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Positive effect of peptide‐calcium chelates from Grifola frondosa on a mouse model of senile osteoporosis
Calcium supplementation has been shown to be efficacious in mitigating the progression of senile osteoporosis (SOP) and reducing the incidence of osteoporotic fractures resulting from prolonged calcium shortage. In this study, Grifola frondosa (GF) peptides‐calcium chelate were synthesized through t...
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Published in: | Journal of food science 2024-06, Vol.89 (6), p.3816-3828 |
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description | Calcium supplementation has been shown to be efficacious in mitigating the progression of senile osteoporosis (SOP) and reducing the incidence of osteoporotic fractures resulting from prolonged calcium shortage. In this study, Grifola frondosa (GF) peptides‐calcium chelate were synthesized through the interaction between peptide from GF and CaCl2. The chelation reaction was shown to involve the participation of the amino and carboxyl groups in the peptide, as revealed by scanning electron microscope, Fourier‐transform infrared, and ultraviolet spectrophotometry. Furthermore, a mouse model of (SOP) induced by d‐galactose was established (SCXK‐2018‐0004). Results demonstrated that low dosage of low‐molecular weight GF peptides‐calcium chelates (LLgps‐Ca) could significantly improve serum index and pathological features of bone tissue and reduce bone injury. Further research suggested that LLgps‐Ca could ameliorate SOP by modulating the disrupted metabolic pathway, which includes focal adhesion, extracellular matrix receptor interaction, and PI3K‐Akt signaling pathway. Using Western blot, the differentially expressed proteins were further confirmed. Thus, calciumchelating peptides from GF could serve as functional calcium agents to alleviate SOP. |
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In this study, Grifola frondosa (GF) peptides‐calcium chelate were synthesized through the interaction between peptide from GF and CaCl2. The chelation reaction was shown to involve the participation of the amino and carboxyl groups in the peptide, as revealed by scanning electron microscope, Fourier‐transform infrared, and ultraviolet spectrophotometry. Furthermore, a mouse model of (SOP) induced by d‐galactose was established (SCXK‐2018‐0004). Results demonstrated that low dosage of low‐molecular weight GF peptides‐calcium chelates (LLgps‐Ca) could significantly improve serum index and pathological features of bone tissue and reduce bone injury. Further research suggested that LLgps‐Ca could ameliorate SOP by modulating the disrupted metabolic pathway, which includes focal adhesion, extracellular matrix receptor interaction, and PI3K‐Akt signaling pathway. Using Western blot, the differentially expressed proteins were further confirmed. Thus, calciumchelating peptides from GF could serve as functional calcium agents to alleviate SOP.</description><identifier>ISSN: 0022-1147</identifier><identifier>ISSN: 1750-3841</identifier><identifier>EISSN: 1750-3841</identifier><identifier>DOI: 10.1111/1750-3841.17073</identifier><identifier>PMID: 38685878</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>1-Phosphatidylinositol 3-kinase ; AKT protein ; Animals ; biochemical pathways ; blood serum ; bones ; calcium ; Calcium - metabolism ; Calcium Chelating Agents - pharmacology ; Calcium chloride ; Chelates ; Chelation ; Disease Models, Animal ; Electron microscopes ; Extracellular matrix ; Female ; femoral proteome ; focal adhesions ; food science ; Fourier transforms ; Fractures ; Galactose ; gene expression regulation ; Grifola frondosa ; Humans ; Infrared spectrophotometers ; Metabolic pathways ; Mice ; Molecular weight ; Osteoporosis ; Peptides ; Peptides - pharmacology ; peptide‐calcium chelates ; Scanning electron microscopy ; senile osteoporosis ; Signal transduction ; Spectrophotometry ; spectroscopy ; Western blotting</subject><ispartof>Journal of food science, 2024-06, Vol.89 (6), p.3816-3828</ispartof><rights>2024 Institute of Food Technologists.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3593-2a5ebee52b0bac0dd77417b750635e170fceafd493411c19acefac49e71e06053</cites><orcidid>0000-0002-6219-3093</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38685878$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xiong, Yu</creatorcontrib><creatorcontrib>Li, Jing‐Ru</creatorcontrib><creatorcontrib>Peng, Pei‐Zhi</creatorcontrib><creatorcontrib>Liu, Bin</creatorcontrib><creatorcontrib>Zhao, Li‐Na</creatorcontrib><title>Positive effect of peptide‐calcium chelates from Grifola frondosa on a mouse model of senile osteoporosis</title><title>Journal of food science</title><addtitle>J Food Sci</addtitle><description>Calcium supplementation has been shown to be efficacious in mitigating the progression of senile osteoporosis (SOP) and reducing the incidence of osteoporotic fractures resulting from prolonged calcium shortage. In this study, Grifola frondosa (GF) peptides‐calcium chelate were synthesized through the interaction between peptide from GF and CaCl2. The chelation reaction was shown to involve the participation of the amino and carboxyl groups in the peptide, as revealed by scanning electron microscope, Fourier‐transform infrared, and ultraviolet spectrophotometry. Furthermore, a mouse model of (SOP) induced by d‐galactose was established (SCXK‐2018‐0004). Results demonstrated that low dosage of low‐molecular weight GF peptides‐calcium chelates (LLgps‐Ca) could significantly improve serum index and pathological features of bone tissue and reduce bone injury. Further research suggested that LLgps‐Ca could ameliorate SOP by modulating the disrupted metabolic pathway, which includes focal adhesion, extracellular matrix receptor interaction, and PI3K‐Akt signaling pathway. Using Western blot, the differentially expressed proteins were further confirmed. Thus, calciumchelating peptides from GF could serve as functional calcium agents to alleviate SOP.</description><subject>1-Phosphatidylinositol 3-kinase</subject><subject>AKT protein</subject><subject>Animals</subject><subject>biochemical pathways</subject><subject>blood serum</subject><subject>bones</subject><subject>calcium</subject><subject>Calcium - metabolism</subject><subject>Calcium Chelating Agents - pharmacology</subject><subject>Calcium chloride</subject><subject>Chelates</subject><subject>Chelation</subject><subject>Disease Models, Animal</subject><subject>Electron microscopes</subject><subject>Extracellular matrix</subject><subject>Female</subject><subject>femoral proteome</subject><subject>focal adhesions</subject><subject>food science</subject><subject>Fourier transforms</subject><subject>Fractures</subject><subject>Galactose</subject><subject>gene expression regulation</subject><subject>Grifola frondosa</subject><subject>Humans</subject><subject>Infrared spectrophotometers</subject><subject>Metabolic pathways</subject><subject>Mice</subject><subject>Molecular weight</subject><subject>Osteoporosis</subject><subject>Peptides</subject><subject>Peptides - pharmacology</subject><subject>peptide‐calcium chelates</subject><subject>Scanning electron microscopy</subject><subject>senile osteoporosis</subject><subject>Signal transduction</subject><subject>Spectrophotometry</subject><subject>spectroscopy</subject><subject>Western blotting</subject><issn>0022-1147</issn><issn>1750-3841</issn><issn>1750-3841</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkc1OxCAUhYnR6PizdmdI3LjpCAVKuzTq-BMTTdQ1ofQSO7alllYzOx_BZ_RJpM7owo0sLrk3HwcOB6F9SqY0rGMqBYlYyumUSiLZGpr8TtbRhJA4jijlcgttez8nY8-STbTF0iQVqUwn6PnO-bIvXwGDtWB67Cxuoe3LAj7fP4yuTDnU2DxBpXvw2HauxhddaV2lx6YpnNfYNVjj2g0eQi2gGkU8NGUF2PkeXOu6cIvfRRtWVx72VvsOepydP5xeRje3F1enJzeRYSJjUawF5AAizkmuDSkKKTmVefCVMAHBpzWgbcEzxik1NNMGrDY8A0mBJESwHXS01G079zKA71VdegNVpRsIj1SMCpYKmhL2P0p4JuOYfKse_kHnbuiaYCRQieQxT2IaqOMlZYJl34FVbVfWulsoStQYmRoDUmNA6juycOJgpTvkNRS__E9GAUiWwFv40MV_eup6dna_VP4CWNihnw</recordid><startdate>202406</startdate><enddate>202406</enddate><creator>Xiong, Yu</creator><creator>Li, Jing‐Ru</creator><creator>Peng, Pei‐Zhi</creator><creator>Liu, Bin</creator><creator>Zhao, Li‐Na</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7QR</scope><scope>7ST</scope><scope>7T7</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><orcidid>https://orcid.org/0000-0002-6219-3093</orcidid></search><sort><creationdate>202406</creationdate><title>Positive effect of peptide‐calcium chelates from Grifola frondosa on a mouse model of senile osteoporosis</title><author>Xiong, Yu ; Li, Jing‐Ru ; Peng, Pei‐Zhi ; Liu, Bin ; Zhao, Li‐Na</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3593-2a5ebee52b0bac0dd77417b750635e170fceafd493411c19acefac49e71e06053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>1-Phosphatidylinositol 3-kinase</topic><topic>AKT protein</topic><topic>Animals</topic><topic>biochemical pathways</topic><topic>blood serum</topic><topic>bones</topic><topic>calcium</topic><topic>Calcium - metabolism</topic><topic>Calcium Chelating Agents - pharmacology</topic><topic>Calcium chloride</topic><topic>Chelates</topic><topic>Chelation</topic><topic>Disease Models, Animal</topic><topic>Electron microscopes</topic><topic>Extracellular matrix</topic><topic>Female</topic><topic>femoral proteome</topic><topic>focal adhesions</topic><topic>food science</topic><topic>Fourier transforms</topic><topic>Fractures</topic><topic>Galactose</topic><topic>gene expression regulation</topic><topic>Grifola frondosa</topic><topic>Humans</topic><topic>Infrared spectrophotometers</topic><topic>Metabolic pathways</topic><topic>Mice</topic><topic>Molecular weight</topic><topic>Osteoporosis</topic><topic>Peptides</topic><topic>Peptides - pharmacology</topic><topic>peptide‐calcium chelates</topic><topic>Scanning electron microscopy</topic><topic>senile osteoporosis</topic><topic>Signal transduction</topic><topic>Spectrophotometry</topic><topic>spectroscopy</topic><topic>Western blotting</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xiong, Yu</creatorcontrib><creatorcontrib>Li, Jing‐Ru</creatorcontrib><creatorcontrib>Peng, Pei‐Zhi</creatorcontrib><creatorcontrib>Liu, Bin</creatorcontrib><creatorcontrib>Zhao, Li‐Na</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Journal of food science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xiong, Yu</au><au>Li, Jing‐Ru</au><au>Peng, Pei‐Zhi</au><au>Liu, Bin</au><au>Zhao, Li‐Na</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Positive effect of peptide‐calcium chelates from Grifola frondosa on a mouse model of senile osteoporosis</atitle><jtitle>Journal of food science</jtitle><addtitle>J Food Sci</addtitle><date>2024-06</date><risdate>2024</risdate><volume>89</volume><issue>6</issue><spage>3816</spage><epage>3828</epage><pages>3816-3828</pages><issn>0022-1147</issn><issn>1750-3841</issn><eissn>1750-3841</eissn><abstract>Calcium supplementation has been shown to be efficacious in mitigating the progression of senile osteoporosis (SOP) and reducing the incidence of osteoporotic fractures resulting from prolonged calcium shortage. In this study, Grifola frondosa (GF) peptides‐calcium chelate were synthesized through the interaction between peptide from GF and CaCl2. The chelation reaction was shown to involve the participation of the amino and carboxyl groups in the peptide, as revealed by scanning electron microscope, Fourier‐transform infrared, and ultraviolet spectrophotometry. Furthermore, a mouse model of (SOP) induced by d‐galactose was established (SCXK‐2018‐0004). Results demonstrated that low dosage of low‐molecular weight GF peptides‐calcium chelates (LLgps‐Ca) could significantly improve serum index and pathological features of bone tissue and reduce bone injury. Further research suggested that LLgps‐Ca could ameliorate SOP by modulating the disrupted metabolic pathway, which includes focal adhesion, extracellular matrix receptor interaction, and PI3K‐Akt signaling pathway. Using Western blot, the differentially expressed proteins were further confirmed. Thus, calciumchelating peptides from GF could serve as functional calcium agents to alleviate SOP.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>38685878</pmid><doi>10.1111/1750-3841.17073</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-6219-3093</orcidid></addata></record> |
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subjects | 1-Phosphatidylinositol 3-kinase AKT protein Animals biochemical pathways blood serum bones calcium Calcium - metabolism Calcium Chelating Agents - pharmacology Calcium chloride Chelates Chelation Disease Models, Animal Electron microscopes Extracellular matrix Female femoral proteome focal adhesions food science Fourier transforms Fractures Galactose gene expression regulation Grifola frondosa Humans Infrared spectrophotometers Metabolic pathways Mice Molecular weight Osteoporosis Peptides Peptides - pharmacology peptide‐calcium chelates Scanning electron microscopy senile osteoporosis Signal transduction Spectrophotometry spectroscopy Western blotting |
title | Positive effect of peptide‐calcium chelates from Grifola frondosa on a mouse model of senile osteoporosis |
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