The anatomy of the sawfly Perga affinis affinis Kirby (Hymenoptera: Symphyta)

1962 ◽  
Vol 10 (4) ◽  
pp. 652 ◽  
Author(s):  
NN Tait
Keyword(s):  
Reproductive System ◽  
No Reduction ◽  
Reproductive Organs ◽  
Male Reproductive System ◽  
Flight Muscles

This paper is an account of the anatomy of the larval and adult stages of the sawfly Perga affinis affinis Kirby. Particular attention has been paid to those structures that seem relevant to the ecology of the animal. In this respect, this work is supplementary to that of Carne (1962) on the ecology of this insect. The external features of the larva and adult are described. Measurements of head capsules of the larvae showed that these could be employed as a method of identifying the various instars. From observations made by Carne (op. cit.) it is probable that the species breeds parthenogenetically. However, the male reproductive system appears quite functional. The structure and musculature of the ovipositor is described, as well as the internal reproductive organs. The muscles of the thorax are compared with those described by Snodgrass (1927) in the generalized insect and by Tiegs (1955) in the various orders. In P. affinis affinis the prothoracic muscles are modified for the movement of the head and prepectus. The development of flight muscles is greatest in the mesothorax where the indirect flight muscles almost completely fill the cavity. The indirect flight muscles of the metathorax are poorly developed. The muscles are composed of numerous fibres. There has been no reduction and enlargement of the fibres as in the Diptera. The coxal muscles have become separated from the flight muscles and are confined to the sterna and furcae.

scholarly journals Bacterial Infections Affect Male Fertility: A Focus on the Oxidative Stress-Autophagy Axis

2021 ◽  
Vol 9 ◽  
Author(s):  
Sutian Wang ◽  
Kunli Zhang ◽  
Yuchang Yao ◽  
Jianhao Li ◽  
Shoulong Deng
Keyword(s):  
Oxidative Stress ◽  
Reproductive System ◽  
Bacterial Infections ◽  
Reproductive Organs ◽  
Innate Immune ◽  
Male Reproductive System ◽  
Pathogenic Microorganisms ◽  
Immune Functions ◽  
Molecular Patterns ◽  
Multiple Signaling

Numerous factors trigger male infertility, including lifestyle, the environment, health, medical resources and pathogenic microorganism infections. Bacterial infections of the male reproductive system can cause various reproductive diseases. Several male reproductive organs, such as the testicles, have unique immune functions that protect the germ cells from damage. In the reproductive system, immune cells can recognize the pathogen-associated molecular patterns carried by pathogenic microorganisms and activate the host’s innate immune response. Furthermore, bacterial infections can lead to oxidative stress through multiple signaling pathways. Many studies have revealed that oxidative stress serves dual functions: moderate oxidative stress can help clear the invaders and maintain sperm motility, but excessive oxidative stress will induce host damage. Additionally, oxidative stress is always accompanied by autophagy which can also help maintain host homeostasis. Male reproductive system homeostasis disequilibrium can cause inflammation of the genitourinary system, influence spermatogenesis, and even lead to infertility. Here, we focus on the effect of oxidative stress and autophagy on bacterial infection in the male reproductive system, and we also explore the crosslink between oxidative stress and autophagy during this process.

scholarly journals Impact of Age on the Male Reproductive System from the Pathologist’s Perspective

2016 ◽  
Vol 45 (1) ◽  
pp. 195-205 ◽  
Author(s):  
Catherine A. Picut ◽  
Amera K. Remick
Keyword(s):  
Postnatal Development ◽  
Reproductive System ◽  
Reproductive Organs ◽  
Male Reproductive System ◽  
Laboratory Animals ◽  
Large Animal ◽  
Age Related ◽  
Organ Systems ◽  
Microscopic Evaluation ◽  
Tissue Changes

Age, and in particular young age, can significantly impact the response to toxicants in animals and can greatly influence the interpretation of tissue changes by the toxicologic pathologist. Although this applies to multiple organ systems, the current review focuses on the male reproductive system. When performing microscopic evaluation of male reproductive organs, the toxicologic pathologist must be aware of the dynamic changes in histomorphology, predominantly driven by timed hormonal alterations, at various life stages. Specific challenges pathologists face are understanding the appearance of male reproductive tissues throughout the neonatal, infantile, and juvenile developmental periods, recognizing when normal looks abnormal during tissue development, defining sexual maturity, and working with high interanimal variability in maturation rate and histologic appearance in developing large laboratory animals, such as nonhuman primates, dogs, and pigs. This review describes postnatal development of the male reproductive system in the rat, demonstrates how assessing toxicity during a defined window of postnatal development in the rat may improve definition of toxicant timing and targets, and discusses challenges associated with the interpretation of toxicity in immature large animal species. The emphasis is on key age-related characteristics that influence the interpretation of tissue changes by the toxicologic pathologist.

Presence of α-glucosidases in the male reproductive system of the rat and hormonal influences

1983 ◽  
Vol 61 (7) ◽  
pp. 764-769 ◽  
Author(s):  
Anne-Marie Grandmont ◽  
Pierre Chapdelaine ◽  
Roland R. Tremblay
Keyword(s):  
Enzyme Activity ◽  
Reproductive System ◽  
Reproductive Organs ◽  
Gonadal Hormones ◽  
Antagonistic Effect ◽  
Seminal Vesicles ◽  
Male Reproductive System ◽  
Male Rat ◽  
Glucosidase Activity ◽  
Estradiol 17Β

The use of a synthetic substrate (p-nitrophenyl-α-D-glucoside) to measure α-glucosidase activity has allowed us to demonstrate the presence of acid and neutral α-glucosidases in the reproductive organs of the male rat. Both enzymes increased in the epididymis, particularly in the caput segment, along with initiation of spermatogenesis at puberty; it then started decreasing after 12 weeks of life. Similar variations were not recorded in testis, prostate, and seminal vesicles. Castration led to a significant decrease of acid and neutral α-glucosidases in all accessory reproductive organs, but administration of testosterone proprionate (50 μg/day for 10 days) restored the enzyme activity to its original level. When estradiol-17β (5 mg) was administered simultaneously with testosterone (500 μg), the antagonistic effect of estradiol on testosterone was particularly evident on the levels of neutral α-glucosidases which reached the castration range, while the acid α-glucosidase remained unchanged in epididymis, prostate, and seminal vesicles. These results show that both acid and neutral α-glucosidases may be influenced by gonadal hormones in the male rat.

scholarly journals Necroptosis promotes the Aging of the Male Reproductive System in Mice

2017 ◽  
Author(s):  
Dianrong Li ◽  
Lingjun Meng ◽  
Tao Xu ◽  
Yaning Su ◽  
Xiao Liu ◽  
...  
Keyword(s):  
Reproductive System ◽  
Accelerated Aging ◽  
Reproductive Organs ◽  
Male Reproductive System ◽  
Necrotic Cell Death ◽  
Wild Type ◽  
Necrotic Cell ◽  
Age Related ◽  
And Function ◽  
Age Related Changes

AbstractNecroptosis is a form of programmed necrotic cell death in mammals that is mediated by a pair of kinases, RIP1 and RIP3, as well as the RIP3 substrate MLKL. We report here that male reproductive organs of both RIP3-and MLKL-knockout mice retain “youthful” morphology and function into advanced age, while those of age-matched wild type mice deteriorate. The RIP3 phosphorylation of MLKL, the activation marker of necroptosis, is detected in spermatogonial stem cells in the testes of old but not in young wild type mice. When the testes of young wild type mice are given a local necroptotic stimulus, their reproductive organs showed accelerated aging. Feeding of wild type mice with an RIP1 inhibitor prior to the normal onset of age-related changes in their reproductive organs blocked the appearance of signs of aging. Thus, necroptosis in testes promotes the aging-associated deterioration of the male reproductive system in mice.

scholarly journals Expression of estrogen receptor-alpha and -beta mRNAs in the male reproductive system of the rat as revealed by in situ hybridization

2001 ◽  
Vol 26 (3) ◽  
pp. 165-174 ◽  
Author(s):  
CN Mowa ◽  
T Iwanaga
Keyword(s):  
Estrogen Receptor ◽  
In Situ Hybridization ◽  
Reproductive System ◽  
Initial Segment ◽  
Vas Deferens ◽  
Perinatal Period ◽  
Reproductive Organs ◽  
Male Reproductive System ◽  
Prenatal Period

We mapped the cellular expression of estrogen receptor (ER) alpha and ERbeta mRNAs in the male reproductive system of the rat during development and adulthood by in situ hybridization. The expression patterns of ERalpha mRNA in the gonad, efferent duct and initial segment of the epididymis during the perinatal period were essentially similar to those of the adult: ERalpha mRNA signals were expressed most intensely in the epithelia of the efferent ducts and initial segment of the epididymis, and in the interstitial cells of the testis from the prenatal period to adulthood. However, ERalpha mRNA signals in the primordial epididymis and vas deferens during the prenatal period were confined to the outermost cellular layer of the ducts, whereas thereafter they were only expressed weakly in the epithelium and stroma of the epididymis and moderately in the muscle layer of the vas deferens. ERbeta signals were expressed intensely (1) in primordial germ and Sertoli cells only during the prenatal period, (2) in arterial walls in the adult testis, and (3) in the epithelium of the sex accessory glands from the perinatal period to adulthood. This report is the first to describe the cellular distribution of ER mRNA in the male reproductive organs during the perinatal period, and complements and confirms earlier data on its distribution in the adult. The broad expression of ERs in male reproductive organs suggests roles for estrogen in regulating tissue development and reproductive events.

scholarly journals RIPK1-RIPK3-MLKL-dependent necrosis promotes the aging of mouse male reproductive system

eLife ◽  
2017 ◽  
Vol 6 ◽  
Author(s):  
Dianrong Li ◽  
Lingjun Meng ◽  
Tao Xu ◽  
Yaning Su ◽  
Xiao Liu ◽  
...  
Keyword(s):  
Reproductive System ◽  
Accelerated Aging ◽  
Reproductive Organs ◽  
Male Reproductive System ◽  
Necrotic Cell Death ◽  
Wild Type ◽  
Necrotic Cell ◽  
Age Related ◽  
And Function ◽  
Age Related Changes

A pair of kinases, RIPK1 and RIPK3, as well as the RIPK3 substrate MLKL cause a form of programmed necrotic cell death in mammals termed necroptosis. We report here that male reproductive organs of both Ripk3- and Mlkl-knockout mice retain ‘youthful’ morphology and function into advanced age, while those of age-matched wild-type mice deteriorate. The RIPK3 phosphorylation of MLKL, the activation marker of necroptosis, is detected in spermatogonial stem cells in the testes of old but not in young wild-type mice. When the testes of young wild-type mice are given a local necroptotic stimulus, their reproductive organs showed accelerated aging. Feeding of wild-type mice with an RIPK1 inhibitor prior to the normal onset of age-related changes in their reproductive organs blocked the appearance of signs of aging. Thus, necroptosis in testes promotes the aging-associated deterioration of the male reproductive system in mice.

scholarly journals Toxicity Investigation of Nano-SiO2 on Male Reproductive System in Pubertal Mice

2021 ◽  
Author(s):  
Fanli Sun ◽  
Xuying Wang ◽  
Pinzheng Zhang ◽  
Ziyun Chen ◽  
Zhiyi Guo ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Reproductive System ◽  
Intraperitoneal Injection ◽  
Sperm Quality ◽  
Underlying Mechanism ◽  
Reproductive Organs ◽  
Male Reproductive System ◽  
Reproductive Capacity ◽  
Apoptotic Pathway ◽  
And Function

Abstract BackgroundPuberty is a crucial stage to gain reproductive capacity, but it is also a period vulnerable to exogenous materials. While exposure to nanoparticles (NPs) has been linked to toxic responses in reproductive system in previous findings, little is known about the age-dependent effect of NPs, let alone the underlying mechanism. In the present study, we assessed male fertility parameters and explored its mechanism following intraperitoneal exposure to Nano-Silicon dioxide (Nano-SiO2) in mice during puberty.Methods40 mice aged 5 weeks were divided into 2 groups after 1 week acclimation and then exposed to 40mg/kg Nano-SiO2 dissolved in saline or vehicle controls by intraperitoneal injection every day over a period of 7-day, respectively. Changes in the structure and function of male reproductive organs were detected after exposure.ResultsNano-SiO2 exposed through intraperitoneal injection could cause damage to the testicular and epididymal histological architecture and reduce the level of sex hormone (testosterone), leading to a decrease in sperm quality and quantity. Furthermore, Nano-SiO2 could induce oxidative stress and inflammation in male reproductive tissues, indicated by reduced activity of antioxidants (superoxide dismutase, SOD) and increased level of the lipid peroxidation marker (malondialdehyde, MDA), which leads to the activation of cell apoptosis.ConclusionExposure to Nano-SiO2 in pubertal mice could cause toxicity on male reproductive system via inducing oxidative stress and activating TNF-α mediated apoptotic pathway.

Sign in / Sign up

Export Citation Format

Share Document