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Exploring mechanisms underlying diabetes comorbidities and strategies to prevent vascular complications
It is important to prevent not only diabetic complications but also diabetic comorbidities in diabetes care. We have elucidated multifaceted insulin action in various tissues mainly by means of model mice, and it was revealed that insulin regulates endoplasmic reticulum (ER) stress response during f...
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Published in: | Diabetology international 2024-01, Vol.15 (1), p.34-40 |
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description | It is important to prevent not only diabetic complications but also diabetic comorbidities in diabetes care. We have elucidated multifaceted insulin action in various tissues mainly by means of model mice, and it was revealed that insulin regulates endoplasmic reticulum (ER) stress response during feeding, whereas ER stress ‘response failure’ contributes to the development of steatohepatitis, one of the major diabetic comorbidities. Insulin regulates gluconeogenesis not only in the liver but also in the proximal tubules of the kidney, which is also suppressed by reabsorbed glucose in the latter. In skeletal muscle, another important insulin-targeted tissue, impaired insulin/IGF-1 signaling leads not only to sarcopenia, an aging-related disease, but also to bone loss and shorter longevity. Aging is regulated by adipokines as well, and it is deemed to be accelerated by ‘imbalanced adipokines’ in combination with genetic background of progeria. Moreover, we reported effects of intensive multifactorial intervention on diabetic complications and mortality in patients with type 2 diabetes in a large-scale clinical trial, the J-DOIT3, followed by reports of subsequent sub-analyses of renal events and fracture events. Various approaches to elucidate the mechanisms underlying the development of diabetes and how it should be treated are expected to help us improve diabetes management. |
doi_str_mv | 10.1007/s13340-023-00677-3 |
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Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c576t-56b540dc9977ca74438e284bb65fe98334d4bb6514cecf7bb50e022de6d24d343</cites><orcidid>0000-0002-7644-309X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10800323/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10800323/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38264227$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sasako, Takayoshi</creatorcontrib><title>Exploring mechanisms underlying diabetes comorbidities and strategies to prevent vascular complications</title><title>Diabetology international</title><addtitle>Diabetol Int</addtitle><addtitle>Diabetol Int</addtitle><description>It is important to prevent not only diabetic complications but also diabetic comorbidities in diabetes care. We have elucidated multifaceted insulin action in various tissues mainly by means of model mice, and it was revealed that insulin regulates endoplasmic reticulum (ER) stress response during feeding, whereas ER stress ‘response failure’ contributes to the development of steatohepatitis, one of the major diabetic comorbidities. Insulin regulates gluconeogenesis not only in the liver but also in the proximal tubules of the kidney, which is also suppressed by reabsorbed glucose in the latter. In skeletal muscle, another important insulin-targeted tissue, impaired insulin/IGF-1 signaling leads not only to sarcopenia, an aging-related disease, but also to bone loss and shorter longevity. Aging is regulated by adipokines as well, and it is deemed to be accelerated by ‘imbalanced adipokines’ in combination with genetic background of progeria. Moreover, we reported effects of intensive multifactorial intervention on diabetic complications and mortality in patients with type 2 diabetes in a large-scale clinical trial, the J-DOIT3, followed by reports of subsequent sub-analyses of renal events and fracture events. Various approaches to elucidate the mechanisms underlying the development of diabetes and how it should be treated are expected to help us improve diabetes management.</description><subject>Aging</subject><subject>Animal models</subject><subject>Bone loss</subject><subject>Comorbidity</subject><subject>Diabetes</subject><subject>Diabetes mellitus (non-insulin dependent)</subject><subject>Endocrinology</subject><subject>Endoplasmic reticulum</subject><subject>Gluconeogenesis</subject><subject>Insulin</subject><subject>Insulin-like growth factor I</subject><subject>Insulin-like growth factors</subject><subject>Kidneys</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metabolic Diseases</subject><subject>Progeria</subject><subject>Proximal tubules</subject><subject>Review</subject><subject>Review Article</subject><subject>Sarcopenia</subject><subject>Skeletal muscle</subject><issn>2190-1678</issn><issn>2190-1686</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9UU1v3CAURFWrJkrzB3KoLPXSi1O-DPapqqK0iRSpl-aMMLzdENngAl41_z6QTbYfh3KBgZl57zEInRF8TjCWnxJhjOMWU9ZiLKRs2St0TMmAWyJ68fpwlv0ROk3pHpfFB4KleIuOWE8Fp1Qeo-3lr2UK0fltM4O5096lOTWrtxCnh3prnR4hQ2pMmEMcnXXZFaS9bVKOOsO2whyaJcIOfG52Opl10rEKlskZnV3w6R16s9FTgtPn_QTdfr38cXHV3nz_dn3x5aY1nRS57cTYcWzNMEhptOSc9UB7Po6i28DQl5HtEyDcgNnIcewwYEotCEu5ZZydoM9732UdZ7CmdBT1pJboZh0fVNBO_f3i3Z3ahp0iuMeYUVYcPj47xPBzhZTV7JKBadIewpoUHUhPBtETXKgf_qHehzX6Ml9lSVq_uxrSPcvEkFKEzaEbglXNUu2zVCVL9ZSlqqL3f85xkLwkVwhsT0hLTQ_i79r_sX0Eoy6skA</recordid><startdate>20240101</startdate><enddate>20240101</enddate><creator>Sasako, Takayoshi</creator><general>Springer Nature Singapore</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-7644-309X</orcidid></search><sort><creationdate>20240101</creationdate><title>Exploring mechanisms underlying diabetes comorbidities and strategies to prevent vascular complications</title><author>Sasako, Takayoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c576t-56b540dc9977ca74438e284bb65fe98334d4bb6514cecf7bb50e022de6d24d343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Aging</topic><topic>Animal models</topic><topic>Bone loss</topic><topic>Comorbidity</topic><topic>Diabetes</topic><topic>Diabetes mellitus (non-insulin dependent)</topic><topic>Endocrinology</topic><topic>Endoplasmic reticulum</topic><topic>Gluconeogenesis</topic><topic>Insulin</topic><topic>Insulin-like growth factor I</topic><topic>Insulin-like growth factors</topic><topic>Kidneys</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metabolic Diseases</topic><topic>Progeria</topic><topic>Proximal tubules</topic><topic>Review</topic><topic>Review Article</topic><topic>Sarcopenia</topic><topic>Skeletal muscle</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sasako, Takayoshi</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Diabetology international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sasako, Takayoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Exploring mechanisms underlying diabetes comorbidities and strategies to prevent vascular complications</atitle><jtitle>Diabetology international</jtitle><stitle>Diabetol Int</stitle><addtitle>Diabetol Int</addtitle><date>2024-01-01</date><risdate>2024</risdate><volume>15</volume><issue>1</issue><spage>34</spage><epage>40</epage><pages>34-40</pages><issn>2190-1678</issn><eissn>2190-1686</eissn><abstract>It is important to prevent not only diabetic complications but also diabetic comorbidities in diabetes care. 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Moreover, we reported effects of intensive multifactorial intervention on diabetic complications and mortality in patients with type 2 diabetes in a large-scale clinical trial, the J-DOIT3, followed by reports of subsequent sub-analyses of renal events and fracture events. Various approaches to elucidate the mechanisms underlying the development of diabetes and how it should be treated are expected to help us improve diabetes management.</abstract><cop>Singapore</cop><pub>Springer Nature Singapore</pub><pmid>38264227</pmid><doi>10.1007/s13340-023-00677-3</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-7644-309X</orcidid></addata></record> |
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subjects | Aging Animal models Bone loss Comorbidity Diabetes Diabetes mellitus (non-insulin dependent) Endocrinology Endoplasmic reticulum Gluconeogenesis Insulin Insulin-like growth factor I Insulin-like growth factors Kidneys Medicine Medicine & Public Health Metabolic Diseases Progeria Proximal tubules Review Review Article Sarcopenia Skeletal muscle |
title | Exploring mechanisms underlying diabetes comorbidities and strategies to prevent vascular complications |
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