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Study · Animal study (in vivo) · rat · 2018

8 results

Lixisenatide, a novel GLP-1 analog, protects against cerebral ischemia/reperfusion injury in diabetic rats.

Abdel-Latif RG, Heeba GH, Taye A, Khalifa MMA

Naunyn-Schmiedeberg's archives of pharmacology18 Apr 2018Cited by 31 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study8

8 results from studies that gave the peptide. No result from this study comes from people.

  1. 01AnimalAnimal study (in vivo)Mechanism

    In diabetic rats with cerebral ischemia/reperfusion injury, lixisenatide ameliorated glucose intolerance.

    In plain wordsIn rats with diabetes and brain injury, lixisenatide improved glucose intolerance.

    Outcome
    DecreaseGlucose intolerance
    Study

    ratn: not reported in source

    Adult male Wistar rats with diabetes and cerebral ischemia/reperfusion injury
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Apart from ameliorating glucose intolerance and insulin resistance,
    2 context sentences
    Summary · context
    This study investigated and compared the neuroprotective effect of lixisenatide against glimepiride on diabetic rats subjected to global cerebral ischemia/reperfusion (I/R) injury.
    Summary · context
    T2DM-induced adult male Wistar rats were administered lixisenatide or glimepiride prior to induction of global cerebral I/R-induced injury.
  2. 02AnimalAnimal study (in vivo)Mechanism

    In diabetic rats with cerebral ischemia/reperfusion injury, lixisenatide ameliorated insulin resistance.

    In plain wordsIn rats with diabetes and brain injury, lixisenatide improved insulin resistance.

    Outcome
    DecreaseInsulin resistance
    Study

    ratn: not reported in source

    Adult male Wistar rats with diabetes and cerebral ischemia/reperfusion injury
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Apart from ameliorating glucose intolerance and insulin resistance,
    2 context sentences
    Summary · context
    This study investigated and compared the neuroprotective effect of lixisenatide against glimepiride on diabetic rats subjected to global cerebral ischemia/reperfusion (I/R) injury.
    Summary · context
    T2DM-induced adult male Wistar rats were administered lixisenatide or glimepiride prior to induction of global cerebral I/R-induced injury.
  3. 03AnimalAnimal study (in vivo)Mechanism

    In diabetic rats with cerebral injury, lixisenatide surpassed glimepiride in neurological function enhancement and suppression of oxidative stress, inflammation and apoptosis.

    In plain wordsIn rats with diabetes and brain injury, lixisenatide surpassed glimepiride in neurological function and suppression of injury processes.

    Outcome
    MixedNeurological function and cerebral injury pathways
    Study

    ratn: not reported in source

    Adult male Wistar rats with diabetes and cerebral ischemia/reperfusion injury
    Comparator
    Glimepiride
    Outcome group
    Neuroprotection · Nervous system and cognition
    Studied dose
    Dose not stated

    Source sentences

    Summary
    lixisenatide was found to be superior to glimepiride as protective treatment in terms of enhancing behavioral/neurological functions and suppressing cerebral oxidative stress, inflammation, and apoptosis in cerebral I/R-injured diabetic rats.
    2 context sentences
    Summary · context
    This study investigated and compared the neuroprotective effect of lixisenatide against glimepiride on diabetic rats subjected to global cerebral ischemia/reperfusion (I/R) injury.
    Summary · context
    T2DM-induced adult male Wistar rats were administered lixisenatide or glimepiride prior to induction of global cerebral I/R-induced injury.
  4. 04AnimalAnimal study (in vivo)Mechanism

    In diabetic rats with cerebral injury, lixisenatide relieved carotid endothelial dysfunction, unlike glimepiride.

    In plain wordsIn rats with diabetes and brain injury, lixisenatide relieved carotid vessel dysfunction, unlike glimepiride.

    Outcome
    DecreaseCarotid endothelial dysfunction
    Study

    ratn: not reported in source

    Adult male Wistar rats with diabetes and cerebral ischemia/reperfusion injury
    Comparator
    Glimepiride
    Outcome group
    Vascular function · Cardiovascular
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Unlike glimepiride, lixisenatide relieved carotid endothelial dysfunction by increasing eNOS expression.
    2 context sentences
    Summary · context
    This study investigated and compared the neuroprotective effect of lixisenatide against glimepiride on diabetic rats subjected to global cerebral ischemia/reperfusion (I/R) injury.
    Summary · context
    T2DM-induced adult male Wistar rats were administered lixisenatide or glimepiride prior to induction of global cerebral I/R-induced injury.
  5. 05AnimalAnimal study (in vivo)Mechanism

    In diabetic rats with cerebral injury, lixisenatide increased carotid eNOS expression, unlike glimepiride.

    In plain wordsIn rats with diabetes and brain injury, lixisenatide increased carotid eNOS expression, unlike glimepiride.

    Outcome
    IncreaseeNOS expression
    Study

    ratn: not reported in source

    Adult male Wistar rats with diabetes and cerebral ischemia/reperfusion injury
    Comparator
    Glimepiride
    Outcome group
    Receptor activity and mechanism · Cardiovascular
    Studied dose
    Dose not stated

    Source sentences

    Summary
    Unlike glimepiride, lixisenatide relieved carotid endothelial dysfunction by increasing eNOS expression.
    2 context sentences
    Summary · context
    This study investigated and compared the neuroprotective effect of lixisenatide against glimepiride on diabetic rats subjected to global cerebral ischemia/reperfusion (I/R) injury.
    Summary · context
    T2DM-induced adult male Wistar rats were administered lixisenatide or glimepiride prior to induction of global cerebral I/R-induced injury.
  6. 06AnimalAnimal study (in vivo)Mechanism

    In diabetic rats with cerebral injury, lixisenatide dampened vascular nitrosative and oxidative stress.

    In plain wordsIn rats with diabetes and brain injury, lixisenatide reduced vascular nitrosative and oxidative stress.

    Outcome
    DecreaseVascular nitrosative and oxidative stress
    Study

    ratn: not reported in source

    Adult male Wistar rats with diabetes and cerebral ischemia/reperfusion injury
    Outcome group
    Oxidative stress · Cardiovascular
    Studied dose
    Dose not stated

    Source sentences

    Summary
    It also dampened vascular nitrosative/oxidative stress via suppression of iNOS and NADPH oxidase expressions.
    2 context sentences
    Summary · context
    This study investigated and compared the neuroprotective effect of lixisenatide against glimepiride on diabetic rats subjected to global cerebral ischemia/reperfusion (I/R) injury.
    Summary · context
    T2DM-induced adult male Wistar rats were administered lixisenatide or glimepiride prior to induction of global cerebral I/R-induced injury.
  7. 07AnimalAnimal study (in vivo)Mechanism

    In diabetic rats with cerebral injury, lixisenatide suppressed vascular iNOS expression.

    In plain wordsIn rats with diabetes and brain injury, lixisenatide reduced vascular iNOS expression.

    Outcome
    DecreaseiNOS expression
    Study

    ratn: not reported in source

    Adult male Wistar rats with diabetes and cerebral ischemia/reperfusion injury
    Outcome group
    Receptor activity and mechanism · Cardiovascular
    Studied dose
    Dose not stated

    Source sentences

    Summary
    It also dampened vascular nitrosative/oxidative stress via suppression of iNOS and NADPH oxidase expressions.
    2 context sentences
    Summary · context
    This study investigated and compared the neuroprotective effect of lixisenatide against glimepiride on diabetic rats subjected to global cerebral ischemia/reperfusion (I/R) injury.
    Summary · context
    T2DM-induced adult male Wistar rats were administered lixisenatide or glimepiride prior to induction of global cerebral I/R-induced injury.
  8. 08AnimalAnimal study (in vivo)Mechanism

    In diabetic rats with cerebral injury, lixisenatide suppressed vascular NADPH oxidase expression.

    In plain wordsIn rats with diabetes and brain injury, lixisenatide reduced vascular NADPH oxidase expression.

    Outcome
    DecreaseNADPH oxidase expression
    Study

    ratn: not reported in source

    Adult male Wistar rats with diabetes and cerebral ischemia/reperfusion injury
    Outcome group
    Receptor activity and mechanism · Cardiovascular
    Studied dose
    Dose not stated

    Source sentences

    Summary
    It also dampened vascular nitrosative/oxidative stress via suppression of iNOS and NADPH oxidase expressions.
    2 context sentences
    Summary · context
    This study investigated and compared the neuroprotective effect of lixisenatide against glimepiride on diabetic rats subjected to global cerebral ischemia/reperfusion (I/R) injury.
    Summary · context
    T2DM-induced adult male Wistar rats were administered lixisenatide or glimepiride prior to induction of global cerebral I/R-induced injury.

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Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    28 Oct 2026, 02:03 UTC

    Study results updated

  2. Version 1

    27 Oct 2026, 16:36 UTC

    First added · source update from Europe PMC

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