Turmeric Bioactive Compounds Alleviate Spinal Nerve Ligation-Induced Neuropathic Pain by Suppressing Glial Activation and Improving Mitochondrial Function in Spinal Cord and Amygdala

This study examined the effects of turmeric bioactive compounds, curcumin C3 complex® (CUR) and bisdemethoxycurcumin (BDMC), on mechanical hypersensitivity and the gene expression of markers for glial activation, mitochondrial function, and oxidative stress in the spinal cord and amygdala of rats wi...

Full description

Bibliographic Details
Main Authors: Julianna M. Santos, Rui Wang, Viren Bhakta, Zarek Driver, Yakhnitsa Vadim, Takaki Kiritoshi, Guangchen Ji, Volker Neugebauer, Chwan-Li Shen
Format: Article
Language:English
Published: MDPI AG 2023-10-01
Series:Nutrients
Subjects:
Online Access:https://www.mdpi.com/2072-6643/15/20/4403
_version_ 1797572717455605760
author Julianna M. Santos
Rui Wang
Viren Bhakta
Zarek Driver
Yakhnitsa Vadim
Takaki Kiritoshi
Guangchen Ji
Volker Neugebauer
Chwan-Li Shen
author_facet Julianna M. Santos
Rui Wang
Viren Bhakta
Zarek Driver
Yakhnitsa Vadim
Takaki Kiritoshi
Guangchen Ji
Volker Neugebauer
Chwan-Li Shen
author_sort Julianna M. Santos
collection DOAJ
description This study examined the effects of turmeric bioactive compounds, curcumin C3 complex® (CUR) and bisdemethoxycurcumin (BDMC), on mechanical hypersensitivity and the gene expression of markers for glial activation, mitochondrial function, and oxidative stress in the spinal cord and amygdala of rats with neuropathic pain (NP). Twenty-four animals were randomly assigned to four groups: sham, spinal nerve ligation (SNL, an NP model), SNL+100 mg CUR/kg BW p.o., and SNL+50 mg BDMC/kg BW p.o. for 4 weeks. Mechanical hypersensitivity was assessed by the von Frey test (VFT) weekly. The lumbosacral section of the spinal cord and the right amygdala (central nucleus) were collected to determine the mRNA expression of genes (IBA-1, CD11b, GFAP, MFN1, DRP1, FIS1, PGC1α, PINK, Complex I, TLR4, and SOD1) utilizing qRT-PCR. Increased mechanical hypersensitivity and increased gene expression of markers for microglial activation (IBA-1 in the amygdala and CD11b in the spinal cord), astrocyte activation (GFAP in the spinal cord), mitochondrial dysfunction (PGC1α in the amygdala), and oxidative stress (TLR4 in the spinal cord and amygdala) were found in untreated SNL rats. Oral administration of CUR and BDMC significantly decreased mechanical hypersensitivity. CUR decreased CD11b and GFAP gene expression in the spinal cord. BDMC decreased IBA-1 in the spinal cord and amygdala as well as CD11b and GFAP in the spinal cord. Both CUR and BDMC reduced PGC1α gene expression in the amygdala, PINK1 gene expression in the spinal cord, and TLR4 in the spinal cord and amygdala, while they increased Complex I and SOD1 gene expression in the spinal cord. CUR and BDMC administration decreased mechanical hypersensitivity in NP by mitigating glial activation, oxidative stress, and mitochondrial dysfunction.
first_indexed 2024-03-10T20:59:38Z
format Article
id doaj.art-6b4dd1601ad14255b1531fa92b017548
institution Directory Open Access Journal
issn 2072-6643
language English
last_indexed 2024-03-10T20:59:38Z
publishDate 2023-10-01
publisher MDPI AG
record_format Article
series Nutrients
spelling doaj.art-6b4dd1601ad14255b1531fa92b0175482023-11-19T17:38:18ZengMDPI AGNutrients2072-66432023-10-011520440310.3390/nu15204403Turmeric Bioactive Compounds Alleviate Spinal Nerve Ligation-Induced Neuropathic Pain by Suppressing Glial Activation and Improving Mitochondrial Function in Spinal Cord and AmygdalaJulianna M. Santos0Rui Wang1Viren Bhakta2Zarek Driver3Yakhnitsa Vadim4Takaki Kiritoshi5Guangchen Ji6Volker Neugebauer7Chwan-Li Shen8Department of Pathology, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USADepartment of Pathology, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USADepartment of Biochemistry, Texas Tech University, Lubbock, TX 79409, USADepartment of Biochemistry, Texas Tech University, Lubbock, TX 79409, USADepartment of Pharmacology and Neurosciences, Texas Tech University Health Science Center, Lubbock, TX 79430, USADepartment of Pharmacology and Neurosciences, Texas Tech University Health Science Center, Lubbock, TX 79430, USADepartment of Pharmacology and Neurosciences, Texas Tech University Health Science Center, Lubbock, TX 79430, USADepartment of Pharmacology and Neurosciences, Texas Tech University Health Science Center, Lubbock, TX 79430, USADepartment of Pathology, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USAThis study examined the effects of turmeric bioactive compounds, curcumin C3 complex® (CUR) and bisdemethoxycurcumin (BDMC), on mechanical hypersensitivity and the gene expression of markers for glial activation, mitochondrial function, and oxidative stress in the spinal cord and amygdala of rats with neuropathic pain (NP). Twenty-four animals were randomly assigned to four groups: sham, spinal nerve ligation (SNL, an NP model), SNL+100 mg CUR/kg BW p.o., and SNL+50 mg BDMC/kg BW p.o. for 4 weeks. Mechanical hypersensitivity was assessed by the von Frey test (VFT) weekly. The lumbosacral section of the spinal cord and the right amygdala (central nucleus) were collected to determine the mRNA expression of genes (IBA-1, CD11b, GFAP, MFN1, DRP1, FIS1, PGC1α, PINK, Complex I, TLR4, and SOD1) utilizing qRT-PCR. Increased mechanical hypersensitivity and increased gene expression of markers for microglial activation (IBA-1 in the amygdala and CD11b in the spinal cord), astrocyte activation (GFAP in the spinal cord), mitochondrial dysfunction (PGC1α in the amygdala), and oxidative stress (TLR4 in the spinal cord and amygdala) were found in untreated SNL rats. Oral administration of CUR and BDMC significantly decreased mechanical hypersensitivity. CUR decreased CD11b and GFAP gene expression in the spinal cord. BDMC decreased IBA-1 in the spinal cord and amygdala as well as CD11b and GFAP in the spinal cord. Both CUR and BDMC reduced PGC1α gene expression in the amygdala, PINK1 gene expression in the spinal cord, and TLR4 in the spinal cord and amygdala, while they increased Complex I and SOD1 gene expression in the spinal cord. CUR and BDMC administration decreased mechanical hypersensitivity in NP by mitigating glial activation, oxidative stress, and mitochondrial dysfunction.https://www.mdpi.com/2072-6643/15/20/4403curcuminpainneuroinflammationbrainanimal
spellingShingle Julianna M. Santos
Rui Wang
Viren Bhakta
Zarek Driver
Yakhnitsa Vadim
Takaki Kiritoshi
Guangchen Ji
Volker Neugebauer
Chwan-Li Shen
Turmeric Bioactive Compounds Alleviate Spinal Nerve Ligation-Induced Neuropathic Pain by Suppressing Glial Activation and Improving Mitochondrial Function in Spinal Cord and Amygdala
Nutrients
curcumin
pain
neuroinflammation
brain
animal
title Turmeric Bioactive Compounds Alleviate Spinal Nerve Ligation-Induced Neuropathic Pain by Suppressing Glial Activation and Improving Mitochondrial Function in Spinal Cord and Amygdala
title_full Turmeric Bioactive Compounds Alleviate Spinal Nerve Ligation-Induced Neuropathic Pain by Suppressing Glial Activation and Improving Mitochondrial Function in Spinal Cord and Amygdala
title_fullStr Turmeric Bioactive Compounds Alleviate Spinal Nerve Ligation-Induced Neuropathic Pain by Suppressing Glial Activation and Improving Mitochondrial Function in Spinal Cord and Amygdala
title_full_unstemmed Turmeric Bioactive Compounds Alleviate Spinal Nerve Ligation-Induced Neuropathic Pain by Suppressing Glial Activation and Improving Mitochondrial Function in Spinal Cord and Amygdala
title_short Turmeric Bioactive Compounds Alleviate Spinal Nerve Ligation-Induced Neuropathic Pain by Suppressing Glial Activation and Improving Mitochondrial Function in Spinal Cord and Amygdala
title_sort turmeric bioactive compounds alleviate spinal nerve ligation induced neuropathic pain by suppressing glial activation and improving mitochondrial function in spinal cord and amygdala
topic curcumin
pain
neuroinflammation
brain
animal
url https://www.mdpi.com/2072-6643/15/20/4403
work_keys_str_mv AT juliannamsantos turmericbioactivecompoundsalleviatespinalnerveligationinducedneuropathicpainbysuppressingglialactivationandimprovingmitochondrialfunctioninspinalcordandamygdala
AT ruiwang turmericbioactivecompoundsalleviatespinalnerveligationinducedneuropathicpainbysuppressingglialactivationandimprovingmitochondrialfunctioninspinalcordandamygdala
AT virenbhakta turmericbioactivecompoundsalleviatespinalnerveligationinducedneuropathicpainbysuppressingglialactivationandimprovingmitochondrialfunctioninspinalcordandamygdala
AT zarekdriver turmericbioactivecompoundsalleviatespinalnerveligationinducedneuropathicpainbysuppressingglialactivationandimprovingmitochondrialfunctioninspinalcordandamygdala
AT yakhnitsavadim turmericbioactivecompoundsalleviatespinalnerveligationinducedneuropathicpainbysuppressingglialactivationandimprovingmitochondrialfunctioninspinalcordandamygdala
AT takakikiritoshi turmericbioactivecompoundsalleviatespinalnerveligationinducedneuropathicpainbysuppressingglialactivationandimprovingmitochondrialfunctioninspinalcordandamygdala
AT guangchenji turmericbioactivecompoundsalleviatespinalnerveligationinducedneuropathicpainbysuppressingglialactivationandimprovingmitochondrialfunctioninspinalcordandamygdala
AT volkerneugebauer turmericbioactivecompoundsalleviatespinalnerveligationinducedneuropathicpainbysuppressingglialactivationandimprovingmitochondrialfunctioninspinalcordandamygdala
AT chwanlishen turmericbioactivecompoundsalleviatespinalnerveligationinducedneuropathicpainbysuppressingglialactivationandimprovingmitochondrialfunctioninspinalcordandamygdala