Effect of Salivariadenectomy and Administration of Salivary Gland Homogenates upon the Reproductive Organs of the Female Rat

1960 ◽  
Vol 39 (3) ◽  
pp. 554-571 ◽  
Author(s):  
Richard P. Suddick
1992 ◽  
Vol 596 (1-2) ◽  
pp. 353-356 ◽  
Author(s):  
Ann Robins ◽  
Karen J. Berkley ◽  
Yuko Sato

1984 ◽  
Vol 247 (5) ◽  
pp. F760-F764 ◽  
Author(s):  
B. H. van Leeuwen ◽  
S. M. Grinblat ◽  
C. I. Johnston

Glandular kallikreins are kinin-generating serine proteases found in the salivary glands, pancreas, reproductive organs, and kidney and in their secretions. They are physico-chemically, enzymatically, and immunologically identical but it is not known whether they perform similar functions at these separate anatomical sites. A specific radioimmunoassay was used to measure immunoreactive kallikrein in these tissues of the rat after various stimuli. Salt depletion significantly increased kallikrein in the kidney from 2.35 +/- 0.17 to 4.11 +/- 0.27 microgram/g tissue (P less than 0.01, 16 DF) and in the salivary glands from 16.8 +/- 2.1 to 24.2 +/- 0.9 mg/g tissue (P less than 0.01, 16 DF), but did not change pancreatic kallikrein. Deoxycorticosterone (2.4 mg s.c. over 8 days) led to a doubling in kidney kallikrein, from 2.35 +/- 0.17 to 5.27 +/- 0.56 microgram/g tissue (P less than 0.01, 18 DF), without changing salivary gland or pancreatic kallikrein, whereas testosterone (240 micrograms/day s.c. over 15 days) significantly increased salivary gland kallikrein from 26.6 +/- 2.1 to 42.2 +/- 1.8 mg/g tissue (P less than 0.01, 18 DF) with no increase in kidney or pancreatic kallikrein. Accordingly, the glandular kallikreins in these tissues vary independently, which suggests they are under different electrolyte and endocrine control and may perform different physiological functions at each anatomical site.


1959 ◽  
Vol 38 (s4) ◽  
pp. 4-22 ◽  
Author(s):  
K. Soiva ◽  
M. Grunroos ◽  
U. K. Rinne ◽  
E. Naatanen

1990 ◽  
Vol 63 (2) ◽  
pp. 256-272 ◽  
Author(s):  
K. J. Berkley ◽  
H. Hotta ◽  
A. Robbins ◽  
Y. Sato

1. Electrophysiological techniques were used to characterize responses of afferent fibers in pelvic nerve of adult, virgin female rats to mechanical or chemical stimulation of internal reproductive organs and to mechanical stimulation of other pelvic organs. 2. In an in vivo barbiturate-anesthetized preparation, pelvic nerve afferent fibers responded to a wide variety of mechanical stimulation applied to restricted regions of the vaginal canal, caudal uterus (body and cervix), bladder, ureter, colon, or anus. 3. Single-fiber mechanoreceptive fields were invariably confined to a single organ. Notably, responses could be evoked not only by gentle stimulation of the unit's receptive field directly on the organ itself, but also by stimulating the field indirectly with intense stimulation through the appropriate part of a contiguous organ. This innervation feature is consistent with the separability of pelvic organ functions under innocuous conditions but their confusion under noxious ones. 4. Receptive fields on the reproductive organs extended from the caudal edge of the vagina to the uterine body (including the cervix) but were most often located in the fornix (vaginocervical junction). Most units had no or low levels of spontaneous activity. Their responses to mechanical stimuli were usually slowly or moderately adapting and time-locked to the stimulus. 5. Fibers with vaginal receptive fields (including the fornix) responded best either to vaginal distension with a balloon or, more often, to a probe moving along the internal vaginal surface in a direction toward the cervix. They were observed most frequently during the proestrus stage of the rat's estrous cycle. These fibers, therefore, seem particularly suited for relaying information about stimuli that occur during mating. 6. Fibers with receptive fields on the uterine cervix and body responded best to static pressure and were observed less frequently than those with vaginal fields, regardless of estrous stage. They were, however, sensitized by hypoxia. In addition, irritation of the uterus increased the probability of observing them. These fibers, therefore, may exert their primary function during reproductive conditions different from those of virgin rats, such as parturition. 7. Response activity of most of the mechanoreceptive afferent fibers supplying reproductive organs increased as the stimulus intensity increased into the noxious range; i.e., into a range in which the stimulus momentarily produced ischemia at the stimulus site. In addition, in an in vitro preparation, pelvic nerve fibers responded in a dose-dependent manner to injections through the uterine artery of bradykinin (BRAD) as well as to other algesic chemicals, 5-hydroxytryptamine (5-HT) and KCl.(ABSTRACT TRUNCATED AT 400 WORDS)


1957 ◽  
Vol 36 (4) ◽  
pp. 559-565 ◽  
Author(s):  
David Bixler ◽  
Richard C. Webster ◽  
Joseph C. Muhler

Endocrinology ◽  
1970 ◽  
Vol 86 (2) ◽  
pp. 429-431 ◽  
Author(s):  
ALFRED BORIS ◽  
JOHN MILMORE ◽  
THELMA TRMAL

2019 ◽  
Vol 42 (2) ◽  
pp. 66-71
Author(s):  
Faraidoon Abdul Sattar Muhamad Amin

The objective of the present study was to assess the effects of various doses of Azorubine which is a food additive on the female reproductive organs in Sprague Dawley rats. Twenty four female Sprgue Dawley rats were divided randomly into 4 equal groups. Group 1(control group), group, 2, 3 and 4 were received Azorubine (5, 10 and 20 mg/kg) orally, daily for 30 days respectively. Blood samples were taken for estimation of white blood cells, red blood cells, hemoglobin and platelets, in addition Luteinizing, follicular stimulation, estrogen and progesterone hormones from the sera. The reproductive hormones levels affected drastically under the effects of different doses of treatment like Luteinizing hormone (0.69±0.25, 0.60±0.75 and 0.55±0.63), Follicular Stimulation hormone (0.17±0.11, 0.13±0.33 and 0.3±0.45), Progesterone hormone (0.50±0.77, 0.14±0.56 and 0.10±0.85), and estrogen hormone (0.45+0.43, 0.30±0.29 and 0.14±0.27) hormones were decreased significantly (P˂0.05) in groups of rats treated with each 5, 10 and 20 mg/kg doses of Azorubine respectively. Histopathologically, the ovaries treated with 5 mg/kg doses of Azorubine showing follicles at the beginning stages of growth with no Graffian follicle while the ovaries with 10 mg/kg doses of Azorubine contain fully grown Graffian follicles with no follicles at various stages as well as those with 20 mg/kg doses of treatment displaying no mature Graffian follicle with many atretic and shrunk follicles. The hematological outcomes are significantly affected by this food additive. The results of this work is concluded that Azorubine can be considered as one of the most important causes of infertility, hormonal disturbances and irregular estrus cycle in the female rat.


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