Single-Pulse and Unidirectional Electrical Activation of the Cervical Vagus Nerve Reduces Tumor Necrosis Factor in Endotoxemia
- 13 Downloads
The inflammatory reflex is a neural circuit defined by action potentials transmitted in the vagus nerve that regulate cytokine production in the spleen. Detailed mechanistic studies implicate the vagus nerve, the splenic nerve, a T-cell subset that produces acetylcholine under the control of adrenergic signals, and alpha7 nicotinic acetylcholine receptors (α7nAChR). expressed on macrophages. This study defines the vagus nerve fibers that transmit the efferent signal in this pathway, a motor arc of the inflammatory reflex. Mice and rats were subjected to electrical cervical vagus nerve stimulation or sham surgery. Cytokine levels in serum were measured in endotoxemic animals or in endotoxin-exposed blood samples. Evoked potentials were measured in the vagus nerve and a portion of the vagus nerve was anesthetized using local application of lidocaine before stimulation. The lowest threshold subdiaphragmatic fibers in the rat vagus nerve have conduction velocities consistent with that of myelinated B fibers. The stimulation current threshold for significant suppression of serum TNF levels was similar in mice and rats (≤500 µA). Blockade of the fibers caudal to the site of vagus nerve stimulation impaired the inhibition of TNF release. A single suprathreshold pulse stimulation was sufficient to suppress TNF release in endotoxemia. These results indicate that single-pulse and unidirectional electrical activation of the cervical vagus nerve reduce TNF in endotoxemia.
Bioelectronic medicine, the interdisciplinary field that brings together neurophysiology, molecular medicine and biomedical engineering, has a significant potential to revolutionize treatment of inflammation and other diseases (1). The inflammatory reflex, a neural circuit that regulates inflammation, includes a sensory arc through the vagus nerve, and an efferent arc termed the cholinergic antiinflammatory pathway. Neurophysiological, genetic and molecular mechanistic studies of the inflammatory reflex have revealed that the integrity of the circuit is dependent upon action potentials descending in the vagus nerve, splenic T cells that express choline acetyltransferase and red pulp macrophages that express alpha7 nicotinic acetylcholine receptors (α7nAChR). Stimulation of the inflammatory reflex attenuates inflammatory disease in arthritis, colitis and other inflammatory diseases in animals (2, 3, 4) and in a clinical trial of rheumatoid arthritis patients (5). Ongoing clinical studies of implanted vagus nerve stimulators are focused on rheumatoid arthritis, inflammatory bowel disease and postoperative ileus (6,7).
Despite the detailed mechanistic understanding of the inflammatory reflex, the neurophysiological identity of the efferent vagus nerve fibers in the motor arc of the inflammatory reflex have not been described. Prior neuroanatomical studies revealed a connection between vagus nerve fibers and prevertebral ganglia, including the celiac and superior mesenteric ganglia, which is the origin of the adrenergic splenic nerve (8, 9, 10, 11). It also has been established that action potentials arising in the splenic nerve as well as activation of acetylcholine-releasing T cells in spleen are required for the integrity of the inflammatory reflex and its ability to inhibit TNF release by splenic macrophages (12, 13, 14). Moreover, activation of isolated splenic neurons inhibits TNF production in isolated spleen preparations (15). The magnitude of the electrical stimulation sufficient to activate the inflammatory reflex is significantly less than the threshold required to induce bradycardia (16,17), suggesting, though not proving, that the fibers that transmit the TNF inhibiting signal are distinct from the fibers that modulate heart rate. The cervical vagus nerve contains a large number of fibers, >100,000 in humans, predominantly unmyelinated C fibers, and a minority of myelinated A and B fibers. Recent observations suggest that therapeutic effects of vagus nerve stimulation are associated with electrical activation of myelinated fibers (18). Accordingly, here we investigated stimulation thresholds and directionality requirements of electrical activation of the cervical vagus nerve to inhibit TNF production in the spleen during endotoxemia.
Materials and Methods
This study was approved by The Feinstein Institute for Medical Research’s Institutional Animal Care and Use Committee.
Vagus Nerve Stimulation
Male balb/C mice and Sprague Dawley rats were obtained from Taconic Farms Inc. (Hudson, NY, USA) and the studies were conducted at The Feinstein Institute for Medical Research (Manhasset, NY, USA). Animal care conformed to the Guide for the Care and Use of Laboratory Animals (19), and the applicable standard operating procedures of The Feinstein Institute for Medical Research. Animals were housed in a laboratory environment on a 12-h light-dark cycle at 19.5 to 24°C room temperature and relative humidity 30%–70% and had free access to food and water.
Electrical pulses were delivered by a custom-built stimulator (SetPoint Medical Inc., Valencia, CA, USA) as 0 to 2,500 µA charge-balanced biphasic square pulses with 200–250 µs pulse width at 10 Hz for 60 s, unless otherwise specified. In some experiments, 1.5 µL of lidocaine 20 mg/mL was applied on the nerve cranial and/or caudal to the cuff electrode for 3 to 5 min prior to stimulation.
Three hours after VNS, endotoxin (LPS from Escherichia coli, 0111:B4; Sigma-Aldrich, St. Louis, MO, USA) was injected intraperitoneally (IP) (1 mg/kg in rats; 5 mg/kg in mice). Rodents were euthanized 90 min later and serum was collected for determination of TNF concentration by ELISA (R&D Systems, Minneaspolis, MN, USA).
Measurement of Evoked Potentials in Rats
A bipolar cuff electrode (MicroProbes) was placed on the left cervical vagus nerve, in isoflurane-anesthetized (1.5%–3%) rats. The ventral trunk of the subdiaphragmatic vagus nerve was isolated through a midline abdominal incision and placed across a bipolar hook electrode (Plastics One Inc., Roanoke, VA, USA). The neural compound action potentials evoked by cervical VNS were sampled at 20 kHz, filtered (100 Hz to 10 kHz, 60 Hz notch), and amplified (50,000×) using an MP150 data acquisition system (Biopac Systems Inc., Goleta, CA, USA). The data was then averaged 60 times to increase signal-to-noise ratios.
Differences between treatment groups were analyzed using analysis of variance (ANOVA) with Holm-Šidák post hoc test. Prism 6.0 (GraphPad software, San Diego, CA, USA) was used for statistical analyses. p < 0.05 was considered significant.
The Threshold of Electrical Cervical Vagus Nerve Stimulation for Inhibition of TNF in Endotoxemia Is Similar in Mice and Rats
Electrical stimulation of the cervical vagus nerve (VNS) in Sprague Dawley rats with a charge-balanced, biphasic pulse (20) delivered through a bipolar stimulating electrode (see Figure 1A) elicited evoked potentials recorded in the subdiaphragmatic vagus nerve; the observed stimulation current threshold is 265 ± 139 µA (Figure 1B). The subdiaphragmatic fibers in the rat vagus nerve have conduction velocities of 4 to 9 m/s, consistent with activation of large myelinated, preganglionic B fibers (Figure 1C).
Unidirectional Efferent Vagus Nerve Signals Are Sufficient to Suppress TNF in Endotoxemia
These results do not exclude the possibility that afferent vagus nerve signals can modulate other pathways that regulate the cytokine response to endotoxin. Accordingly, we next blocked the efferent vagus nerve signals by applying anesthesia caudal to the stimulation cuff. Afferent vagus nerve stimulation under these experimental conditions also significantly reduced TNF release (Figure 3C), despite blockade of the efferent portion of the vagus nerve relative to the site of stimulation. Inhibition of TNF release in these experiments was not significantly different between caudal and cranial vagus nerve anesthesia. These data reveal additional TNF-inhibiting pathways mediated by afferent, or incoming signals, in the vagus nerve that can, in turn, activate descending, antiinflammatory mechanisms that are independent of the complete inflammatory reflex.
These results indicate that single-pulse and unidirectional electrical activation of the cervical vagus nerve reduces TNF in endotoxemia.
As defined here and previously, the motor arc of the inflammatory reflex comprises action potentials in the vagus nerve that travel to the celiac ganglia to activate the adrenergic splenic nerve. The isolated motor arc is termed “the cholinergic antiinflammatory pathway,” because neurotransmitter release from the splenic nerve triggers choline acetyltransferase+ T cells in the spleen to release acetylcholine (23) which inhibits TNF release by activating α7nAChR on monocytes and macrophages in the spleen (12,24, 25, 26). Multiple studies have confirmed and extended the original observations that signals in the vagus nerve reduce cytokine release in various inflammatory conditions by activating this efferent pathway that functionally connects the vagus nerve with immune cells in the spleen (3,8–11,21,27–29). Until now, the functional anatomy of the efferent vagus nerve pathway in the inflammatory reflex had been partially addressed, primarily in experiments of surgically dividing the nerve and assessing the effects on TNF release. In the present study, electrical propagation of vagus nerve signals was temporarily disabled by application of a local anesthetic. This approach offers the advantage of controlling the experimental conditions without permanently disrupting normal vagus neurophysiology. In agreement with previous findings, the present study shows that electrical stimulation of the efferent arc of the inflammatory reflex is sufficient to reduce TNF release in endotoxemia (21). The conduction velocity of the evoked potentials in the subdiaphragmatic vagus is consistent with the notion that large myelinated vagus nerve B fibers propagate the signals in this efferent arc of the inflammatory reflex. This observation does not, however, exclude the existence of other reflexively activated efferent nerves that regulate cytokine production and release.
Anesthetizing the vagus nerve caudal to the stimulation electrodes did not abolish the effect of cervical vagus nerve stimulation on inhibition of TNF release in mice. This observation supports the presence of other antiinflammatory pathways from the central nervous system (CNS) that can inhibit cytokine release independently of the prototypical inflammatory reflex (reviewed in [30,31]). Such putative mechanisms include both signaling via the sympathetic chain to the splenic nerve and spleen and also activation of the hypothalamic-pituitary-adrenal axis to release glucocorticoids that, in turn, inhibit serum TNF (9,31, 32, 33). As we and others have discussed elsewhere, the inflammatory reflex is a prototypical cytokine-regulating circuit, but not an exclusive one, and a number of neural reflexes have now been identified that can regulate inflammation and immunity (4,34).
Other neural pathways that regulate immune cell activity and cytokine release includes vagus nerve-dependent inhibition of intestinal inflammation, which is independent of splenic signaling and, therefore, independent of the inflammatory reflex (35). Entry of pathogenic T cells across the blood brain barrier into the CNS is modulated by adrenergic efferent signals activated in response to proprioceptive signals originating in the lumbar spinal cord (36,37). Sensory nerves in skin can be activated directly by bacterial products (38) and nociceptive neurons also can promote skin inflammation (39). Signals arising in adrenergic nerves are known to have important effects on immune cell activity (40,41) and electric stimulation of the sciatic nerve regulates adrenal catecholamine-production via the vagus nerve (42). Together with other findings, these studies reveal that specific neural circuits regulate activation of immunity. As with other reflexes, which do not function in isolation, immune-regulating neural reflex pathways are not mutually exclusive. Rather, neural reflexes are integrated to maintain immunological homeostasis under a wide range of invasive and injurious threat.
Another major finding in this study is that a single electrical pulse applied to the vagus nerve significantly reduced serum TNF levels. The single-pulse experiments were performed in mice at a supra-threshold current of 750 µA, corresponding to a total cathodal charge delivery of 150 pC. This discovery is important, because it suggests that a very short activation of implanted vagus nerve stimulators may be sufficient to have a treatment effect on inflammatory disease. Limited and ultralow duty cycle “on” time of an implanted stimulator will likely not only reduce unwanted side effects, but the low energy requirement will demand less stimulator battery power and may allow for new miniaturized form factors and longer intervals between device servicing. Furthermore, the vagus nerve stimulation threshold current for inhibition of TNF release in our experiments was 250–500 µA in mice and rats. The current requirements reported here at 10 Hz are significantly below the levels that previously have been described to reduce heart rate in rodents (13,16,17). Together, these findings suggest that the motor arc of the inflammatory reflex is transmitted by motor fibers that are distinct from those that regulate heart rate.
Vagus nerve stimulation is emerging as a potential treatment for human inflammatory diseases (5,6,43,44). The growing understanding of the components and signals that constitute the inflammatory reflex is driving the development of a potentially revolutionary line of novel therapeutic opportunities. This study shows that a single-pulse electrical activation of the vagus nerve is sufficient to reduce cytokine release, and that efferent and afferent vagus nerve signals have a separate capacity to regulate immunity. The implications of fiber specificity and the potential to target afferent and efferent pathways separately should inform development of future neuromodulation techniques to treat disease.
YA Levine, A Caravaca, and M Faltys are full time employees of SetPoint Medical Corporation.
We thank Warren M Grill for his insightful comments. This study was funded by SetPoint Medical Corporation, by the National Institute of General Medical Sciences (R01GM057226 to KJ Tracey and R01GM089807 to VA Pavlov) and by Svenska Läkaresällskapet.
- 5.Koopman FA, et al. (2012) Pilot study of stimulation of the cholinergic anti-inflammatory pathway with an implantable vagus nerve stimulation device in patients with rheumatoid arthritis [abstract]. Arthritis Rheum. 64:S195.Google Scholar
- 19.Committee for the Update of the Guide for the Care and Use of Laboratory Animals, Institute for Laboratory Animal Research, Division on Earth and Life Studies, National Research Council of the National Academies. (2011) Guide for the Care and Use of Laboratory Animals. 8th edition. Washington (DC): The National Academies Press.Google Scholar
- 44.Olofsson PS. (2014) A stimulating concept: bioelectronic medicine in inflammatory disease. Bioelectron. Med. 1:30–3.Google Scholar
Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, and provide a link to the Creative Commons license. You do not have permission under this license to share adapted material derived from this article or parts of it.
The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.
To view a copy of this license, visit (https://doi.org/creativecommons.org/licenses/by-nc-nd/4.0/)