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Notes: The arterial system of the gills of carp and its histological structure were studied light and electron microscopically by making Mercox or Neoplane Latex corrosion cast preparations. Four pairs of afferent and efferent branchial arteries, and a pair of afferent and efferent pseudobranchial arteries were identified in the branchial arterial system. The 1st and 2nd afferent branchial arteries are given off directly from the ventral aorta, and the 3rd and 4th afferent arteries originate from their common trunk, which is branched off from the ventral aorta caudal to the origin of the former branchial arteries. Numerous afferent filamental arteries are connected to the lamellar blood capillary networks in the gill lamellae via afferent lamellar arterioles, and efferent filamental arteries followed the efferent lamellar arterioles are converged into four efferent branchial arteries that are connected to the dorsal aorta. To the pseudobranchia, afferent pseudobranchial arteries are connected with the ventral branches of the 1st efferent branchial arteries to provide arterial blood to the organ through the afferent mandibular arteries. Afferent pseudobranchial lamellar arterioles originating from the afferent pseudobranchial filamental arteries are connected with the blood capillary networks in the pseudobranchial lamellae, and blood in the capillary networks is drained into the efferent pseudobranchial filamental arteries via 2-4 pseudobranchial lamellar arterioles. Branches of the efferent pseudobranchial filamental arteries are connected with the arteries to the eyeballs and provide blood to choroid of the vascular tunic of them. Pseudobranchial cells surrounding lamellar capillaries in the pseudobranchia are furnished with abundant mitochondria and tubular structures, and the histological findings suggest the cells may share an ability to exchange physiological materials between the cells and the blood in the capillary networks of pseudobranchia.

Notes: After the initial discovery that, in vivo, mammalian skin both transcribes and translates the proopiomelanocortin (POMC) gene, and processes its product into melanocortins (Slominski et al., Experientia 1992), it has become increasingly appreciated that the hair follicle – including the human one – is a prime source and target not only of POMC-derived “pituitary” hormones, e.g. alpha-MSH, ACTH and ß-endorphin, but also expresses the most proximal control element of the hypothalamic-pituitary-adrenal (HPA) axis, corticotropin-releasing hormone (CRH) and its receptor (e.g. Roloff et al. FASEB J 1998, Ito et al. J Invest Dermatol 2004). However, while all proximal elements of the HPA are expressed in both murine and human hair follicles (CRH, CHR-R, POMC, ACTH and ACTH-R), it has neither been shown that these are functionally linked (i.e., is CRH actually capable of modulating intrafollicular POMC gene expression and ACTH production?), nor has it been known whether the most distal HPA component – cortisol synthesis – is also present in the hair follicle. Therefore, we have investigated whether the stimulation of microdissected, organ-cultured human hair follicles with CRH or ACTH elicits responses inside this peripheral miniorgan that imitate a functional HPA – in the absence of any systemic or neural connections and under serum-free culture conditions. Here, we show that CRH stimulation of organ-cultured human scalp hair follicles in the anagen VI stage of the hair cycle indeed results in significant upregulation of POMC transcription, and of alpha-MSH, ACTH, MC1, MC2 and glucocorticoid receptor (GR) immunoreactivity in situ (immunofluorescence). ACTH stimulation, in turn, significantly up-regulates the – already constitutively present!– cortisol-immunoreactivity as well as cortisol secretion into the culture medium. This represents the first available evidence that normal human skin (more precisely: the hair follicle) can actually synthesize the “adrenal” steroid hormone cortisol in situ, and that this acticity is regulated by the same “hypothalamic” and “pituitary” hormones that operate as key controls of adrenal cortisol synthesis. Moreover, we show that cortisol stimulation exerts classical feedback responses inside the human anagen hair follicle recognized for the central HPA: cortisol up-regulates GR, while it down-regulates CRH expression. Given that the HPA operates as the major system for coordinating stress-responses of the mammalian organism and for integrating them into changing metabolic demands and neuro-endocrine-immune signaling circuits, it has fascinating implications (e.g. for general skin physiology and dermatological therapy), and raises most intriguing questions, that human hair follicles are utilizing a fully functional peripheral equivalent of the central HPA.

Notes: Background  Interferon (IFN)-γ appears to be an important hair cycle modulator in mice. It is unclear whether it has similar hair growth modulatory functions in human hair follicles.Objectives  To study whether IFN-γ can be exploited to modulate the growth, pigmentation and/or cycling of organ-cultured human anagen scalp hair follicles, as an in vitro indicator system for how IFN-γ affects human hair growth in vivo. This was correlated with the hair follicle expression patterns of IFN-γ receptors α and β. In addition, we wanted to establish a new, simple tool for the rapid experimental induction of catagen in vitro.Methods  Normal human scalp hair follicles in the anagen VI stage of the hair cycle were cultured according to the method of Philpott et al., with or without IFN-γ (50–1000 IU mL−1). Hair shaft elongation and pigmentation changes were measured, complemented by quantitative histomorphometry to assess changes in hair follicle cycling (hair cycle score), proliferation (Ki-67), melanogenesis (Masson–Fontana) and apoptosis (TUNEL). IFN-γ receptors were also localized by immunofluorescence and EnVision technique. As transforming growth factor (TGF)-β2 is a recognized key inducer of catagen in human hair follicles, TGF-β2 expression was investigated by tyramide signal amplification and reverse transcription-polymerase chain reaction in anagen hair follicles treated with vehicle (phosphate-buffered saline) or IFN-γ.Results  IFN-γ rapidly inhibited hair elongation in cultured human anagen hair follicles and induced morphological signs of catagen transformation after only 4 days of culture, i.e. faster than with other reported catagen-inducers (e.g. TGF-β2). Proliferation was inhibited, apoptosis was increased and follicular melanogenesis was switched off in hair bulb keratinocytes treated in situ with IFN-γ. Anagen hair follicles displayed strong IFN-γ receptor α-like immunoreactivity, while the immunoreactivity for IFN-γ receptor β in the hair matrix was only weak. TGF-β2 immunoreactivity and mRNA transcript levels were enhanced in hair follicles treated with IFN-γ.Conclusions  These data suggest that IFN-γ is a potent catagen inducer in normal human scalp hair follicles, which express cognate receptors, and show that IFN-γ administration offers an excellent tool for experimental catagen induction in organ-cultured human hair follicles. This catagen induction probably occurs at least in part via upregulation of the recognized catagen-stimulatory growth factor TGF-β2.

Notes: Summary After severe dietary calcium-magnesium deficiency in rats, succinic dehydrogenase and acetylcholinesterase enzyme activity of gastrocnemius muscle showed a neurogenic atrophy. This alteration was associated with a high concentration of calcium in the spinal cord.

Notes: Summary The carcinogenicity of sodium nitrite and methylguanidine singly and together were examined in rats. A hepatocellular carcinoma, a hemangiosarcoma and a spindle cell sarcoma were found in 3 of 15 rats fed continuously on pellet diet containing 0.16% sodium nitrite and 0.16% methylguanidine. Hemangiomas and bile duct adenomas of the liver were also found in 6 and 8, respectively, of the 15 rats in this group. Hemangiomas and bile duct adenomas of the liver were found in 2 and 3, respectively, of the 4 rats fed on pellet diet containing 0.16% sodium nitrite. Only 1 of 5 rats fed on pellet diet containing 0.16% methylguanidine developed a hemangioma. No tumor was found in the control group. All the tumors were found in rats that survived for over 12 months. No significant changes were detected in the esophagus or stomach.