In vitro chondroprotective potential of Senna alata and Senna tora in porcine cartilage explants and their species differentiation by DNA barcoding-high resolution melting (Bar-HRM) analysis

Senna species and anthraquinone derivatives generated by these organisms, rhein and aloe-emodin, exert anti-inflammatory effects. These species present a similar morphology but produce different ingredients when they are used as medicinal products. In this study, a DNA barcoding- (Bar-) high-resolut...

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Veröffentlicht in:PloS one 2019-04, Vol.14 (4), p.e0215664-e0215664
Hauptverfasser: Ongchai, Siriwan, Chokchaitaweesuk, Chatchadawalai, Kongdang, Patiwat, Chomdej, Siriwadee, Buddhachat, Kittisak
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Chokchaitaweesuk, Chatchadawalai
Kongdang, Patiwat
Chomdej, Siriwadee
Buddhachat, Kittisak
description Senna species and anthraquinone derivatives generated by these organisms, rhein and aloe-emodin, exert anti-inflammatory effects. These species present a similar morphology but produce different ingredients when they are used as medicinal products. In this study, a DNA barcoding- (Bar-) high-resolution melting (HRM) technique was developed using internal transcribed sequence 2 (ITS2) to differentiate between Senna alata and Senna tora as a result of significant differences in their melting profiles. We used this approach for confirmation of S. alata and S. tora raw materials, and we examined the chondroprotective properties of the ethanolic extracts of S. alata and S. tora using a porcine model of cartilage degradation induced by a combination of interleukin-17A (IL-17A) and IL-1β. We found that both Senna ethanolic extracts, at a concentration of 25 μg/mL, effectively prevented cartilage degradation. Rhein and aloe-emodin were present in the extract of S. alata but not in that of S. tora. We observed a reduction in the release of sulfated glycosaminoglycans (S-GAGs) and hyaluronic acid (HA) into media in both treatments of Senna extracts, which indicated proteoglycan preservation in explant tissues. These results suggest that neither rhein nor aloe-emodin are the main factors responsible for cartilage-protecting properties. Taken together, results show that both S. alata and S. tora are promising for further development as anti-osteoarthritic agents and that Bar-HRM using ITS2 could be applied for species confirmation with Senna products.
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These species present a similar morphology but produce different ingredients when they are used as medicinal products. In this study, a DNA barcoding- (Bar-) high-resolution melting (HRM) technique was developed using internal transcribed sequence 2 (ITS2) to differentiate between Senna alata and Senna tora as a result of significant differences in their melting profiles. We used this approach for confirmation of S. alata and S. tora raw materials, and we examined the chondroprotective properties of the ethanolic extracts of S. alata and S. tora using a porcine model of cartilage degradation induced by a combination of interleukin-17A (IL-17A) and IL-1β. We found that both Senna ethanolic extracts, at a concentration of 25 μg/mL, effectively prevented cartilage degradation. Rhein and aloe-emodin were present in the extract of S. alata but not in that of S. tora. We observed a reduction in the release of sulfated glycosaminoglycans (S-GAGs) and hyaluronic acid (HA) into media in both treatments of Senna extracts, which indicated proteoglycan preservation in explant tissues. These results suggest that neither rhein nor aloe-emodin are the main factors responsible for cartilage-protecting properties. 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Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health &amp; Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Applied &amp; Life Sciences</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ongchai, Siriwan</au><au>Chokchaitaweesuk, Chatchadawalai</au><au>Kongdang, Patiwat</au><au>Chomdej, Siriwadee</au><au>Buddhachat, Kittisak</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In vitro chondroprotective potential of Senna alata and Senna tora in porcine cartilage explants and their species differentiation by DNA barcoding-high resolution melting (Bar-HRM) analysis</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2019-04-19</date><risdate>2019</risdate><volume>14</volume><issue>4</issue><spage>e0215664</spage><epage>e0215664</epage><pages>e0215664-e0215664</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Senna species and anthraquinone derivatives generated by these organisms, rhein and aloe-emodin, exert anti-inflammatory effects. These species present a similar morphology but produce different ingredients when they are used as medicinal products. In this study, a DNA barcoding- (Bar-) high-resolution melting (HRM) technique was developed using internal transcribed sequence 2 (ITS2) to differentiate between Senna alata and Senna tora as a result of significant differences in their melting profiles. We used this approach for confirmation of S. alata and S. tora raw materials, and we examined the chondroprotective properties of the ethanolic extracts of S. alata and S. tora using a porcine model of cartilage degradation induced by a combination of interleukin-17A (IL-17A) and IL-1β. We found that both Senna ethanolic extracts, at a concentration of 25 μg/mL, effectively prevented cartilage degradation. Rhein and aloe-emodin were present in the extract of S. alata but not in that of S. tora. We observed a reduction in the release of sulfated glycosaminoglycans (S-GAGs) and hyaluronic acid (HA) into media in both treatments of Senna extracts, which indicated proteoglycan preservation in explant tissues. These results suggest that neither rhein nor aloe-emodin are the main factors responsible for cartilage-protecting properties. Taken together, results show that both S. alata and S. tora are promising for further development as anti-osteoarthritic agents and that Bar-HRM using ITS2 could be applied for species confirmation with Senna products.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>31002692</pmid><doi>10.1371/journal.pone.0215664</doi><orcidid>https://orcid.org/0000-0003-4746-9861</orcidid><oa>free_for_read</oa></addata></record>
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1932-6203
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subjects Aloe
Animals
Anthraquinone
Anthraquinones
Anti-inflammatory agents
Arthritis
Backup software
Bar codes
Base Sequence
Biochemistry
Biocompatibility
Biomedical materials
Cartilage
Cartilage - drug effects
Cartilage - metabolism
Cartilage - pathology
Cartilage diseases
Collagen Type II - metabolism
Cytokines
Degradation
Deoxyribonucleic acid
Disease Models, Animal
DNA
DNA Barcoding, Taxonomic - methods
DNA, Ribosomal Spacer - genetics
Drugs
EDTA
Emodin
Ethanol - chemistry
Explants
Gene sequencing
Genetic aspects
Genetic research
Glycosaminoglycans
Herbal medicine
High resolution
Hyaluronic acid
IL-1β
Inflammation
Interleukins
Leaves
Medicine
Melting
Morphology
Mucopolysaccharides
Osteoarthritis
Osteoarthritis - metabolism
Osteoarthritis - prevention & control
Phytotherapy - methods
Preservation
Protective Agents - pharmacology
Proteoglycans
Proteoglycans - metabolism
Raw materials
Senna alata
Senna Extract - chemistry
Senna Extract - pharmacology
Senna Plant - chemistry
Senna Plant - classification
Senna Plant - genetics
Senna tora
Sequence Homology, Nucleic Acid
Species
Species Specificity
Stem cells
Sulfates
Swine
Tissue engineering
title In vitro chondroprotective potential of Senna alata and Senna tora in porcine cartilage explants and their species differentiation by DNA barcoding-high resolution melting (Bar-HRM) analysis
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