The DOI matches its Crossref record; 25 of the 25 references it cites were found in a registry or an index.
Two types of hippocampal rhythmical slow activity in both the rabbit and the rat: Relations to behavior and effects of atropine, diethyl ether, urethane, and pentobarbital
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In the citing paper
“Classical work in rodents has demonstrated the existence of two mechanistically distinct types of theta oscillations: fast Type-1 (atropine-insensitive) theta oscillations (7–11 Hz), which are observed during locomotion, and slower Type-2 (atropine-sensitive) oscillations (4–7 Hz), which are thought to preferentially occur during immobility26–28,42,50,97.”
From Place and behavioral modulation of hippocampal neurons during immobility (2026) · cites this paper as [97]
In the citing paper
“the in vivo theta rhythm has been reported to be either atropine resistant or atropine sensitive”
From Interneuronal mechanisms of hippocampal theta oscillations in a full-scale model of the rodent CA1 circuit (2016) · cites this paper as Kramis et al., 1975
In the citing paper
“the former is typically associated with walking and may not be dependent on neuromodulatory inputs”
From Interneuronal mechanisms of hippocampal theta oscillations in a full-scale model of the rodent CA1 circuit (2016) · cites this paper as Kramis et al., 1975
In the citing paper
“the latter requires intact, rhythmic cholinergic inputs”
From Interneuronal mechanisms of hippocampal theta oscillations in a full-scale model of the rodent CA1 circuit (2016) · cites this paper as Kramis et al., 1975
Citations
Cites
The rat brain: A stereotaxic atlas of the forebrain and lower parts of the brain stem
König, J. F. R., & Klippel, R. (1986) · Medical Entomology and Zoology · Cited by 4,134
Hippocampal electrical activity and voluntary movement in the rat
Vanderwolf, C. H. (1969) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(69)90092-3 · Cited by 1,928
Self-citationStudies on single neurons in dorsal hippocampal formation and septum in unrestrained rats
Ranck, J. B. (1973) · Experimental Neurology · doi:10.1016/0014-4886(73)90290-2 · Cited by 1,322
THE ASCENDING CHOLINERGIC RETICULAR SYSTEM: NEOCORTICAL, OLFACTORY AND SUBCORTICAL PROJECTIONS
Shute, C. C. D., & Lewis, P. R. (1967) · Brain · doi:10.1093/brain/90.3.497 · Cited by 1,120
Lewis, P. R., & Shute, C. C. D. (1967) · Brain · doi:10.1093/brain/90.3.521 · Cited by 969
Whishaw, I. Q., & Vanderwolf, C. H. (1973) · Behavioral Biology · doi:10.1016/s0091-6773(73)80041-0 · Cited by 508
Self-citationVanderwolf, C. H. (1975) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0076211 · Cited by 420
Self-citationPatterns of hippocampal theta rhythm in the freely moving rat
Winson, J. (1974) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/0013-4694(74)90171-0 · Cited by 332
Hippocampal Rhythmic Slow Activity and Neocortical Low-Voltage Fast Activity: Relations to Behavior
Vanderwolf, C. H., Kramis, R. C., Gillespie, L. A., & Bland, B. H. (1975) · Springer eBooks · doi:10.1007/978-1-4684-2979-4_3 · Cited by 253
Self-citationInterspecies differences in the occurrence of theta
Winson, J. (1972) · Behavioral Biology · doi:10.1016/s0091-6773(72)80210-4 · Cited by 231
Research works printed but not linked: 3
- Bennett, 1969, Evidence against the theory that hippocampal theta is a correlate of voluntary movement, Commun. Behav. Biol., 4, 165
- Bennett, 1971, Hippocampal theta activity and behavior—A review, Comm. Behav. Biol., 6, 37
- Kim, 1956, Electroencephalographic study comparing effects of neuropharmacological agents on limbic and neocortical structures, Electroenceph. Clin. Neurophysiol., 8, 524
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Metadata
- Authors
- Kramis, R., Vanderwolf, C. H., & Bland, B. H.
- Affiliations
- Western University (CA)
- Corresponding author
- Vanderwolf, C.H.
- Venue
- Experimental Neurology
- Publisher
- Elsevier BV
- Published
- 1975-10
- Volume
- 49
- Issue
- 1
- Pages
- 58-85
- ISSN
- 0014-4886 (ISSN-L)
- OpenAlex
- W2049289902
- Cited by
- 791
- References
- 25
- Citations by year
- 2026: 16 · 2025: 26 · 2024: 15 · 2023: 23 · 2022: 25 · 2021: 28 · 2020: 23 · 2019: 19 · 2018: 20 · 2017: 31 · 2016: 15 · 2015: 22 · 2014: 24 · 2013: 29 · 2012: 24
- FWCI
- 8.10
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Experimental Neurology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Sleep and Wakefulness Research
- Keywords
- hippocampal theta rhythm, atropine sensitivity, urethane anesthesia, pentobarbital, hypothalamic stimulation, midbrain reticular formation, drug effects on behavior
- MeSH terms
- Animals, Atropine, Dose-Response Relationship, Drug, Drinking Behavior, Electroencephalography, Ether, Ethyl Ethers, Feeding Behavior, Grooming, Hippocampus, Hypothalamus, Mesencephalon, Motor Activity, Neural Pathways, Pentobarbital, Posture, Rabbits, Reticular Formation, Theta Rhythm, Urethane, Rats
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