The evaluation of 2.3-diazepine influence on tissue respiration of the liver and its exocrine function in rats with a rotenone model of Parkinson’s disease
Parkinson’s disease (PD) is a progressive neurodegenerative disorder, characterized by the loss of dopaminergic neurons in the substantia nigra pars compacta. The causes of PD are not fully understood; however, increasing evidence implicates disturbed respiratory function of the mitochondria and a l...
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| Veröffentlicht in: | Biopolimery i kletka 2019, Vol.35 (5), p.356-370 |
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| creator | Khilya, V. P. Yanchuk, I. P. Shtanova, L. Ya Veselsky, S. P. Vovkun, T. V. Tsymbalyuk, O. V. Moskvina, V. S. Shablykina, O. V. Bogza, S. L. |
| description | Parkinson’s disease (PD) is a progressive neurodegenerative disorder, characterized by the loss of dopaminergic neurons in the substantia nigra pars compacta. The causes of PD are not fully understood; however, increasing evidence implicates disturbed respiratory function of the mitochondria and a lack of energy in cells. Aim. To study the effects of 2.3-diazepine (2.3-DP), a new derivative of benzodiazepine, on liver tissue respiration (LTR) and energy dependent processes of bile and bile acids (BAs) production in a rat model of PD. Methods. PD was induced by intraperitoneal injections of rotenone (ROT). LTR (the intensity of the oxygen uptake) was assessed using the polarograph LP-9 (Czech Republic). Secreted bile was collected during 1 hour of the experiment through the polyethylene catheter inserted into the common bile duct. BAs were separated by the method of thin layer chromatography. Results. ROT diminished the index of liver oxygen consumption by 34 % (p |
| doi_str_mv | 10.7124/bc.000A13 |
| format | Article |
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P. ; Yanchuk, I. P. ; Shtanova, L. Ya ; Veselsky, S. P. ; Vovkun, T. V. ; Tsymbalyuk, O. V. ; Moskvina, V. S. ; Shablykina, O. V. ; Bogza, S. L.</creator><creatorcontrib>Khilya, V. P. ; Yanchuk, I. P. ; Shtanova, L. Ya ; Veselsky, S. P. ; Vovkun, T. V. ; Tsymbalyuk, O. V. ; Moskvina, V. S. ; Shablykina, O. V. ; Bogza, S. L.</creatorcontrib><description>Parkinson’s disease (PD) is a progressive neurodegenerative disorder, characterized by the loss of dopaminergic neurons in the substantia nigra pars compacta. The causes of PD are not fully understood; however, increasing evidence implicates disturbed respiratory function of the mitochondria and a lack of energy in cells. Aim. To study the effects of 2.3-diazepine (2.3-DP), a new derivative of benzodiazepine, on liver tissue respiration (LTR) and energy dependent processes of bile and bile acids (BAs) production in a rat model of PD. Methods. PD was induced by intraperitoneal injections of rotenone (ROT). LTR (the intensity of the oxygen uptake) was assessed using the polarograph LP-9 (Czech Republic). Secreted bile was collected during 1 hour of the experiment through the polyethylene catheter inserted into the common bile duct. BAs were separated by the method of thin layer chromatography. Results. ROT diminished the index of liver oxygen consumption by 34 % (p<0.001), reduced bile flow by 33.8 % (p<0.001) and disturbed the conjugation of cholic acid with amino acids taurine and glycine reducing the index of conjugation by 29.2 % (p<0.001). ROT also increased by 25.6 % (p<0.001) the part of acidic pathway in the biosynthesis of BAs. The application of 2.3-DP results in full or partial recovery of LTR, bile flow, concentrations of BAs and their ratio in the bile of rats with PD. Conclusion. 2.3-DP markedly affected function of the liver parenchyma in a rat model of PD. This drug changed the intensity of LTR, bile flow and notably modified bile chemical compositions.</description><identifier>ISSN: 0233-7657</identifier><identifier>EISSN: 1993-6842</identifier><identifier>DOI: 10.7124/bc.000A13</identifier><language>eng</language><publisher>Kiev: Natsional'na Akademiya Nauk Ukrainy - National Academy of Sciences of Ukraine</publisher><subject>Benzodiazepines ; Bile ; Bile acids ; Bile ducts ; Cholic acid ; Dopamine receptors ; Glycine ; Liver ; Mitochondria ; Movement disorders ; Neurodegenerative diseases ; Oxygen consumption ; Parenchyma ; Parkinson's disease ; Polyethylene ; Respiration ; Respiratory function ; Rot ; Rotenone ; Substantia nigra ; Taurine</subject><ispartof>Biopolimery i kletka, 2019, Vol.35 (5), p.356-370</ispartof><rights>2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2073-e393105d0d93b53cbf71b2ae87f59f9473f64014e1ee389fc86824ed28102f1a3</citedby><cites>FETCH-LOGICAL-c2073-e393105d0d93b53cbf71b2ae87f59f9473f64014e1ee389fc86824ed28102f1a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,4010,27904,27905,27906</link.rule.ids></links><search><creatorcontrib>Khilya, V. P.</creatorcontrib><creatorcontrib>Yanchuk, I. P.</creatorcontrib><creatorcontrib>Shtanova, L. Ya</creatorcontrib><creatorcontrib>Veselsky, S. P.</creatorcontrib><creatorcontrib>Vovkun, T. V.</creatorcontrib><creatorcontrib>Tsymbalyuk, O. V.</creatorcontrib><creatorcontrib>Moskvina, V. S.</creatorcontrib><creatorcontrib>Shablykina, O. V.</creatorcontrib><creatorcontrib>Bogza, S. L.</creatorcontrib><title>The evaluation of 2.3-diazepine influence on tissue respiration of the liver and its exocrine function in rats with a rotenone model of Parkinson’s disease</title><title>Biopolimery i kletka</title><description>Parkinson’s disease (PD) is a progressive neurodegenerative disorder, characterized by the loss of dopaminergic neurons in the substantia nigra pars compacta. The causes of PD are not fully understood; however, increasing evidence implicates disturbed respiratory function of the mitochondria and a lack of energy in cells. Aim. To study the effects of 2.3-diazepine (2.3-DP), a new derivative of benzodiazepine, on liver tissue respiration (LTR) and energy dependent processes of bile and bile acids (BAs) production in a rat model of PD. Methods. PD was induced by intraperitoneal injections of rotenone (ROT). LTR (the intensity of the oxygen uptake) was assessed using the polarograph LP-9 (Czech Republic). Secreted bile was collected during 1 hour of the experiment through the polyethylene catheter inserted into the common bile duct. BAs were separated by the method of thin layer chromatography. Results. ROT diminished the index of liver oxygen consumption by 34 % (p<0.001), reduced bile flow by 33.8 % (p<0.001) and disturbed the conjugation of cholic acid with amino acids taurine and glycine reducing the index of conjugation by 29.2 % (p<0.001). ROT also increased by 25.6 % (p<0.001) the part of acidic pathway in the biosynthesis of BAs. The application of 2.3-DP results in full or partial recovery of LTR, bile flow, concentrations of BAs and their ratio in the bile of rats with PD. Conclusion. 2.3-DP markedly affected function of the liver parenchyma in a rat model of PD. This drug changed the intensity of LTR, bile flow and notably modified bile chemical compositions.</description><subject>Benzodiazepines</subject><subject>Bile</subject><subject>Bile acids</subject><subject>Bile ducts</subject><subject>Cholic acid</subject><subject>Dopamine receptors</subject><subject>Glycine</subject><subject>Liver</subject><subject>Mitochondria</subject><subject>Movement disorders</subject><subject>Neurodegenerative diseases</subject><subject>Oxygen consumption</subject><subject>Parenchyma</subject><subject>Parkinson's disease</subject><subject>Polyethylene</subject><subject>Respiration</subject><subject>Respiratory function</subject><subject>Rot</subject><subject>Rotenone</subject><subject>Substantia nigra</subject><subject>Taurine</subject><issn>0233-7657</issn><issn>1993-6842</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNo9kLtOwzAUhi0EEqUw8AaWmBhSbJ9cnLGquEmVYIA5cpxj1SW1i52Uy8RrMPByPAkpRUxn-L_vP9JPyClnk4KL9KLWE8bYlMMeGfGyhCSXqdgnIyYAkiLPikNyFOOSsTyVQozI18MCKW5U26vOeke9oWICSWPVO66tQ2qdaXt0GumQdjbGHmnAuLbhX-iGitZuMFDlGmq7SPHV67C1Te_0L2YdHYRIX2y3oIoG36HzA7DyDbbbknsVnqyL3n1_fEba2Igq4jE5MKqNePJ3x-Tx6vJhdpPM765vZ9N5ogUrIEEogbOsYU0JdQa6NgWvhUJZmKw0ZVqAyVPGU-SIIEujZS5Fio2QnAnDFYzJ2a53Hfxzj7Grlr4PbnhZCeB5CpnMYKDOd5QOPsaAploHu1LhreKs2q5f1brarQ8_v2J6DA</recordid><startdate>2019</startdate><enddate>2019</enddate><creator>Khilya, V. P.</creator><creator>Yanchuk, I. P.</creator><creator>Shtanova, L. Ya</creator><creator>Veselsky, S. P.</creator><creator>Vovkun, T. V.</creator><creator>Tsymbalyuk, O. V.</creator><creator>Moskvina, V. S.</creator><creator>Shablykina, O. V.</creator><creator>Bogza, S. 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P. ; Vovkun, T. V. ; Tsymbalyuk, O. V. ; Moskvina, V. S. ; Shablykina, O. V. ; Bogza, S. L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2073-e393105d0d93b53cbf71b2ae87f59f9473f64014e1ee389fc86824ed28102f1a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Benzodiazepines</topic><topic>Bile</topic><topic>Bile acids</topic><topic>Bile ducts</topic><topic>Cholic acid</topic><topic>Dopamine receptors</topic><topic>Glycine</topic><topic>Liver</topic><topic>Mitochondria</topic><topic>Movement disorders</topic><topic>Neurodegenerative diseases</topic><topic>Oxygen consumption</topic><topic>Parenchyma</topic><topic>Parkinson's disease</topic><topic>Polyethylene</topic><topic>Respiration</topic><topic>Respiratory function</topic><topic>Rot</topic><topic>Rotenone</topic><topic>Substantia nigra</topic><topic>Taurine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Khilya, V. P.</creatorcontrib><creatorcontrib>Yanchuk, I. P.</creatorcontrib><creatorcontrib>Shtanova, L. Ya</creatorcontrib><creatorcontrib>Veselsky, S. P.</creatorcontrib><creatorcontrib>Vovkun, T. V.</creatorcontrib><creatorcontrib>Tsymbalyuk, O. V.</creatorcontrib><creatorcontrib>Moskvina, V. S.</creatorcontrib><creatorcontrib>Shablykina, O. V.</creatorcontrib><creatorcontrib>Bogza, S. 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P.</au><au>Yanchuk, I. P.</au><au>Shtanova, L. Ya</au><au>Veselsky, S. P.</au><au>Vovkun, T. V.</au><au>Tsymbalyuk, O. V.</au><au>Moskvina, V. S.</au><au>Shablykina, O. V.</au><au>Bogza, S. L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The evaluation of 2.3-diazepine influence on tissue respiration of the liver and its exocrine function in rats with a rotenone model of Parkinson’s disease</atitle><jtitle>Biopolimery i kletka</jtitle><date>2019</date><risdate>2019</risdate><volume>35</volume><issue>5</issue><spage>356</spage><epage>370</epage><pages>356-370</pages><issn>0233-7657</issn><eissn>1993-6842</eissn><abstract>Parkinson’s disease (PD) is a progressive neurodegenerative disorder, characterized by the loss of dopaminergic neurons in the substantia nigra pars compacta. The causes of PD are not fully understood; however, increasing evidence implicates disturbed respiratory function of the mitochondria and a lack of energy in cells. Aim. To study the effects of 2.3-diazepine (2.3-DP), a new derivative of benzodiazepine, on liver tissue respiration (LTR) and energy dependent processes of bile and bile acids (BAs) production in a rat model of PD. Methods. PD was induced by intraperitoneal injections of rotenone (ROT). LTR (the intensity of the oxygen uptake) was assessed using the polarograph LP-9 (Czech Republic). Secreted bile was collected during 1 hour of the experiment through the polyethylene catheter inserted into the common bile duct. BAs were separated by the method of thin layer chromatography. Results. ROT diminished the index of liver oxygen consumption by 34 % (p<0.001), reduced bile flow by 33.8 % (p<0.001) and disturbed the conjugation of cholic acid with amino acids taurine and glycine reducing the index of conjugation by 29.2 % (p<0.001). ROT also increased by 25.6 % (p<0.001) the part of acidic pathway in the biosynthesis of BAs. The application of 2.3-DP results in full or partial recovery of LTR, bile flow, concentrations of BAs and their ratio in the bile of rats with PD. Conclusion. 2.3-DP markedly affected function of the liver parenchyma in a rat model of PD. This drug changed the intensity of LTR, bile flow and notably modified bile chemical compositions.</abstract><cop>Kiev</cop><pub>Natsional'na Akademiya Nauk Ukrainy - National Academy of Sciences of Ukraine</pub><doi>10.7124/bc.000A13</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record> |
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| subjects | Benzodiazepines Bile Bile acids Bile ducts Cholic acid Dopamine receptors Glycine Liver Mitochondria Movement disorders Neurodegenerative diseases Oxygen consumption Parenchyma Parkinson's disease Polyethylene Respiration Respiratory function Rot Rotenone Substantia nigra Taurine |
| title | The evaluation of 2.3-diazepine influence on tissue respiration of the liver and its exocrine function in rats with a rotenone model of Parkinson’s disease |
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