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. 2020 Apr 2;14:264. doi: 10.3389/fnins.2020.00264

TABLE 2.

Summary of experimental procedures and stimulation parameters for reviewed studies concerning both invasive and non-invasive stimulation.

Evoked Cell Potentials
Authors Species Strain Type of Stimulation Bilateral or Unilateral Stimulation? Structures Stimulated Time of Day of Stimulation Overall Stimulation Time Period Stimulus Pulse Duration Stimulation Frequency/voltage Stimulation Current Lighting Conditions During Stimulation Anaesthesia Used During Stimulation Time of Sacrifice Lighting Conditions During Sacrifice Substance Measured Collection Method
Brooks et al., 1975 Rat White Invasive electrical Bilateral Cervical sympathetic trunks Not described 48 s 1 every 1.25 s 30 Hz Not described Not described Urethane Not described Not described N/A N/A
Ronnekleiv et al., 1980 Rat Sprague Dawley Invasive Electrical Not described Medial habenular nucleus Usually > 18:00 Not described 50– 200 μs Up to 10 Hz 0.001− 0.1 mA Darkened room Urethane Following stimulation Not described N/A N/A
Pazo, 1981 Rat Wistar Invasive electrical Habenular complex: bilaterally, sciatic nerve: unilaterally, septal area: unclear, optic tract: unclear Sciatic nerve, habenular complex and adjacent stria medullary, septal area, optic tract 10:00– 18:00 Not described 0.5 ms Not described Variable intensity Relatively dark room with no direct light on the animals Ether Not described Not described N/A N/A
Semm et al., 1981 Guinea-pig N/A Invasive electrical Bilateral Lateral habenular nuclei Daytime 50−100 ms (train) 0.5 ms 100 Hz 0.5 mA Darkened room Urethane, pentobarbitone. glucose, gallamine triethiodide mixture Not described Not described N/A N/A
Bowers and Zigmond, 1982 Rat Sprague Dawley Invasive Electrical Bilateral Cervical sympathetic trunks Night-time Not described 0.5, 1.0, 3.0, 5.0, and 20 ms 10 Hz ∼5 – 60 μA Not described Chloral Hydrate Not described Not described N/A N/A
Reuss et al., 1984 Rat Not described Invasive Electrical Bilateral Lateral habenular nuclei Daytime Not described 0.1– 0.5 ms 1–10 Hz 0.1–0.5 mA (occasionally up to 5 mA) Darkened room Urethane and pentobarbital Not described Not described N/A N/A
Reuss et al., 1985b Rat Sprague Dawley Invasive electrical Both SCG 09:00–18:00 Not described 0.2 ms 10 Hz 0.1–0.5 mA “Natural lighting conditions” Urethane Not described Not described N/A N/A
Reyes-Vazquez et al., 1986 Rat Sprague Dawley Invasive electrical Bilateral Postganglionic nerve fibres of the SCG Not described Not described 0.2 ms 1 Hz 0.1– 0.6 mA Ordinary room illumination during light cycle Urethane Following stimulation Not described N/A N/A
Stehle et al., 1987 Hamster Golden Invasive electrical SCG: unilateral, habenular nuclei: bilateral SCG and lateral habenular nuclei During the dark and light periods <17 h 0.2ms 2–20 Hz 0.2 mA for habenular and optic but up to 2mA for the SCG Not described Urethane Not described Not described N/A N/A
Evoked Cell Potentials
Patel and Demaine, 1990 Hamster Golden Invasive electrical Both SCG up to 6 h after 15:30 Not described 0.5–1 ms 10–20 Hz 0.5–1 mA Artificial lab lighting Urethane Not described Not described N/A N/A
Pazo and Gonzalez, 1991 Rat Wistar Invasive electrical Unilateral SCG and sciatic nerve 09:00–18:00 Not described 0.5 ms Not described Up to 0.5 mA “Relatively dark room with no direct light on the animal during daylight” Urethane Not described Not described N/A N/A
Indoleamine Output and Enzymatic Activity
Brownstein and Heller, 1968 Rat Holtzman Invasive electrical Unilateral Preganglionic cervical sympathetic fibres Not described 4 h 9 s on; 51 s off 10 Hz 3–5 mA Not described but animals blinded Ether 4-h post-op Not described but animals blinded HIOMT Pineal homogenization
Volkman and Heller, 1971 Rat Holtzman Invasive electrical Unilateral Preganglionic cervical sympathetic trunk Daytime/light phase 1, 2, or 3 h 10 ms for 9 s every min 10 Hz 2x that required to produce maximal exophthalmos in the eye (2 × 0.23 mA) Not described Ether Immediately or 1-h post-stimulation cessation Not described AANAT Pineal homogenization
Bowers and Zigmond, 1980 Rat Sprague Dawley Invasive electrical Bilateral Cervical sympathetic trunks >4 h after darkness onset Animals were not stimulated past the time were lights would normally turn on 0.5 ms 5 Hz 0.4–2.0 mA Exposed to light for 15 min prior to anaesthetic administration for SCG exposure to reduce night-time AANAT levels by more than 95% Chloral hydrate Immediately post-stimulation – before the onset of the light period Dim red light AANAT Pineal homogenization
Heydorn et al., 1981 Rat (ex vivo) Sprague Dawley Invasive electrical Bilateral SCG Not described 1 min 10 ms 10 Hz (10 V) Not described Not described Not described Not described Not described cAMP Pineal homogenization
Evoked Cell Potentials
Bowers and Zigmond, 1982 Rat Sprague Dawley Invasive electrical Both Cervical sympathetic trunks Night (>4 h into night period) AND day (>4 h into light period) 0.5, 1, 1.5, and 2 h 0.5 ms 10 Hz 2x that require to produce maximal exophthalmos of the ipsilateral eye (values ranged for each nerve from 100–1000uA) Not described Chloral hydrate Immediately following stimulation Not described AANAT Pineal homogenization
Bowers et al., 1984a Rat Sprague Dawley Invasive electrical Bilateral Cervical sympathetic trunks >4 h into light period 3 h Not described 5 Hz 2x that required to produce maximal exophthalmos in the ipsilateral eye >4 h into light period Chloral hydrate >7 h into light period Dimred light AANAT Pineal homogenization
Reuss et al., 1985a Rats Sprague Dawley Invasive electrical Bilateral PVN Daytime experiments: 11:00–13:00; Night-time experiments: 00:00–06:00 15, 30, 60 min 0.2 ms 10 Hz 0.1 mA Normal artificial light Urethane Following stimulation Normal artificial light but animals blinded for night-time experiments AANAT, melatonin Pineal homogenization
Olcese et al., 1987 Rat Sprague Dawley Invasive electrical Bilateral PVN >02:00 2 min 0.2 ms 10 Hz 0.1 mA Yes, but all animals blinded surgically Urethane 30 min post-stimulation Artificial light but animals are blinded Melatonin, NE Pineal homogenization
Reuss et al., 1989 Rat Sprague Dawley Invasive electrical Bilateral SCG 10:00–14:00 (1) 120 min; (2a + b) 15 min (1) 0.5 ms; (2a) 0.5 ms; (2b) 1 ms (1) 10 Hz; (2a) 10 Hz; (2b) 25 Hz (1) 0.5 mA; (2a + b) 0.5 mA Not described Urethane (1) 2 h after stimulation onset; (2) immediately following stimulation Not described AANAT Pineal homogenization of 2/3 of each gland
Chan et al., 1989 Rabbit New Zealand Invasive electrical Unilateral Left preganglionic cervical sympathetic trunk Light phase 24– 60 min 60 ms every 2 s OR 7.5 s every 20 s 300 Hz 1–5 mA Not described Pentobarbital Not described Not described Melatonin Blood (plasma) sampling from the confluens sinuum
Lingappa and Zigmond, 2013 Rat Sprague Dawley Invasive electrical Bilateral Cervical sympathetic trunks 4–8 h into daytime 3 h 0.5 ms 10, 5, 2.5, and 1 Hz (10 Hz was considered optimal for AANAT stimulation) 0.2–0.8 mA Not described Chloral hydrate Immediately after stimulation (stimulation carried out 4–8 h into daytime) Not described AANAT Pineal homogenization
Non-invasive Stimulation
McIntyre and Oxenkrug, 1984 Rat Sprague Dawley Non-invasive electrical Bilateral Ears Before 12:00 One shock every day for 7 days 0.75 s 130 V Not described Not described Not described 2100h Dim red light 5-HT, melatonin, NAS Pineal homogenization
Nowak et al., 1988 Rat Wistar Non-invasive electrical Bilateral Ears At the end of the light phase with the very final treatment being given at 22:00 A single electric sock or 10 shocks per day over 10 consecutive days 500 ms 50 Hz 70 mA (to induce tonic-clonic seizures) Not described Not described 1 or 2 h after the final stimulation Light or dim-red light AANAT, HIOMT Pineal homogenization
Oxenkrug et al., 1991 Rat Sprague Dawley Non-invasive electrical Bilateral Ears 10:00 Not described 0.75 s 130 V Not described Not described Not described 90 min after stimulation Not described Melatonin, serotonin, 5-HIAA. NAS Pineal homogenization
Chao et al., 2001 Rat Wistar Percutaneous electrical nerve stimulation N/A Fengfu DU16 and Jinsuo DU8 Not described 30 or 60 min Not described 80 Hz 1.7–2.5 mA Not described Sodium pentobarbital After stimulation Not described Melatonin Pineal homogenization
Spence et al., 2004 Humans Humans with anxiety and insomnia (but no diagnosed anxiety disorder) Acupuncture Not described Not described Not described 2× a week for 5 weeks 1 hr per session N/A N/A N/A N/A N/A N/A Melatonin Measurement of urinary melatonin metabolite aMT6s
Kayumov et al., 2003 Humans Humans with insomnia and anxiety Acupuncture Not described Not described Not described 2× a week for 5 weeks N/A N/A N/A Not described N/A N/A N/A Melatonin Measurement of urinary melatonin metabolite aMT6s
Li et al., 2014 Rat Zucker diabetic fatty and Zucker lean Non-invasive electrical Bilateral Right side auricular concha region 14:00–17:00 30 min for 34 consecutive days Not described 2 and 15 Hz alternating every sec 2 mA Not described Isoflurane Not described Not described Melatonin Blood (plasma) sampling from the tail vein
Wang et al., 2015 Rat Zucker diabetic fatty Non-invasive electrical Bilateral Right side auricular concha region Afternoon 30 min Not described 2 and 15 Hz switched every sec 2 mA Not described Isoflurane Not described Not described Melatonin Blood (plasma) sampling from the tail vein