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PAN-811 prevents chemotherapy-induced cognitive impairment and preserves neurogenesis in the hippocampus of adult rats
Chemotherapy-induced cognitive impairment (CICI) occurs in a substantial proportion of treated cancer patients, with no drug currently available for its therapy. This study investigated whether PAN-811, a ribonucleotide reductase inhibitor, can reduce cognitive impairment and related suppression of...
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Published in: | PloS one 2018-01, Vol.13 (1), p.e0191866-e0191866 |
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description | Chemotherapy-induced cognitive impairment (CICI) occurs in a substantial proportion of treated cancer patients, with no drug currently available for its therapy. This study investigated whether PAN-811, a ribonucleotide reductase inhibitor, can reduce cognitive impairment and related suppression of neurogenesis following chemotherapy in an animal model. Young adult rats in Chemo and Chemo+PAN-811 groups received 3 intraperitoneal (i.p.) injections of methotrexate (MTX) and 5-fluorouracil (5-FU), and those in Saline and Saline+PAN-811 groups received equal volumes of physiological saline at 10-day intervals. PAN-811 in saline was delivered through i.p. injection, 10 min following each saline (Saline+PAN-811 group) or MTX/5-FU (Chemo+PAN-811 group) treatment, while equal volumes of saline were delivered to Saline and Chemo groups. Over Days 31-66, rats were administered tests of spatial memory, nonmatching-to-sample rule learning, and discrimination learning, which are sensitive to dysfunction in hippocampus, frontal lobe and striatum, respectively. On Day 97, neurogenesis was immnunohistochemically evaluated by counting doublecortin-positive (DCX+) cells in the dentate gyrus (DG). The results demonstrated that the Chemo group was impaired on the three cognitive tasks, but co-administration of PAN-811 significantly reduced all MTX/5-FU-induced cognitive impairments. In addition, MTX/5-FU reduced DCX+ cells to 67% of that in Saline control rats, an effect that was completely blocked by PAN-811 co-administration. Overall, we present the first evidence that PAN-811 protects cognitive functions and preserves neurogenesis from deleterious effects of MTX/5-FU. The current findings provide a basis for rapid clinical translation to determine the effect of PAN-811 on CICI in human. |
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This study investigated whether PAN-811, a ribonucleotide reductase inhibitor, can reduce cognitive impairment and related suppression of neurogenesis following chemotherapy in an animal model. Young adult rats in Chemo and Chemo+PAN-811 groups received 3 intraperitoneal (i.p.) injections of methotrexate (MTX) and 5-fluorouracil (5-FU), and those in Saline and Saline+PAN-811 groups received equal volumes of physiological saline at 10-day intervals. PAN-811 in saline was delivered through i.p. injection, 10 min following each saline (Saline+PAN-811 group) or MTX/5-FU (Chemo+PAN-811 group) treatment, while equal volumes of saline were delivered to Saline and Chemo groups. Over Days 31-66, rats were administered tests of spatial memory, nonmatching-to-sample rule learning, and discrimination learning, which are sensitive to dysfunction in hippocampus, frontal lobe and striatum, respectively. On Day 97, neurogenesis was immnunohistochemically evaluated by counting doublecortin-positive (DCX+) cells in the dentate gyrus (DG). The results demonstrated that the Chemo group was impaired on the three cognitive tasks, but co-administration of PAN-811 significantly reduced all MTX/5-FU-induced cognitive impairments. In addition, MTX/5-FU reduced DCX+ cells to 67% of that in Saline control rats, an effect that was completely blocked by PAN-811 co-administration. Overall, we present the first evidence that PAN-811 protects cognitive functions and preserves neurogenesis from deleterious effects of MTX/5-FU. The current findings provide a basis for rapid clinical translation to determine the effect of PAN-811 on CICI in human.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0191866</identifier><identifier>PMID: 29370277</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>5-Fluorouracil ; Animal cognition ; Animal models ; Animals ; Antineoplastic Agents - administration & dosage ; Antineoplastic Agents - adverse effects ; Biology and Life Sciences ; Cancer therapies ; Chemotherapy ; Cognitive ability ; Cognitive Dysfunction - chemically induced ; Cognitive Dysfunction - prevention & control ; Cognitive tasks ; Dentate gyrus ; Dentate Gyrus - drug effects ; Discrimination learning ; Discrimination Learning - drug effects ; Disease Models, Animal ; Doublecortin protein ; Drugs ; Enzyme Inhibitors - pharmacology ; Female ; Fluorouracil - administration & dosage ; Fluorouracil - adverse effects ; Frontal lobe ; Hippocampus ; Hippocampus - drug effects ; Hippocampus - pathology ; Hippocampus - physiopathology ; Humans ; Impairment ; Laboratories ; Learning ; Learning - drug effects ; Medicine and Health Sciences ; Memory ; Memory tasks ; Methotrexate ; Methotrexate - administration & dosage ; Methotrexate - adverse effects ; Neostriatum ; Neurogenesis ; Neurogenesis - drug effects ; Neuroprotective Agents - pharmacology ; Neurotoxicity ; Pharmaceuticals ; Physiology ; Pyridines - pharmacology ; Quality of life ; Rats ; Rats, Long-Evans ; Reductase ; Reductases ; Ribonucleotide Reductases - antagonists & inhibitors ; Social Sciences ; Spatial analysis ; Spatial discrimination learning ; Spatial memory ; Spatial Memory - drug effects ; Thiosemicarbazones - pharmacology ; Young adults</subject><ispartof>PloS one, 2018-01, Vol.13 (1), p.e0191866-e0191866</ispartof><rights>2018 Jiang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2018 Jiang et al 2018 Jiang et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-10384511e5d78aab8368d32d3b66e758a91be85ebd77440fdc1919397344d2403</citedby><cites>FETCH-LOGICAL-c526t-10384511e5d78aab8368d32d3b66e758a91be85ebd77440fdc1919397344d2403</cites><orcidid>0000-0002-1101-4040</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2390634144/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2390634144?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29370277$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Kavushansky, Alexandra</contributor><creatorcontrib>Jiang, Zhi-Gang</creatorcontrib><creatorcontrib>Winocur, Gordon</creatorcontrib><creatorcontrib>Wojtowicz, J Martin</creatorcontrib><creatorcontrib>Shevtsova, Olga</creatorcontrib><creatorcontrib>Fuller, Steven</creatorcontrib><creatorcontrib>Ghanbari, Hossein A</creatorcontrib><title>PAN-811 prevents chemotherapy-induced cognitive impairment and preserves neurogenesis in the hippocampus of adult rats</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Chemotherapy-induced cognitive impairment (CICI) occurs in a substantial proportion of treated cancer patients, with no drug currently available for its therapy. This study investigated whether PAN-811, a ribonucleotide reductase inhibitor, can reduce cognitive impairment and related suppression of neurogenesis following chemotherapy in an animal model. Young adult rats in Chemo and Chemo+PAN-811 groups received 3 intraperitoneal (i.p.) injections of methotrexate (MTX) and 5-fluorouracil (5-FU), and those in Saline and Saline+PAN-811 groups received equal volumes of physiological saline at 10-day intervals. PAN-811 in saline was delivered through i.p. injection, 10 min following each saline (Saline+PAN-811 group) or MTX/5-FU (Chemo+PAN-811 group) treatment, while equal volumes of saline were delivered to Saline and Chemo groups. Over Days 31-66, rats were administered tests of spatial memory, nonmatching-to-sample rule learning, and discrimination learning, which are sensitive to dysfunction in hippocampus, frontal lobe and striatum, respectively. On Day 97, neurogenesis was immnunohistochemically evaluated by counting doublecortin-positive (DCX+) cells in the dentate gyrus (DG). The results demonstrated that the Chemo group was impaired on the three cognitive tasks, but co-administration of PAN-811 significantly reduced all MTX/5-FU-induced cognitive impairments. In addition, MTX/5-FU reduced DCX+ cells to 67% of that in Saline control rats, an effect that was completely blocked by PAN-811 co-administration. Overall, we present the first evidence that PAN-811 protects cognitive functions and preserves neurogenesis from deleterious effects of MTX/5-FU. The current findings provide a basis for rapid clinical translation to determine the effect of PAN-811 on CICI in human.</description><subject>5-Fluorouracil</subject><subject>Animal cognition</subject><subject>Animal models</subject><subject>Animals</subject><subject>Antineoplastic Agents - administration & dosage</subject><subject>Antineoplastic Agents - adverse effects</subject><subject>Biology and Life Sciences</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Cognitive ability</subject><subject>Cognitive Dysfunction - chemically induced</subject><subject>Cognitive Dysfunction - prevention & control</subject><subject>Cognitive tasks</subject><subject>Dentate gyrus</subject><subject>Dentate Gyrus - drug effects</subject><subject>Discrimination learning</subject><subject>Discrimination Learning - drug effects</subject><subject>Disease Models, Animal</subject><subject>Doublecortin protein</subject><subject>Drugs</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Female</subject><subject>Fluorouracil - administration & dosage</subject><subject>Fluorouracil - adverse effects</subject><subject>Frontal lobe</subject><subject>Hippocampus</subject><subject>Hippocampus - drug effects</subject><subject>Hippocampus - pathology</subject><subject>Hippocampus - physiopathology</subject><subject>Humans</subject><subject>Impairment</subject><subject>Laboratories</subject><subject>Learning</subject><subject>Learning - drug effects</subject><subject>Medicine and Health Sciences</subject><subject>Memory</subject><subject>Memory tasks</subject><subject>Methotrexate</subject><subject>Methotrexate - administration & dosage</subject><subject>Methotrexate - adverse effects</subject><subject>Neostriatum</subject><subject>Neurogenesis</subject><subject>Neurogenesis - drug effects</subject><subject>Neuroprotective Agents - pharmacology</subject><subject>Neurotoxicity</subject><subject>Pharmaceuticals</subject><subject>Physiology</subject><subject>Pyridines - pharmacology</subject><subject>Quality of life</subject><subject>Rats</subject><subject>Rats, Long-Evans</subject><subject>Reductase</subject><subject>Reductases</subject><subject>Ribonucleotide Reductases - 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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>Jiang, Zhi-Gang</au><au>Winocur, Gordon</au><au>Wojtowicz, J Martin</au><au>Shevtsova, Olga</au><au>Fuller, Steven</au><au>Ghanbari, Hossein A</au><au>Kavushansky, Alexandra</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PAN-811 prevents chemotherapy-induced cognitive impairment and preserves neurogenesis in the hippocampus of adult rats</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2018-01-01</date><risdate>2018</risdate><volume>13</volume><issue>1</issue><spage>e0191866</spage><epage>e0191866</epage><pages>e0191866-e0191866</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Chemotherapy-induced cognitive impairment (CICI) occurs in a substantial proportion of treated cancer patients, with no drug currently available for its therapy. This study investigated whether PAN-811, a ribonucleotide reductase inhibitor, can reduce cognitive impairment and related suppression of neurogenesis following chemotherapy in an animal model. Young adult rats in Chemo and Chemo+PAN-811 groups received 3 intraperitoneal (i.p.) injections of methotrexate (MTX) and 5-fluorouracil (5-FU), and those in Saline and Saline+PAN-811 groups received equal volumes of physiological saline at 10-day intervals. PAN-811 in saline was delivered through i.p. injection, 10 min following each saline (Saline+PAN-811 group) or MTX/5-FU (Chemo+PAN-811 group) treatment, while equal volumes of saline were delivered to Saline and Chemo groups. Over Days 31-66, rats were administered tests of spatial memory, nonmatching-to-sample rule learning, and discrimination learning, which are sensitive to dysfunction in hippocampus, frontal lobe and striatum, respectively. On Day 97, neurogenesis was immnunohistochemically evaluated by counting doublecortin-positive (DCX+) cells in the dentate gyrus (DG). The results demonstrated that the Chemo group was impaired on the three cognitive tasks, but co-administration of PAN-811 significantly reduced all MTX/5-FU-induced cognitive impairments. In addition, MTX/5-FU reduced DCX+ cells to 67% of that in Saline control rats, an effect that was completely blocked by PAN-811 co-administration. Overall, we present the first evidence that PAN-811 protects cognitive functions and preserves neurogenesis from deleterious effects of MTX/5-FU. The current findings provide a basis for rapid clinical translation to determine the effect of PAN-811 on CICI in human.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>29370277</pmid><doi>10.1371/journal.pone.0191866</doi><orcidid>https://orcid.org/0000-0002-1101-4040</orcidid><oa>free_for_read</oa></addata></record> |
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recordid | cdi_plos_journals_2390634144 |
source | Open Access: PubMed Central; Publicly Available Content Database |
subjects | 5-Fluorouracil Animal cognition Animal models Animals Antineoplastic Agents - administration & dosage Antineoplastic Agents - adverse effects Biology and Life Sciences Cancer therapies Chemotherapy Cognitive ability Cognitive Dysfunction - chemically induced Cognitive Dysfunction - prevention & control Cognitive tasks Dentate gyrus Dentate Gyrus - drug effects Discrimination learning Discrimination Learning - drug effects Disease Models, Animal Doublecortin protein Drugs Enzyme Inhibitors - pharmacology Female Fluorouracil - administration & dosage Fluorouracil - adverse effects Frontal lobe Hippocampus Hippocampus - drug effects Hippocampus - pathology Hippocampus - physiopathology Humans Impairment Laboratories Learning Learning - drug effects Medicine and Health Sciences Memory Memory tasks Methotrexate Methotrexate - administration & dosage Methotrexate - adverse effects Neostriatum Neurogenesis Neurogenesis - drug effects Neuroprotective Agents - pharmacology Neurotoxicity Pharmaceuticals Physiology Pyridines - pharmacology Quality of life Rats Rats, Long-Evans Reductase Reductases Ribonucleotide Reductases - antagonists & inhibitors Social Sciences Spatial analysis Spatial discrimination learning Spatial memory Spatial Memory - drug effects Thiosemicarbazones - pharmacology Young adults |
title | PAN-811 prevents chemotherapy-induced cognitive impairment and preserves neurogenesis in the hippocampus of adult rats |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T23%3A10%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=PAN-811%20prevents%20chemotherapy-induced%20cognitive%20impairment%20and%20preserves%20neurogenesis%20in%20the%20hippocampus%20of%20adult%20rats&rft.jtitle=PloS%20one&rft.au=Jiang,%20Zhi-Gang&rft.date=2018-01-01&rft.volume=13&rft.issue=1&rft.spage=e0191866&rft.epage=e0191866&rft.pages=e0191866-e0191866&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0191866&rft_dat=%3Cproquest_plos_%3E2390634144%3C/proquest_plos_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c526t-10384511e5d78aab8368d32d3b66e758a91be85ebd77440fdc1919397344d2403%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2390634144&rft_id=info:pmid/29370277&rfr_iscdi=true |