EFFECT OF SEX HORMONES ON EHRLICH MOUSE ASCITES CANCER

1960 ◽  
Vol XXXIV (III) ◽  
pp. 437-448
Author(s):  
C. G. Ahlström ◽  
N. Jonsson
Keyword(s):  
Cancer Cells ◽  
Sex Hormones ◽  
Previous Investigation ◽  
Early Growth ◽  
Male Mice ◽  
Female Mice ◽  
Small Doses ◽  
Mouse Ascites ◽  
Males And Females ◽  
The Difference

ABSTRACT Ehrlich mouse ascites cancer grew better during the first 3 days after inoculation in female than in male mice. The difference was only demonstrable on inoculation with small doses of cancer cells and could not be seen when large doses were used. On the 5th day after inoculation no difference could be observed in the growth of the cancer between males and females. Gonadectomy had no influence on the growth of the cancer. Testosterone inhibited the growth of the cancer in castrated male mice. It had no effect on the growth of the cancer in castrated female mice. Oestradiol did not influence the growth of the cancer in castrated male or female mice. It is noteworthy that the results obtained in a previous investigation on the growth of the Ehrlich mouse ascites cancer in hamsters revealed a hormonal influence which was only discernible in its natural host during the early growth of the cancer and then only after transplantation of a relatively small number of cancer cells.

scholarly journals MOUSE COMPLEMENT: THE EFFECT OF SEX HORMONES AND CASTRATION ON TWO OF THE LATE-ACTING COMPONENTS

1967 ◽  
Vol 125 (4) ◽  
pp. 657-672 ◽  
Author(s):  
Winthrop H. Churchill ◽  
Ronald M. Weintraub ◽  
Tibor Borsos ◽  
Herbert J. Rapp
Keyword(s):  
Sex Hormones ◽  
Male Mice ◽  
Complement Components ◽  
Female Mice

The titer of late-acting complement components in sera from male mice is 8–10 times higher than the titer of sera from female mice. Using assays developed to measure the serum content of two of the late-acting components, we have shown that this difference is due to the effect of androgen and estrogen on these two late-acting complement components. These two components have been tentatively identified as C'5 and C'6. Androgen and estrogen have greater effect on C'6 than on C'5. The possibility has not been excluded that still other of the late-acting complement components are affected by androgens and estrogens. The course of homograft rejection was unchanged in mice deficient in C'5 and C'6.

scholarly journals Leptin pharmacokinetics in male mice

2017 ◽  
Vol 6 (1) ◽  
pp. 20-26 ◽  
Author(s):  
Robert A Hart ◽  
Robin C Dobos ◽  
Linda L Agnew ◽  
Neil A Smart ◽  
James R McFarlane
Keyword(s):  
Digestive Tract ◽  
Time Course ◽  
Normal Male ◽  
Male Mice ◽  
Male And Female ◽  
Female Mice ◽  
Males And Females ◽  
High Degree ◽  
The Brain ◽  
Major Target

Pharmacokinetics of leptin in mammals has not been studied in detail and only one study has examined more than one time point in non-mutant mice and this was in a female mice. This is the first study to describe leptin distribution over a detailed time course in normal male mice. A physiologic dose (12 ng) of radiolabelled leptin was injected into adult male mice via the lateral tail vein and tissues were dissected out and measured for radioactivity over a time course of up to two hours. Major targets were the digestive tract, kidneys, skin and lungs. The brain was not a major target, and 0.15% of the total dose was recovered from the brain 5 min after administration. Major differences appear to exist in the distribution of leptin between the male and female mice, indicating a high degree of sexual dimorphism. Although the half-lives were similar between male and female mice, almost twice the proportion of leptin was recovered from the digestive tract of male mice in comparison to that reported previously for females. This would seem to indicate a major difference in leptin distribution and possibly function between males and females.

scholarly journals Male sex hormones promote vagally mediated reflex airway responsiveness to cholinergic stimulation

2007 ◽  
Vol 292 (4) ◽  
pp. L908-L914 ◽  
Author(s):  
Jeffrey W. Card ◽  
James W. Voltz ◽  
Catherine D. Ferguson ◽  
Michelle A. Carey ◽  
Laura M. DeGraff ◽  
...  
Keyword(s):  
Sex Hormones ◽  
Ex Vivo ◽  
Airway Responsiveness ◽  
Male Mice ◽  
Cholinergic Stimulation ◽  
Intact Female ◽  
Reflex Mechanism ◽  
Female Mice ◽  
Male Sex

A sex disparity in airway responsiveness to cholinergic stimulation has been observed in laboratory mice in that males are considerably more responsive than females, but the basis for this difference is unclear. In this report, we demonstrate that male sex hormones promote murine airway responsiveness to cholinergic stimulation via vagus nerve-mediated reflex mechanisms. In tissue bath preparations, no sex-based differences were observed in the contractile responses of isolated tracheal and bronchial ring segments to carbachol, indicating that the mechanism(s) responsible for the in vivo sex difference is (are) absent ex vivo. Bilateral cervical vagotomy was found to abolish in vivo airway responsiveness to methacholine in male mice, whereas it did not alter the responses of females, suggesting a regulatory role for male sex hormones in promoting reflex airway constriction. To test this possibility, we next studied mice with altered circulating male sex hormone levels. Castrated male mice displayed airway responsiveness equivalent to that observed in intact females, whereas administration of exogenous testosterone to castrated males restored responsiveness, albeit not to the level observed in intact males. Administration of exogenous testosterone to intact female mice similarly enhanced responsiveness. Importantly, the promotive effects of exogenous testosterone in castrated male and intact female mice were absent when bilateral vagotomy was performed. Together, these data indicate that male sex hormones promote cholinergic airway responsiveness via a vagally mediated reflex mechanism that may be important in the regulation of airway tone in the normal and diseased lung.

scholarly journals Evaluation of Sex Differences in Murine Diabetic Ketoacidosis and Neutropenic Models of Invasive Mucormycosis

2021 ◽  
Author(s):  
Teclegiorgis Gebremariam ◽  
Sondus Alkhazraji ◽  
Abdullah Alqarihi ◽  
Nathan P. Wiederhold ◽  
Laura K. Najvar ◽  
...  
Keyword(s):  
Mouse Model ◽  
Mucor Circinelloides ◽  
Male Mice ◽  
Rhizopus Delemar ◽  
Female Mice ◽  
Pulmonary Mucormycosis ◽  
Susceptibility To Infection ◽  
Cytokine Levels ◽  
Untreated Female ◽  
The Difference

There is increased concern that the quality, generalizability, and reproducibility of biomedical research can be influenced by the sex of animals used. We studied the differences between male and female mice in response to invasive pulmonary mucormycosis including susceptibility to infection, host immune reaction, and responses to antifungal therapy. We used diabetic ketoacidotic (DKA) or neutropenic mice infected with either Rhizopus delemar or Mucor circinelloides. The only difference detected was that when DKA mice were infected with M. circinelloides, female mice were more resistant to infection than male mice (median survival time of 5 vs. 2 days for female and male mice, respectively). However, a 100% lethality was detected among infected animals of both sexes. Treatment with either liposomal amphotericin B (L-AMB) or posaconazole (POSA) protected mice from infection and eliminated the difference seen between infected but untreated female and male mice. Treatment with L-AMB consistently outperformed POSA in prolonging survival and reducing tissue fungal burden of DKA and neutropenic mice infected with R. delemar or M. circinelloides, in both mouse sexes. Although little difference was detected in cytokine levels among both sexes, mucormycosis infection in the DKA mouse model induced more inflammatory cytokines/chemokines involved in neutrophil (CXCL1) and macrophage (CXCL2) recruitment vs. uninfected mice. As expected, this inflammatory response was reduced in the neutropenic mouse model. Our studies show that there are few differences between female and male DKA or neutropenic mice infected with mucormycosis with no effect on the outcome of treatment or host immune response.

scholarly journals Evaluation of Sex Differences in Murine Diabetic Ketoacidosis and Neutropenic Models of Invasive Mucormycosis

2021 ◽  
Vol 7 (4) ◽  
pp. 313
Author(s):  
Teclegiorgis Gebremariam ◽  
Sondus Alkhazraji ◽  
Abdullah Alqarihi ◽  
Nathan P. Wiederhold ◽  
Laura K. Najvar ◽  
...  
Keyword(s):  
Mouse Model ◽  
Mucor Circinelloides ◽  
Male Mice ◽  
Rhizopus Delemar ◽  
Female Mice ◽  
Pulmonary Mucormycosis ◽  
Susceptibility To Infection ◽  
Cytokine Levels ◽  
Untreated Female ◽  
The Difference

There is increased concern that the quality, generalizability and reproducibility of biomedical research can be influenced by the sex of animals used. We studied the differences between male and female mice in response to invasive pulmonary mucormycosis including susceptibility to infection, host immune reaction and responses to antifungal therapy. We used diabetic ketoacidotic (DKA) or neutropenic mice infected with either Rhizopus delemar or Mucor circinelloides. The only difference detected was that when DKA mice were infected with M. circinelloides, female mice were more resistant to infection than male mice (median survival time of 5 vs. 2 days for female and male mice, respectively). However, a 100% lethality was detected among infected animals of both sexes. Treatment with either liposomal amphotericin B (L-AMB) or posaconazole (POSA) protected mice from infection and eliminated the difference seen between infected but untreated female and male mice. Treatment with L-AMB consistently outperformed POSA in prolonging survival and reducing tissue fungal burden of DKA and neutropenic mice infected with R. delemar or M. circinelloides, in both mouse sexes. While little difference was detected in cytokine levels among both sexes, mucormycosis infection in the DKA mouse model induced more inflammatory cytokines/chemokines involved in neutrophil (CXCL1) and macrophage (CXCL2) recruitment vs. uninfected mice. As expected, this inflammatory response was reduced in the neutropenic mouse model. Our studies show that there are few differences between female and male DKA or neutropenic mice infected with mucormycosis with no effect on the outcome of treatment or host immune response.

scholarly journals Divergent strategies for learning in males and females

2019 ◽  
Author(s):  
Cathy S. Chen ◽  
R. Becket Ebitz ◽  
Sylvia R. Bindas ◽  
A. David Redish ◽  
Benjamin Y. Hayden ◽  
...  
Keyword(s):  
Decision Making ◽  
Male Mice ◽  
Female Mice ◽  
Multiple Dimensions ◽  
Males And Females ◽  
Immediate Experience ◽  
Feature Dimension ◽  
Individual Strategies ◽  
Correct Image ◽  
Do So

AbstractA frequent assumption in value-based decision-making tasks is that agents make decisions based on the feature dimension that reward probabilities vary on. However, in complex, multidimensional environments, stimuli can vary on multiple dimensions at once, meaning that the feature deserving the most credit for outcomes is not always obvious. As a result, individuals may vary in the strategies used to sample stimuli across dimensions, and these strategies may have an unrecognized influence on decision-making. Sex is a proxy for multiple genetic and endocrine influences that can influence decision-making strategies, including how environments are sampled. In this study, we examined the strategies adopted by female and male mice as they learned the value of stimuli that varied in both image and location in a visually-cued two-armed bandit, allowing two possible dimensions to learn about. Female mice acquired the correct image-value associations more quickly than male mice, and they used a fundamentally different strategy to do so. Female mice constrained their decision-space early in learning by preferentially sampling one location over which images varied. Conversely, male strategies were inconsistent, changing frequently and strongly influenced by the immediate experience of stochastic rewards. Individual strategies were related to sex-gated changes in neuronal activation in early learning. Together, we find that in mice, sex is linked with divergent strategies for sampling and learning about the world, revealing substantial unrecognized variability in the approaches implemented during value-based decision-making.

scholarly journals Sex Differences in Head-fixed Running Behavior

2019 ◽  
Author(s):  
Emily J. Warner ◽  
Krishnan Padmanabhan
Keyword(s):  
Sex Differences ◽  
Male Mice ◽  
Specific Difference ◽  
Running Wheel ◽  
Female Mice ◽  
In The Wild ◽  
Males And Females ◽  
Neural Underpinnings ◽  
Divergent Behavior ◽  
Almost All

ABSTRACTSex differences in running behaviors between male and female mice occur naturally in the wild. Recent experiments using head restrained mice on a running wheel have exploited locomotion to provide insight in the neural underpinnings of a number of behaviors ranging from spatial navigation to decision making. However, it is largely unknown how males and females behave differently in this experimental paradigm. We found that in head-fixed mice that were initially exposed to a running wheel, all female mice ran forward naturally within the first two days, while almost all male mice scurried backward for up to 4 days. With daily exposure, male mice progressively learned to naturally run forward, with this transition occurring over the course of a 7-day period. Taken together, we have identified a sexually divergent behavior in head-fixed running that should be considered in experiments that use this experimental design. Furthermore, this sex-specific difference could serve as a new way to interrogate the neural underpinnings of a number of behaviors such as anxiety or fear.

scholarly journals Bridging Sex-Specific Differences in the CAR-Mediated Hepatocarcinogenesis of Nitrapyrin Using Molecular and Apical Endpoints

2021 ◽  
Vol 3 ◽  
Author(s):  
Lynea Murphy ◽  
Matthew J. LeBaron ◽  
Kamin Johnson ◽  
Reza J. Rasoulpour ◽  
Xiujuan Wang ◽  
...  
Keyword(s):  
Mode Of Action ◽  
Liver Tumors ◽  
Constitutive Androstane Receptor ◽  
Nitrification Inhibitor ◽  
Tumor Formation ◽  
Male Mice ◽  
Female Mice ◽  
Increased Sensitivity ◽  
Males And Females ◽  
Related Increase

Nitrapyrin, a nitrification inhibitor, produces liver tumors in B6C3F1 mice. In a 2-year oncogenicity study, increased incidence of mice with hepatocellular tumors was observed following exposure to 125 (females only) or 250 mg/kg/day (males and females) nitrapyrin in the diet. Previous data was generated in male mice to support a mode-of-action (MoA) characterized by constitutive androstane receptor (CAR) nuclear receptor (NR) activation, increased hepatocellular proliferation, and subsequent hepatocellular foci and tumor formation. Uncertainty as to the relevance of this MoA for females remained given the increased sensitivity to tumor formation in female mice. A targeted MoA study was conducted to evaluate CAR activation and hepatic responses in female mice treated with the female carcinogenic dose of nitrapyrin for 4 days. Nitrapyrin induced a treatment-related increase in hepatocellular hypertrophy and hepatocellular proliferation. Nitrapyrin also induced a dose-related increase in the Cyp2b10/CAR-associated transcript and liver weights. Nitrapyrin-induced liver weights and Cyp2b10 gene expression for both males and females were compared to data generated from three other established CAR activators; methyl isobutyl ketone, phenobarbital, and sulfoxaflor. The response observed in female mice following exposure to nitrapyrin was within range of the degree of change observed in mice following exposure to tumorigenic doses of other CAR activators. Consistent with the liver MoA in male mice, these data support a CAR-mediated mode of action for nitrapyrin-induced liver tumors in female mice, with the understanding that a focused approach minimizing animal use can bridge male and female datasets when sex-specific carcinogenic differences are observed.

Hexachlorocyclohexane-Induced Tumorigenicity in Mice under Different Experimental Conditions

1983 ◽  
Vol 69 (5) ◽  
pp. 383-386 ◽  
Author(s):  
Khan Md. Munir ◽  
Chitralekha Sudhakar Soman ◽  
Sumati Vasudeo Bhide
Keyword(s):  
Sex Hormones ◽  
Liver Tumors ◽  
Age Groups ◽  
Tumor Incidence ◽  
Male Mice ◽  
Experimental Conditions ◽  
Continuous Administration ◽  
Female Mice

Continuous administration of 500 ppm hexachlorocyclohexane (HCH) in the diet induced 100 % liver tumors in mice, but none were observed in rats and hamsters treated with the same dose of HCH. In Swiss male mice, tumor incidence at earlier ages was greater than that observed in corresponding age groups of Swiss female mice. It was further observed that in Swiss females, sex hormones retarded the tumorigenic effect of HCH; in BALB/c mice a similar phenomenon was not observed.

scholarly journals The Impact of Sex on Changes in Plasma Corticosterone and Cotinine Levels Induced by Nicotine in C57BL/6J Mice

2020 ◽  
Vol 10 (10) ◽  
pp. 705
Author(s):  
Khoa Nguyen ◽  
Keiko Kanamori ◽  
Chang Sung Shin ◽  
Abdul Hamid ◽  
Kabirullah Lutfy
Keyword(s):  
Plasma Corticosterone ◽  
Male Mice ◽  
Once Daily ◽  
Female Mice ◽  
Nicotine Administration ◽  
Corticosterone Secretion ◽  
Males And Females ◽  
Repeated Dosing ◽  
The Impact ◽  
First Time

We assessed if there were any sex-related differences in the ability of nicotine to increase plasma corticosterone secretion after single or repeated nicotine administration. For single-dose studies, male and female mice were habituated to the test room for 1 h and injected with saline or nicotine (0.25 or 1 mg/kg, subcutaneously (s.c.)). In repeated-dosing studies, mice were injected with saline or nicotine (1 mg/kg, s.c.) once daily for six days, and, on day 7, received nicotine (1 mg/kg, s.c.). Mice were then euthanized 15 min later, and trunk blood was collected for the measurement of corticosterone, nicotine, and cotinine. Our results showed that saline or nicotine each significantly increased plasma corticosterone levels in both males and females, with a greater response in female mice. Plasma corticosterone levels were increased in male but not female mice after being treated repeatedly compared to single nicotine administration. The level of cotinine, a biomarker of nicotine use, was significantly higher in female than in male mice. Taken together, these novel findings suggest that female mice respond to nicotine and the stress of handling more than male mice and provide for the first-time quantitative data on male–female differences in nicotine-induced elevations of corticosterone and cotinine plasma levels.

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