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Transient Neonatal-Onset Hypothyroidism Boosts Estradiol Synthesis in the Testis of Adult Wistar Rat 短暂性新生儿甲状腺功能减退症促进成年Wistar大鼠睾丸雌二醇合成
Pub Date : 2015-06-01 DOI: 10.18519/JER/2014/V18/67732
N. Venkatesh, M. K. Kumar, S. Sambavi, N. Kalpana, A. M. S. John, J. Anbalagan, R. Ilangovan, M. Aruldhas
Transient neonatal hypothyroidism is known to boost Sertoli cell (SC), Leydig cell (LC) and germ cell (GC) number at adult age. Existing reports attribute decreased steroidogenic potential of LCs to unaltered/decreased serum testosterone in such rats, despite a boost in the cell number. However, these studies have ignored the status of estradiol in such conditions. In this present study, we tested the hypothesis "transient neonatal-onset hypothyroidism may lead to a temporal shift in adult rat testicular steroidogenesis towards estradiol production". Hypothyroidism was induced in neonates by providing methimazole (MMI) in drinking water (0.05%) to lactating mothers and pups for a transient period from postnatal day 1 (PND 1) to PND 14 or from PND 1 to PND 29. After the experimental period, the pups were provided drinking water free of MMI and sacrificed on PND 91. Coeval rats without MMI exposure served as control. Radioimmunoassay revealed decreased serum titres of luteinizing hormone (LH), follicle stimulating hormone (FSH), growth hormone (GH) and prolactin (PRL); while serum testosterone remained unaltered, its level in testicular interstitial fluid (TIF) decreased. Between the two major metabolites of testosterone, 5α-dihydrotestosterone (DHT) concentration decreased in serum and TIF, whereas estradiol recorded a significant increase in both. Transient neonatal-onset hypothyroidism decreased 3β-hydroxy steroid dehydrogenase (3β-HSD) in LCs but augmented 17β-HSD activity. Radio-receptor assay revealed decreased concentration of LHR and ER in LCs of hypothyroid groups, whereas AR and PRLR increased. While aromatase activity decreased in LCs, it increased along with FSHR in SCs, when compared to control rats. The changes in LHR and FSHR levels and aromatase were consistent with the expression level of the respective genes. The present study supports the proposed hypothesis and suggests that transient neonatal-onset hypothyroidism-induced boost in estradiol in adult rat testis may be due to augmented expression and activity of aromatase, and FSHR content in SCs of these rats.
一过性新生儿甲状腺功能减退症可增加成年时的支持细胞(SC)、间质细胞(LC)和生殖细胞(GC)数量。现有的报告将LCs的类固醇生成潜力降低归因于这类大鼠的血清睾酮未改变/降低,尽管细胞数量增加。然而,这些研究忽略了雌二醇在这种情况下的地位。在本研究中,我们验证了“短暂性新生儿甲状腺功能减退可能导致成年大鼠睾丸激素生成向雌二醇生成的时间转移”的假设。从出生后第1天(PND 1)到第14天或从第1天到第29天,通过在饮用水中添加0.05%的甲巯咪唑(MMI)诱导新生儿甲状腺功能减退。试验期结束后,给予不含MMI的饮水,用PND 91处死。未接触MMI的同龄大鼠作为对照。放射免疫分析显示血清促黄体生成素(LH)、促卵泡激素(FSH)、生长激素(GH)和催乳素(PRL)滴度降低;血清睾酮维持不变,但睾丸间质液(TIF)睾酮水平下降。在睾酮的两种主要代谢物中,血清和TIF中5α-二氢睾酮(DHT)浓度下降,而雌二醇在两者中均显著升高。新生儿发作的短暂性甲状腺功能减退降低了LCs中3β-羟基类固醇脱氢酶(3β-HSD)的活性,但增加了17β-HSD的活性。放射受体测定显示,甲状腺功能减退组LHR和ER浓度降低,AR和PRLR浓度升高。与对照大鼠相比,LCs的芳香酶活性下降,而SCs的芳香酶活性随着FSHR的增加而增加。LHR和FSHR水平以及芳香化酶的变化与各自基因的表达水平一致。本研究支持上述假设,并提示新生儿发作性甲状腺功能减退引起的成年大鼠睾丸中一过性雌二醇升高可能是由于这些大鼠sc中芳香化酶的表达和活性以及FSHR含量的增强。
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引用次数: 1
Effect of Trigonella foenum Graecum (Fenugreek)-Loaded PLGA Nanoparticles on Non-Specific Esterase Enzyme Activity in Salivary Glands of Aging-Accelerated Male Mice 胡芦巴负载PLGA纳米颗粒对衰老加速雄性小鼠唾液腺非特异性酯酶活性的影响
Pub Date : 2015-06-01 DOI: 10.18519/JER/2015/V19/86058
V. Deshmukh, M. Walvekar, S. S. Desai
During oxidative stress, the reactive oxygen species (ROS) generally produce structural and biochemical alterations in cells and cell organelles. Impairment of lysosomal and mitochondrial function is the key for understanding the degenerative changes due to aging. Nonspecific esterase enzyme is particularly present in lysosomes and microsomes. In order to find the antioxidant property of fenugreek, non-specific esterase activity was measured to study the lysosomal membrane integrity in submandibular and sublingual salivary glands of D-galactose-induced aging male mice without and with supplementation of fenugreek. Adult male albino mice ( Mus musculus ) were divided in to six groups of five each and treated as follows: a) control for D-galactose (Dg) treatment; b) Dgtreated; c) Dg + fenugreek seed extract (FSE) treated concurrently; d) treated with Dg first, followed by treatment of FSE; e) Dg + FSE-loaded PLGA nanoparticle treated concurrently; and f) treated with Dg first followed by treatment of FSE-loaded PLGA nanoparticle. A significant decrease in non-specific esterase activity was observed in D-galactose treated mice, whereas FSE and FSE-PGLA groups of mice indicated protection against Dg-induced aging related oxidative stress in salivary glands. Thus, it is shown that fenugreek seed possesses antioxidant property, whereby non-specific esterase activity in salivary glands is increased but in a manner dependent on the treatment pattern, and the best result is obtained when FSE is administered post-treatment as loaded in PGLA nanoparticles.
在氧化应激过程中,活性氧(ROS)通常会在细胞和细胞器中产生结构和生化改变。溶酶体和线粒体功能损伤是了解衰老引起的退行性变化的关键。非特异性酯酶尤其存在于溶酶体和微粒体中。为了研究胡芦巴的抗氧化作用,我们测定了非特异性酯酶活性,研究了d -半乳糖诱导的衰老雄性小鼠在不添加胡芦巴和补充胡芦巴的情况下下颌和舌下唾液腺溶酶体膜的完整性。将成年雄性白化小鼠(小家鼠)分为6组,每组5只,按如下方法处理:a)对照组给予d -半乳糖(Dg)处理;b) Dgtreated;c)同时处理Dg +葫芦巴籽提取物(FSE);d)先用Dg处理,再用FSE处理;e)同时处理负载Dg + fse的PLGA纳米颗粒;f)先用Dg处理,再用负载fse的PLGA纳米颗粒处理。d -半乳糖处理小鼠的非特异性酯酶活性显著降低,而FSE和FSE- pgla组小鼠的唾液腺显示出对dg诱导的衰老相关氧化应激的保护作用。因此,研究表明葫芦巴种子具有抗氧化特性,因此唾液腺中的非特异性酯酶活性增加,但其方式取决于处理模式,并且当FSE在处理后加载PGLA纳米颗粒时获得最佳效果。
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引用次数: 1
Neuropeptide Y (NPY) Distribution in the Forebrain of Adult Spiny Eel, Macrognathus pancalus 成鱼前脑神经肽Y (NPY)的分布
Pub Date : 2015-06-01 DOI: 10.18519/JER/2014/V18/67734
M. Zahid, S. Malik, S. Rani
In the present study, the distribution of neuropeptide Y (NPY)-immunoreactive neurons and fibers in the forebrain of adult spiny eel, Macrognathus pancalus , which is a bottom-dwelling nocturnal fish, was investigated. Serial Nissl-stained brain sections were used to demarcate forebrain regions and neuronal structures. NPY peptidecontaining cell bodies and fibers localized immunocytochemically were found widely distributed throughout the forebrain. The brain areas showing NPY distribution included predominant cell groups in the telencephalon (nucleus entopeduncularis, NE; nucleus of area ventralis telencephali, Vn), diencephalon (nucleus preopticus, pars parvocellularis, NPOp; nucleus preopticus, pars magnocellularis, NPOm; nucleus lateralis tuberis, NLT) and mesencephalon (midbrain tegmentum, MT). The important areas with only NPY-immunoreactive (-ir) fibers included olfactory bulb (OB), area dorsalis telencephali pars anterioris (Da), dorsal part of Dmd (Dmdd), ventral subdivision of Dl (Dlv), anterior subdivision of Dl (Dla), preoptic area (POA), optic tectum (OTec) and nucleus recessi lateralis (NRL). The pattern of NPY distribution in the forebrain of M. pancalus suggests its role in processing of many physiological functions (viz., feeding, daily activities, reproduction and other metabolic processes). The basic information on anatomical localization of NPY in eel will help to understand better the seasonal variations of NPY and its interaction with other reproductive hormones.
本研究研究了成年底栖夜行鱼大刺鳗前脑中神经肽Y (NPY)免疫反应神经元和纤维的分布。连续使用nissl染色的脑切片来划分前脑区域和神经元结构。含NPY肽的细胞体和纤维广泛分布于前脑。显示NPY分布的脑区包括远脑的优势细胞群(内脑髓核,NE;端脑腹侧核(Vn)、间脑(眼前核,旁细胞部,NPOp);视前核,大细胞部,NPOm;结节外侧核(NLT)和中脑(中脑被盖)。只有npy免疫反应(-ir)纤维的重要区域包括嗅球(OB)、远端脑前部背区(Da)、Dmd背区(Dmdd)、Dl腹侧亚区(Dlv)、Dl前亚区(Dla)、视前区(POA)、视顶叶(OTec)和外侧隐核(NRL)。NPY在pancalus前脑的分布模式表明它在处理许多生理功能(即摄食、日常活动、繁殖和其他代谢过程)中的作用。研究NPY在鳗鱼体内的解剖定位,有助于更好地了解NPY的季节变化及其与其他生殖激素的相互作用。
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引用次数: 2
Short-Term in Situ Action of Melatonin on Ion Transport in Mice Kept at Restraint Stress 褪黑素对抑制应激小鼠离子转运的短期原位作用
Pub Date : 2015-06-01 DOI: 10.18519/JER/2015/V19/86052
A. Khan, M. Peter
Melatonin, a pleiotropic hormone, is involved in many physiological functions including combating oxidative stress. However, its role in ion transport during stress response is not yet understood. The dose-dependent effect of in situ melatonin was examined in Swiss albino mice. Perfusion of melatonin at 10 -7 M for 20 minutes produced a significant decrease in Na + , K + -ATPase activity in the kidney, liver, stomach and intestinal tissues. A dose-responsive decrease in cytosolic and mitochondrial H + ATPase activity was found in these tissues after melatonin perfusion. Likewise, the cytosolic and mitochondrial Ca 2+ ATPase activities decreased in the kidney, liver, stomach and intestine. The mitochondrial Mg 2+ ATPase activity decreased in the tested tissues in a dose-responsive manner. Subjecting mice to restraint stress for seven days increased the Na + , K + -ATPase, H + ATPase, Ca 2+ ATPase and Mg 2+ ATPase activities to significant levels in kidney, liver, stomach and intestinal tissues. On the contrary, in-situ perfusion of melatonin to stressed mice at 10 -9 M caused decrease in the stress-induced hyperactivity of these transmembrane ion transporters. These results provide evidence for a role of melatonin in ion transporter activity and point to a protective role of melatonin in ion transport during stress response in mice.
褪黑素是一种多效性激素,参与许多生理功能,包括对抗氧化应激。然而,其在应激反应中离子转运中的作用尚不清楚。在瑞士白化病小鼠体内观察原位褪黑素的剂量依赖性。褪黑素在10 -7 M灌注20分钟后,肾、肝、胃、肠组织中Na +、K + - atp酶活性显著降低。褪黑激素灌注后,这些组织的胞浆和线粒体H + atp酶活性呈剂量反应性降低。同样,肾、肝、胃和肠的胞质和线粒体ca2 + atp酶活性降低。线粒体mg2 + atp酶活性在被试组织中呈剂量反应性下降。抑制应激7 d后,小鼠肾、肝、胃、肠组织中Na +、K + - atp酶、H + atp酶、ca2 + atp酶和Mg 2+ atp酶活性显著升高。相反,应激小鼠在10 -9 M时原位灌注褪黑素可使应激诱导的这些跨膜离子转运体的过度活性降低。这些结果为褪黑激素在离子转运体活性中的作用提供了证据,并指出了褪黑激素在小鼠应激反应中对离子转运的保护作用。
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引用次数: 3
The Constitutive Androstane Receptor (CAR): A Nuclear Receptor in Health and Disease 组成型雄甾受体(CAR):健康和疾病中的核受体
Pub Date : 2014-06-01 DOI: 10.18519/JER/2014/V18/67731
A. K. Dash, A. Yende, Sudhir Kumar, Shashi Singh, Deepak Kotiya, Manjul Rana, R. Tyagi
Constitutive Androstane Receptor (CAR, NR1I3), a member of the nuclear receptor superfamily of transcription factors, has emerged as one of the key regulators of the drug and xenobiotic metabolism. The unique feature that separates CAR from other members of the superfamily is that it remains active in the absence of ligand and is further regulated by activators. From its first isolation in 1994, a number of studies related to its distribution, characteristics, functions, and relation to other members of the superfamily have been conducted that place it centrally, governing many key events of the body. Human CAR is expressed relatively higher in liver and epithelial cells of the small intestine villi and less in heart, muscle, kidney, brain and lung. Though there are some controversies regarding its subcellular localization in different cell lines, in general, the subcellular localization of CAR is reported to be predominantly cytoplasmic, in complex with co-chaperone partners HSP90 and CCRP (cytoplasmic CAR retention protein). To execute transcription functions, nuclear translocation is a prerequisite event for a NR, including CAR. In this context, existence of two pathways is suggested, i) direct mechanism of action; and ii) indirect mechanism of action that is governed via nuclear translocation of CAR. Additionally, existence of species-specific differences in its modulation with ligands acting either as an agonist, antagonist or inverse agonist is also apparent. Like the other xenobiotic receptor PXR, CAR also functions as an alternative 'xenosensor' to defend the body against persistent chemical insults. It responds to diverse array of chemically distinct compounds, including endobiotics and xenobiotics, to regulate the clearance of noxious chemicals and toxic metabolites in liver and intestine via induction of genes involved in their metabolism. The usefulness of targeting CAR in metabolic diseases including bilirubinemia, obesity, type 2 diabetes mellitus, atherosclerosis, preeclampsia, hypertension, cholestasis and also in liver cancer is being extensively studied in animal models. However, to determine the human relevance it requires further investigation. Though a large number of natural and synthetic compounds act as modulators of CAR, designing new derivatives with defined therapeutic benefit need to be investigated. The purpose of this review is to highlight the general aspects of nuclear receptor CAR, its mechanism of action and importance in human health and disease.
组成型雄甾烷受体(constituent Androstane Receptor, CAR, NR1I3)是核受体转录因子超家族的成员之一,已成为药物和外源代谢的关键调控因子之一。将CAR与其他超家族成员区分开来的独特特征是,它在没有配体的情况下保持活性,并由激活剂进一步调节。自1994年首次分离以来,对其分布、特征、功能以及与超家族其他成员的关系进行了大量研究,将其置于中心位置,控制着身体的许多关键事件。人类CAR在肝脏和小肠绒毛上皮细胞中的表达相对较高,在心脏、肌肉、肾脏、脑和肺中的表达较少。尽管关于其在不同细胞系中的亚细胞定位存在一些争议,但总的来说,CAR的亚细胞定位主要是在细胞质中,与共伴侣HSP90和CCRP(细胞质CAR保留蛋白)复杂。为了执行转录功能,核易位是包括CAR在内的NR的先决条件。在此背景下,建议存在两种途径:i)直接作用机制;ii)由CAR的核易位控制的间接作用机制。此外,在其作为激动剂、拮抗剂或反激动剂的配体的调节中,存在物种特异性差异也是显而易见的。像其他的异种受体PXR一样,CAR也可以作为一种替代的“异种传感器”来保护身体免受持续的化学伤害。它对包括内源性和外源性在内的多种化学成分作出反应,通过诱导参与代谢的基因来调节肝脏和肠道中有毒化学物质和有毒代谢物的清除。靶向CAR在代谢性疾病(包括胆红素血症、肥胖、2型糖尿病、动脉粥样硬化、子痫前期、高血压、胆汁淤积症和肝癌)中的有效性正在动物模型中得到广泛研究。然而,要确定它与人类的关系,还需要进一步的调查。虽然大量的天然和合成化合物作为CAR的调节剂,但设计具有明确治疗效益的新衍生物需要进行研究。本综述的目的是强调核受体CAR的一般方面,其作用机制和在人类健康和疾病中的重要性。
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引用次数: 6
Effect of Gonadotropins and Gonadal Steroids (17β-Estradiol and Testosterone) on Harderian Gland Porphyrin Content and Circulatory Hormones in Indian Palm Squirrel Funambulus pennanti 促性腺激素和性腺类固醇(17β-雌二醇和睾酮)对棕榈松鼠哈德腺卟啉含量和循环激素的影响
Pub Date : 2014-01-01 DOI: 10.18519/JER/2014/V18/71547
S. Dubey, R. Verma, S. Rastogi, C. Haldar
Mostly studied in the hamster, the Harderian gland (HG, an extra-orbital gland) has been shown to be capable of melatonin (MEL) synthesis and to possess steroid receptor binding sites. Sexual dimorphism and ability to respond to steroid hormones have been reported for HG of some temperate zone mammals. However, to date there is no report on functional relation of HG with pineal, pituitary and gonad in any rodent. Hence, we tested the effect of gonadotropins [FSH (10μg) + LH (10μg)] and steroids [testosterone (100μg) and 17-β estradiol (50μg)] on HG function in relation to the activities of the pineal gland and gonad in both sexes of Indian palm squirrel Funambulus pennanti during the sexually quiescent phase. In general, squirrels treated with gonadotropins and gonadal steroids showed a significant increase in gonadal weight and decrease in pineal weight and plasma melatonin level in LH- and testosterone-treated groups only. There was no change in the weight of HG on FSH treatment. Porphyrin content of HG decreased after testosterone and estradiol treatment. Pineal gland weight invariably decreased after treatment with gonadotropins and testosterone. Plasma testosterone and estradiol levels increased but melatonin level decreased in all treated groups. Our data suggest that in this tropical rodent gonadotropins have an indirect effect on HG and that gonadal steroids have significant effect on HG through the influence on gonadal and pineal functions.
哈德氏腺(HG,一种眶外腺)已被证明能够合成褪黑激素(MEL)并具有类固醇受体结合位点,这一研究主要在仓鼠身上进行。据报道,一些温带哺乳动物的HG具有两性二态性和对类固醇激素的反应能力。然而,目前还没有关于HG与松果体、垂体和性腺功能关系的报道。因此,我们测试了促性腺激素[FSH (10μg) + LH (10μg)]和类固醇[睾酮(100μg)和17-β雌二醇(50μg)]对印度棕榈松鼠两性在性静止期松果体和性腺活性的影响。总的来说,仅在LH和睾酮处理组,促性腺激素和性腺激素处理组,松鼠的性腺重量显著增加,松果体重量和血浆褪黑素水平显著降低。在FSH处理下,HG的重量没有变化。经睾酮和雌二醇治疗后,HG的卟啉含量降低。用促性腺激素和睾酮治疗后,松果体的重量总是下降。所有治疗组血浆睾酮和雌二醇水平均升高,但褪黑激素水平下降。我们的数据表明,在这种热带啮齿动物中,促性腺激素对HG有间接影响,而性腺类固醇通过影响性腺和松果体功能对HG有显著影响。
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引用次数: 2
Effect of Exogenous Gonadal Steroids on Reproductive Functions of the Indian Pygmy Field Mouse Mus terricolor 外源性性腺类固醇对印度侏儒田鼠生殖功能的影响
Pub Date : 2014-01-01 DOI: 10.18519/JER/2014/V18/71440
S. Arora, P. Singh, P. Basu, C. Haldar
Different thresholds of gonadal steroids exert stimulatory or inhibitory effects on GnRH and gonadotropin release. During the reproductively active phase (RAP), the concentration of endogenous gonadal steroids remains high while, during reproductively inactive phase (RIP), it remains low. During RIP the HPG axis is sensitive to gonadal steroids but the circulatory levels of testosterone and estradiol remain low. During this phase one can observe conveniently the effects of gonadal steroids on the HPG axis in male or female rodents. Therefore, the aim of the present study was to find the effects of testosterone and estradiol on the reproductive functions of male and female Indian pygmy field mouse, Mus terricolor , during RIP. The male mice were injected aquaviron (commercially available testosterone, 1mg/100g body weight) while the female mice received estradiol-benzoate (25μg/100g body weight) for 15 consecutive days during the RIP. After completion of the treatment, a significant increase in the weights of gonads and accessory sex organs was noted in both the sexes. The biochemical constituents of accessory sex organs such as epididymal sialic acid, seminal vesicular fructose and uterine protein content reflected significant elevation accompanied by increased levels of plasma testosterone, estradiol and progesterone. Histologically, the gonads and accessory sex organs exhibited increased cellular activity. However, the gonadal cholesterol was significantly decreased in both the sexes. Over all, administration of gonadal steroids to both male and female mice accelerated the gonadal recrudescence but did not inhibit the reproductive functions when administered during the RIP. Therefore, it can be inferred from the present study that during the RIP the HPG axis is sensitive to gonadal steroids and, hence, exogenous gonadal steroids induce gonadal activity.
不同的促性腺激素阈值对GnRH和促性腺激素的释放有刺激或抑制作用。在生殖活跃期(RAP),内源性性腺激素浓度保持较高,而在生殖非活跃期(RIP),内源性性腺激素浓度保持较低。在RIP期间,HPG轴对性腺类固醇敏感,但循环中的睾酮和雌二醇水平仍然很低。在这一阶段,我们可以方便地观察性腺类固醇对雄性或雌性啮齿动物HPG轴的影响。因此,本研究的目的是发现睾酮和雌二醇对雄性和雌性印度侏儒田鼠(Mus terricolor) RIP期间生殖功能的影响。在RIP期间,雄性小鼠连续15天注射阿卡铁(市售睾酮,1mg/100g体重),雌性小鼠连续15天注射雌二醇-苯甲酸酯(25μg/100g体重)。治疗结束后,两性性腺和附属性器官的重量显著增加。附睾唾液酸、精囊果糖、子宫蛋白等副性器官生化成分含量显著升高,血浆睾酮、雌二醇、黄体酮水平升高。组织学上,性腺和附属性器官表现出细胞活性增加。然而,两性的性腺胆固醇明显下降。总体而言,在RIP期间,雄性和雌性小鼠服用性腺类固醇加速了性腺复发,但没有抑制生殖功能。因此,从本研究可以推断,在RIP过程中,HPG轴对性腺类固醇敏感,因此外源性性腺类固醇诱导性腺活动。
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引用次数: 0
Fertility Suppression by the Fruit Extract of Opuntia elatior in the Male Rat: Possible Extragonadal Action 果提取物对雄性大鼠生育能力的抑制作用:可能的外用作用
Pub Date : 2014-01-01 DOI: 10.18519/JER/2014/V18/71441
Ramya M. Chamundaiah, Shivabasavaiah, T. Shivanandappa
Plant - derived male antifertility agents need to address the basic requirements of reversibility and fertility suppression without affecting libido. This study was undertaken to evaluate the male antifertility potential of the fruit extract of Opuntia elatior in the male rat and its reversibility. The methanolic extract was administered through oral route (300, 900 mg/kg bw) to male rats for 30 and 60 days, and fertility was assessed by analysing spermatogenesis, sperm count and testosterone levels. Reversibility of fertility suppression was studied by withdrawal of treatment for two weeks and mating with normally cycling virgin females. Sperm count and motility were markedly reduced in both the groups of treated rats, without commensurate decline in serum testosterone levels and testicular hydroxysteroid dehydrogenase (HSDH) activity. Fertility of the treated rats was suppressed when mated with normally cycling virgin female rats without affecting libido. Withdrawal of treatment for two weeks restored the sperm count, testicular HSDH activity, serum testosterone levels and fertility. The methanolic extract of the fruit of O. elatior produces reversible male antifertility effect without affecting the testosterone levels and libido.
植物性雄性抗生育药物需要在不影响性欲的情况下满足可逆性和抑制生育的基本要求。本研究旨在评价牛蒡子提取物对雄性大鼠的雄性抗生育潜力及其可逆性。雄性大鼠口服甲醇提取物(300、900 mg/kg bw) 30和60天,通过分析精子发生、精子数量和睾丸激素水平来评估其生育能力。通过停止治疗两周并与正常周期的处女交配来研究生育抑制的可逆性。两组大鼠的精子数量和活力均显著降低,血清睾酮水平和睾丸羟类固醇脱氢酶(HSDH)活性未见相应下降。在不影响性欲的情况下,治疗后的大鼠与正常循环的雌性大鼠交配,其生育能力受到抑制。停止治疗两周后,精子数量、睾丸HSDH活性、血清睾酮水平和生育能力恢复。该果实的甲醇提取物产生可逆的男性抗生育作用,而不影响睾酮水平和性欲。
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引用次数: 0
Effect of L-tryptophan feeding on brain mitochondrial ion transport in net- confined climbing perch (Anabas testudineus Bloch) l -色氨酸摄食对网闭攀鲈脑线粒体离子运输的影响
Pub Date : 2014-01-01 DOI: 10.18519/JER/2014/V18/71439
S. Anupriya, V. S. Peter, M. Peter
Serotonin (5-HT), a neurohormone with many physiological actions, is synthesized from the dietary essential amino acid tryptophan (TRP). However, the effects of TRP on neuronal ion transporters and its role in stress response have not yet been identified in the teleost fish. The effects of varied doses of TRP on the activities of mitochondrial (m) and cytosolic (c) ion transporters were examined in the forebrain (FB), midbrain (MB) and hindbrain (HB) segments of an air-breathing fish Anabas testudineus Bloch kept either in non-stressed or in stressed condition. Feeding the fish with varied doses of TRP (1, 2 and 4 mg g -1 feed) for seven days produced dose-dependent effects on Na + , K + -ATPase and H + -ATPase activities in different regions of fish brain. A decrease in (P<0.001) Na + , K + -ATPase activity was found in FB and MB after seven days of TRP treatment. TRP decreased (P<0.001) H + -ATPase activity in the FB but increased Na + , K + ATPase activity in all the three regions of the brain. In non-stressed fish, feeding 20 mg g -1 TRP for two days produced a substantial rise (P<0.001) in cH + -ATPase activity in the FB and HB of the fish. But mH + -ATPase showed a reversed response to TRP feeding. On the contrary, TRP treatment in net-confined fish showed a decrease (P<0.001) in the cH + -ATPase activity in the FB and HB, whereas it produced an increase (P<0.001) in the MB. In non-stressed fish, cytosolic and mitochondrial Ca 2+ -ATPase activities in FB and MB decreased (P<0.001) after TRP feeding. Feeding TRP in stressed fish reduced (P<0.001) cCa 2+ - ATPase activity in the MB but produced an increase (P<0.001) in its activity in mitochondria. In non-stressed fish, TRP feeding decreased (P<0.001) mMg 2+ -ATPase activity in the FB and MB segments. TRP treatment, in stressed fish, however decreased (P<0.001) Mg 2+ -ATPase activity in the MB but not in other brain segments. The data indicate that TRP can regulate brain mitochondrial ion transport, and induction of stress may modify the TRP-induced mitochondrial ion transport response of air-breathing fish.
5-羟色胺(5-HT)是一种具有多种生理作用的神经激素,由膳食必需氨基酸色氨酸(TRP)合成。然而,色氨酸对硬骨鱼神经离子转运体的影响及其在应激反应中的作用尚未被确定。研究了不同剂量的TRP对无应激和应激条件下呼吸鱼testudineus Bloch前脑(FB)、中脑(MB)和后脑(HB)段线粒体(m)和细胞质(c)离子转运蛋白活性的影响。用不同剂量的TRP(1、2和4 mg g -1饲料)喂养鱼7天,对鱼脑不同区域的Na +、K + - atp酶和H + - atp酶活性产生剂量依赖性。TRP治疗7天后,FB和MB的Na +、K + - atp酶活性降低(P<0.001)。TRP降低了FB的H + - atp酶活性(P<0.001),但增加了脑内所有三个区域的Na +、K + atp酶活性。在非应激鱼中,喂食20 mg g -1 TRP 2天后,鱼FB和HB中cH + - atp酶活性显著升高(P<0.001)。而mH + - atp酶则对TRP的摄食表现出相反的反应。与之相反,TRP使网闭鱼FB和HB的cH + - atp酶活性降低(P<0.001),而使MB的cH + - atp酶活性升高(P<0.001)。在非应激鱼中,TRP饲喂后FB和MB的胞质和线粒体ca2 + - atp酶活性降低(P<0.001)。应激鱼饲喂TRP降低了线粒体ccca2 + - atp酶活性(P<0.001),提高了线粒体ccca2 + - atp酶活性(P<0.001)。在非应激鱼中,TRP摄食降低了FB和MB段的mMg 2+ - atp酶活性(P<0.001)。然而,在应激鱼中,TRP处理降低了MB中Mg 2+ - atp酶的活性(P<0.001),而在其他脑段中没有。上述数据表明,TRP可以调节脑线粒体离子转运,应激诱导可能会改变TRP诱导的呼吸鱼线粒体离子转运反应。
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引用次数: 2
Short-Term in Situ Effects of Prolactin and Insulin on Ion Transport in Liver and Intestine of Freshwater Climbing Perch ( Anabas testudineus Bloch) 催乳素和胰岛素对淡水攀鲈肝脏和肠道离子转运的短期原位影响
Pub Date : 2014-01-01 DOI: 10.18519/JER/2014/V18/71719
M. Peter, V. Mini, D. S. Bindulekha, V. S. Peter
The short-term in situ effects of prolactin and insulin on the transport of monovalent and divalent cations were examined in climbing perch Anabas testudineus to infer upon how these hormones regulate ion transport in the metabolic and osmoregualtory tissues of freshwater fish. Varied doses (10 -9 , 10 -8 and 10 -7 M) of ovine prolactin (oPRL) and insulin were infused in these fish for 20 min and the specific activities of ion-specific ATPases were analyzed. The Na + , K + -ATPase activity in the intestine and liver showed significant increase after oPRL infusion. Infusion of oPRL significantly decreased the cytosolic H + -ATPase activity in the intestine and liver, but increased the cytosolic Ca 2+ -ATPase activity in these tissues. Infusion of oPRL decreased the mitochondrial Mg 2+ -ATPase and H + -ATPase activities in the liver but the activities of these transporters increased in the intestine. Similar to oPRL, insulin infusion produced dose-dependent effects on the transporter activities in the liver and intestinal tissues. The mitochondrial Mg 2+ -ATPase activity in the liver significantly decreased at 10 -9 and 10 -7 M insulin infusion whereas its activity increased significantly in intestine at 10 -8 M insulin. Likewise, insulin infusion produced significant increases in the activities of all tested transporters except the cytosolic H + -ATPase activity in the intestine. A direct action of insulin on ion transport was found in both liver and intestinal tissues, as evident in the activity patterns of ion-specific ATPases. Taken together the results point to vital roles of PRL and insulin in ion transport in both liver and intestinal tissues of climbing perch.
研究了催乳素和胰岛素对龙尾鲈鱼一价和二价阳离子运输的短期原位影响,以推断这些激素如何调节淡水鱼代谢和渗透组织中的离子运输。将不同剂量(10 -9、10 -8和10 -7 M)的绵羊催乳素(oPRL)和胰岛素注入这些鱼体内20 min,分析离子特异性atp酶的特异性活性。oPRL输注后,小肠和肝脏内Na +、K + - atp酶活性显著升高。灌注oPRL可显著降低肠、肝组织胞浆中H + -ATPase活性,但提高这些组织胞浆中ca2 + -ATPase活性。输注oPRL降低了肝脏线粒体Mg 2+ - atp酶和H + - atp酶活性,但增加了肠道转运体活性。与oPRL相似,胰岛素输注对肝脏和肠道组织的转运蛋白活性产生剂量依赖效应。胰岛素注射10 -9和10 -7 M时,肝脏线粒体Mg 2+ - atp酶活性显著降低,而胰岛素注射10 -8 M时,肠道线粒体Mg 2+ - atp酶活性显著升高。同样,胰岛素输注显著增加了除肠内胞浆H + - atp酶活性外的所有被测转运蛋白的活性。在肝脏和肠道组织中发现了胰岛素对离子运输的直接作用,这在离子特异性atp酶的活性模式中是显而易见的。综上所述,这些结果表明PRL和胰岛素在攀鲈肝脏和肠道组织的离子运输中起着重要作用。
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引用次数: 2
期刊
Journal of Endocrinology and Reproduction
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