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Low and medium Frequency Electrotherapy - Implox

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2.2.2 Endorphin release theory (Sjölund <strong>and</strong> Eriksson)<br />

This theory (27) is based on the assumption that, in chronic pain, there is either hypoactivity of the endorphin system,<br />

or an increased consumption of the endorphins released. The central nervous system can be stimulated to produce<br />

these endogenous opiates, resulting in pain suppression, by applying a ‘Burst-TENS’ current (also referred to as ‘lowfrequency,<br />

high-intensity TENS’ or ‘acupuncture-like TENS’). According to Sjölund <strong>and</strong> Eriksson, endorphins are only<br />

released at a burst frequency of 2-5 Hz, <strong>and</strong> 7 pulses per burst. The amplitude in Burst-TENS should be such that<br />

local muscle contractions occur, without discomfort (limit of tolerance).<br />

Pain reduction in conventional TENS (‘high-frequency, low-intensity TENS’) is ascribed to local, spinal release of<br />

endogenous opiates (encephalins) (27,32,34) .<br />

2.2.3 Postexcitation depression of the sympathetic nervous system (Sato <strong>and</strong> Schmidt)<br />

This theory (26) states that a postexcitation depression of the sympathetic nervous system can be obtained by<br />

stimulating the type II <strong>and</strong> type III nerve fibres. In this case, excessive stimulation of the type IV nerve fibres must be<br />

avoided. In conditions involving overactivity of the sympathetic nervous system the emphasis should therefore be on<br />

stimulating the type II <strong>and</strong> type III fibres.<br />

Trauma with<br />

nerve lesion<br />

Abnormal state of<br />

afferent neurons<br />

Sympathetic<br />

block<br />

Pain<br />

Distorted information<br />

processing in spinal cord<br />

Dysregulation of sympathetic<br />

activity (vasomotor, sudomotor)<br />

Trophic<br />

changes<br />

Fig. 2. Sympathetic reflex dystrophy.<br />

2.3 Selective stimulation<br />

From the foregoing it can be seen that there is a preference for stimulating the type II <strong>and</strong> type III nerve fibres. In<br />

addition, for muscle stimulation, selective stimulation of the type I (Aα) motor neurons is preferred.<br />

Investigators who have concerned themselves with selective stimulation of the peripheral nerves are Howson (8) ,<br />

Lullies (18,19) <strong>and</strong> Wyss (18,35) .<br />

8

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