Berberine Hydrochloride Improves Cognitive Function and Hippocampal Antioxidant Status in Subchronic and Chronic Lead Poisoning

To determine the neuroprotective effects of berberine hydrochloride (BBR) against lead-induced injuries on the hippocampus of rats. Wistar rats were exposed orally to doses of 100 and 500 ppm lead acetate for 1 and 2 months to develop subchronic and chronic lead poisening models, respectively. For t...

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Published in:Chinese journal of integrative medicine
Main Authors: Mehrjerdi, Fatemeh Zare, Raeini, Azadeh Shahrokhi, Zebhi, Fatemeh Sadate, Hafizi, Zeynab, Mirjalili, Reyhaneh, Aghda, Faezeh Afkhami
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Abstract To determine the neuroprotective effects of berberine hydrochloride (BBR) against lead-induced injuries on the hippocampus of rats. Wistar rats were exposed orally to doses of 100 and 500 ppm lead acetate for 1 and 2 months to develop subchronic and chronic lead poisening models, respectively. For treatment, BBR (50 mg/kg daily) was injected intraperitoneally to rats poisoned with lead. At the end of the experiment, the spatial learning and memory of rats were assessed using the Morris water maze test. Hippocampal tissue changes were examined by hematoxylin and eosin staining. The activity of antioxidant enzymes catalase, superoxide dismutase, glutathione peroxidase, and malondialdehyde levels as parameters of oxidative stress and antioxidant status of the hippocampus were evaluated. BBR reduced cognitive impairment in rats exposed to lead (P<0.05 or P<0.01). The resulting biochemical changes included a decrease in the activity of antioxidants and an increase in lipid peroxidation of the hippocampus of lead-exposed rats (P<0.05 or P<0.01), which were significantly modified by BBR (P<0.05). BBR also increased the density of healthy cells in the hippocampus of leadexposed rats (P<0.05). Significant changes in tissue morphology and biochemical factors of the hippocampus were observed in rats that received lead for 2 months (P<0.05). Most of these changes were insignificant in rats that received lead for 1 month. BBR can improve oxidative tissue changes and hippocampal dysfunction in lead-exposed rats, which may be due to the strong antioxidant potential of BBR.
AbstractList To determine the neuroprotective effects of berberine hydrochloride (BBR) against lead-induced injuries on the hippocampus of rats.OBJECTIVESTo determine the neuroprotective effects of berberine hydrochloride (BBR) against lead-induced injuries on the hippocampus of rats.Wistar rats were exposed orally to doses of 100 and 500 ppm lead acetate for 1 and 2 months to develop subchronic and chronic lead poisening models, respectively. For treatment, BBR (50 mg/kg daily) was injected intraperitoneally to rats poisoned with lead. At the end of the experiment, the spatial learning and memory of rats were assessed using the Morris water maze test. Hippocampal tissue changes were examined by hematoxylin and eosin staining. The activity of antioxidant enzymes catalase, superoxide dismutase, glutathione peroxidase, and malondialdehyde levels as parameters of oxidative stress and antioxidant status of the hippocampus were evaluated.METHODSWistar rats were exposed orally to doses of 100 and 500 ppm lead acetate for 1 and 2 months to develop subchronic and chronic lead poisening models, respectively. For treatment, BBR (50 mg/kg daily) was injected intraperitoneally to rats poisoned with lead. At the end of the experiment, the spatial learning and memory of rats were assessed using the Morris water maze test. Hippocampal tissue changes were examined by hematoxylin and eosin staining. The activity of antioxidant enzymes catalase, superoxide dismutase, glutathione peroxidase, and malondialdehyde levels as parameters of oxidative stress and antioxidant status of the hippocampus were evaluated.BBR reduced cognitive impairment in rats exposed to lead (P<0.05 or P<0.01). The resulting biochemical changes included a decrease in the activity of antioxidants and an increase in lipid peroxidation of the hippocampus of lead-exposed rats (P<0.05 or P<0.01), which were significantly modified by BBR (P<0.05). BBR also increased the density of healthy cells in the hippocampus of leadexposed rats (P<0.05). Significant changes in tissue morphology and biochemical factors of the hippocampus were observed in rats that received lead for 2 months (P<0.05). Most of these changes were insignificant in rats that received lead for 1 month.RESULTSBBR reduced cognitive impairment in rats exposed to lead (P<0.05 or P<0.01). The resulting biochemical changes included a decrease in the activity of antioxidants and an increase in lipid peroxidation of the hippocampus of lead-exposed rats (P<0.05 or P<0.01), which were significantly modified by BBR (P<0.05). BBR also increased the density of healthy cells in the hippocampus of leadexposed rats (P<0.05). Significant changes in tissue morphology and biochemical factors of the hippocampus were observed in rats that received lead for 2 months (P<0.05). Most of these changes were insignificant in rats that received lead for 1 month.BBR can improve oxidative tissue changes and hippocampal dysfunction in lead-exposed rats, which may be due to the strong antioxidant potential of BBR.CONCLUSIONBBR can improve oxidative tissue changes and hippocampal dysfunction in lead-exposed rats, which may be due to the strong antioxidant potential of BBR.
To determine the neuroprotective effects of berberine hydrochloride (BBR) against lead-induced injuries on the hippocampus of rats. Wistar rats were exposed orally to doses of 100 and 500 ppm lead acetate for 1 and 2 months to develop subchronic and chronic lead poisening models, respectively. For treatment, BBR (50 mg/kg daily) was injected intraperitoneally to rats poisoned with lead. At the end of the experiment, the spatial learning and memory of rats were assessed using the Morris water maze test. Hippocampal tissue changes were examined by hematoxylin and eosin staining. The activity of antioxidant enzymes catalase, superoxide dismutase, glutathione peroxidase, and malondialdehyde levels as parameters of oxidative stress and antioxidant status of the hippocampus were evaluated. BBR reduced cognitive impairment in rats exposed to lead (P<0.05 or P<0.01). The resulting biochemical changes included a decrease in the activity of antioxidants and an increase in lipid peroxidation of the hippocampus of lead-exposed rats (P<0.05 or P<0.01), which were significantly modified by BBR (P<0.05). BBR also increased the density of healthy cells in the hippocampus of leadexposed rats (P<0.05). Significant changes in tissue morphology and biochemical factors of the hippocampus were observed in rats that received lead for 2 months (P<0.05). Most of these changes were insignificant in rats that received lead for 1 month. BBR can improve oxidative tissue changes and hippocampal dysfunction in lead-exposed rats, which may be due to the strong antioxidant potential of BBR.
Author Mirjalili, Reyhaneh
Raeini, Azadeh Shahrokhi
Hafizi, Zeynab
Mehrjerdi, Fatemeh Zare
Aghda, Faezeh Afkhami
Zebhi, Fatemeh Sadate
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  givenname: Fatemeh Zare
  surname: Mehrjerdi
  fullname: Mehrjerdi, Fatemeh Zare
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  organization: Yazd Neuroendocrine Research Center, School of Medicine, Shahid Sadoughi University of Medical Sciences and Health Services, Yazd, 8915133149, Iran. mehzaref@gmail.com
– sequence: 2
  givenname: Azadeh Shahrokhi
  surname: Raeini
  fullname: Raeini, Azadeh Shahrokhi
  organization: Yazd Neuroendocrine Research Center, School of Medicine, Shahid Sadoughi University of Medical Sciences and Health Services, Yazd, 8915133149, Iran
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  givenname: Fatemeh Sadate
  surname: Zebhi
  fullname: Zebhi, Fatemeh Sadate
  organization: Yazd Neuroendocrine Research Center, School of Medicine, Shahid Sadoughi University of Medical Sciences and Health Services, Yazd, 8915133149, Iran
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  givenname: Zeynab
  surname: Hafizi
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  givenname: Reyhaneh
  surname: Mirjalili
  fullname: Mirjalili, Reyhaneh
  organization: Yazd Neuroendocrine Research Center, School of Medicine, Shahid Sadoughi University of Medical Sciences and Health Services, Yazd, 8915133149, Iran
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  givenname: Faezeh Afkhami
  surname: Aghda
  fullname: Aghda, Faezeh Afkhami
  organization: Yazd Neuroendocrine Research Center, School of Medicine, Shahid Sadoughi University of Medical Sciences and Health Services, Yazd, 8915133149, Iran
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Cites_doi 10.1016/j.joim.2019.01.002
10.2147/CMAR.S242329
10.1007/s10534-021-00360-7
10.1016/j.pharep.2015.03.002
10.3389/fphar.2021.631100
10.21608/zjfm.2019.14504.1033
10.3390/toxics9020023
10.1016/j.tox.2023.153654
10.1016/j.isci.2020.101005
10.1002/ptr.6252
10.1016/j.bjorl.2016.12.004
10.2131/jts.46.345
10.14202/vetworld.2016.660-671
10.4103/1673-5374.297086
10.3390/nu13082550
10.1016/j.plaphy.2016.05.019
10.1016/j.pediatrneurol.2020.08.005
10.1016/j.ecoenv.2020.110358
10.1142/S0192415X21500658
10.3390/cells11050796
10.1007/s00210-021-02182-3
10.1515/jbcpp-2020-0173
10.1007/s00210-019-01754-8
10.1111/jcmm.13930
10.4103/jrms.JRMS_810_19
10.1007/s11655-022-3720-7
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Keywords Morris water maze
hippocampus
oxidative stress
berberine
lead acetate
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References DR da Silva (3907_CR13) 2020; 194
GPS Sidhu (3907_CR16) 2016; 105
Y Cai (3907_CR24) 2021; 12
I Ilieva (3907_CR4) 2022; 29
Y Wang (3907_CR6) 2020; 12
Z Pirmoradi (3907_CR9) 2019; 22
J Fan (3907_CR30) 2019; 23
ML Aski (3907_CR11) 2018; 21
F Zucki (3907_CR14) 2018; 84
LJ Bandaru (3907_CR20) 2022; 35
DR Ortega (3907_CR15) 2021; 9
JW Shou (3907_CR27) 2022; 11
JZ Bo (3907_CR18) 2021; 16
K Rajasekhar (3907_CR26) 2020; 23
VI Naranjo (3907_CR3) 2020; 113
S Nakhaee (3907_CR12) 2020; 25
JH Zhang (3907_CR29) 2021; 49
M Imenshahidi (3907_CR22) 2019; 33
R Mohi-Ud-Din (3907_CR8) 2022; 25
SA Adefegha (3907_CR28) 2022; 33
H Chen (3907_CR17) 2023; 499
3907_CR23
JV Zhao (3907_CR25) 2021; 13
M Awaga (3907_CR2) 2020; 18
Q Han (3907_CR21) 2021; 46
MA Assi (3907_CR1) 2016; 9
T Ahmed (3907_CR7) 2015; 67
AS Raeini (3907_CR10) 2020; 393
MA Okesola (3907_CR19) 2019; 17
MA Mombeini (3907_CR5) 2022; 395
References_xml – volume: 17
  start-page: 125
  year: 2019
  ident: 3907_CR19
  publication-title: J Integr Med
  doi: 10.1016/j.joim.2019.01.002
  contributor:
    fullname: MA Okesola
– volume: 12
  start-page: 695
  year: 2020
  ident: 3907_CR6
  publication-title: Cancer Manag Res
  doi: 10.2147/CMAR.S242329
  contributor:
    fullname: Y Wang
– volume: 35
  start-page: 1
  year: 2022
  ident: 3907_CR20
  publication-title: Biometals
  doi: 10.1007/s10534-021-00360-7
  contributor:
    fullname: LJ Bandaru
– volume: 67
  start-page: 970
  year: 2015
  ident: 3907_CR7
  publication-title: Pharmacol Rep
  doi: 10.1016/j.pharep.2015.03.002
  contributor:
    fullname: T Ahmed
– volume: 12
  start-page: 631100
  year: 2021
  ident: 3907_CR24
  publication-title: Front Pharmacol
  doi: 10.3389/fphar.2021.631100
  contributor:
    fullname: Y Cai
– volume: 18
  start-page: 21
  year: 2020
  ident: 3907_CR2
  publication-title: Zagazig J Forensic Med Toxicol
  doi: 10.21608/zjfm.2019.14504.1033
  contributor:
    fullname: M Awaga
– volume: 21
  start-page: 53
  year: 2018
  ident: 3907_CR11
  publication-title: Iran J Basic Med Sci
  contributor:
    fullname: ML Aski
– volume: 9
  start-page: 23
  year: 2021
  ident: 3907_CR15
  publication-title: Toxics
  doi: 10.3390/toxics9020023
  contributor:
    fullname: DR Ortega
– volume: 499
  start-page: 153654
  year: 2023
  ident: 3907_CR17
  publication-title: Toxicology
  doi: 10.1016/j.tox.2023.153654
  contributor:
    fullname: H Chen
– volume: 23
  start-page: 101005
  year: 2020
  ident: 3907_CR26
  publication-title: iScience
  doi: 10.1016/j.isci.2020.101005
  contributor:
    fullname: K Rajasekhar
– volume: 33
  start-page: 504
  year: 2019
  ident: 3907_CR22
  publication-title: Phytother Res
  doi: 10.1002/ptr.6252
  contributor:
    fullname: M Imenshahidi
– volume: 84
  start-page: 150
  year: 2018
  ident: 3907_CR14
  publication-title: Braz J Otorhinolaryngol
  doi: 10.1016/j.bjorl.2016.12.004
  contributor:
    fullname: F Zucki
– volume: 46
  start-page: 345
  year: 2021
  ident: 3907_CR21
  publication-title: J Toxicol Sci
  doi: 10.2131/jts.46.345
  contributor:
    fullname: Q Han
– volume: 9
  start-page: 660
  year: 2016
  ident: 3907_CR1
  publication-title: Vet World
  doi: 10.14202/vetworld.2016.660-671
  contributor:
    fullname: MA Assi
– volume: 16
  start-page: 836
  year: 2021
  ident: 3907_CR18
  publication-title: Neural Regen Res
  doi: 10.4103/1673-5374.297086
  contributor:
    fullname: JZ Bo
– volume: 29
  start-page: 69
  year: 2022
  ident: 3907_CR4
  publication-title: Acta Morphol Anthropol
  contributor:
    fullname: I Ilieva
– volume: 13
  start-page: 2550
  year: 2021
  ident: 3907_CR25
  publication-title: Nutrients
  doi: 10.3390/nu13082550
  contributor:
    fullname: JV Zhao
– volume: 105
  start-page: 290
  year: 2016
  ident: 3907_CR16
  publication-title: Plant Physiol Biochem
  doi: 10.1016/j.plaphy.2016.05.019
  contributor:
    fullname: GPS Sidhu
– volume: 113
  start-page: 51
  year: 2020
  ident: 3907_CR3
  publication-title: Pediatr Neurol
  doi: 10.1016/j.pediatrneurol.2020.08.005
  contributor:
    fullname: VI Naranjo
– volume: 194
  start-page: 110358
  year: 2020
  ident: 3907_CR13
  publication-title: Ecotoxicol Environ Saf
  doi: 10.1016/j.ecoenv.2020.110358
  contributor:
    fullname: DR da Silva
– volume: 49
  start-page: 1399
  year: 2021
  ident: 3907_CR29
  publication-title: Am J Chin Med
  doi: 10.1142/S0192415X21500658
  contributor:
    fullname: JH Zhang
– volume: 11
  start-page: 796
  year: 2022
  ident: 3907_CR27
  publication-title: Cells
  doi: 10.3390/cells11050796
  contributor:
    fullname: JW Shou
– volume: 395
  start-page: 187
  year: 2022
  ident: 3907_CR5
  publication-title: Naunyn Schmiedebergs Arch Pharmacol
  doi: 10.1007/s00210-021-02182-3
  contributor:
    fullname: MA Mombeini
– volume: 33
  start-page: 389
  year: 2022
  ident: 3907_CR28
  publication-title: J Basic Clin Physiol Pharmacol
  doi: 10.1515/jbcpp-2020-0173
  contributor:
    fullname: SA Adefegha
– volume: 25
  start-page: 616
  year: 2022
  ident: 3907_CR8
  publication-title: Comb Chem
  contributor:
    fullname: R Mohi-Ud-Din
– volume: 393
  start-page: 581
  year: 2020
  ident: 3907_CR10
  publication-title: Naunyn Schmiedebergs Arch Pharmacol
  doi: 10.1007/s00210-019-01754-8
  contributor:
    fullname: AS Raeini
– volume: 22
  start-page: 154
  year: 2019
  ident: 3907_CR9
  publication-title: Iran J Basic Med Sci
  contributor:
    fullname: Z Pirmoradi
– volume: 23
  start-page: 21
  year: 2019
  ident: 3907_CR30
  publication-title: J Cell Mol Med
  doi: 10.1111/jcmm.13930
  contributor:
    fullname: J Fan
– volume: 25
  start-page: 68
  year: 2020
  ident: 3907_CR12
  publication-title: J Res Med Sci
  doi: 10.4103/jrms.JRMS_810_19
  contributor:
    fullname: S Nakhaee
– ident: 3907_CR23
  doi: 10.1007/s11655-022-3720-7
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Snippet To determine the neuroprotective effects of berberine hydrochloride (BBR) against lead-induced injuries on the hippocampus of rats. Wistar rats were exposed...
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Title Berberine Hydrochloride Improves Cognitive Function and Hippocampal Antioxidant Status in Subchronic and Chronic Lead Poisoning
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