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The Head, Education Division, African Union Commission, Ms Sophia Ashipala, has urged African leaders to fashion out measures that address the challenge of skills mismatch on the continent.
According to her, there was an increasing gap between the skills provided by the education system and those required by industry and this must be addressed if the issue of unemployment was to be addressed on the continent.
“The growing gap between the skills provided by the global Technical Vocational Education and Training (TVET) agenda must address this mismatch through constant dialogue between education providers as well as local governments,” she emphasised.
Ms Ashipala made the call at the opening of the third day of the maiden edition of the Africa Skills Week (ASW) currently underway in Accra.
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Speaking on the theme for the day “Rethinking TVET and skill development: Effective models for implementation in Africa”, she said stronger partnerships between governments, educational institutions and industries was essential for curriculum relevance and practical change.
“The private sector must be engaged, not just as a beneficiary, but as a co-creator of programmes, ensuring that the skills taught are the skills that are needed,” she said.
Ms Ashipala noted that for TVET to truly be a force for change, the negative perception that served as a barrier would have to change, adding that “We need to change the perception, because too often, and this has also been alluded to at several discussions yesterday, TVET is seen as a second-tier educational chain, overshadowed by academic pathways.
She said TVET must not be seen only an alternative, but as an equal, prestigious, and rewarding pathway to national development.
Ms Ashipala explained that the 21st century workplace was widely driven by technology and African nations must leverage emerging technology in TVET to bridge the gaps in infrastructure, quality, and access.
“E-learning platforms, augmented reality, and mobile training units are just some examples of how we can bring vocational skills to even the most remote areas,” she said.
She said the continent was blessed with green and abundant resources, however, the future required a shift towards a more sustainable, eco-friendly industry and this must not be lost on leaders.
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“Green skills, those that support environmental sustainability, are becoming increasingly important,” she said.
The Director-General of the Commission for TVET, Dr Fred Kyei Asamoah, said the major gap militating against TVET on the continent was the lack of political will on the part of some African leaders and funding.
“The major gap we have got from the perspective of Africa is the political commitment that we need to really keep to what we put to people. You can see that most African countries may have fantastic policies, such as France, however, the only way we can bridge the gap in the situation is by showing commitment,” he said.
Dr Kyei Asamoah said Africa’s huge youthful population implied that the continent would have to recommit and focus on TVET education since it remained the only means of addressing unemployment
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Binance创建账户 on May 16, 2025
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Registrieren on September 6, 2025
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PedsElite on November 1, 2025
As I stated, Dianabol is ideally used alongside other compounds,
so your dosage can vary tremendously relying on your targets and what different steroids are in the cycle.
To steadiness advantages and unwanted effects well, 15 or 20mg every day is not going
to disappoint, particularly if it’s your first time.
This period is optimal because it lets you make features for
the longest time till you reach the purpose the place gaining
muscle starts to decrease, plateau, and potentially
stop altogether.
Steroids reduce the breakdown of muscle tissue (catabolism) by suppressing cortisol, a
stress hormone that may degrade muscle. He reported that he felt deep regret for his
actions and could not comprehend how he may have
dedicated such a felony offense. With the abrupt discontinuation of AAS, his feelings of
invincibility vanished, and he appeared back with disbelief on what he
had carried out. Though the federal government sought a life sentence, Mr.
A received a prison sentence of 20 years, which was judged by
his legal team to represent a comparatively lenient outcome that resulted partially from consideration of the mitigating effect of AAS.
AB was the project supervisor of the study,
coordinated recruitment and collection of biometrical knowledge.
All individuals have been examined as described by Bjørnebekk et
al.34, encompassing urine samples, questionnaire, and interviews to substantiate alleged AAS
use.
We detected an abnormally high glutamine/glutamate metabolite ratio (Kaufman et al.,
2015). As A End Result Of glutamine is a catabolite of glutamate, we interpreted the high
glutamine/glutamate ratios in AAS customers to reflect increased glutamate
turnover (e.g., higher glutamate release and/or lower glutamate reuptake, resulting in increased glutamate catabolism to glutamine).
Nandrolone, like a variety of different AAS, induces excess oxidative stress (see section 6.1 and Desk 1), which reduces GLT-1 expression and performance (Trotti
et al., 1996, 1997; Blanc et al., 1998; Keller et al., 1997).
Excessive glutamate ranges inhibit protein phosphatase 2A (Yi
et al., 2005, 2008), an enzyme that reduces tau-P levels by dephosphorylation (see
section 7.7), and thus high glutamate levels in AAS users may improve tau-P levels
and danger for creating AD/ADRD.
With such medical presentations, elevated bilirubin values are
additionally to be anticipated. Other reviews in literature have also documented peliosis hepatis (102, 103), hepatocellular carcinoma (104) and adenoma (105, 106) in affiliation with AAS use.
The incidence is probably (very) low and a firm causal hyperlink has not
been established. Excessive doses of oral AAS compounds may
cause liver harm.[5] Peliosis hepatis has been more
and more recognised with the utilization of AAS. For the continual,
high-dosage AAS male user who isn’t involved fertility
in the close to future, the writer typically prescribes comparatively excessive dosages of injectable
testosterone with a tapering of testosterone over several months.
This strategy may help facilitate convincing a man to
stop AAS use and mitigates AAS withdrawal syndrome.
Men (and a very small number of women) might use AASs to reinforce
their look or enhance efficiency in nonelite athletic competitors.
By doing so, these persons aim to boost their bodily efficiency in athletic endeavors or improve
their physique. Tales of Eastern-bloc athletes receiving testosterone and AASs as
a half of their training regimens as early because the Nineteen Fifties abound.
The Eastern-bloc weightlifters and observe athletes subsequently ruled the athletic stage
for decades.
AR expression was significantly downregulated with METH administration with
or without train in adult male Wistar rats (27, 32). Moreover, two rodent studies utilized murine C6C12 cells in vitro (10,
22). Muscle phenotypic changes in human topics were measured in the
vastus lateralis in three research (14, 20, 35);
additionally, one examine utilized human skeletal myoblasts in vitro
(41). A full itemizing of phenotypes, intervention variables, and genes investigated may be found in Table 5.
In basic, the long-term effects of performance-enhancing drugs haven’t been studied sufficient.
Over the years, it has turn into apparent that the endocrinology of
skeletal muscle is highly complex, and there
could be a delicate stability between synthesis and breakdown during development, well being, disease and
ageing, as thought of by Sheffield-Moore
and Urban (2004). Steroids are comparatively small molecules, for example, testosterone has a molecular weight of 288, they usually can passively diffuse into cells.
In target tissues, that is, the cells that comprise steroid receptors, the hormone binds to the receptor ligand-binding domain, inflicting dissociation of
the receptor–Hsp90 advanced, the resultant conformational (allosteric) change making the receptor
active. In the case of the androgen (and glucocorticoid) receptor,
the chaperone advanced resides within the cytoplasm, and following dissociation from the chaperone the activated receptor is translocated into the nucleus.
Activated receptors work together as homodimers with the steroid
response component on the chromatin, the impact of two receptors binding being cooperative
(greater affinity and stability). This attachment to the DNA,
in turn, triggers the formation of a transcription complex,
a cluster of coregulators (also referred to as comodulators) that fit around the receptors like ‘pieces in a jigsaw puzzle’.
Coregulators can be either optimistic or negative regulatory proteins, known as co-activators or corepressors, respectively (Perissi and
Rosenfeld, 2005).
On-treatment Total Testosterone Concentrations in a dose-response study in postmenopausal ladies
with androgen deficiency. Information characterize imply and
normal errors at baseline and on-treatment for each testosterone dose group
(Adapted from Huang et al., 2014). AASs have also been shown to alter fasting blood glucose levels and reduce glucose tolerance, presumably as a end result
of either a hepatic effect or adjustments in the insulin receptor.
Thyroxine-binding globulin (TBG) may be lowered by AASs and lead to lowered
total T4 ranges, with free T4 levels remaining regular.
An up-regulation of sex-hormone binding globulin, with a concomitant lower in TBG, is
assumed to cause the changes in complete T4 ranges.
In common, the objective of altering an AAS is to increase its
anabolic traits and to lower its androgenic options, thus multiplying the compound’s fascinating, anabolic, nitrogen-sparing effects and minimizing its generally undesirable, androgenic, virilizing results.
The HAARLEM examine, nevertheless, found no interaction between blood strain and echocardiographic parameters – most likely because the rise was
mild and of relatively brief duration (97). Future analysis is necessary to explore
the efficacy of blood pressure-lowering treatment on this
group of patients as no trial to date has evaluated this.
When considering pharmacological remedy, angiotensin-converting enzyme
(ACE) inhibitors and angiotensin II receptor blockers (ARBs) might be
preferrable over different blood pressure-lowering medication as they don’t have an result on exercise capacity (98).
Additionally, they do not seem to be on the present record of prohibited substances and methods of
the World Anti-Doping Affiliation, which could – ironically –
be relevant for some AAS customers. Alternatively,
or additionally, calcium channel blockers are a preferred selection in athletes (98).
References:
PedsElite
PedsElite on November 1, 2025
With the liver being the principle website of steroid clearance, hepatotoxicity
is probably certainly one of the main antagonistic effects
of chronic AAS use. The purpose of this paper is to
give consideration to the newest research and information obtained relating to AAS-induced liver harm.
It reduces male libido and fertility and is used to scale back high T
levels, male hypersexuality, prostate most cancers, early puberty,
androgen-dependent skin and hair situations (such as zits, hirsutism, female baldness), and
in transgender hormone therapy. Cyproterone is relatively well tolerated,
but patients may develop hypogonadism, infertility, osteoporosis, breast enlargement, gynecomastia, obesity,
fatigue, melancholy, vitamin B12 deficiency, and reduced
glucocorticoid activity.
In hamsters, aggressive habits has usually been the dependent variable
(DeLeon et al., 2002; Ricci et al., 2009),
although one research has examined the effect of AAS on sexual habits (Salas-Ramirez et al., 2008).
In rats, aggression has been studied intimately (Cunningham and McGinnis, 2006, 2007; Farrell and McGinnis, 2003; Frahm et al.,
2011; Keleta et al., 2007; Kubala et al., 2008;
Wesson and McGinnis, 2006). In addition, the effects
of AAS on sexual habits and two androgen-dependent behaviors, scent marking and ultrasonic
vocalizations have been examined. A steroid’s energy is decided by
things like its androgenic and anabolic ratio, the individual’s genetic response to the compound, how delicate they are to estrogenic and DHT related results, and whether they’re using different
steroids.
Roughly 3% of our examine individuals at present use AASs—all men—which is low compared to the findings of different research where the prevalence was 18%, 23%, and 9%
in Eastern SA, Kuwait, and Sweden, respectively23. Moreover, the Riyadh
studies performed by Al Jabri et al. and Al Harbi et al.
had excessive prevalence rates of 30.5% and 29.3%, respectively24,25.
This might be attributed to the fact that the inhabitants in these
studies was composed of male gymnasts who have
been older than our study individuals.
Cardiovascular problems, hepatotoxicity, and
the event of some mind tumours had been reported as rare opposed effects.
Sure sufferers might develop withdrawal signs and adrenal insufficiency [110].
Finasteride and dutasteride (67 and 68, Figure 12) are both 4-aza-derived 5α-reductase inhibitors that find use within the treatment of prostate cancer, and
enlarged prostate (benign prostatic hyperplasia). Continuous use of
finasteride for up to six months is required
to scale back an enlarged prostate, however the results can final for as much as twelve months after the drug is discontinued.
Each compounds are also indicated in male sample baldness, excessive hair development, and transgender hormone
therapy. Frequent antagonistic results embody increased danger
of high-grade prostate cancer because of the reducing impact on prostate-specific antigen (PSA), gastrointestinal distress, dizziness, headache, gynecomastia,
and sexual dysfunctions [111]. Abiraterone (69, Figure 12) is a CYP17 inhibitor and is especially useful in some forms of prostate most cancers, together with castration-resistant and castration-sensitive variants
(mCRPC and mCSPC, respectively).
Larger doctor information could be helpful in precisely
screening these sufferers prior to serious complications.
More analysis is needed to provide higher insight on addressing this
patient inhabitants. This chronology has essential implications for assessing the long-term medical and psychiatric consequences of
AAS use. As A Outcome Of AAS use was unusual within the general inhabitants prior to the 1980’s,
till lately there have been relatively few men over the age of 45 who used AAS when they were youthful.
ND didn’t restore atrogin-1 ranges in comparison with a management group of adult mice
and reduced its expression by 69% in comparison with
a sham group of eight-week-old male C57BL/6
mice (3, 39). There was a main effect of ND to extend Cyclin D1 mRNA expression after 14 days of restoration post-injury in eight-week-old male C57BL/6 mice,
but no impact was current after 42 days (38). ND brought on the expression of HBS1,
GAL, ADAMTS1, SERPINE1, NR4A1-3, ATF3, BTG2, TCF4, and USP 12 to be downregulated at seven days
post-administration in male Wistar-Hannover rats however
upregulated at 35 days post-administration (31).
TPM, BCL6, TLE1, and UBE2E2 were downregulated at each seven- and
35-days post-administration in male Wistar-Hannover rats (31).
BHLHB3 and SFRS10 expression was upregulated at
seven days post-administration in male Wistar-Hannover
rats however downregulated at 35 days post-administration (31).
ND affected general TGFB1 mRNA ranges in 7.5-week-old matched mutSOD1 and NTg mice (11).
The final query was about the legality of the usage of these agents for bodybuilding.
These questions inquired in regards to the previous,
current or future use of AASs and the source of information about
these brokers. In addition, the questionnaire asked them whether or not users would
advise different schools to make use of AASs. An additional question regarding
using nutritional vitamins and minerals before asking about
AAS was asked to guarantee that members knew what was meant and that
it differed from minerals and nutritional vitamins.
Passable information of the AAS was identified as having a score
of 80% or more within the third section that measured knowledge in regards
to the AAS. The adverse events for long-term utilization amongst adolescents are similar to those of adults, even when doses and period
are considerably less.
In first users or prudent people, cycles generally comprise solely oral anabolic steroids, largely a single agent,
in a low to average daily dose (20–50 mg). Extra
frequent, oral anabolic steroids are added to injectable ones, as an example, in the first
few weeks of the cycle, known as a ‘kick start’.
Some have adopted the so-called ‘blast and cruise’ technique, during which cycles with multiple
excessive dose AAS are alternated with a lower upkeep dose, to stop muscle loss in between cycles.
In addition, the variation in time scale of the metrics included (i.e.
lifetime dependence, ASEBA based on earlier
six months) indicates that the outcomes introduced
ought to be interpreted with caution.
A current cause for concern is the latest manufacture of analogues of established anabolic steroids
to tap into the bodybuilding market. These steroids are
supplied for oral administration, and are therefore subject to first-pass metabolism, a
very important factor as to the extent the steroid is deactivated or transformed to a more active type.
This evaluation suggests that AAS misuse and abuse lead to
opposed results in all physique tissues and organs. This evaluation exhibits that long-term administration of excessive doses of AASs might lead to
serious penalties, corresponding to hypogonadism, cardiac
impairment, neurodegeneration, coronary artery illness
and sudden cardiac dying. The most reported long-term side effects have an result on the cardiovascular system, corresponding to
cardiomyopathy and atherosclerotic disease.
Hypogonadism is a frequent finding in AAS abusers and have to be taken into consideration when AAS use is suspected to have the ability to
undertake aggressive therapy [8,120].
In grownup rodents, AAS decreased GABA-A subunit expression within the amygdala and hypothalamus (McIntyre et al., 2002) (Table
1). These findings indicate that AAS can modulate neurotransmission through the glutamatergic and GABAergic techniques,
however the results of AAS on the GABAergic system varies for
pubertal and grownup animals. Dihydrotestosterone (DHT) is one other hormone that Testosterone can convert into.
In most people, an enzyme known as 5-alpha reductase in the body converts a small portion of Testosterone into DHT.
Just like with estrogenic compounds, this distinction in conversion can significantly impression the efficiency of DHT-based steroids, corresponding to
Masteron. A Number Of antagonistic effects on the liver are associated to AAS use/abuse, corresponding
to hepatic peliosis, cholestatic jaundice and hepatic neoplasms.
This latter pathology was not clinical relevant
throughout topic lifetime, however it was diagnosed solely during autopsies (Søe et al., 1994; Neri et al., 2011; Turillazzi et al., 2011).
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