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Pathogen research abs 1 || Pathogen research abs 2 || Pathogen research abs 3 || Pathogen research abs 4 || Pathogen research abs 5 || Hormone and endocrine research abs 1 || Hormone and endocrine research abs 2 || Hormone and endocrine research abs 3 || Hormone and endocrine research abs 4 || Hormone and endocrine research abs 5





Clin Sci (Lond). 2003 Jun 18 [Epub ahead of print].
Exaggerated postprandial lipaemia and lower postheparin lipoprotein lipase activity in middle-aged men.

Jackson KG, Knapper-Francis JM, Morgan LM, Webb DH, Zampelas A, Williams CM.

An exaggerated postprandial lipaemic response is thought to play a central role in the development of an atherogenic lipoprotein phenotype, a recognised lipid risk factor for coronary heart disease. A small number of studies have compared postprandial lipaemia in subjects of varying age but have not investigated mechanisms underlying age-associated changes in postprandial lipaemia. In order to test the hypothesis that impaired lipaemia in older subjects is associated with loss of insulin sensitivity, this study compared the postprandial lipaemic and hormone responses for 9 h following a standard mixed meal in healthy young and middle-aged men. Lipoprotein lipase (LPL) and hepatic lipase (HL) activities were determined in postheparin plasma 9 h postprandially and on another occasion under fasting conditions. Postprandial plasma glucose (P<0.02), retinyl ester (RE; indirect marker for chylomicron particles) (P<0.005) and triacylglycerol (TAG)-rich lipoprotein (d<1.006 g/ml fraction of plasma) TAG (P<0.05) and RE (P<0.005) responses were higher in middle-aged men, whilst plasma insulin responses were lower (P<0.001). Fasting and 9 h postprandial LPL and HL activities were also significantly lower in the middle-aged compared with the young men (P<0.006). In conclusion, the higher incremental postprandial TAG response in middle-aged than young men, was attributed to the accumulation of dietary derived TAG-rich lipoproteins (d<1.006 g/ml fraction of plasma) and occurred in the absence of marked differences in fasting TAG levels between the two groups. Fasting and postprandial LPL and HL activities were markedly lower in middle-aged men, but lack of statistical associations between measures of insulin response and postheparin lipase activities, as well as between insulin and measures of postprandial lipaemia, suggest that this lower activity cannot be attributed to lack of sensitivity of lipases to activation by insulin. Alternatively, postheparin lipase activities may not be good markers for the insulin sensitive component of lipase that is activated postprandially.


online pharmacy ref. source: www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12812518&dopt=Abstract [PubMed - as supplied by publisher]



Biochem J. 2003 Sep 15;374(Pt 3):779-84.
Suppression by polycyclic compounds of the conversion of human amylin into insoluble amyloid.

Aitken JF, Loomes KM, Konarkowska B, Cooper GJ.

Biochemistry and Molecular Biology Group, School of Biological Sciences, University of Auckland, Auckland, New Zealand.

There is a significant correlation between the occurrence of pancreatic islet amyloid and beta-cell failure in advanced type II diabetes mellitus. Islet amyloid is composed primarily of the fibrillar form of the pancreatic hormone, amylin. Using thioflavin-T fluorescence binding and radioprecipitation assays, we investigated whether or not a series of small tricyclic compounds, tetracycline or Congo Red could interfere with the conversion of synthetic human amylin into its insoluble amyloid form. Of the compounds investigated, incubation of human amylin with a 20-fold molar excess of either Congo Red or Acridine Orange resulted in significant inhibition in the rate of amyloid formation. With Congo Red, maximal inhibition effectively occurred at a 1:1 molar ratio or greater over human amylin, whereas inhibition by Acridine Orange was dose-dependent. A 20-fold molar excess of the compound tetracycline also decreased insoluble amyloid content after extended incubation periods of approx. 20 h. Amyloid fibril morphology in the presence of tetracycline, as measured by transmission electron microscopy, was characterized by short fragmented fibrils compared with the longer and denser appearance of fibrils formed by amylin alone. These findings show that polycyclic compounds can suppress the formation of amyloid by human amylin, providing support for an alternative approach to peptide-based strategies by which islet amyloid formation could be modulated.


online pharmacy ref. source: www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12812521&dopt=Abstract [PubMed - in process]



Gen Comp Endocrinol. 2003 Jun 15;132(2):241-7.
Maternal androgens in egg yolks: relation with sex, incubation time and embryonic growth.

Eising CM, Muller W, Dijkstra C, Groothuis TG.

Department of Animal Behaviour, University of Groningen, P.O. Box 14, 9750 AA Haren, The Netherlands. C.M.Eisiniol.rug.ac.nl

Hormones of maternal origin are known to be transferred to the egg yolks of oviparous species. Several studies have shown that within and between clutch variation of maternal androgens may be adaptively tuned. Moreover, it has recently been hypothesized that sex steroids of maternal origin may play a role in adaptive sex ratio manipulation. For sex determination the eggs have to be incubated to allow the germinal disc to grow and thus extract sufficient DNA. This means that yolk hormone levels are determined after a number of days of incubation and this may hamper interpretation of the data. If yolk utilization or embryonic hormone production are influenced by the sex of the embryo, differences in hormone content at a certain stage of incubation do not reflect the mother's initial allocation. In this experiment we show that testosterone levels in chicken eggs do not change with incubation period. A4 levels decrease between 3 and 5 days of incubation, which we cannot explain. Male eggs did not contain higher levels of testosterone or androstenedione than female eggs, in contrast to the data reported for another galliform species, the peacock. We conclude that it is unlikely that maternal androgens are a key factor in the avian sex determination mechanism.


online pharmacy ref. source: www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12812771&dopt=Abstract [PubMed - in process]



Gen Comp Endocrinol. 2003 Jun 15;132(2):272-7.
In vitro study of corticotropin-releasing hormone-induced thyrotropin release: ontogeny and inhibition by somatostatin.

Geris KL, De Groef B, Kuhn ER, Darras VM.

Laboratory of Comparative Endocrinology, Zoological Institute, K.U. Leuven, Naamsestraat 61, B-3000 Leuven, Belgium.

Recent research has shown that in the chicken important interactions take place between the adrenal and the thyroidal axis both at the central and the peripheral level. In vivo as well as in vitro experiments showed that ovine corticotropin-releasing hormone (oCRH) clearly increases thyrotropin (TSH) secretion in late embryonic and early posthatch chicks. In vivo experiments in older chickens, however, suggested that this response might disappear at a later stage. Therefore we started to study in detail the ontogeny of the TSH releasing activity of oCRH using the in vitro perifusion technique. Several embryonic stages (E14, E16, and E18) as well as posthatch stages (C1, C8, C22, and adult chickens) were included in the study. We also investigated the possible regulatory role of somatostatin (SRIH) in this specific endocrine function of CRH. The perifusion studies show that CRH stimulated the TSH release at all stages tested. The 10 and 100 nM oCRH doses were almost equally effective at the early embryonic stages while in most posthatch stages the higher oCRH dose was significantly more effective than the lower one. The stimulation factor, representative for the relative increase in TSH secretion following oCRH challenge, was high at early embryonic stages and clearly lower in adult animals. This seemed to be related to an age-dependent increase in basal TSH secretion levels. In both embryonic (E19) and posthatch (C8) chicks a pretreatment of the pituitaries with SRIH lowered the sensitivity of the thyrotropes to an oCRH challenge. This effect was more pronounced in the posthatch chicks compared to the embryos. The results show that CRH is capable of stimulating the TSH secretion during the entire life cycle of the chicken and that SRIH may play an important role in the fine-tuning of this response by lowering the sensitivity of the thyrotropes to CRH.


online pharmacy ref. source: www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12812775&dopt=Abstract [PubMed - in process]



Gen Comp Endocrinol. 2003 Jun 15;132(2):278-83.
Localization of the neuronal form of nitric oxide synthase (bNOS) in the diencephalon and pituitary gland of the catfish, Synodontis multipunctatus: an immunocytochemical study.

Jadhao AG, Malz CR.

Department of Anatomy and Embryology, School of Medicine, University of Goettingen, Kreuzbergring 36, D-37075 Goettingen, Germany. arun_jadhaotmail.com

The distribution of the neuronal form of nitric oxide synthase (bNOS) was investigated in the brain and pituitary gland of the catfish, Synodontis multipunctatus. Immunoreactive neurons were found mainly in the nucleus praeopticus periventricularis, the parvocellular and supraoptic subdivisions of the nucleus praeopticus, the nucleus recessus lateralis and the nucleus recessus posterioris. In addition, some scattered bNOS labeled somata were noted in the dorsal hypothalamic area. A few positive cells in the adenohypophysis and some reactive fibers in the pituitary stalk were also seen. Our results are compatible with the notion that the cells expressing bNOS in the diencephalon and hypophysis are involved in the control of hormone regulation. Moreover, the presence of bNOS positive cells in the rostral pars distalis of the pituitary gland supports a role of nitric oxide in osmoregulation.


online pharmacy ref. source: www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12812776&dopt=Abstract [PubMed - in process]







Vitamins, amino acids, oils for topical application, and prescription medications...
There are a number of approaches to hair loss problems.
Hair Million is an herbal alternative. It is a formula made of traditional, edible herbs and has been anecdotally demonstrated the efficacy to ward off hair loss problems.

There is no singular medical or alternative cure for hair loss since the biology of hair growth is a highly complicated phenomenon. It is unknown how Hair Million stops hair loss, and promotes hair restoration. The advantages of Hair Million over other approaches are, firstly, Hair Million is comparatively inexpensive, and secondly, it is made only of traditionally used safe and healthy herbs that promote hair growth according to Chinese pharmacopoeia. In addition, Hair Million is cardiotonic, meaning that Hair Million consists of herbs that strengthens your heart, according to Chinese medicine. There is an interesting research paper which correlates baldness to heart diseases: people with alopecia or hair loss problems are significantly more likely to develop heart attacks.












DHEA is a natural hormone, and it is produced in our body by the adrenal glands. DHEA has been suggested to provide numerous potential benefits. DHEA (or dehydroepiandrosterone) is converted into androgens (male hormones) or estrogens (female hormones) in the cells.





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