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1

Oikawa, Hirobumi, Makoto Sasaki, Shigeru Ehara, and Takashi Abe. "Substantia innominata: MR findings in Parkinson?s disease." Neuroradiology 46, no. 10 (2004): 817–21. http://dx.doi.org/10.1007/s00234-004-1257-4.

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2

Grove, Elizabeth A. "Efferent connections of the substantia innominata in the rat." Journal of Comparative Neurology 277, no. 3 (1988): 347–64. http://dx.doi.org/10.1002/cne.902770303.

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3

WENK, G. L. "Pharmacological Manipulation of the Substantia Innominata-Cortical Cholinergic Pathway." Annals of the New York Academy of Sciences 444, no. 1 Memory Dysfun (1985): 541–42. http://dx.doi.org/10.1111/j.1749-6632.1985.tb37640.x.

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4

Mori, Norio, Shuzo Hoshino, and Hisashi Kumashiro. "Comparison between substantia innominata and amygdala kindling in rats." Brain Research 534, no. 1-2 (1990): 329–31. http://dx.doi.org/10.1016/0006-8993(90)90151-z.

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5

Ota, Kazuki, Takanari Kitazono, Hiroaki Ooboshi, et al. "Role of substantia innominata in cerebral blood flow autoregulation." Brain Research 1135 (March 2007): 146–53. http://dx.doi.org/10.1016/j.brainres.2006.12.017.

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6

Khanamiryan, T. V. "Participation of the substantia innominata in differential inhibition in cats." Neuroscience and Behavioral Physiology 18, no. 1 (1988): 4–9. http://dx.doi.org/10.1007/bf01186898.

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7

Zhu, Zhenggang, Qingqing Ma, Lu Miao, et al. "A substantia innominata-midbrain circuit controls a general aggressive response." Neuron 109, no. 9 (2021): 1540–53. http://dx.doi.org/10.1016/j.neuron.2021.03.002.

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8

Hanyu, Haruo, Soichiro Shimizu, Yuriko Tanaka, Kentaro Hirao, Toshihiko Iwamoto, and Kimihiko Abe. "MR features of the substantia innominata and therapeutic implications in dementias." Neurobiology of Aging 28, no. 4 (2007): 548–54. http://dx.doi.org/10.1016/j.neurobiolaging.2006.02.009.

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9

Formaggio, E., A. C. Dalfini, F. Fazzini, G. Fumagalli, and C. Chiamulera. "GABAergic neurons expressing p75 in rat substantia innominata and nucleus basalis." Molecular and Cellular Neuroscience 46, no. 3 (2011): 625–32. http://dx.doi.org/10.1016/j.mcn.2011.01.002.

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10

Grove, Elizabeth A. "Neural associations of the substantia innominata in the rat: Afferent connections." Journal of Comparative Neurology 277, no. 3 (1988): 315–46. http://dx.doi.org/10.1002/cne.902770302.

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11

Storozhuk, V. M., and L. �. Zinyuk. "Neuronal responses in the cat substantia innominata during instrumental conditioned reflex." Neurophysiology 21, no. 6 (1990): 568–74. http://dx.doi.org/10.1007/bf01051955.

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12

Austin, Mark C., and Peter W. Kalivas. "Dopaminergic involvement in locomotion elicited from the ventral pallidum/substantia innominata." Brain Research 542, no. 1 (1991): 123–31. http://dx.doi.org/10.1016/0006-8993(91)91005-l.

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13

Cui, Yuting, Guanghui Lv, Sen Jin, et al. "A Central Amygdala-Substantia Innominata Neural Circuitry Encodes Aversive Reinforcement Signals." Cell Reports 21, no. 7 (2017): 1770–82. http://dx.doi.org/10.1016/j.celrep.2017.10.062.

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14

Zhu, Zhenggang, Yanqin Yu, and Shumin Duan. "Universal control of diverse aggressive behaviors by the posterior substantia innominata." IBRO Reports 6 (September 2019): S407. http://dx.doi.org/10.1016/j.ibror.2019.07.1297.

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15

Osman, Nadir I., Helen A. Baghdoyan, and Ralph Lydic. "Morphine Inhibits Acetylcholine Release in Rat Prefrontal Cortex When Delivered Systemically or by Microdialysis to Basal Forebrain." Anesthesiology 103, no. 4 (2005): 779–87. http://dx.doi.org/10.1097/00000542-200510000-00016.

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Background Cortical acetylcholine originates in the basal forebrain and is essential for maintaining normal cognition and arousal. Morphine impairs these cholinergically mediated cortical functions. The current study tested the hypothesis that morphine decreases prefrontal cortical acetylcholine release by acting at the level of the basal forebrain. Methods Adult male Sprague-Dawley rats (n = 18) were anesthetized with isoflurane. One microdialysis probe was placed in the substantia innominata region of the basal forebrain and perfused with Ringer's solution (control) followed by one concentra
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16

Gauthier, Elizabeth A., Sarah E. Guzick, Chad M. Brummett, Helen A. Baghdoyan, and Ralph Lydic. "Buprenorphine Disrupts Sleep and Decreases Adenosine Concentrations in Sleep-regulating Brain Regions of Sprague Dawley Rat." Anesthesiology 115, no. 4 (2011): 743–53. http://dx.doi.org/10.1097/aln.0b013e31822e9f85.

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Background Buprenorphine, a partial μ-opioid receptor agonist and κ-opioid receptor antagonist, is an effective analgesic. The effects of buprenorphine on sleep have not been well characterized. This study tested the hypothesis that an antinociceptive dose of buprenorphine decreases sleep and decreases adenosine concentrations in regions of the basal forebrain and pontine brainstem that regulate sleep. Methods Male Sprague Dawley rats were implanted with intravenous catheters and electrodes for recording states of wakefulness and sleep. Buprenorphine (1 mg/kg) was administered systemically via
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17

Heimer, L., R. E. Harlan, G. F. Alheid, M. M. Garcia, and J. de Olmos. "Substantia innominata: a notion which impedes clinical–anatomical correlations in neuropsychiatric disorders." Neuroscience 76, no. 4 (1997): 957–1006. http://dx.doi.org/10.1016/s0306-4522(96)00405-8.

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18

Mariotti, Maurizio, Ivana Gritti, and Mauro Mancia. "The synchronising influence of Substantia Innominata on the thalamus of the cat." Journal of Sleep Research 10, no. 2 (2001): 143–52. http://dx.doi.org/10.1046/j.1365-2869.2001.00246.x.

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19

Russchen, F. T., D. G. Amaral, and J. L. Price. "The afferent connections of the substantia innominata in the monkey,Macaca fascicularis." Journal of Comparative Neurology 242, no. 1 (1985): 1–27. http://dx.doi.org/10.1002/cne.902420102.

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20

Sotorzhuk, V. M., and L. E. Zinyuk. "Neocortex neuron reactions caused by stimulation of the substantia innominata in cats." Neurophysiology 24, no. 1 (1992): 7–14. http://dx.doi.org/10.1007/bf01053476.

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21

Sarter, Martin. "The substantia innominata remains incognita: pressing research themes on basal forebrain neuroanatomy." Brain Structure and Function 213, no. 1-2 (2008): 11–15. http://dx.doi.org/10.1007/s00429-007-0165-x.

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22

Napier, T. Celeste, and Pamela E. Potter. "Dopamine in the rat ventral pallidum/substantia innominata: Biochemical and electrophysiological studies." Neuropharmacology 28, no. 7 (1989): 757–60. http://dx.doi.org/10.1016/0028-3908(89)90163-9.

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23

Marazioti, A., A. Kastellakis, K. Antoniou, D. Papasava, and K. Thermos. "Somatostatin receptors in the ventral pallidum/substantia innominata modulate rat locomotor activity." Psychopharmacology 181, no. 2 (2005): 319–26. http://dx.doi.org/10.1007/s00213-005-2237-z.

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24

Peruzzi, Philippe, Pierre Lacombe, Véronique Moro, Elvire Vaucher, Françoise Levy, and Jacques Seylaz. "The Cerebrovascular Effects of Physostigmine Are Not Mediated through the Substantia Innominata." Experimental Neurology 122, no. 2 (1993): 319–26. http://dx.doi.org/10.1006/exnr.1993.1131.

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25

MORITA, Kyohei. "GABAergic system in substantia innominata inhibits the secondary generalization of amygdaloid kindled seizure." Okayama Igakkai Zasshi (Journal of Okayama Medical Association) 97, no. 11-12 (1985): 973–91. http://dx.doi.org/10.4044/joma1947.97.11-12_973.

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26

Storozhuk, Victor M., and Larissa E. Zinjuk. "Influence of substantia innominata neuronal activity on neocortex neuronal reactions during conditioned reflex." Brain Research 550, no. 1 (1991): 169–71. http://dx.doi.org/10.1016/0006-8993(91)90424-t.

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27

van den Bos, Ruud, and Alexander R. Cools. "Motor activity and the GABAA-receptor in the ventral pallidum/substantia innominata complex." Neuroscience Letters 124, no. 2 (1991): 246–50. http://dx.doi.org/10.1016/0304-3940(91)90105-3.

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28

de Belleroche, J., I. M. Gardiner, M. H. Hamilton, and N. J. M. Birdsall. "Analysis of muscarinic receptor concentration and subtypes following lesion of rat substantia innominata." Brain Research 340, no. 2 (1985): 201–9. http://dx.doi.org/10.1016/0006-8993(85)90915-1.

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29

Sarter, M., and H. H. Schneider. "High density of benzodiazepine binding sites in the substantia innominata of the rat." Pharmacology Biochemistry and Behavior 30, no. 3 (1988): 679–82. http://dx.doi.org/10.1016/0091-3057(88)90083-4.

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30

George, S., E. J. Mufson, S. Leurgans, R. C. Shah, C. Ferrari, and L. deToledo-Morrell. "MRI-based volumetric measurement of the substantia innominata in amnestic MCI and mild AD." Neurobiology of Aging 32, no. 10 (2011): 1756–64. http://dx.doi.org/10.1016/j.neurobiolaging.2009.11.006.

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31

Kunimoto, Masayuki, Shigeya Tanaka, Tatsuya Tanaka, and Yukichi Yonemasu. "Ibotenic Acid-Induced Lesions of Substantia Innominata on Focal Limbic Seizures in Chronic Cats." Psychiatry and Clinical Neurosciences 41, no. 3 (1987): 508–9. http://dx.doi.org/10.1111/j.1440-1819.1987.tb01747.x.

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32

Ellison, David W., Neil W. Kowall, and Joseph B. Martin. "Subset of neurons characterized by the presence of NADPH-diaphorase in human substantia innominata." Journal of Comparative Neurology 260, no. 2 (1987): 233–45. http://dx.doi.org/10.1002/cne.902600207.

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33

Napier, T. Celeste, James J. Chrobak, and Jay Yew. "Systemic and microiontophoretic administration of morphine differentially effect ventral pallidum/substantia innominata neuronal activity." Synapse 12, no. 3 (1992): 214–19. http://dx.doi.org/10.1002/syn.890120306.

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34

Benzing, William C., and Elliott J. Mufson. "Increased number of NADPH-d-positive neurons within the substantia innominata in Alzheimer's disease." Brain Research 670, no. 2 (1995): 351–55. http://dx.doi.org/10.1016/0006-8993(94)01362-l.

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35

Mihara, Ban. "Effects of lesions in the substantia innominata on active avoidance task and cerebral glucose metabolism." Keio Journal of Medicine 38, no. 4 (1989): 419–31. http://dx.doi.org/10.2302/kjm.38.419.

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36

Choi, Seo Hee, Tae Min Jung, Ji E. Lee, Seung-Koo Lee, Young H. Sohn, and Phil Hyu Lee. "Volumetric analysis of the substantia innominata in patients with Parkinson's disease according to cognitive status." Neurobiology of Aging 33, no. 7 (2012): 1265–72. http://dx.doi.org/10.1016/j.neurobiolaging.2010.11.015.

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37

Numan, Michael, Keith P. Corodimas, Marilyn J. Numan, Elizabeth M. Factor, and Wayne D. Piers. "Axon-sparing lesions of the preoptic region and substantia innominata disrupt maternal behavior in rats." Behavioral Neuroscience 102, no. 3 (1988): 381–96. http://dx.doi.org/10.1037/0735-7044.102.3.381.

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38

Knox, Dayan, Holly Brothers, Greg J. Norman, and Gary G. Berntson. "Nucleus basalis magnocellularis and substantia innominata corticopetal cholinergic lesions attenuate freezing induced by predator odor." Behavioral Neuroscience 122, no. 3 (2008): 601–10. http://dx.doi.org/10.1037/0735-7044.122.3.601.

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39

Shreve, Paul E., and Norman J. Uretsky. "GABA and glutamate interact in the substantia innominata/lateral preoptic area to modulate locomotor activity." Pharmacology Biochemistry and Behavior 38, no. 2 (1991): 385–88. http://dx.doi.org/10.1016/0091-3057(91)90296-e.

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40

Morita, K., M. Okamoto, K. Seki, and J. A. Wada. "Suppression of amygdala-kindled seizure in cats by enhanced GABAergic transmission in the substantia innominata." Experimental Neurology 89, no. 1 (1985): 225–36. http://dx.doi.org/10.1016/0014-4886(85)90278-x.

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41

Vaucher, Elvire, François Dauphin, Jacques Seylaz, and Pierre Lacombe. "Autoradiographic study of the cerebrovascular effects of stimulation of the substantia innominata: convenient stimulation paradigm." Journal of the Autonomic Nervous System 49 (September 1994): 43–47. http://dx.doi.org/10.1016/0165-1838(94)90085-x.

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42

Stær, Kristian, Alex Iranzo, Morten G. Stokholm, et al. "Cortical cholinergic dysfunction correlates with microglial activation in the substantia innominata in REM sleep behavior disorder." Parkinsonism & Related Disorders 81 (December 2020): 89–93. http://dx.doi.org/10.1016/j.parkreldis.2020.10.014.

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43

Wright, Christopher I., Brian Martis, Carl E. Schwartz, et al. "Novelty responses and differential effects of order in the amygdala, substantia innominata, and inferior temporal cortex." NeuroImage 18, no. 3 (2003): 660–69. http://dx.doi.org/10.1016/s1053-8119(02)00037-x.

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44

Gasbarri, A., A. Sulli, C. Pacitti, and J. L. McGaugh. "Serotonergic input to cholinergic neurons in the substantia innominata and nucleus basalis magnocellularis in the rat." Neuroscience 91, no. 3 (1999): 1129–42. http://dx.doi.org/10.1016/s0306-4522(98)00672-1.

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45

Holland, P. C. "Different Roles for Amygdala Central Nucleus and Substantia Innominata in the Surprise-Induced Enhancement of Learning." Journal of Neuroscience 26, no. 14 (2006): 3791–97. http://dx.doi.org/10.1523/jneurosci.0390-06.2006.

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46

Gomi, Shintaro, Fumio Gotoh, Naoki Ishihara, et al. "Effects of Lesioning of the Substantia Innominata on Autoregulation of Local Cerebral Blood Flow in Rats." Journal of Cerebral Blood Flow & Metabolism 11, no. 1 (1991): 66–71. http://dx.doi.org/10.1038/jcbfm.1991.7.

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Recently, accumulated data have suggested that the nucleus basalis magnocellularis, i.e., the substantia innominata (SI), may represent the primary source of central cholinergic innervation in the rat cortical vasculature. We therefore examined the effects of unilateral lesion of the SI on the autoregulation of local CBF (1CBF) during induced hypotension in rats. Male Wistar rats were divided into three groups. The animals of groups 1 and 2 received an injection of 5 μg of ibotenate into the right SI stereotaxically. At 7 days after the injection, the 1CBF was measured by the [14C]iodoantipyri
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47

KIM, HACKJIN, LEAH H. SOMERVILLE, ASHLY A. McLEAN, TOM JOHNSTONE, LISA M. SHIN, and PAUL J. WHALEN. "Functional MRI Responses of the Human Dorsal Amygdala/Substantia Innominata Region to Facial Expressions of Emotion." Annals of the New York Academy of Sciences 985, no. 1 (2006): 533–35. http://dx.doi.org/10.1111/j.1749-6632.2003.tb07120.x.

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48

Barbeliview, Alexandra, Eric T. MacKenzie, and François Dauphin. "Regional cerebral blood flow responses to neurochemical stimulation of the substantia innominata in the anaesthetized rat." Neuroscience Letters 190, no. 2 (1995): 81–84. http://dx.doi.org/10.1016/0304-3940(95)11506-r.

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49

Kowall, Neil W., and M. Flint Beal. "Galanin-like immunoreactivity is present in human substantia innominata and in senile plaques in Alzheimer's disease." Neuroscience Letters 98, no. 1 (1989): 118–23. http://dx.doi.org/10.1016/0304-3940(89)90384-4.

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50

Cromwell, Howard C., and Kent C. Berridge. "Where does damage lead to enhanced food aversion: the ventral pallidum/substantia innominata or lateral hypothalamus?" Brain Research 624, no. 1-2 (1993): 1–10. http://dx.doi.org/10.1016/0006-8993(93)90053-p.

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