Knock-out of the critical nitric oxide synthase regulator DDAH1 in mice impacts amphetamine sensitivity and dopamine metabolism
© 2023. The Author(s)..
The enzyme dimethylarginine dimethylaminohydrolase 1 (DDAH1) plays a pivotal role in the regulation of nitric oxide levels by degrading the main endogenous nitric oxide synthase inhibitor asymmetric dimethylarginine (ADMA). Growing evidence highlight the potential implication of DDAH/ADMA axis in the etiopathogenesis of several neuropsychiatric and neurological disorders, yet the underlying molecular mechanisms remain elusive. In this study, we sought to investigate the role of DDAH1 in behavioral endophenotypes with neuropsychiatric relevance. To achieve this, a global DDAH1 knock-out (DDAH1-ko) mouse strain was employed. Behavioral testing and brain region-specific neurotransmitter profiling have been conducted to assess the effect of both genotype and sex. DDAH1-ko mice exhibited increased exploratory behavior toward novel objects, altered amphetamine response kinetics and decreased dopamine metabolite 3,4-dihydroxyphenylacetic acid (DOPAC) level in the piriform cortex and striatum. Females of both genotypes showed the most robust amphetamine response. These results support the potential implication of the DDAH/ADMA pathway in central nervous system processes shaping the behavioral outcome. Yet, further experiments are required to complement the picture and define the specific brain-regions and mechanisms involved.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2023 |
---|---|
Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:130 |
---|---|
Enthalten in: |
Journal of neural transmission (Vienna, Austria : 1996) - 130(2023), 9 vom: 16. Sept., Seite 1097-1112 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Kozlova, Alena A [VerfasserIn] |
---|
Links: |
---|
Anmerkungen: |
Date Completed 30.08.2023 Date Revised 30.08.2023 published: Print-Electronic Citation Status MEDLINE |
---|
doi: |
10.1007/s00702-023-02597-7 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM35299357X |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM35299357X | ||
003 | DE-627 | ||
005 | 20231226055001.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231226s2023 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1007/s00702-023-02597-7 |2 doi | |
028 | 5 | 2 | |a pubmed24n1176.xml |
035 | |a (DE-627)NLM35299357X | ||
035 | |a (NLM)36792833 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Kozlova, Alena A |e verfasserin |4 aut | |
245 | 1 | 0 | |a Knock-out of the critical nitric oxide synthase regulator DDAH1 in mice impacts amphetamine sensitivity and dopamine metabolism |
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 30.08.2023 | ||
500 | |a Date Revised 30.08.2023 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a © 2023. The Author(s). | ||
520 | |a The enzyme dimethylarginine dimethylaminohydrolase 1 (DDAH1) plays a pivotal role in the regulation of nitric oxide levels by degrading the main endogenous nitric oxide synthase inhibitor asymmetric dimethylarginine (ADMA). Growing evidence highlight the potential implication of DDAH/ADMA axis in the etiopathogenesis of several neuropsychiatric and neurological disorders, yet the underlying molecular mechanisms remain elusive. In this study, we sought to investigate the role of DDAH1 in behavioral endophenotypes with neuropsychiatric relevance. To achieve this, a global DDAH1 knock-out (DDAH1-ko) mouse strain was employed. Behavioral testing and brain region-specific neurotransmitter profiling have been conducted to assess the effect of both genotype and sex. DDAH1-ko mice exhibited increased exploratory behavior toward novel objects, altered amphetamine response kinetics and decreased dopamine metabolite 3,4-dihydroxyphenylacetic acid (DOPAC) level in the piriform cortex and striatum. Females of both genotypes showed the most robust amphetamine response. These results support the potential implication of the DDAH/ADMA pathway in central nervous system processes shaping the behavioral outcome. Yet, further experiments are required to complement the picture and define the specific brain-regions and mechanisms involved | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 4 | |a Amphetamine | |
650 | 4 | |a Behaviour | |
650 | 4 | |a DDAH1 | |
650 | 4 | |a Dopamine | |
650 | 4 | |a Knock-out mice | |
650 | 4 | |a Nitric oxide | |
650 | 7 | |a Amidohydrolases |2 NLM | |
650 | 7 | |a EC 3.5.- |2 NLM | |
650 | 7 | |a Amphetamine |2 NLM | |
650 | 7 | |a CK833KGX7E |2 NLM | |
650 | 7 | |a Dopamine |2 NLM | |
650 | 7 | |a VTD58H1Z2X |2 NLM | |
650 | 7 | |a Enzyme Inhibitors |2 NLM | |
650 | 7 | |a Nitric Oxide |2 NLM | |
650 | 7 | |a 31C4KY9ESH |2 NLM | |
650 | 7 | |a Nitric Oxide Synthase |2 NLM | |
650 | 7 | |a EC 1.14.13.39 |2 NLM | |
650 | 7 | |a dimethylargininase |2 NLM | |
650 | 7 | |a EC 3.5.3.18 |2 NLM | |
700 | 1 | |a Rubets, Elena |e verfasserin |4 aut | |
700 | 1 | |a Vareltzoglou, Magdalini R |e verfasserin |4 aut | |
700 | 1 | |a Jarzebska, Natalia |e verfasserin |4 aut | |
700 | 1 | |a Ragavan, Vinitha N |e verfasserin |4 aut | |
700 | 1 | |a Chen, Yingjie |e verfasserin |4 aut | |
700 | 1 | |a Martens-Lobenhoffer, Jens |e verfasserin |4 aut | |
700 | 1 | |a Bode-Böger, Stefanie M |e verfasserin |4 aut | |
700 | 1 | |a Gainetdinov, Raul R |e verfasserin |4 aut | |
700 | 1 | |a Rodionov, Roman N |e verfasserin |4 aut | |
700 | 1 | |a Bernhardt, Nadine |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Journal of neural transmission (Vienna, Austria : 1996) |d 1998 |g 130(2023), 9 vom: 16. Sept., Seite 1097-1112 |w (DE-627)NLM087117487 |x 1435-1463 |7 nnns |
773 | 1 | 8 | |g volume:130 |g year:2023 |g number:9 |g day:16 |g month:09 |g pages:1097-1112 |
856 | 4 | 0 | |u http://dx.doi.org/10.1007/s00702-023-02597-7 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 130 |j 2023 |e 9 |b 16 |c 09 |h 1097-1112 |