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 |
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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 |
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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)
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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 |
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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 |
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