<i>Escherichia coli</i> (Lilly) and <i>Saccharomyces cerevisiae</i> (Novo) rDNA Glucagon: An Assessment of Their Actions When Supplied Selectively to Periportal Cells in the Bivascularly Perfused Rat Liver

The actions of Eli Lilly-rDNA glucagon and Novo Nordisk-rDNA glucagon on glycogen catabolism and related parameters were investigated using the bivascularly perfused rat liver. The technique allows glucagon to be supplied to a selective portion of the hepatic periportal region (≈39%) when the former...

Full description

Bibliographic Details
Main Authors: Lívia Bracht, Jorgete Constantin, Rosane Marina Peralta, Adelar Bracht
Format: Article
Language:English
Published: MDPI AG 2023-06-01
Series:Scientia Pharmaceutica
Subjects:
Online Access:https://www.mdpi.com/2218-0532/91/3/29
_version_ 1797577104995385344
author Lívia Bracht
Jorgete Constantin
Rosane Marina Peralta
Adelar Bracht
author_facet Lívia Bracht
Jorgete Constantin
Rosane Marina Peralta
Adelar Bracht
author_sort Lívia Bracht
collection DOAJ
description The actions of Eli Lilly-rDNA glucagon and Novo Nordisk-rDNA glucagon on glycogen catabolism and related parameters were investigated using the bivascularly perfused rat liver. The technique allows glucagon to be supplied to a selective portion of the hepatic periportal region (≈39%) when the former is infused into the hepatic artery in retrograde perfusion. Both glucagon preparations were equally effective in influencing metabolism (glucose output, glycolysis and O<sub>2</sub> uptake) when supplied to all cells along the liver sinusoids. When only a selective periportal region of the liver was supplied with the hormone, however, the action of Novo Nordisk-rDNA glucagon was proportional to the accessible cell space, whereas the action of Eli Lilly-rDNA glucagon greatly exceeded the action that was expected for the accessible space. Chromatographically, both rDNA preparations were not pure, but their impurities were not the same. The impurities in Eli Lilly-rDNA glucagon resembled those found in the similarly acting pancreatic Eli Lilly glucagon. It was concluded that the space-extrapolating action of Eli Lilly-rDNA glucagon is caused by a yet-to-be-identified impurity. The hypothesis was raised that an impurity in certain glucagon preparations can enhance cell-to-cell propagation of the glucagon signal, possibly via gap junctional communication.
first_indexed 2024-03-10T22:03:19Z
format Article
id doaj.art-5edfcdb2fa344b2692aa4b6126caea7f
institution Directory Open Access Journal
issn 0036-8709
2218-0532
language English
last_indexed 2024-03-10T22:03:19Z
publishDate 2023-06-01
publisher MDPI AG
record_format Article
series Scientia Pharmaceutica
spelling doaj.art-5edfcdb2fa344b2692aa4b6126caea7f2023-11-19T12:52:03ZengMDPI AGScientia Pharmaceutica0036-87092218-05322023-06-019132910.3390/scipharm91030029<i>Escherichia coli</i> (Lilly) and <i>Saccharomyces cerevisiae</i> (Novo) rDNA Glucagon: An Assessment of Their Actions When Supplied Selectively to Periportal Cells in the Bivascularly Perfused Rat LiverLívia Bracht0Jorgete Constantin1Rosane Marina Peralta2Adelar Bracht3Department of Biochemistry, State University of Maringá, Maringá 87020900, BrazilDepartment of Biochemistry, State University of Maringá, Maringá 87020900, BrazilDepartment of Biochemistry, State University of Maringá, Maringá 87020900, BrazilDepartment of Biochemistry, State University of Maringá, Maringá 87020900, BrazilThe actions of Eli Lilly-rDNA glucagon and Novo Nordisk-rDNA glucagon on glycogen catabolism and related parameters were investigated using the bivascularly perfused rat liver. The technique allows glucagon to be supplied to a selective portion of the hepatic periportal region (≈39%) when the former is infused into the hepatic artery in retrograde perfusion. Both glucagon preparations were equally effective in influencing metabolism (glucose output, glycolysis and O<sub>2</sub> uptake) when supplied to all cells along the liver sinusoids. When only a selective periportal region of the liver was supplied with the hormone, however, the action of Novo Nordisk-rDNA glucagon was proportional to the accessible cell space, whereas the action of Eli Lilly-rDNA glucagon greatly exceeded the action that was expected for the accessible space. Chromatographically, both rDNA preparations were not pure, but their impurities were not the same. The impurities in Eli Lilly-rDNA glucagon resembled those found in the similarly acting pancreatic Eli Lilly glucagon. It was concluded that the space-extrapolating action of Eli Lilly-rDNA glucagon is caused by a yet-to-be-identified impurity. The hypothesis was raised that an impurity in certain glucagon preparations can enhance cell-to-cell propagation of the glucagon signal, possibly via gap junctional communication.https://www.mdpi.com/2218-0532/91/3/29rDNA glucagonliverbivascular perfusionsignaling propagationglycogenolysisglycolysis
spellingShingle Lívia Bracht
Jorgete Constantin
Rosane Marina Peralta
Adelar Bracht
<i>Escherichia coli</i> (Lilly) and <i>Saccharomyces cerevisiae</i> (Novo) rDNA Glucagon: An Assessment of Their Actions When Supplied Selectively to Periportal Cells in the Bivascularly Perfused Rat Liver
Scientia Pharmaceutica
rDNA glucagon
liver
bivascular perfusion
signaling propagation
glycogenolysis
glycolysis
title <i>Escherichia coli</i> (Lilly) and <i>Saccharomyces cerevisiae</i> (Novo) rDNA Glucagon: An Assessment of Their Actions When Supplied Selectively to Periportal Cells in the Bivascularly Perfused Rat Liver
title_full <i>Escherichia coli</i> (Lilly) and <i>Saccharomyces cerevisiae</i> (Novo) rDNA Glucagon: An Assessment of Their Actions When Supplied Selectively to Periportal Cells in the Bivascularly Perfused Rat Liver
title_fullStr <i>Escherichia coli</i> (Lilly) and <i>Saccharomyces cerevisiae</i> (Novo) rDNA Glucagon: An Assessment of Their Actions When Supplied Selectively to Periportal Cells in the Bivascularly Perfused Rat Liver
title_full_unstemmed <i>Escherichia coli</i> (Lilly) and <i>Saccharomyces cerevisiae</i> (Novo) rDNA Glucagon: An Assessment of Their Actions When Supplied Selectively to Periportal Cells in the Bivascularly Perfused Rat Liver
title_short <i>Escherichia coli</i> (Lilly) and <i>Saccharomyces cerevisiae</i> (Novo) rDNA Glucagon: An Assessment of Their Actions When Supplied Selectively to Periportal Cells in the Bivascularly Perfused Rat Liver
title_sort i escherichia coli i lilly and i saccharomyces cerevisiae i novo rdna glucagon an assessment of their actions when supplied selectively to periportal cells in the bivascularly perfused rat liver
topic rDNA glucagon
liver
bivascular perfusion
signaling propagation
glycogenolysis
glycolysis
url https://www.mdpi.com/2218-0532/91/3/29
work_keys_str_mv AT liviabracht iescherichiacoliilillyandisaccharomycescerevisiaeinovordnaglucagonanassessmentoftheiractionswhensuppliedselectivelytoperiportalcellsinthebivascularlyperfusedratliver
AT jorgeteconstantin iescherichiacoliilillyandisaccharomycescerevisiaeinovordnaglucagonanassessmentoftheiractionswhensuppliedselectivelytoperiportalcellsinthebivascularlyperfusedratliver
AT rosanemarinaperalta iescherichiacoliilillyandisaccharomycescerevisiaeinovordnaglucagonanassessmentoftheiractionswhensuppliedselectivelytoperiportalcellsinthebivascularlyperfusedratliver
AT adelarbracht iescherichiacoliilillyandisaccharomycescerevisiaeinovordnaglucagonanassessmentoftheiractionswhensuppliedselectivelytoperiportalcellsinthebivascularlyperfusedratliver