Systemic Nitric Oxide Synthase Inhibition Suppresses Apelin-Induced Rise in Body Temperature in Rats
Apelin is a peptide involved in the regulation of various physiological processes, including thermoregulation, metabolism, and energy balance. This study investigates the role of nitric oxide (NO) in mediating apelin’s effects on body temperature, food intake, and body mass gain in rats. Using the n...
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Sciendo
2025-06-01
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| Series: | Acta Medica Bulgarica |
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| Online Access: | https://doi.org/10.2478/amb-2025-0046 |
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| author | Hristov M. Andreeva-Gateva P. |
| author_facet | Hristov M. Andreeva-Gateva P. |
| author_sort | Hristov M. |
| collection | DOAJ |
| description | Apelin is a peptide involved in the regulation of various physiological processes, including thermoregulation, metabolism, and energy balance. This study investigates the role of nitric oxide (NO) in mediating apelin’s effects on body temperature, food intake, and body mass gain in rats. Using the non-selective nitric oxide synthase (NOS) inhibitor L-NAME and the selective inducible NOS inhibitor aminoguanidine (AG), we assessed how systemic inhibition of NO synthesis modulates apelin-induced responses. Male Wistar rats were administered intraperitoneal injections of [Pyr1]apelin-13 following pre-treatment with L-NAME or AG. Our results show that both L-NAME and AG suppressed the apelin-induced rise in body temperature, with L-NAME having a more pronounced effect. Additionally, L-NAME significantly reduced apelin-induced food intake and body mass gain, while AG had a lesser impact. These findings suggest that NO plays a key role in mediating the apelin’s thermoregulatory and metabolic effects. The differential outcomes between L-NAME and AG highlight the potential involvement of multiple NOS isoforms in these processes. Further investigation into the distinct roles of NOS isoforms may provide deeper insights into NO-apelin interactions and their relevance to metabolic regulation, offering potential therapeutic targets for metabolic disorders. |
| format | Article |
| id | doaj-art-8adebbddee70497690f21bc100e53339 |
| institution | OA Journals |
| issn | 2719-5384 |
| language | English |
| publishDate | 2025-06-01 |
| publisher | Sciendo |
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| series | Acta Medica Bulgarica |
| spelling | doaj-art-8adebbddee70497690f21bc100e533392025-08-20T02:10:28ZengSciendoActa Medica Bulgarica2719-53842025-06-01522626710.2478/amb-2025-0046Systemic Nitric Oxide Synthase Inhibition Suppresses Apelin-Induced Rise in Body Temperature in RatsHristov M.0Andreeva-Gateva P.11Department of Pharmacology and Toxicology, Faculty of Medicine, Medical University – Sofia, Bulgaria1Department of Pharmacology and Toxicology, Faculty of Medicine, Medical University – Sofia, BulgariaApelin is a peptide involved in the regulation of various physiological processes, including thermoregulation, metabolism, and energy balance. This study investigates the role of nitric oxide (NO) in mediating apelin’s effects on body temperature, food intake, and body mass gain in rats. Using the non-selective nitric oxide synthase (NOS) inhibitor L-NAME and the selective inducible NOS inhibitor aminoguanidine (AG), we assessed how systemic inhibition of NO synthesis modulates apelin-induced responses. Male Wistar rats were administered intraperitoneal injections of [Pyr1]apelin-13 following pre-treatment with L-NAME or AG. Our results show that both L-NAME and AG suppressed the apelin-induced rise in body temperature, with L-NAME having a more pronounced effect. Additionally, L-NAME significantly reduced apelin-induced food intake and body mass gain, while AG had a lesser impact. These findings suggest that NO plays a key role in mediating the apelin’s thermoregulatory and metabolic effects. The differential outcomes between L-NAME and AG highlight the potential involvement of multiple NOS isoforms in these processes. Further investigation into the distinct roles of NOS isoforms may provide deeper insights into NO-apelin interactions and their relevance to metabolic regulation, offering potential therapeutic targets for metabolic disorders.https://doi.org/10.2478/amb-2025-0046apelinaminoguanidinel-namemetabolismnitric oxide synthasethermoregulation |
| spellingShingle | Hristov M. Andreeva-Gateva P. Systemic Nitric Oxide Synthase Inhibition Suppresses Apelin-Induced Rise in Body Temperature in Rats Acta Medica Bulgarica apelin aminoguanidine l-name metabolism nitric oxide synthase thermoregulation |
| title | Systemic Nitric Oxide Synthase Inhibition Suppresses Apelin-Induced Rise in Body Temperature in Rats |
| title_full | Systemic Nitric Oxide Synthase Inhibition Suppresses Apelin-Induced Rise in Body Temperature in Rats |
| title_fullStr | Systemic Nitric Oxide Synthase Inhibition Suppresses Apelin-Induced Rise in Body Temperature in Rats |
| title_full_unstemmed | Systemic Nitric Oxide Synthase Inhibition Suppresses Apelin-Induced Rise in Body Temperature in Rats |
| title_short | Systemic Nitric Oxide Synthase Inhibition Suppresses Apelin-Induced Rise in Body Temperature in Rats |
| title_sort | systemic nitric oxide synthase inhibition suppresses apelin induced rise in body temperature in rats |
| topic | apelin aminoguanidine l-name metabolism nitric oxide synthase thermoregulation |
| url | https://doi.org/10.2478/amb-2025-0046 |
| work_keys_str_mv | AT hristovm systemicnitricoxidesynthaseinhibitionsuppressesapelininducedriseinbodytemperatureinrats AT andreevagatevap systemicnitricoxidesynthaseinhibitionsuppressesapelininducedriseinbodytemperatureinrats |