Median nerve diadynamic current stimulation for blood pressure modulation
Authors
- Rajan Soundarpandian SenthilkumarDepartment of Physiotherapy, Saveetha College of Physiotherapy, Thandalam, Chennai, Tamil Nadu, Indiahttps://orcid.org/0009-0000-5626-6842
- Ramana KameswaranDepartment of Physiotherapy, Saveetha College of Physiotherapy, Thandalam, Chennai, Tamil Nadu, Indiahttps://orcid.org/0000-0003-2332-2187
- Priyadarshini Babu Rajendra PrasadDepartment of Physiotherapy, Saveetha College of Physiotherapy, Thandalam, Chennai, Tamil Nadu, Indiahttps://orcid.org/0009-0006-7300-6720
DOI:
https://doi.org/10.3329/bsmmuj.v18i4.84473Keywords
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Published by Bangladesh Medical University (former Bangabandhu Sheikh Mujib Medical University).
Electrical stimulation modifies peripheral nerve function and neuromuscular activity by applying controlled electrical currents through the skin [1]. Peripheral neuromodulation offers therapeutic promise for reestablishing physiological balance by using targeted nerve stimulation to control organ and tissue function through bidirectional brain–periphery transmission [2]. The somato-autonomic reflex involves central pathways in which somatosensory stimulation activates autonomic efferents through spinal and brainstem circuits, resulting in organ-specific or systemic cardiovascular responses [3]. The axon reflex is a peripheral process in which neuropeptides such as substance P and calcitonin gene-related peptide are released by sensory neurones antidromically to produce localised vasodilation or vasoconstriction without engaging the central nervous system [4]. Through somato-autonomic reflexes, median nerve stimulation may affect blood pressure. Axon-reflex activity and neurotransmitter release further limit presympathetic drive, supporting physiological blood pressure regulation, while afferent input activates central autonomic nuclei projecting to the rostral ventrolateral medulla, suppressing sympathetic outflow [5]. This study uniquely investigates diadynamic median nerve stimulation as a non-invasive method of reducing the sympathetic outflow and modulating blood pressure in a healthy adult.
An apparently healthy 19-year-old man with a body mass index of 23.5kg/m2, leading a healthy lifestyle was selected. Comorbid conditions like hypertension, diabetes, and autonomic dysfunction were excluded to provide more reliable physiological responses [6]. Ethical guidelines were adhered to, and an informed consent was obtained prior to commencing the study. This experimental design was adopted to evaluate the effects of diadynamic stimulation on blood pressure regulation. Systolic and diastolic blood pressure were measured using a digital sphygmomanometer (Omron HEM-7120).
Table 1 Intervention phases and blood pressure measurements of a 19-year-old man
Week | Phase |
| Blood pressure (mmHg) | |
|
|
| Systolic | Diastolic |
Pre-test | Baseline | – | 121 | 65 |
Week 1 | Intervention | Pre | 127 | 67 |
|
| Post | 119 | 66 |
Week 2 | Washout | – | 128 | 69 |
Week 3 | Intervention | Pre | 131 | 78 |
|
| Post | 134 | 64 |
Week 4 | Washout | – | 124 | 67 |
Post-test | Follow-up | – | 118 | 69 |
Categories | Number (%) |
Sex |
|
Male | 36 (60.0) |
Female | 24 (40.0) |
Age in yearsa | 8.8 (4.2) |
Education |
|
Pre-school | 20 (33.3) |
Elementary school | 24 (40.0) |
Junior high school | 16 (26.7) |
Cancer diagnoses |
|
Acute lymphoblastic leukemia | 33 (55) |
Retinoblastoma | 5 (8.3) |
Acute myeloid leukemia | 4 (6.7) |
Non-Hodgkins lymphoma | 4 (6.7) |
Osteosarcoma | 3 (5) |
Hepatoblastoma | 2 (3.3) |
Lymphoma | 2 (3.3) |
Neuroblastoma | 2 (3.3) |
Medulloblastoma | 1 (1.7) |
Neurofibroma | 1 (1.7) |
Ovarian tumour | 1 (1.7) |
Pancreatic cancer | 1 (1.7) |
Rhabdomyosarcoma | 1 (1.7) |
aMean (standard deviation) | |
Categories | Number (%) |
Sex |
|
Male | 36 (60.0) |
Female | 24 (40.0) |
Age in yearsa | 8.8 (4.2) |
Education |
|
Pre-school | 20 (33.3) |
Elementary school | 24 (40.0) |
Junior high school | 16 (26.7) |
Cancer diagnoses |
|
Acute lymphoblastic leukemia | 33 (55) |
Retinoblastoma | 5 (8.3) |
Acute myeloid leukemia | 4 (6.7) |
Non-Hodgkins lymphoma | 4 (6.7) |
Osteosarcoma | 3 (5) |
Hepatoblastoma | 2 (3.3) |
Lymphoma | 2 (3.3) |
Neuroblastoma | 2 (3.3) |
Medulloblastoma | 1 (1.7) |
Neurofibroma | 1 (1.7) |
Ovarian tumour | 1 (1.7) |
Pancreatic cancer | 1 (1.7) |
Rhabdomyosarcoma | 1 (1.7) |
aMean (standard deviation) | |
Pain level | Number (%) | P | ||
Pre | Post 1 | Post 2 | ||
Mean (SD)a pain score | 4.7 (1.9) | 2.7 (1.6) | 0.8 (1.1) | <0.001 |
Pain categories | ||||
No pain (0) | - | 1 (1.7) | 31 (51.7) | <0.001 |
Mild pain (1-3) | 15 (25.0) | 43 (70.0) | 27 (45.0) | |
Moderete pain (4-6) | 37 (61.7) | 15 (25.0) | 2 (3.3) | |
Severe pain (7-10) | 8 (13.3) | 2 (3.3) | - | |
aPain scores according to the visual analogue scale ranging from 0 to 10; SD indicates standard deviation | ||||
Following diadynamic current median nerve stimulation, an effect on blood pressure regulation appeared to manifest across the subsequent intervention phases but none of them were sustained for statistical significance. Contrary to the findings of other studies, the diastolic pressure increased paradoxically. This divergent diastolic response may suggest our inability to control extraneous factors in the statistical analysis.
It is hypothesised that diadynamic current changes the autonomic outflow by exciting cuta-neous and afferent nerve fibers. Thus, the balance shifts to increased parasympathetic and reduced sympathetic activity [9]. However, the present findings indicate a possible autonomic influence of diadynamic current stimulation, which requires further controlled studies to recommend any therapeutic indication. Subsequent studies may require an adjustment of dosages of electrical stimulation and other indices such as intensity, frequency and duration of the sessions that cause maximal blood pressure changes without provoking side effect or discomfort using a design that can adjust the results for extraneous factors such as objectively measured caffeine and salt intake and physical activity before the measurement of blood pressure.

