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Brain Research | 1983

Effects of estrogen on the excitability of neurons projecting from the noradrenergic A1 region to the preoptic and anterior hypothalamic area

Hideto Kaba; Hideo Saito; Kuniaki Otsuka; Katsuo Seto; Masazumi Kawakami

Estradiol benzoate administered to ovariectomized female rats significantly elevated the mean spontaneous firing rate and frequency of successful antidromic propagation into the somatodendritic spike and significantly reduced the strength of post-stimulus inhibition in presumed A1 noradrenergic neurons projecting directly to the preoptic and anterior hypothalamic area. The occurrence of both antidromic spikes and post-stimulus inhibition of the majority of these neurons was completely abolished by the injection of 6-hydroxydopamine but not by 5, 7-dihydroxytryptamine directly into the medial forebrain bundle.


Progress in Brain Research | 1967

Mechanisms in the Limbic System Controlling Reproductive Functions of the Ovary with Special Reference to the Positive Feedback of Progestin to the Hippocampus

Masazumi Kawakami; Katsuo Seto; Ei Terasawa; Kazuchika Yoshida

Publisher Summary The purpose of this chapter is to discuss mechanisms in the limbic system controlling reproductive functions of the ovary with special reference to the positive feedback of progestin to the hippocampus. The mechanism by which limbic structures modulate the function of the hypothalamo-hypophysial system is undoubtedly neural in character. On the other hand, it is inferred that the sex hormone and gonadotrophin act on the excitabilities of the limbic structures. The experiments are given in the chapter is designed to demonstrate the existence of positive feedback control of the hippocampus on ovarian progesterone formation and its output, as well as the existence of negative feedback control of the amygdala on ovarian progesterone formation and its output. In conclusion, the results of these experiments support the presumption that the hippocampus and the amygdala are the critical areas of feedback control of progesterone: the hippocampo-hypothalamo-pituitary-gonad axis is a loop of the positive feedback of progesterone and the medial amygdaloid complex a loop of the negative feedback of progesterone.


Neuroendocrinology | 1972

Influence of Repeated Immobilization Stress upon the Circadian Rhythmicity of Adrenocorticoid Biosynthesis

M. Kawvakami; Katsuo Seto; Fukuko Kimura

Experiments were carried out to elucidate the influence of stress on the diurnal change in adrenal biosynthetic activity during controlled 24 h light-dark cycles. stress Groups of 10 rabbits were deca


Neuroendocrinology | 1969

Biosynthesis of Ovarian Steroids in the Rabbit: Influence of Progesterone or Estradiol Implantation into the Hypothalamus and Limbic Structures

Masazumi Kawakami; Katsuo Seto; K. Yoshida; T. Miyamoto

The feedback action of progesterone and estradiol implants in the hippocampus amygdala and hypothalamus was investigated and their influence on the incorporation of acetate-1-carbon-14 into ovarian steroids by ovarian homogenate in rabbits was estimated. Progesterone implants in the alverus of the hippocampus markedly increased carbon-14 progestin formation. This region may be part of a positive feedback mechanism that regulates progestin production. Carbon-14-estrogen formation was markedly suppressed by estradiol implants in the medial nucleus of the amygadala which implies that the site is related to the negative feedback control of estrogen formation. Estradiol implants in various sites of the amygdala resulted in a decrease in progestin labeling. Progesterone implants in the medial preoptic area suppressed carbon-14-estrogen formation and those placed in the periventricular arcuate nucleus and the ventromedial hypothalamus nucleus encouraged carbon-14-estrogen formation. It is suggested that the periventricular arcuate nucleus and ventromedial hypothalamus nucleus are involved in different feedback mechanisms for progestin and estrogen formaton and that the medial preoptic area is involved in the reciprocal feedback control of estrogen formation. Estrogen implants inhibited estrogen formation in the medial preoptic area anterior hypothalamic area ventromedial hypothalamic nucleus and periventricular arcuate nucleus and facilitated estrogen formation in the supraoptic nucleus. Estradiol implants in the medial preoptic area anterior hypothalamic area and ventromedial hypothalamic nucleus facilitated progestin periventricular arcuate nucleus.


Neuroendocrinology | 1968

Influence of electrical stimulation and lesion in limbic structure upon biosynthesis of adrenocorticoid in the rabbit.

Masazumi Kawakami; Katsuo Seto; E. Terasawa; K. Yoshida; T. Miyamoto; M. Sekiguchi; Y. Hattori


Neuroendocrinology | 1968

Influence of Corticosterone Implantation in Limbic Structure upon Biosynthesis of Adrenocortical Steroid

Masazumi Kawakami; Katsuo Seto; K. Yoshida


Japanese Journal of Physiology | 1966

INFLUENCE OF THE LIMBIC SYSTEM ON OVULATION AND ON PROGESTERONE AND ESTROGEN FORMATION IN RABBIT'S OVARY

Masazumi Kawakami; Katsuo Seto; Kazuchika Yoshida


Endocrinologia Japonica | 1971

Effect of Electrical Stimulation of the Medial Preoptic Area on Hypothalamic Multiple Unit Activity in Relation to LH Release

Masazumi Kawakami; Ei Terasawa; Katsuo Seto; Katsumi Wakabayashi


Japanese Journal of Physiology | 1968

INFLUENCES OF THE LIMBIC STRUCTURE ON BIOSYNTHESIS OF OVARIAN STEROIDS IN RABBITS

Masazumi Kawakami; Katsuo Seto; Kazuchika Yoshida


Endocrinologia Japonica | 1972

Influence of the fornix section on the biosynthesis of ovarian steroids in the rabbit.

Masazumi Kawakami; Katsuo Seto; Fukuko Kimura; Masahiro Yanase

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Fukuko Kimura

Yokohama City University

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K. Yoshida

Yokohama City University

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T. Miyamoto

Yokohama City University

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Ei Terasawa

University of Wisconsin-Madison

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E. Terasawa

Yokohama City University

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Hideo Saito

Yokohama City University

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Hideto Kaba

Yokohama City University

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Katsumi Wakabayashi

National Institute of Radiological Sciences

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