Peripheral Neuropathy Presents Similar Symptoms and Pathological Changes in Both High-Fat Diet and Pharmacologically Induced Pre- and Diabetic Mouse Models
The objective of the study was to compare the effects of experimentally induced type 1 or type 2 diabetes (T1D or T2D) on the functional, structural and biochemical properties of mouse peripheral nerves. Eight-week-old C57BL/6 mice were randomly assigned into three groups, including the control (CTR...
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2021
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oai:doaj.org-article:f256b20a853941649fc3d8db76f583592021-11-25T18:11:42ZPeripheral Neuropathy Presents Similar Symptoms and Pathological Changes in Both High-Fat Diet and Pharmacologically Induced Pre- and Diabetic Mouse Models10.3390/life111112672075-1729https://doaj.org/article/f256b20a853941649fc3d8db76f583592021-11-01T00:00:00Zhttps://www.mdpi.com/2075-1729/11/11/1267https://doaj.org/toc/2075-1729The objective of the study was to compare the effects of experimentally induced type 1 or type 2 diabetes (T1D or T2D) on the functional, structural and biochemical properties of mouse peripheral nerves. Eight-week-old C57BL/6 mice were randomly assigned into three groups, including the control (CTRL, chow-fed), STZ (streptozotocin (STZ)-injected), and HFD (high-fat diet (HFD)-fed) group. After 18-weeks of experimental treatment, HFD mice had higher body weights and elevated levels of plasma lipids, while STZ mice developed hyperglycemia. STZ-treated mice, after an extended period of untreated diabetes, developed motor and sensory nerve conduction-velocity deficits. Moreover, relative to control fibers, pre- and diabetic axons were lower in number and irregular in shape. Animals from both treatment groups manifested a pronounced overexpression of nNOS and a reduced expression of SOD1 proteins in the sciatic nerve, indicating oxidative–nitrosative stress and ineffective antioxidant protection in the peripheral nervous system of these mice. Collectively, STZ- and HFD-treated mice revealed similar characteristics of peripheral nerve damage, including a number of morphological and electrophysiological pathologies in the sciatic nerve. While hyperglycemia is a large component of diabetic neuropathy pathogenesis, the non-hyperglycemic effects of diabetes, including dyslipidemia, may also be of importance in the development of this condition.Julia JaroslawskaAgnieszka KorytkoKamila Zglejc-WaszakTomasz AntonowskiAndrzej S. PomianowskiKrzysztof WasowiczJoanna WojtkiewiczJudyta K. JuranekMDPI AGarticlediabetic peripheral neuropathysciatic nervediabetic mouse modelsstreptozotocinhigh-fat dietScienceQENLife, Vol 11, Iss 1267, p 1267 (2021) |
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diabetic peripheral neuropathy sciatic nerve diabetic mouse models streptozotocin high-fat diet Science Q |
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diabetic peripheral neuropathy sciatic nerve diabetic mouse models streptozotocin high-fat diet Science Q Julia Jaroslawska Agnieszka Korytko Kamila Zglejc-Waszak Tomasz Antonowski Andrzej S. Pomianowski Krzysztof Wasowicz Joanna Wojtkiewicz Judyta K. Juranek Peripheral Neuropathy Presents Similar Symptoms and Pathological Changes in Both High-Fat Diet and Pharmacologically Induced Pre- and Diabetic Mouse Models |
description |
The objective of the study was to compare the effects of experimentally induced type 1 or type 2 diabetes (T1D or T2D) on the functional, structural and biochemical properties of mouse peripheral nerves. Eight-week-old C57BL/6 mice were randomly assigned into three groups, including the control (CTRL, chow-fed), STZ (streptozotocin (STZ)-injected), and HFD (high-fat diet (HFD)-fed) group. After 18-weeks of experimental treatment, HFD mice had higher body weights and elevated levels of plasma lipids, while STZ mice developed hyperglycemia. STZ-treated mice, after an extended period of untreated diabetes, developed motor and sensory nerve conduction-velocity deficits. Moreover, relative to control fibers, pre- and diabetic axons were lower in number and irregular in shape. Animals from both treatment groups manifested a pronounced overexpression of nNOS and a reduced expression of SOD1 proteins in the sciatic nerve, indicating oxidative–nitrosative stress and ineffective antioxidant protection in the peripheral nervous system of these mice. Collectively, STZ- and HFD-treated mice revealed similar characteristics of peripheral nerve damage, including a number of morphological and electrophysiological pathologies in the sciatic nerve. While hyperglycemia is a large component of diabetic neuropathy pathogenesis, the non-hyperglycemic effects of diabetes, including dyslipidemia, may also be of importance in the development of this condition. |
format |
article |
author |
Julia Jaroslawska Agnieszka Korytko Kamila Zglejc-Waszak Tomasz Antonowski Andrzej S. Pomianowski Krzysztof Wasowicz Joanna Wojtkiewicz Judyta K. Juranek |
author_facet |
Julia Jaroslawska Agnieszka Korytko Kamila Zglejc-Waszak Tomasz Antonowski Andrzej S. Pomianowski Krzysztof Wasowicz Joanna Wojtkiewicz Judyta K. Juranek |
author_sort |
Julia Jaroslawska |
title |
Peripheral Neuropathy Presents Similar Symptoms and Pathological Changes in Both High-Fat Diet and Pharmacologically Induced Pre- and Diabetic Mouse Models |
title_short |
Peripheral Neuropathy Presents Similar Symptoms and Pathological Changes in Both High-Fat Diet and Pharmacologically Induced Pre- and Diabetic Mouse Models |
title_full |
Peripheral Neuropathy Presents Similar Symptoms and Pathological Changes in Both High-Fat Diet and Pharmacologically Induced Pre- and Diabetic Mouse Models |
title_fullStr |
Peripheral Neuropathy Presents Similar Symptoms and Pathological Changes in Both High-Fat Diet and Pharmacologically Induced Pre- and Diabetic Mouse Models |
title_full_unstemmed |
Peripheral Neuropathy Presents Similar Symptoms and Pathological Changes in Both High-Fat Diet and Pharmacologically Induced Pre- and Diabetic Mouse Models |
title_sort |
peripheral neuropathy presents similar symptoms and pathological changes in both high-fat diet and pharmacologically induced pre- and diabetic mouse models |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/f256b20a853941649fc3d8db76f58359 |
work_keys_str_mv |
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