of the Samarkand region at the end of May and the beginning of June in the phase flowering 2018-2019 (<xref ref-type="fig" rid="fig2">Figure 2</xref>).</p><p>Astragalus pterocephalus grows on gravel, rocky and fine-grained slopes, on shale’s, at heights of 1500 - 2000 m. to the mountains of Amankutan, Samarkand region.</p><p>Amankutan is a mountain tract in the Zerafshan ridge with absolute elevations of 1000 - 2000 m. the highest point of 2015 m, low 1000 m above the sea. The difference in height is 1000 m, which is typical of a typical mid-mountain relief.</p><p>The climate of Amankutan is sharply continental. The amplitudes of temperature fluctuations day and night, winter and summer are more pronounced than in the Zerafshan valley. Humidity here also changes more sharply than in the irrigated zone. Summer in Amankutan is cool, almost without precipitation with low relative humidity. At the end of May, all signs of summer, which lasts until mid-September, are already showing. The average July temperature is 24.5˚C, the maximum for the summer is +35˚C. During this period, no more than 200 mm of atmospheric precipitation falls. The hottest month—July.</p><p>For the purpose of anatomical study and morphological description of the leaf and thorn, the plant was fixed in 70˚ ethanol. The epidermis was studied on paradermal and transverse sections, transverse sections of the leaf were made through the middle, thorns from the base. Descriptions of the main tissues and cells are given according to C. Esau [<xref ref-type="bibr" rid="scirp.99763-ref16">16</xref>], N. S. Kiseleva [<xref ref-type="bibr" rid="scirp.99763-ref17">17</xref>] and the epidermis according to S. F. Zakharevich [<xref ref-type="bibr" rid="scirp.99763-ref18">18</xref>]. Manual preparations were stained with methylene blue, followed by gluing in glycerol-gelatin [<xref ref-type="bibr" rid="scirp.99763-ref19">19</xref>]. Microphotographs were taken using a computer microphotograph of a Canon A123 digital camera under a Motic B1-220A-3 microscope.</p></sec><sec id="s3"><title>3. Results and Discussion</title><p>The leaf is a vegetative organ of the plant, performing the function of photosynthesis, transpiration and gas exchange.</p><p>On the paradermal section, the outlines of the epidermal cells of the leaf are rectilinear, the projection is polygonal. However, the upper epidermis is somewhat different from the lower epidermis. The cells of the upper epidermis are larger than the lower. The leaves are amphystomatic, stomata are located on both sides of the leaf blade, located transversely to the longitudinal axis of the leaf. The shape of the stomata is round. The upper (adaxial) epidermis has a significantly smaller number of stomata compared to the lower (abaxial) epidermis. All this leads to a reduction in water loss from the surface of the sheet. The closing stomata cells on both sides of the leaf are almost the same length. Stomata submerged, hemiparacytic and anomocytic types (<xref ref-type="fig" rid="fig3">Figure 3</xref> and <xref ref-type="fig" rid="fig4">Figure 4</xref>).</p><p>The mesophyll of the leaf on the cross-section of the isolate-palisade type, is represented by 2 rows of palisade cells on both sides of the leaf and a spongy layer of different thickness between them. The epidermis is represented by one row of cells with a thick-walled cuticle layer. Adaxial epidermal cells are larger than abaxial.</p><p>An assimilation tissue consisting of palisade and spongy cells is located between the adaxial and abaxial epidermis. The palisade parenchyma is chlorophyll-bearing, large and elongated, which consists of 2 rows of cells and is located</p><p>between the adaxial and abaxial leaf epidermis.</p><p>The spongy chlorophyll-bearing parenchyma consists of 3 - 4 rows and is located between the palisade parenchyma. The spongy parenchyma is round, small-cell with small cavities. Between palisade and spongy cells, the main and lateral vascular bundles are located.</p><p>The main and lateral conducting bundles protrude on the abaxial side and are located in the central part of the leaf mesophyll. Vascular bundles are most sclerified, due to the presence of mechanical tissues (sclerenchyma) in them (<xref ref-type="fig" rid="fig4">Figure 4</xref>).</p><p>Under the abaxial epidermis and above the main vascular bundles, there is a 2-row lamellar collenchyma. Large and small conductive beams alternate with each other. Vascular bundles of closed collateral type, numerous, consisting of phloem and xylem (<xref ref-type="fig" rid="fig4">Figure 4</xref>).</p><p>Thorn. On the cross-section, oval or heart-shaped, parenchymal-beam type of structure. The epidermis is single-row, oval and thin-walled. Collenchyma lamellar, thickened consists of 3 - 4 rows. Under the collenchyma is a rounded oval cortex parenchyma, which consists of 5 - 6 rows (<xref ref-type="fig" rid="fig5">Figure 5</xref>).</p><p>Vascular bundles of a circular arrangement, the phloem is extensive, the xylem is round-oval, large and small. Vascular bundles are most sclerified, due to the presence of mechanical tissues (sclerenchyma) in them.</p><p>Large and small conductive beams alternate with each other. Vascular bundles of closed collateral type, numerous, consisting of a phloem and xylem. The core is extensive, parenchymal cells are round, thick-walled, among which there are</p><p>hydrocytic cells (<xref ref-type="fig" rid="fig5">Figure 5</xref>).</p><p>Thus, the anatomical structure of the leaf and spines of Astragalus pterocephalus was studied and the following diagnostic signs were determined: leaf—isolateral-palisade type of mesophyll leaf; thick-walled outer walls of the epidermis; the outline of epidermal cells is rectilinear, the projection is polygonal; amphystomatic leaves; submerged numerous stomata of hemiparacitic and anomocytic type; chlorophyll-bearing palisade and spongy parenchyma; closed collateral type of vascular bundles and more sclerified, due to sclerenchymal cells. Thorn—parenchymal-beam type of structure; thin-walled outer walls of the</p><p>epidermis; under the epidermis is a lamellar collenchyma; closed collateral type of vascular bundles and more sclerified, due to sclerenchymal cells. The diagnostic characters that we have identified reflect more xeromorphicity of this species and can be used in the taxonomy of the studied tribes, and can also serve to identify plant materials.</p></sec><sec id="s4"><title>Acknowledgements</title><p>The work was carried out with financial support from the State Foundation for Basic Research of the Republic of Uzbekistan (under grant No. VA-FA-F7-009).</p></sec><sec id="s5"><title>Conflicts of Interest</title><p>The authors declare no conflicts of interest regarding the publication of this paper.</p></sec><sec id="s6"><title>Cite this paper</title><p>Agzamova, M.A., Duschanova, G.M., Rakhmatov, H.A. and Janibekov, A.A. (2020) The Anatomical Structure of Leaves and Thorns Plants Astragalus pterocephalus Bunge, Growing in Uzbekistan. 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