Dysfunction in Cardiovascular Autonomic Modulation Caused by Chronic Use of Ketamine Hydrochloride Can Be Prevented by Aerobic Exercise Training in Wistar Rats.
Adriano Dos-Santos, Lucas Porto Fernandes Dos Santos, Gabriela Da Silva-Santos, Bruno Durante Da Silva, Bruno Nascimento-Carvalho, Hunter Douglas De Souza-Lima, Nicolas Da Costa-Santos, Erico Chagas Caperuto, Nathalia Bernardes, Katia De Angelis, Maria Claudia Irigoyen, Katia Bilhar Scapini, Iris Callado Sanches
Journal of Clinical Medicine October 24, 2025 DOI: 10.3390/jcm14217548 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Randomized controlled trial Peer reviewed |
|---|---|
| Sample size | 24 |
| Population | Wistar rats |
| Interventions | Aerobic exercise training Ketamine |
| Dose | 10 mg/kg |
| Duration | 6-week intervention |
| Topics | Ketamine Esketamine |
| Keywords | Cardiovascular autonomic control Ketamine: ketamine Chronic ketamine exposure Long-term ketamine-related issues Regular physical activity Aerobic exercise training Non-pharmacological strategy Healthier heart function Heart health Vital heart regulation Elevated blood pressure Heart protection |
| Key findings | Aerobic training attenuated the elevated systolic blood pressure and reduced baroreflex sensitivity caused by chronic ketamine administration in rats. |
Abstract
Background/Objectives: Ketamine, widely used for its anesthetic and analgesic properties, has been linked to cardiotoxic effects, particularly with chronic use. Prolonged ketamine exposure may impair cardiovascular function, while aerobic exercise is known to promote protective cardiovascular adaptations. This study aimed to evaluate whether aerobic training can mitigate the deleterious cardiovascular effects of chronic ketamine administration in rats.
Methods: Twenty-four Wistar rats were randomly assigned to four groups: sedentary control (S), trained control (T), sedentary with ketamine (S-ket), and trained with ketamine (T-ket). Ketamine was administered intraperitoneally at a dose of 10 mg/kg, three times per week for six weeks. Aerobic training was conducted on a treadmill in the trained groups throughout the protocol. At the end of the experiment, cardiac function was assessed by echocardiography. Additionally, animals were cannulated in the carotid artery and jugular vein to measure blood pressure, baroreflex sensitivity, and heart rate variability using a data acquisition system (2 kHz, Windaq DATAQ).
Results: Rats in the S-ket group showed elevated systolic arterial pressure and reduced baroreflex sensitivity compared to controls. Aerobic training attenuated these effects. Baroreflex sensitivity improved (bradycardic reflex-S: -1.7 ± 0.3; S-ket: -0.7 ± 0.1; T: -1.3 ± 0.2; T-ket: -1.3 ± 0.1), and cardiovascular autonomic function was preserved (total power-S: 45.6 ± 6.3; S-ket: 18.3 ± 2.1; T: 44.1 ± 5.7; T-ket: 38.9 ± 8.4) in trained animals.
Conclusions: Aerobic exercise mitigates cardiovascular impairments caused by chronic ketamine exposure in rats, suggesting its potential as a non-pharmacological intervention to counteract ketamine-induced cardiotoxicity. These findings support incorporating exercise into treatment strategies for individuals chronically exposed to ketamine.
Comparable studies
Other preclinical and animal studies on ketamine, most cited first.
| Study | Year | Design | Participants |
|---|---|---|---|
| mTOR-Dependent Synapse Formation Underlies the Rapid Antidepressant Effects of NMDA Antagonists Rats | 2010 | Observational study | |
| Activation of Glutamatergic Neurotransmission by Ketamine: A Novel Step in the Pathway from NMDA Receptor Blockade to Dopaminergic and Cognitive Disruptions Associated with the Prefrontal Cortex Conscious rats | 1997 | Dose-response study with microdialysis and behavioral testing | |
| NMDAR inhibition-independent antidepressant actions of ketamine metabolites Mice | 2016 | Preclinical study | |
| The dissociative anaesthetics, ketamine and phencyclidine, selectively reduce excitation of central mammalian neurones by N‐methyl‐aspartate Spinal neurons in decerebrate or pentobarbitone-anaesthetized cats and rats | 1983 | Experimental study | |
| R-ketamine: a rapid-onset and sustained antidepressant without psychotomimetic side effects Mice | 2015 | Experimental study |
Citations in the library
Cites 8
- Side-effects associated with ketamine use in depression: a systematic review. The Lancet Psychiatry 2018
- Ketamine for chronic pain: risks and benefits British Journal of Clinical Pharmacology February 21, 2013
- Ketamine: 50 Years of Modulating the Mind Frontiers in Human Neuroscience November 29, 2016
- Oral Ketamine for Depression The Journal of Clinical Psychiatry April 15, 2019
- Metabolomic signatures of drug response phenotypes for ketamine and esketamine in subjects with refractory major depressive disorder: new mechanistic insights for rapid acting antidepressants Translational Psychiatry September 20, 2016
and 3 more in the library