The Potential Neuroprotective Effect of Thymoquinone on Scopolamine-Induced In Vivo Alzheimer's Disease-like Condition : Mechanistic Insights
BACKGROUND: Alzheimer's disease (AD) is a common neurodegenerative disorder without effective treatment. Thymoquinone (TQ) has demonstrated potential in exhibiting anti-inflammatory, anti-cancer, and antioxidant characteristics. Despite TQ's neuroprotection effect, there is a scarcity of information regarding its application in AD research, and its molecular trajectories remain ambiguous. Thus, the objective of the current investigation was to examine the potential beneficial effects and underlying mechanisms of TQ in scopolamine (SCOP)-induced neuronal injury to mimic AD in vivo model.
METHODS: Thirty mice were divided into normal, SCOP, and TQ groups. The Y-maze and pole climbing tests were performed to measure memory and motor performance. Afterwards, histopathological and immunohistochemical examinations were carried out. Furthermore, peroxisome proliferator-activated receptor gamma (PPAR-γ) signaling pathway-related proteins and genes were detected with an emphasis on the role of miR-9.
RESULTS: TQ has the potential to ameliorate cognitive deficits observed in SCOP-induced AD-like model, as evidenced by the improvement in behavioral outcomes, histopathological changes, modulation of the expression pattern of PPAR-γ downstream targets with a significant decrease in the deposition of amyloid beta (Aβ).
CONCLUSIONS: TQ provided meaningful multilevel neuroprotection through its anti-inflammatory and its PPAR-γ agonist activity. Consequently, TQ may possess a potential beneficial role against AD development.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2023 |
---|---|
Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:28 |
---|---|
Enthalten in: |
Molecules (Basel, Switzerland) - 28(2023), 18 vom: 11. Sept. |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Abo Mansour, Hend E [VerfasserIn] |
---|
Links: |
---|
Themen: |
Alzheimer’s disease |
---|
Anmerkungen: |
Date Completed 29.09.2023 Date Revised 03.10.2023 published: Electronic Citation Status MEDLINE |
---|
doi: |
10.3390/molecules28186566 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM362606102 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM362606102 | ||
003 | DE-627 | ||
005 | 20231226091604.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231226s2023 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.3390/molecules28186566 |2 doi | |
028 | 5 | 2 | |a pubmed24n1208.xml |
035 | |a (DE-627)NLM362606102 | ||
035 | |a (NLM)37764343 | ||
035 | |a (PII)6566 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Abo Mansour, Hend E |e verfasserin |4 aut | |
245 | 1 | 4 | |a The Potential Neuroprotective Effect of Thymoquinone on Scopolamine-Induced In Vivo Alzheimer's Disease-like Condition |b Mechanistic Insights |
264 | 1 | |c 2023 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 29.09.2023 | ||
500 | |a Date Revised 03.10.2023 | ||
500 | |a published: Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a BACKGROUND: Alzheimer's disease (AD) is a common neurodegenerative disorder without effective treatment. Thymoquinone (TQ) has demonstrated potential in exhibiting anti-inflammatory, anti-cancer, and antioxidant characteristics. Despite TQ's neuroprotection effect, there is a scarcity of information regarding its application in AD research, and its molecular trajectories remain ambiguous. Thus, the objective of the current investigation was to examine the potential beneficial effects and underlying mechanisms of TQ in scopolamine (SCOP)-induced neuronal injury to mimic AD in vivo model | ||
520 | |a METHODS: Thirty mice were divided into normal, SCOP, and TQ groups. The Y-maze and pole climbing tests were performed to measure memory and motor performance. Afterwards, histopathological and immunohistochemical examinations were carried out. Furthermore, peroxisome proliferator-activated receptor gamma (PPAR-γ) signaling pathway-related proteins and genes were detected with an emphasis on the role of miR-9 | ||
520 | |a RESULTS: TQ has the potential to ameliorate cognitive deficits observed in SCOP-induced AD-like model, as evidenced by the improvement in behavioral outcomes, histopathological changes, modulation of the expression pattern of PPAR-γ downstream targets with a significant decrease in the deposition of amyloid beta (Aβ) | ||
520 | |a CONCLUSIONS: TQ provided meaningful multilevel neuroprotection through its anti-inflammatory and its PPAR-γ agonist activity. Consequently, TQ may possess a potential beneficial role against AD development | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Alzheimer’s disease | |
650 | 4 | |a NF-κB | |
650 | 4 | |a PPAR-γ | |
650 | 4 | |a miR-9 | |
650 | 4 | |a scopolamine | |
650 | 4 | |a thymoquinone | |
650 | 7 | |a Neuroprotective Agents |2 NLM | |
650 | 7 | |a Amyloid beta-Peptides |2 NLM | |
650 | 7 | |a thymoquinone |2 NLM | |
650 | 7 | |a O60IE26NUF |2 NLM | |
650 | 7 | |a PPAR gamma |2 NLM | |
650 | 7 | |a Scopolamine |2 NLM | |
650 | 7 | |a DL48G20X8X |2 NLM | |
700 | 1 | |a Elberri, Aya Ibrahim |e verfasserin |4 aut | |
700 | 1 | |a Ghoneim, Mai El-Sayed |e verfasserin |4 aut | |
700 | 1 | |a Samman, Waad A |e verfasserin |4 aut | |
700 | 1 | |a Alhaddad, Aisha A |e verfasserin |4 aut | |
700 | 1 | |a Abdallah, Mahmoud S |e verfasserin |4 aut | |
700 | 1 | |a El-Berri, Eman I |e verfasserin |4 aut | |
700 | 1 | |a Salem, Mohamed A |e verfasserin |4 aut | |
700 | 1 | |a Mosalam, Esraa M |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Molecules (Basel, Switzerland) |d 2004 |g 28(2023), 18 vom: 11. Sept. |w (DE-627)NLM172073448 |x 1420-3049 |7 nnns |
773 | 1 | 8 | |g volume:28 |g year:2023 |g number:18 |g day:11 |g month:09 |
856 | 4 | 0 | |u http://dx.doi.org/10.3390/molecules28186566 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 28 |j 2023 |e 18 |b 11 |c 09 |