Role of corpora-allata and brain of adult female Lohita grandis gray

Removal of the corpora allata from the emerging female adults of L. grandis caused a rapid and significant increase in the contents of total carbohydrate, glycogen, total lipids, cholesterol, total proteins and RNA in the fat body, and a significant drop in the contents of trehalose free fatty acids (FFA), phospholipids, free amino acids (FAA) and also in the activity of acid and alkaline phosphatase, glutamate oxaloacetate transaminase (GOT), glutamate pyruvate transaminase (GPT) and exterase in the fat body, in comparison with the sham-operated controls. Treatment with juvenile hormone analogue (JHa) of the allatectomized insects significantly reverses the effects produced by allatectomy (P less than or equal to 0.01). Similarly, removal of the brain produced similar responses in the fat-body but with some exceptions such as the decrease of total protein and RNA and increase significant of FAA as compared to the sham-operated controls. Simultaneous removal of corpora-allata and brain produces a rapid increase in the contents of total carbohydrate, glycogen, total lipid, cholesterol, FAA and the activity of acid phosphatase in comparison with all other treatments performed in this study, while the contents of trehalose, phospholipid, FFA, total protein, RNA and the activity of GOT, GPT, general esterase and alkaline phosphatase in the fat-body decreased compared to all other treatments. The results obtained are discussed in relation to the neuro-endocrine control of metabolism in insects.     

Ecdysterone and an analogue of juvenile hormone on the autophagy in the cells of fat body of mamestra brassicae.

The effect of ecdysterone and a juvenile hormone analogue (JHa) on autophagy and heterophagy was investigated in the fat body cells of the last larval instar of Mamestra brassicae. In the course of normal development autophagic vacuoles and protein granules of heterophagic origin begin to accumulate in these cells, on the 4th and 5th day of the last larval stage respectively. When ecdysterone (10 mug/g body weight) was administered to the larvae for 24 h either on the 1st or on the 2nd day of the last larval stage, autophagic and heterophagic vacuoles appeared in the cells as early as on the 2nd or 3rd days. Autophagy was also observed in the cells of one-or two-day-old last larval fat body after a 5 h incubation in a medium containing 10 mug/ml ecdysterone, in vitro. Ligation of the last thoracic segment resulted in inhibition of metamorphic changes in the fat body lobules of the isolated abdomen. Injection of 10 mug ecdysterone into the isolated abdomen resulted in an appearence of autophagic vacuoles in these cells, too. JHa treatment, when started on the 2nd or 3rd day of the last larval stage, inhibited both auto- and heterophagy and the fat bodies maintained their larval character. Treatment started on the 4th or 5th day proved either ineffective or lethal. It is concluded that the auto- and heterophagy taking place in the larval fat body cells are stimulated by ecdysterone and inhibited by JHa. Experiments performed in vitro or on ligated animals in vivo provided evidence for a direct action of ecdysterone at the cellular level.     

Melatonin produced metabolic changes in testis and did not prevent indomethacin-induced testicular lipid peroxidation in adult rat

Melatonin was orally given to rats at the dosage of 0.75 mg/rat/day for 7 days and challenged on the day 7 with a single toxic dose of indomethacin (20 mg/kg, intramuscularly) to test either protection afforded by melatonin against indomethacin-induced oxidative tissue damage or effects of repeated administration of this hormone on some testicular metabolic parameters. The results showed increased lipid peroxidation, as evidenced by the formation of thiobarbituric acid reactive substances, accompanied by non-significantly decreased glutathione content in the testis of rats treated with indomethacin. However, prior administration of melatonin failed to prevent indomethacin-induced testicular lipid peroxidation. No change in the production of lipid peroxidation and glutathione was observed as well after treatment with melatonin alone. Meanwhile, exogenous melatonin inhibited testicular levels of total lipid, total protein, and activity of aspartate aminotransferase, alanine aminotransferase, and alkaline phosphatase. All treated rats exhibited unchanged activity of both acid phosphatase and lactate dehydrogenase. The results indicated inability of oral administration of melatonin to prevent some of the oxidative damaging effects of indomethacin in the rat testis. In addition, the study provided an evidence that melatonin has an inhibitory action on the testicular metabolism in adult rats and thereby suggests a possible role of this hormone in modulating functions of rat testis.     

Acute and sub-acute effects of 2-butenoic acid-3-(diethoxy phosphinothioyl) methyl ester (RPR-II) on testis of albino rat

Acute and sub-acute toxic effects of a novel phosphorothionate coded as RPR-II on testis of albino rats were studied. In acute study rats received a single dose of 12.3 mg/kg of RPR-II and sacrificed after 24 hr. For sub-acute study 0.58 mg/kg/day was administered orally to rats for 10 and 21 days. Acute exposure of rats to RPR-II brought no change either in the gonadosomatic index (GSI) or in the structure of testis or in the serum levels of testosterone. Testis glutathione (GSH) level and glutathione S-transferase (GST) activity was significantly decreased whereas, acid phosphatase (AcP) levels increased significantly at 24 hr post-treatment. On 7th day (withdrawal period) after the cessation of the treatment the GSH, GST, AcP, and AkP levels reached to near control. The sub-acute study revealed a significant decrease in GSI on 10th and 21st day of the treatment. In contrast, a time-dependent and significant increased in GSH level and GST activity was observed on 100th and 21st day of post-treatment, except GSH level on 10th day, which was declined. Due to RPR-II treatment the testis AcP and alkaline phosphatase (AkP) levels were significant at both 10th and 21st day of medication but AcP levels were increased whereas AkP levels decreased. The histopathological studies on day 10th showed considerable loss of spermatozoids in testis and at 21st day complete derangement of cellular organization was observed. Testosterone levels decreased significantly on 10th day and remained significantly low at 21st day. However, withdrawal studies showed a recovery in testis of rat treated with RPR-II. GST, GSH, GSI, AcP and AkP values recovered, testosterone levels were also well recovered but recovery in testis structure remained at a low profile. The present study suggests that RPR-II may cause testicular toxicity in rats affecting the normal functioning of testis and it also gave some new information in withdrawal studies.     

Antifertility effect of Piper betle Linn. extract on ovary and testis of albino rats

Chronic administration (sc) of the extract of the stalk of P. betle at 30 mg/kg body weight daily for 21 days produced significant decrease in oestrogen and androgen dependent target organ weights along with increase in cholesterol in adrenal, ovary and testis. Acid and alkaline phosphatase activities in serum, liver and kidney did not exhibit any toxic effect. There was marked change in morphology of testis and ovary. Vaginal smear showed prolonged dioestrus in treated female. The treated male showed decreased number and motility of sperm. Both male and female remained infertile after treatment suggesting antifertility activity of the extract on both sexes of albino rats.     

Effects of ovine LH, GH and prolactin, and testosterone on serum testosterone and estradiol-17 beta levels, and seminal vesicle and testicular activity in the catfish Clarias batrachus (L.)

Intraperitoneal administrations of testosterone (0.5 microgram/g body wt), and ovine LH (1.0 microgram/g body wt), GH (5 micrograms/g body wt) and prolactin (10 micrograms/g body wt) daily for 7 days during early prespawning phase (May) in C. batrachus produced varied effects on seminal vesicle (SVSI) and testicular (GSI) weights and biochemical correlates. Testosterone and LH treatments significantly increased serum testosterone level and concentrations of total proteins, fructose, hexosamines and sialic acid in both seminal vesicles and testis. Serum E2 levels increased significantly only after testosterone treatment. GH treatment increased significantly serum testosterone level and only the concentrations of SV hexosamines and testicular protein. Prolactin, however, significantly lowered serum testosterone level and concentrations of total protein, hexosamines in both SV and testis, and testicular fructose and sialic acid levels. The results show that the stimulating effect of LH and GH on SV and testicular activity is mediated through the increased secretion of testosterone and the inhibitory effect of prolactin by decreased testosterone secretion.     

Partial suppressive effect of melatonin on indomethacin-induced renal injury in rat

Intramuscular injection of a single high dose of indomethacin (20 mg/kg) in fasted rats produced renal injury. The results showed increases in the level of lipid peroxidation and cholesterol, and activity of acid phosphatase and alkaline phosphatase in the kidney. Also, the renal contents of both reduced glutathione and activity of total adenosine triphosphatase were decreased by the toxicant. In serum, indomethacin increased activity of lactate dehydrogenase and acid phosphatase, and levels of creatinine and inorganic phosphorus. Paradoxically, administration of melatonin (0.75 mg/rat/day) alone for 7 days decreased significantly the activity of lipid peroxidation and acid phosphatase, and increased, but not significantly, the level of reduced glutathione in the kidney. Also, serum level of creatinine tended to decrease, but not significantly. Pretreatment with melatonin prevented the increase by subsequently administered indomethacin in the renal activity of lipid peroxidation and acid phosphatase. However, this pretreatment regimen partially suppressed the adverse changes in the remaining analyzed cytotoxic parameters induced by indomethacin in both serum and kidney. These results indicate that oral administration of melatonin at a low dose level exerted moderate antioxidant action, thereby it protected against some of the renal detrimental effects produced by indomethacin.     

卡麦角林对黄毛鼠睾丸组织结构及四种标志酶活力的影响

为探讨卡麦角林剂量和处理后时间对雄性黄毛鼠睾丸组织结构和相关酶活力的影响,以50μg/kg和100mg/kg卡麦角林连续3d灌胃雄鼠,在处理后第7d和24 d镜检睾丸组织并分析组织中酸性磷酸酶（Acid phosphatase,ACP）、碱性磷酸酶（Alkaline phosphatase,AKP）、乳酸脱氢酶（Lactate dehydrogenase,LDH）、谷胱甘肽过氧化物酶（Glutathione peroxidase,GSH-Px）的活力。结果发现：卡麦角林可使曲细精管内生精细胞、间质细胞和支持细胞受损,脱落解体。100µg/kg卡麦角林可降低ACP酶活力,处理后24 d时恢复;处理后AKP酶与对照无显著差异。处理组LDH酶活力显著增加,但剂量增加导致LDH活力增加幅度下降,且处理后24 d时恢复。100 µg/kg卡麦角林处理后24 d 时,GSH-Px酶活力显著高于对照组,且高于同浓度处理组第7d时的酶活力。处理后相同时间检测的GSH-Px活力高于50µg/kg处理组。结果表明卡麦角林对雄鼠生殖系统有一定的影响,可明显影响睾丸标志酶的活力。     

Changes in phosphatases and lipids following scrotal gamma irradiation in adult rat testis.

Effects of localized low (2.5 Gy) and high (10 Gy) levels of gamma irradiation on the testis of albino rats were studied. A marked increase in the testicular total lipid, phospholipid and cholesterol content was observed at all post-treatment intervals except at 16 weeks where the contents decreased. A significant decrease in the activity of acid phosphatase/g of testis was seen at both the doses, the minimum value being at 4 weeks. The decrease in acid phosphatase activity is correlated with the state of germ cell population in seminiferous tubule which is found to be depleted at 4 week interval. The alkaline phosphatase activity/g testis however, showed a significant increase, the maximum being at 4 weeks post-treatment. Thereafter, the values of the enzyme activity showed a slight recovery at 16 weeks post-irradiation. ATPase activity increased initially followed by a significant decrease at all post-treatment intervals.     

施用生物炭6年后对稻田土壤酶活性及肥力的影响

利用田间定位试验,研究0(BC₀)、7.5(BC₁)、15(BC₂)和22.5(BC₃)t·hm^-2水稻秸秆生物炭及3.75 t·hm^-2水稻秸秆(STR)一次性施加6年后对稻田土壤肥力及酶活性的影响.结果表明: 施用生物炭6年后土壤有机碳、有效磷和速效钾含量显著增加,增幅分别为34.6%、12.4%和26.2%,土壤pH值和容重显著降低,但对土壤全氮含量无显著影响.土壤脲酶和酸性磷酸酶的活性显著增加,土壤荧光素二乙酸酯酶(FDA水解酶)和芳基硫酸酯酶的活性受到不同程度的抑制,其中,BC₂处理的土壤脲酶活性增加量最大,增幅为36.5%.土壤酸性磷酸酶活性随着生物炭施加量的增加而增加,与土壤速效磷含量呈显著正相关关系;土壤FDA水解酶和脲酶主要与土壤速效钾含量有关;酸性磷酸酶和芳基硫酸酯酶与土壤容重呈显著正相关.施用生物炭6年后土壤脱氢酶和多酚氧化酶活性明显升高,增幅分别为48.8%和27.5%,而过氧化氢酶活性逐渐下降,且显著低于对照BC₀.STR处理显著增加了土壤脲酶、FDA水解酶、脱氢酶、酸性磷酸酶和芳基硫酸酯酶的活性,降低了过氧化氢酶和多酚氧化酶的活性,降幅分别为23.4%和15.9%.     

Acid and alkaline phosphatase activities in lithium treated testis, prostate and seminal vesicles of adult albino rats: evidence of duration and dose dependent response

Changes in the activities of acid and alkaline phosphatase were observed in the testis, prostate and seminal vesicle after the injection of lithium chloride at the doses of 100, 200 and 400 micrograms/100 g body weight/day for 7, 14 and 21 days. The studies indicate that 200 and 400 micrograms/100 g body weight for 14 days and 21 days showed a significant inhibition in the activity of acid phosphatase in all the above reproductive organs. There is a significant stimulation of alkaline phosphatase activity at the doses of 200 and 400 micrograms of lithium after 21 days of treatment in testis, prostate and seminal vesicle along with significant decrease in accessory sex organs weight in comparison to control animal. Therefore, it is evident that the effect of lithium on male reproductive organs mainly depends on the amount of the drug being injected and the duration of treatment to it.     

Ecdysteroids in the ovary and the egg of the greater wax moth

Galleria mellonella eggs exhibit a remarkably high molting hormone activity, equivalent to 74 μg/g fresh wt of ecdysone or ecdysterone. The activity in the ovary was also substantial, averaging 0.4 and 0.58 μg/female, respectively, in the pharate adults and in the 1-day-old adults. Seven ecdysteroids were isolated from the eggs. Ecdysone and ecdysterone were the principal components, comprising 80% of the total biological activity, followed by their 3-epimers and three unidentified ecdysteroids with less biological activity. Five of the seven ecdysteroids were found in the ovaries of the pharate adults and six in the 1-day-old adults. In both the ovary and the egg, 80–85% of these ecdysteroids existed in the conjugated form, mainly as sulphates, and were partitioned in both the n-butanol and the water phases. The ratio of these ecdysteroids changed significantly from the ovary to the egg, with ecdysone decreasing, ecdysterone increasing, and the others increasing slightly. The results suggest that these ecdysteroids exist in a dynamic state and are not merely inactivation products or storage forms.     

Juvenile hormone as a regulator of the trade-off between reproduction and life span in Drosophila melanogaster

Trade-offs between reproduction and life span are ubiquitous, but little is known about their underlying mechanisms. Here we combine treatment with the juvenile hormone analog (JHa) methoprene and experimental evolution in Drosophila melanogaster to study the potential role of juvenile hormone (JH) in mediating such trade-offs at both the physiological and evolutionary level. Exposure to JHa in the larval medium (and up to 24 h posteclosion) increased early life fecundity but reduced life span of normal (unselected) flies, supporting the physiological role of JH in mediating the trade-off. This effect was much smaller for life span, and not detectable for fecundity, in fly lines previously bred for 19 generations on a medium containing JHa. Furthermore, these selection lines lived longer than unselected controls even in the absence of JHa treatment, without a detectable reduction in early life fecundity. Thus, selection for resistance to JHa apparently induced some evolutionary changes in JH metabolism or signaling, which led to longer life span as a correlated response. This supports the hypothesis that JH may mediate evolution of longer life span, but--contrary to our expectation-this apparently does not need to trade--off with fecundity.     

Distribution of cadmium in selected organs of mice: effects of cadmium on organ contents of retinoids and beta-carotene

Cadmium was administered to 32 adult ICR mice i.p. in two single doses (0.25 and 0.5 mg CdCl2, per kg of b.w.). After 48 hours concentrations of cadmium in kidneys, liver, spleen, muscle (m. quadriceps femoris), ovaries and testes and the concentration of retinyl palmitate, retinol and beta-carotene in kidney, liver and testes were determined. Significantly higher cadmium concentration was found in liver, kidney and ovary in both experimental groups in comparison with the control group (p<0.001). In muscle, spleen and testis the cadmium level was higher, however not significantly. No significant differences in the concentration of retinyl palmitate, retinol and alpha-carotene in liver were found. Concentration of alpha-carotene in kidney and testis was significantly decreased in both groups administered with cadmium (p<0.001). Concentration of retinyl palmitate was significantly lower in testis in the group with higher cadmium level (p<0.001) and the concentration of retinol significantly decreased in kidney and testis of mice after an administration of 0.5 mg CdCl2/kg b.w.     

Ascorbic acid induces alkaline phosphatase, type X collagen, and calcium deposition in cultured chick chondrocytes

During the process of endochondral bone formation, proliferating chondrocytes give rise to hypertrophic chondrocytes, which then deposit a mineralized matrix to form calcified cartilage. Chondrocyte hypertrophy and matrix mineralization are associated with expression of type X collagen and the induction of high levels of the bone/liver/kidney isozyme of alkaline phosphatase. To determine what role vitamin C plays in these processes, chondrocytes derived from the cephalic portion of 14-day chick embryo sternae were grown in the absence or presence of exogenous ascorbic acid. Control untreated cells displayed low levels of type X collagen and alkaline phosphatase activity throughout the culture period. However, cells grown in the presence of ascorbic acid produced increasing levels of alkaline phosphatase activity and type X collagen mRNA and protein. Both alkaline phosphatase activity and type X collagen mRNA levels began to increase within 24 h of ascorbate treatment; by 9 days, the levels of both alkaline phosphatase activity and type X collagen mRNA were 15-20-fold higher than in non-ascorbate-treated cells. Ascorbate treatment also increased calcium deposition in the cell layer and decreased the levels of types II and IX collagen mRNAs; these effects lagged significantly behind the elevation of alkaline phosphatase and type X collagen. Addition of beta-glycerophosphate to the medium increased calcium deposition in the presence of ascorbate but had no effect on levels of collagen mRNAs or alkaline phosphatase. The results suggest that vitamin C may play an important role in endochondral bone formation by modulating gene expression in hypertrophic chondrocytes.     

Radioprotective properties of ATP and modification of acid phosphatase response after a lethal dose of whole body p(66MeV)/Be neutron radiation to BALB/c mice.

The intraperitoneal administration of exogenous ATP prior to a lethal dose (7 Gy) of whole body neutron irradiation increased the radioresistance of BALB/c mice. This radiation used the beam from a neutron therapy facility produced by the reaction p(66 MeV)/Be. Survival of the mice, determined 7 days post-irradiation as the endpoint, was increased from 26% to 86% by the action of the exogenous ATP. Furthermore, the response of acid phosphatase activity as an indicator of the acute radiation effects showed a marked augmentation in both tissues studied, testes and small intestine. The activity of the enzyme after neutron irradiation with prior administration of ATP showed smaller increases when compared with the increases observed after neutron irradiation alone. This implies that exogenous ATP reduces the effect of the lytic enzyme and, hence, damage. Finally, changes were observed in the activity of acid phosphatase in the testes and intestine with different concentrations of exogenous ATP. In both tissues there was a monotonic decrease in the activity of the enzyme with increase of the concentration of exogenous ATP administrated before radiation. These results reflect the protective ability of exogenous ATP as an adaptive defence mechanism to reduce radiation damage in normal tissues after a lethal dose of neutron radiation.     

外源施加AsA和MeJA对乙烯利诱导水稻叶片衰老的影响

以野生型水稻(Oryza sativa)株系中花11(ZH-11)及其抗坏血酸合成关键酶基因GLDH下调株系(GI-2)为材料,研究了外源抗坏血酸(AsA)与茉莉酸甲酯(MeJA)对乙烯利诱导下水稻叶片早衰现象的影响。结果表明,外源AsA提高了水稻GI-2中的抗坏血酸含量、Rubisco含量及叶绿素的含量,减缓了其光合特性参数的下降速率,但对水稻ZH-11没有显著影响。外源MeJA降低了两株系的抗坏血酸、Rubisco及叶绿素含量,加快了叶内光合特性参数的下降速率,且对ZH-11的影响大于GI-2。因此,外源AsA处理能有效缓解乙烯利诱导的水稻叶片早衰现象,使叶片的衰老进程得以延缓,而外源MeJA作用相反。     

Effects of diallyl sulfide and zinc on testicular steroidogenesis in cadmium-treated male rats

Cadmium (Cd) is one of the environmental pollutants that affect various tissues and organs including testis. Harmful effect of cadmium on testis is known to be germ cell degeneration and impairment of testicular steroidogenesis. In the present study, the effect of diallyl sulfide (DAS), a sulfur-containing volatile compound present in garlic, and zinc (Zn) was investigated on cadmium-induced testicular toxicity in rats. Male adult Wistar rats treated with cadmium (2.5 mg/kg body wt, five times a week for 4 weeks) showed decreased body weight, paired testicular weight, relative testicular weight, serum testosterone, luteinizing hormone, follicle-stimulating hormone, and testicular total antioxidant capacity (TAC) and protein levels. Testicular steroidogenic enzymes, such as 3beta-hydroxysteroid dehydrogenase (3beta-HSD) and 17beta-hydroxysteroid dehydrogenase (17beta-HSD), and marker enzymes, such as sorbitol dehydrogenase (SDH), lactate dehydrogenase (LDH), acid phosphatase (ACP), alkaline phosphatase (ALP), and glucose-6-phosphate dehydrogenase (G6PD), showed a significant decrease in activities whereas that of gamma-glutamyl transferase was significantly increased after cadmium exposure. The results have revealed that concurrent treatment with DAS or zinc restored key steroidogenic enzymes, SDH, LDH, and G6PD and increased testicular weight significantly. DAS restored the TAC level and increased testosterone level and relative testicular weight significantly. Zinc restored testicular protein level and body weight. It can be concluded that cadmium causes testicular toxicity and inhibits androgen production in adult male rats probably by affecting pituitary gonadotrophins and that concurrent administration of DAS or zinc provides protection against cadmium-induced testicular toxicity.     

The release of superoxide anion from granulocytes: effect of inhibitors of anion permeability.

In vivo administration of ecdysterone produced a decrease in cyclic AMP levels and cyclic AMP-binding protein activity in mouse liver 40 min after injection. These changes were accompanied by a concomitant decrease in cyclic AMP-dependent protein kinase. The effect on phosphoprotein phosphatase was the opposite pattern of that on protein kinase. These results support the idea that the cyclic AMP-protein kinase system may be involved in the heterophylic action of ecdysterone.